|Year : 2016 | Volume
| Issue : 1 | Page : 1-12
Cichorium intybus: A concise report on its ethnomedicinal, botanical, and phytopharmacological aspects
Sneha Das, Neeru Vasudeva, Sunil Sharma
Department of Pharmaceutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar, Haryana, India
|Date of Web Publication||13-Apr-2016|
Department of Pharmaceutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar - 125 001, Haryana
Source of Support: None, Conflict of Interest: None
Cichorium intybus L. (chicory) is a Mediterranean plant species belonging to the Asteraceae family. Chicory is gaining interests because of its culinary features, nutritional values and medicinal characteristics. C. intybus has been implemented in folk medicine from North Africa to South Asia for several 100 years. In Indian medicine, it has been used to treat fever, diarrhea, spleen enlargement, jaundice, liver enlargement, gout, and rheumatism. In China, it is valued for its tonic effects upon the liver and digestive tract. In Germany, chicory has been used as a folk medicine for everyday ailments. Thus, C. intybus is a plant of great economic potential due to high concentrations of fructooligosacharide, known as inulin, in its roots, used as a replacement ingredient for sugar and fat. The other various phytoconstituents reported in chicory are sucrose, cellulose, proteins, caffeic acid derivatives, flavonoids, polyphenols, carotenoids, anthocyanins, tannins, coumarins, sesquiterpene lactones, fatty acids, pectin, cholins, benzo-isochromenes, alkaloids, vitamins, amino acids, and minerals. The therapeutic investigations reveal that C. intybus is useful for maintaining normal health and has nematicidal, antihepatotoxic, antidiabetic, cardioprotective, antiallergic, antihyperlipidemic, anti-inflammatory, antineoplastic, calcium homeostater, bulking agent, immunostimulatory, prebiotic, protective against pancreatitis, antimicrobial, and antioxidant effects. This review encompasses botany, ethnomedicinal uses, phytoconstituents, pharmacological uses, and toxicity studies of C. intybus L.
Keywords: Chicory, Cichorium, herbal medicine, pharmacological uses, phytochemicals, review
|How to cite this article:|
Das S, Vasudeva N, Sharma S. Cichorium intybus: A concise report on its ethnomedicinal, botanical, and phytopharmacological aspects. Drug Dev Ther 2016;7:1-12
|How to cite this URL:|
Das S, Vasudeva N, Sharma S. Cichorium intybus: A concise report on its ethnomedicinal, botanical, and phytopharmacological aspects. Drug Dev Ther [serial online] 2016 [cited 2019 Aug 21];7:1-12. Available from: http://www.ddtjournal.org/text.asp?2016/7/1/1/180157
| Introduction|| |
Cichorium intybus L. (chicory) is a Mediterranean plant species belonging to the Asteraceae family. Cichorieae tribe includes approximately hundred genera and many hundreds species of which some genera are used as salad vegetables. This crop is widely cultivated in a number of temperate regions around the world including South Africa but has its origins in Europe, Central Russia, Western Asia, and also found in Egypt and North America. Although leaf chicory is often called “endive,” true endive (Cichorium endivia) is a different species in the genus.
In traditional Indian medicine, chicory has been used to treat fever, diarrhea, spleen enlargement, jaundice, liver enlargement, gout, and rheumatism., This plant is also used to treat AIDS, cancer, diabetes, dysmenorrhea, impotence, insomnia, splenitis, tachycardia, gallstones, gastroenteritis, sinus problems, and cuts and bruises. It is also used as a tonic. In China, it is valued for its tonic effects upon the liver and digestive tract. In Germany, chicory (especially the flower) has been used as a folk medicine for everyday ailments. The roasted roots are used as the traditional coffee substitute with no caffeine and less well known as grazed forage for ruminants.
C. intybus is a plant of great economic potential due to high concentrations of fructooligosaccharide (FOS), known as inulin, in its roots, used as a replacement ingredient for sugar and fat. Inulin is a polysaccharide consisting of a chain of fructose units with a terminal glucose unit. Vegetables such as asparagus, onion, garlic, dahlia, and chicory are the predominant source for commercial inulin. Inulin is particularly suitable for fat replacement in low-fat or fat-free products, such as chocolate, confectionery, cheese, and ice cream dressing, as it has a fat creamy form, gelling capacity and good body, texture, and mouthfeel. Raftiline and raftilose are used as dietary fiber, having the additional advantages of being able to replace fat and sugar in foods.
The present review has been written as chicory is gaining increasing interests because of the culinary features, nutritional values and medicinal characteristics. Hence, the need was felt to prepare a manuscript based upon its botany, cultivation, collection, storage, and pharmacological uses.
| Botany|| |
Scientific name and classification
It can be classified as kingdom: Plantae-plants; Subkingdom: Tracheobionta – vascular plants; Superdivision: Spermatophyta – seed plants; Division: Magnoliophyta – flowering plants; Class: Magnoliopsida – dicotyledons; Subclass: Asteridae; Phylum: Angiosperms; Order: Asterales; Family: Asteraceae; Tribe: Cichorieae; Genus: Cichorium; Species: Intybus [Figure 1].
|Figure 1: (a) Chicory flower; (b) seeds of Puna chicory; (c) blanched leaves and roots of Belgian endive (source: www.wikipedia.com)|
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Common names and varieties
Commonly it is known as chicory, blue sailors, succory, coffee weed, cornflower, wild chicory, wild succory, garden endive, garden chicory, endive, blue daisy, blue dandelion, blue weed, bunk, hendibeh, horseweed, ragged sailors, wild bachelor's buttons, and wild endive. Common names for varieties of var. foliosum include endive, radicchio, Belgian endive, French endive, red endive, sugarloaf, and witloof (or witlof).
There are mainly three subspecies of C. intybus namely C. intybus L. var. foliosum (Hegi) Bisch., C. intybus L. var. silvestre Bisch, and C. intybus L. var. sativus Bishoff.
C. intybus L. var. foliosum (Hegi) Bisch. known as botanical variety salad chicory include three types of this plant: Belgian endive (also called witloof), sugar chicory (sugarloaf), and radicchio chicory (Italian/red chicory). There are eleven types and cultivars of C. intybus L. var. foliosum (Hegi) (red chicory), i.e., “Palla Rossa 3,” “Orchidea Rossa,” “Indigo,” “Fidelio,” “Rosso di Verona,” green – leaf: “Grumolo bionda,” “Capotta di mantovana” and “Pan di Zucchero” (sugarloaf type), then 3 containing anthocyanins coloration of leaves: “Rosso di Chioggia,” “Rosso di Treviso 2,” and “Variegato di Castelfranco.”
C. intybus L. var. silvestre Bisch known as wild red variety have been used in New Zealand to produce following varieties: (i) Puna (grasslands Puna) - It is resistant to bolting, resistance to grazing pressure and is an excellent companion to clover. (ii) Forage Feast - It is lower in tannins than Puna and more palatable. (iii) Choice - It has lower rates of lactucin and lactone for the dairy industry, compounds believed to taint the milk. (iv) Oasis - It has increased lactone rates for the forage industry and for higher resistance to fungal diseases such as Sclerotinia. (v) Puna II - It has greater persistence and longevity. (vi) Grouse - It is considered to be a better companion to brassicas; also have higher rates of bolting and higher crowns susceptible to over browsing. (vii) Six point - This variety is produced in the USA and is similar to Puna. (viii) Inia Le Certa and La Ninia - These varieties are very useful for food plots where conditions are too hot and dry to grow perennials. (ix) Chico - A short-term cultivar, better suited as an annual with very low spring and summer production levels. (x) Forager - This variety is very similar to Chico and (xi) WINA-100. (xii) Plot enhancer.
The third variety is C. intybus L. var. sativus Bishoff commonly known as Belgian endive.
Natural Habitat: Europe, North America, and Australia
It is an erect, bushy perennial herb having rhizome which is light yellow from outside and white from within containing bitter milky juice; stems are 0.3–0.9 m. in length, angled are grooved; branched are tough, rigid, and spreading. Radical and lower leaves are 7.5–15 cm. in length while upper leaves are alternate, small, entire, and their bases clasp the stem. Heads are ligulate 2.5–3.8 cm. in diameter, terminal and solitary or axillary's and clustered, sessile or on short, thick stalks. Flowers are white to light blue and lavender, toothed at the ends. There are two rows of involucral bracts; the inner are longer and erect in comparison to the outer bracts which are shorter and spreading. Flowering occurs from July to October. Achene's are smooth, angled, crowned with the ring of pappus scales.
Parts generally used are roots, seeds, and herb during blooming period.
Propagation, cultivation, collection, and storage
It is a vegetable known as endive (American) or witloof (Australian). Chicory is grown for a number of reasons in different countries. In Brazil, it is cultivated for the production of leaves, while in India, South Africa, and Belgium roasted chicory is mixed with coffee seeds for the preparation of coffee powder. Recently, Belgium has been active in processing the root for the production of inulin (fructose polymer) and its hydrolysis products such as oligofructose and fructose.,,, It has been cultivated as both summer forage and as “coffee substitute” for centuries and was introduced into Australia in the 19th century.C. intybus is now a domesticated plant cultivated for food, fodder, and medicine. Phytochemicals are distributed in whole plant. C. intybus var. sativum Hegi (Belgian endives) is a leafy vegetable with a limited production Area.
In temperate environments, where there is adequate summer rainfall, chicory grows actively from early spring to late autumn. In winter, growth is checked by frosts, but it continues to grow slowly if the soil temperature is more than 9°C. In a given season, not all the plants will be reproductive and those that are vegetative in 1 year are more likely to be reproductive in the following year. Chicory plants require both vernalization and long days to flower. In order to be florally induced, chicory must undergo exposure to low temperature (3 weeks at 4°C) that can be applied to germinating seeds or to the entire plant.
Seed should be sown at a depth of 10 mm, with a seeding rate of 4–5 kg/ha (seed size 830,000/kg). A residual insecticide is essential as it is susceptible to red-legged earth mites. To maintain production and quality, the key is to maximize leaf growth (highly palatable) and minimize stem growth (reduced palatability). A ratio of 70% leaf to 30% stem is regarded as optimal in terms of production and feed quality. The main diseases of chicory are Sclerotinia (Sclerotinia sclerotiorum) and charcoal rot caused by Fusarium spp. where the lower stem and tap-root darken in color until they appear black. Thus, sowing of chicory should be avoided following crops susceptible to Sclerotinia, like the pulse crops and canola. If it is sown too early the plant shows bolting. To obtain roots of a large size, the ground must be rich, light, and well manured. The leaves are used in salads, for which they must be cut and used from young plants, which have been generally blanched, as the unblanched leaves are bitter. For blanching, the soil is dugged up around October and after cutting off the leaves, the roots are exposed to the air for a fortnight or 3 weeks; then they are planted in deep boxes or pots of sand or light soil, leaving 8 inches between the soil and the top of the box. A cover of some sort is put on the box to exclude the light and the box is kept into a warm place where frost is excluded. Deprived of light, the young oncoming leaves become blanched and greatly elongated, and in this state are cut and sent to the market. If light is totally debarred, the produce will be of a beautiful creamy white color, soft, and nearly destitute of the bitter flavor present when the plants are grown in the open air.
Chicory requires rainfall more than 500 mm. It has good tolerance capacity to aluminum, moderate to drought and frost and low tolerance against waterlogging and salt. It requires deep, well-drained fertile soil with good nitrogen content and pH should be around 4.3 for a good yield.
Cultivation of red chicory, also known as radicchio (C. intybus L. var. silvestre Bisch.), may be of greater commercial importance. The expansion of its cultivation is determined by the marketing success of freshly cut salad. Radicchio is a red, broad leaf, heading form of chicory. Its leaf colors range from pink to maroon with white midribs. All the red types of radicchio now being cultivated derive from red-leaved individuals belonging to C. intybus L. var. foliosum (Hegi) Bischoff, while the types with spotted or variegated leaves originated from spontaneous or controlled crosses between these individuals and members of the species C. intybus L. var. latifolium Hegi, commonly known as broad-leaved endive. Some cultivars form loose heads while others have folded leaves and resemble small cabbages. The red coloration increases during the colder months. Production problems including the early stalk development (bolting) greatly reduce the marketable produce. Bolting of radicchio depend on vernalization and photoperiod. Many studies reported about the effect of environmental conditions on bolting and flowering of chicory, but all information were derived from in vitro cultivation of root tissue. However, little information is available on the response of radicchio to temperature and photoperiod in natural field conditions. Low temperature between sowing and germination (below 8°C), long days (above 13 h), and the age of seedlings at transplanting (above 35 days) are known to be a primary environmental factor associated with flower stalk initiation in radicchio. Summer heat can also cause bolting. The crops could not tolerate high ambient temperatures and promote stalk elongation when the temperature exceeded 32°C.
C. intybus has been implemented in folk medicine from North Africa to South Asia for several 100 years. Aqua distillate of aerial parts of C. intybus (Aragh-e-Kasni) is used to purify blood and liver disease in different parts of Iran. In the Persian folk medicine, the seeds and leaves of the plant have been considered to be hepatoprotective and blood purifier. The seeds of the plant are used in hepatobiliary disorders in Ayurvedic medicine. Whole plant, especially root, contains volatile oils, which produce high toxicity to internal parasites. Chicory is used as a tonic in the treatment of gallstones, gastroenteritis, sinus problems, cuts, and bruises. Inulin, the dietary fiber found in chicory is a helpful ingredient in treating diabetes and constipation. Chicory is also often recommended for jaundice and spleen problems. The juice made of leaves and a tea made from the blooming plant help the release of gallstones, elimination of internal mucus, and production of bile. They are also useful for gastrointestinal problems: digestive difficulties, gastritis, and lack of appetite. The plant root is used as antihepatotoxic, antiulcerogenic, anti-inflammatory, appetizer, digestive, stomachic, liver tonic, cholagogue, cardiotonic, depurative, diuretic, emmenagogue, febrifuge, alexeteric, and also as tonic. It is useful in vitiated conditions of Kapha and Pitta, cephalalgia, hepatomegaly, inflammations, anorexia, dyspepsia, flatulence, colic, gout, burning sensation, allergic conditions of skin, jaundice, splenomegaly, hyperdipsia, skin diseases, leprosy, strangury, amenorrhea, chronic and bilious fevers, ophthalmia, pharyngitis, vomiting, arthralgia, lumbago, asthma, and general debility.,
The fresh root is bitter, with a milky juice which is somewhat aperient and is slightly sedative. A decoction of 1 oz. of the root to a pint of boiling water, taken freely, has been found effective in jaundice, liver enlargements, gout and rheumatic complaints, and a decoction of the plant freshly gathered has been recommended for gravel. Syrup of succory acts without irritation, so it is an excellent laxative for children. An infusion of the herb is useful for skin eruptions in connection with gout. The old herbalists described the use of leaves as a good poultice for swellings, inflammations, and inflamed eyes, and that “when boiled in broth for those that have hot, weak, and feeble stomachs do strengthen the same.” The leaves have been used to dye blue.
Fresh chicory root typically contains, by dry weight, 68% inulin, 14% sucrose, 5% cellulose, 6% protein, 4% ash, and 3% other compounds. Dried chicory root extract contains, by weight, approximately 98% inulin and 2% other compounds. Fresh chicory root may contain between 13 and 23% inulin, by total weight which is a polysaccharide similar to starch. Inulin is mainly found in the plant family Asteraceae as a storage carbohydrate (e.g., Jerusalem artichoke, dahlia, yacon, etc. ). It is used as a sweetener in the food industry with a sweetening power 1/10 that of sucrose and is sometimes added to yogurts as a prebiotic. Inulin can be converted to fructose and glucose through hydrolysis. Inulin is also gaining popularity as a source of soluble dietary fiber and functional food., It is used to replace fat or sugar and reduce the calories of food. Thus suitable for consumption by diabetics  and is also used in inulin clearance test to measure glomerular filtration rate. Chicory root extract is a dietary supplement or food additive produced by mixing dried, ground chicory root with water, and removing the insoluble fraction by filtration and centrifugation. Other methods may be used to remove pigments and sugars. It is used as a source of soluble fiber.
Chicory has high fructose content (about 94%). It is a reserve carbohydrate, which consists of a long chain made up of 22–60 fructose molecules with a terminal glucose molecule. Inulin is a blend of fructan chains found widely distributed in nature as plant storage carbohydrate. It may be classified as a FOS and is present in more than 36,000 plant species, mainly plants of the Asteraceae and Graminae families., Chemically, inulin is polydisperse -(2,1) fructan. The fructose units in this mixture of linear fructose polymers and oligomers are linked to each other by -(2,1) bonds. A glucose molecule typically resides at the end of each fructose chain and is linked by an -(1,2) bond, as in sucrose. Fructans have been extracted from chicory roots. The seeds contain abundantly demulcent oil, while the petals furnish a glucoside which is colorless unless treated with alkalies, when it becomes of a golden yellow.
It is well-known from the literature that the main active compounds of chicory are: inulin, FOS, coffee acid derivatives, flavonoids, and polyphenols. Oligofructose significantly alters liver lipid metabolism, resulting over time in a significant reduction in plasma triacylglycerols, phospholipids, and cholesterol levels. Red chicory also features considerable antioxidant properties, and it contains carotenoids, Vitamins: A, B6, K, as well as macro- and micro-elements, such as phosphorus, potassium, zinc, copper, or iron.,
The root extracts have volatile oils, fatty acids, alkaloids, triterpenes, flavonoids, latex, tannins, and saponins. Other compounds which have been isolated and identified from chicory, include flavone derivatives, saccharides, anthocyanins, sesquiterpenes, and vitamins.,
Chicory is well-known to contain several sesquiterpene lactones, especially in the roots., Two guaianolides having different chemical structures, including 8-deoxylactucin and 11 β, 13-dihydrolactucin, from the root extracts of C. intybus var. “Rosso di Chioggia.”, An antimicrobial sesquiterpenoid, 8α-angeloyloxycichoralexin exhibits antifungal activities. Two kinds of guaianolides cichoralexin and 10α hydroxycichopumilide have been isolated and identified. This bitterness is due to the presence of large quantities of sesquiterpene lactones, such as lactucin, 8-desoxylactuctin, lactucopicrin, and 11ß-dihydro-derivates.
The root also contains fatty acids (mostly palmitic and linoleic), cichoriin (esculetin-7-glucoside), α-lactucerol (taraxasterol), tannins, sugars (fructose, mannose, etc. ), pectin, fixed oils, choline, and others. Cichorins A, B, and C, three new benzo-isochromenes have been isolated from C. intybus.,
The roasted root contains a steam-distillable fraction (aroma), composed of pyrazines, benzothiazoles, aldehydes, aromatic hydrocarbons, furans, phenols, organic acids, and others. Other constituents of the roasted root include 2-acetylpyrrole, furfural, phenyl acetaldehyde, phenyl acetic acid, and vanillin. Small amounts of two insole alkaloid (β carbolines), harman and norharman, have also been isolated from the roasted root. The herb (leaves, flowers, shoots, etc. ) contains inulin, fructose, choline, resin, chicoric acid (dicaffeoyl tartaric acid), esculetin, esculin (esculetin-6-glucoside), cichoriin, umbelliferone, scopoletin and 6,7-dihydrocoumarin, and further sesquiterpene lactones and their glycosides. Presence of sesquiterpene lactones has been confirmed by the isolation of a (+)-germacrene, which is a synthase from chicory roots.
C. intybus L. contained alpha-amyrin, taraxerone, baurenyl acetate and beta-sitosterol. Inulooligosaccharides production from chicory extract was carried out using endoinulinase obtained from a new isolate, xanthomonas oryzae number 5. The roots of C. intybus contain 2, 3, 4, 9-tetrahydro-1H-pyrido-(3,4-b) indole-3-carboxylic acid [Figure 2].
Chicory seeds contain amino acids arginine, histidine, isoleucine, leucine, lysine, methionine, cysteine, phenylalanine, tyrosine, threonine, valine, serine, glutamic acid, glycine, alanine, aspartic acid, and proline. Various minerals present in seeds are phosphorus, potassium, calcium, magnesium, sodium (mg g-1), iron (mg g-1), copper (μg g-1), zinc (μg g-1), manganese (μg g-1), molybdenum (μg g-1), selenium (μg g-1), strontium (mg g-1), and cadmium (μg g-1).
The presence of flavones and flavonols in C. intybus has also been reported.
The phenolic content in the aerial parts of different varieties of chicory and presence of 2S, 3S-O-di-caffeoyl tartaric acid (chicoric acid), cyanidin-3-O-(6” malonyl)-glucoside, quercetin-3-O-glucuronide, and chlorogenic acid has been reported. A transformed root culture of C. intybus L. (Asteraceae) was found to produce sesquiterpene lactones of guaiane and germacrane type. Lactucopicrin, 8-desoxylactucin, and three sesquiterpene lactone glycosides: Crepidiaside B, sonchuside A, and ixerisoside D were isolated from the roots.
| Pharmacological Activities|| |
Chicory contains inulin,, which may help humans with weight loss and weight control through the promotion of satiety, constipation, improving bowel function, and general health. In rats, it may increase calcium absorption and bone mineral density. Moreover, cichory has a potent hepatoprotective, antioxidant, hypoglycemic, diuretic, antitesticular toxicity, and immunomodulatory effects.,,
Chicory is well-known for its toxicity to internal parasites. Ether-soluble phenolics from the chicory rhizome possess nematicidal activity and that the addition of dry powder from chicory rhizome to foods elongates food preservation time. Studies indicate that ingestion of chicory by farm animals resulted in reduction of worm burdens which has prompted its widespread use as a forage supplement.,,
Chicory roots and seeds have demonstrated antihepatotoxic potential in animal studies.,,,, Naseem et al. studied the hepatocurative effects (posttreatment study) of aqueous and alcoholic extracts of seeds against carbon tetrachloride (CCl4) induced hepatotoxicity in the albino rats of Sprague-Dawley strain and found that alcoholic extract exhibited more significant hepatocurative effect., Many evidence showed that leaves alcoholic extract, natural root, and root callus extracts possessed potent hepatoprotective activity in rats against CCl4 induced hepatic damage., In line with that the cichotyboside, a sesquiterpene glycoside from seeds of C. intybus was also verified to have antihepatotoxic activity comparable to the standard drug silymarin.,
Hassan investigated the modulating effect of chicory supplemented diet against nitrosamnine-induced oxidative stress and hepatotoxicity in male rats and concluded that chicory can ameliorate any oxidative stress and hepatic injury induced by nitrosamine compounds.
Atta et al., 2010, also investigated the effect of chicory extract on CCl4 induced hepatotoxicity in Sprague-Dawley rats whilst acute toxicity was assessed in Swiss mice over a 5 days period. Rodents were orally administered CCl4 (2.5 ml/kg, 50% CCl4 in corn oil), and treated rodents with 250 or 500 mg/kg chicory extract. This suggested that doses up to 5 g/kg showed no symptoms of morbidity or mortality and so an LD50 of C. intybus is >5g/kg.
Chicory root contains dietary inulin-type fructans, which modulate the production of peptides, such as incretins, by endocrine cells present in the intestinal mucosa. This effect may play a role in the management of obesity and diabetes through its capacity to promote secretion of endogenous gastrointestinal peptides involved in appetite regulation. Kaskoos found that the induction of diabetes in rats with streptozotocin elevated the circulating lipids levels, and administration of extract of C. intybus decreased the levels of circulating lipids. They also lowered the atherogenic index and increased the high-density lipoprotein to much higher level. The aqueous extract possessed antidiabetic activity. Chicory extract (mainly inulin) may have a potential for reducing postprandial hyperglycemia by decreasing intestinal absorption of glucose. This might be due to an increase in the mucosal unstirred layer thickness due to the increased viscosity of chicory extract and inulin., Chicory was also widely used to treat diabetes mellitus, and one recent research supported the traditional belief that ethanol extract of C. intybus could ameliorate a diabetic state by reducing the hepatic glucose-6-phosphatase activity.
The cardioprotective effects of the aqueous extracts of the leaves of C. intybus have been proved by Nayeemunnisa on the ageing myocardium of albino rats by administering shade-dried powdered leaves 500 mg twice daily of C. intybus for 30 days and found that C. intybus ameliorate the age induced injury and offered protection to the heart from oxidative damage, suggestive of ageing.
Kim et al. reported that the aqueous extracts of C. intybus dose dependently inhibited mast cell immediate-type reactions to compound 48/80 in mice with a dose of 1000 mg/kg. Plasma histamine levels were reduced in a dosage related fashion to antidinitrophenol when administered at concentrations between 1 and 1000 mg/kg. C. intybus aqueous extract inhibits mast cell-mediated immediate-type allergic reactions in vivo and in vitro.
Inulin decreases serum triglycerides by decreasing fatty acid synthesis and reducing production of low-density lipoproteins. Chicory root extracts affect reduce cholesterol uptake.
Chicory has been found to inhibit prostaglandin E (2) and cyclooxygenase 2) and prevents immunotoxicity induced by ethanol and have anti-inflammatory properties.,
Chicory derived beta (2-1) fructans have been shown to exert cancer protective effects in animal models. The tumor inhibition of chicory root extracts against Ehrlich ascites carcinoma were tested in mice. Significant results were reported for doses obtained between 300 and 700 mg/kg. The chicory fructan supplements inhibit aberrant crypt foci formation, an early preneoplastic marker of malignant potential in the process of colon carcinogenesis.,
Calcium homeostasis activity
The leaves of chicory maintain calcium levels by heterologous expression of total RNA.,, In addition, inulin also has the capability for enhancement of calcium absorption.,,
Cytochrome P450 activity
Chicory is known to contain guaianolides, eudesmanolides, and germacranolides. The biosynthesis of these sesquiterpene lactones are involved with the cytochrome P450 enzyme.,
Fecal bulking properties
Inulin and oligofructose are considered dietary fibers. They share the basic common characteristics of dietary fibers including saccharides of plant origin, resistance to digestion and absorption in the small intestine, and fermentation in the colon to produce short-chain fatty acids that are absorbed and metabolized in various parts of the body. Moreover, fermentation induced by difidobacteria has a bulking effect. Fermentation of inulin decreases fecal pH and increases fecal volume.
Oligofructose and inulin, selective fermentable chicory fructans, have been shown to stimulate the growth of bifidobacteria, which are regarded as beneficial strains in the colon.,,
Chicory and mannan-oligosaccharide alter fecal microbial populations and certain indices of the immune system.
Menne et al. assessed the prebiotic effect of an Fn-type chicory inulin hydrolysate product. The F is for fructose, and n is the number of β(2->1) bound fructose moieties. Fecal samples of eight subjects (5 females and 3 males) who consumed 8 g daily of an Fn-rich chicory inulin product for up to 5 weeks were collected and analyzed for total anaerobes, bifidobacteria, lactobacilli, Bacteroides, coliforms, and Clostridium perfringens. Both 2 and 5 weeks of oligofructose feeding resulted in a selective increase in bifidobacteria (P < 0.01). A daily intake of 8g of Fn-type oligofructose preparation reduced fecal pH and caused little intestinal discomfort.
Protective in pancreatitis
Minaiyan et al. demonstrated that C. intybus hydroalcoholic extracts possess protective therapy in cerulein-induced acute pancreatitis in mice when given at a dose of 200 mg/kg i.p and suggested a therapeutic potential for pretreatment in this inflammatory disease condition in a clinical setting. Kocsis et al. reported that chicory exhibited a positive effect on the pancreas in experimental dislipidemia.
The cell wall of Gram-negative bacteria is composed fundamentally of a lipopolysaccharide which stops the accumulation of phenolic compounds in a target cell membrane. The seed extract of C. intybus in methanol, ethyl acetate, chloroform, n-butanol, n-hexane and was found to be useful in the treatment of bacterial infections. The antibacterial activity can also be ascribed to the polyphenols, tannins, and coumarins found in crude extracts of herbal plants.,,
Root extracts of chicory in water, ethanol, and ethyl acetate exhibited potent activity against Escherichia coli, Salmonella typhi, Bacillus thuringiensis, and Staphylococcus aureus while some reports suggested that inhibitory effect of chicory root extract against E. coli was not confirm., The fungi Penicillium sp. and Aspergillus sp. were the most resistant to all the extracts. No inhibition activity was found against Penicillium sp. and Aspergillus sp. Chicory extracts can inhibit growth of Sarcina lutea, Agrobacterium tumefaciens, Erwinia carotovora, Pseudomonas aeruginosa, Pseudomonas fluorescens, zoophilic, and anthropophilic dermatophytes. The root extracts have more intensive antibacterial activity than extracts from whole plant. Phenolic compounds could attack cell walls and cell membranes by affecting their permeability, enabling the release of intracellular constituents, and interfering with membrane functionality of the microbe. Aqueous extracts of red chicory can inhibit cell division, DNA, and RNA synthesis and elongate cells of Prevotella intermedia.
Gazzani has studied the water-soluble antioxidant properties of C. intybus var. silvestre and found that chicory contained both pro- and antioxidant compounds that can act in both chemical and biological systems. Antioxidants also possess antimicrobial abilities. Lavelli has studied red chicory products (C. intybus L.var. silvestre) to evaluate the relationship between their polyphenol contents and antioxidant activities. They found that the total amount of phenolics was significantly correlated with antioxidant activity when evaluated with both synthetic radical and enzyme-catalyzed reactions.
Other studies suggesting dosage
Jindal et al. examined the toxicity of alcoholic and water extracts of the crude powder and the roasted roots, there was reported to be a mean LD50 via the i.p. route of the aqueous extract of 8.7 and 9.3 g/kg for the ethanol extract. Both extracts reported to have significant anticonvulsant activity to a range of compounds that act on the higher centers of the brain. Both ethanolic and aqueous extracts had significant anticotine activity the mean ED50 (i.p. mg/kg) was reported to be for aqueous extracts was 510 mg/kg and for ethanol extracts 565 mg/kg. The analgesic effects of both extracts appeared to be similar to morphine. On the neuromuscular junction, the chicory extracts were reported to result in a blockade due to the persistent depolarization. The average daily consumption of chicory fructooligosaccharides (fructans extracted on a commercial basis from the chicory root) in the USA has been reported to be 1–4 g and between 3 and 11 g in Europe.
Reproductive and developmental toxicity
Roy-Choudhury and Venkatakrishna-Bhatt reported on a study where an aqueous suspension of chicory root powder extract was administered to male Swiss mice at 4.3 or 8.7 g/kg for 10 days. A decreased body weight gain was reported for both treated groups. The high dose group also exhibited a decreased testicular weight, degenerated seminiferous tubules with atrophied leydig cells. The seminiferous tubules were reported to be full of desquamated cells and debris. No spermatogenic effect upon the low dose group was reported. Crude ethanol extracts of the seeds of C. intybus were tested for their ability to inhibit postcoital conception in adult female Sprague-Dawley rats. The dose not specified was administered to female rats from days 1 to 10 postcoitum, significant contraceptive activity was observed. The activity of the butanol/chloroform insoluble fractions significantly reduced the numbers of implantation.
| Dosage|| |
C. intybus generally administered at a dose of 3–6 g of powdered seeds or powdered roots.
| Toxicological Assessment|| |
Willi et al. reported a 35-year-old Caucasian male cook with a 6-year history of chronic eczema on his hands and distal forearms, which markedly improved on vacations. Skin prick testing gave a strongly positive reaction to C. intybus (common chicory). The patient confirmed regular contact with chicory and on avoidance of chicory the patient's eczema disappeared quickly. Sometime later, the patient reported developing generalized pruritus, facial erythema, and dyspnea when standing next to a colleague who was handling chicory, but without any direct contact with himself. The diagnosis of anaphylactic type I-allergy to chicory was confirmed.
Escudero et al. reported a study in which sensitization was observed to lettuce and chicory. The patient who had worked in a grocery store for a period of eight years showed symptoms of rhinitis, asthma and chronic eczematous lesions which were clearly related to lettuce and chicory handling, (the patient also gave a positive skin prick test to commercial lettuce extract, leaves and stems of fresh lettuce and chicory). The plants in the Asteraceae family may become sensitizing not only through its wind-pollinated members such as mugwort and ragweed, but also through foods such as lettuce or chicory and commented that 'this is important for elimination diets, for subjects with a known respiratory pollen allergy, and for people highly exposed as a result of their job.
Nemery and Demedts reported occupational asthma in a 55-year-old woman that had reported symptoms of wheezing bronchitis due to “chicory allergy.” The symptoms were only reported by the patient 2-years after she had stared cultivating chicory. The patient was reported to have a delayed cutaneous reaction to a patch test with chicory root and leaves and also had a slightly positive patch test to substances in the rubber gloves used by the grower. The authors suggested that contact dermatitis to chicory is thought to be due to a sesquiterpene lactone. Bronchospasmic reactions along with irritant dermatitis have been noted in workers from a chicory processing unit, but occupational asthma had not been reported.
The safety of a chicory root extract was evaluated by Schmidt et al., on a 28-day sub-chronic toxicity study in male and female Sprague-Dawley rats. The measurements included clinical observations, body weights, food consumption, clinical pathology, gross necropsy and histology. There were no treatment-related toxic effects from chicory extract administered orally at 70, 350, or 1000 mg/kg/day. There were no observed adverse effects of chicory extract in these studies.
The chicory leaves extract were also confirmed without any toxic effects at acute and sub chronic toxicity levels, and free of any cytotoxicity towards rat's lymphocytes.
| Conclusion|| |
Chicory has been described in different system of medicine viz., Ayurvedic, Chinese for treatment of various disorders. The toxicity studies reveal it to be a very safe drug. Most of the investigations carried out are directed toward the presence of major constituent inulin in the root. However certain traditional uses as reported in Indian traditional medicine viz., gout, rheumatism, etc., is yet to be scientifically authenticated. More research should be directed towards scientific authentication of these traditional uses.
We are grateful to Department of Pharmaceutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar, Haryana, for providing infrastructure and laboratories to carry out this research. Moreover, we would like to acknowledge DST, New Delhi, for providing financial support to Ms. Sneha Das, as DST INSPIRE Fellowship.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Hazra B, Sarkar R, Bhattacharyya S, Roy P. Tumour inhibitory activity of chicory root extract against Ehrlich ascites carcinoma in mice. Fitoterapia 2002;73:730-3.
Koch K, Anderson R, Rydberg I, Aman P. Influence of harvest date on inulin chain length distribution and sugar profile for six chicory (Cichorium intybus
L.) cultivars. J Sci Food Agric1999;79:1503-6.
Mulabagal V, Wang H, Ngouajino M, Nair M. Characterization and quantification health of beneficial anthocyanins in leaf chicory (C. intybus
) varieties. Eur Food Res Technol 2009;230:47-53.
Ramalakshmi K, Rao PG, Abraham KO. Chemical analysis of chicory root samples. Indian Coffee 1994;58:3-22.
Schmidt BM, Ilic N, Poulev A, Raskin I. Toxicological evaluation of a chicory root extract. Food Chem Toxicol 2007;45:1131-9.
Silva RF. Use of inulin as a natural texture modifier. Cereal Foods World 1996;41:792-4.
Hewitt L. Fight the good fat. Food Manuf 1994;69:20.
Barcaccia G, Lucchin M, Lazzarin R, Parrini P. Relationships among radicchio (Cichorium intybus
L.) types grown in Veneto and diversity between local varieties and selected lines an assessed by molecular markers. In: Van Hintumn TJ, Lebeda A, Pink D, Schut JW, editors. Eucarpia Leafy Vegetables. Centre for Genetic Resources, The Netherlands (CGN); 2003. p. 105-11.
Biesiada A, Tomczak A. Usability of different types and cultivars of salad chicory (Cichorium intybus
L. var. foliosum
(Hegi) Bish.) for spring cultivation. Acta Sci Pol 2012;11:193-204.
Moore G, Sanford P, Wiley T. Perennial Pastures for Western Australia. Department of Agriculture and Food, Government of Western Australia; 2006. [Bulletin 4690, Perth].
Dragan Z, Joze O, Stanislav T. Plant characteristics for distinction of red chicory (Cichorium intybus
L. var. silvestre
Bisch.) cultivars grown in central Slovenia. Acta Agric Slov 2004;83:251-60.
Rose F. The Wild Flower Key: British Isles and North West Europe: A Guide to Plant Identification in the Field, with and Without Flowers Frederick Warne and Co. Rossendale, LANCS, United Kingdom; 1981. p. 390-1.
Figueira GM, Park KJ, Brod FP, Honorio SL. Evaluation of desorption isotherms, drying rates and inulin concentration of chicory roots (Cichorium intybus
L.) with and without enzymatic activation. J Food Eng 2003;63:273-80.
Zhang M, De Baerdemaeker J, Schrevens E. Effects of different varieties and shelf storage conditions of chicory on deteriotative colour changes using digital image processing and analysis. Food Res Int 2003;36:669-76.
Gadgoli C, Mishra SH. Antihepatotoxic activity of Cichorium intybus
. J Ethnopharmacol 1997;58:131-4.
Baert JR, Van Bockstaele EJ. Cultivation and breeding of root chicory for inulin production. Ind Crops Prod 1992;1:229-34.
Zafar R, Mujahid Ali S. Anti-hepatotoxic effects of root and root callus extracts of Cichorium intybus
L. J Ethnopharmacol 1998;63:227-31.
Maurice DP, Nico VS, Noten V. Breeding and cultivar identification of Cichorium intybus
L. var. foliosum
Hegi. In: Eucarpia Leafy Vegetables. Centre for Genetic Resources, The Netherlands (CGN); 2003. p. 83-90.
Demeulemeester MA, De Proft MP.In vivo
and in vitro
flowering response of chicory (Cichorium intybus
L.): Influence of plant age and vernalization. Plant Cell Rep 1999;18:781-5.
Rangarajan A, Ingall B. Mulch colour affects radicchio quality and yield. HortScience 2001;36:1240-3.
Bertolini P, Baraldi M, Mari B, Truffeli B, Lazzarin R. Effects of long term exposure to high-CO2
during storage at 0°C on biology and infectivity of Botrytis cinerea
in red chicory. J Phytopathol 2003;151:201-7.
Perkinz-Veazie PM, Russo VM, Collins JK. Postharvest changes during storage of packaged radicchio. J Food Qual 1991;15:111-8.
Badila P, Lawnac M, Paulet P. The characteristics of light in floral induction in vitro
of Cichorium intybus
. The possible role of phytochrome. Physiol Plant 1985;65:305-9.
Aktay G, Deliorman D, Ergun E, Ergun F, Yesilada E, Cevik C. Hepatoprotective effects of Turkish folk remedies on experimental liver injury. J Ethnopharmacol 2000;73:121-9.
Nadkarni AK. Indian Materia Medica. Bombay: Popular Prakasam Pvt. Ltd.; 1976.
Varier's PS. Cichorium intybus. Linn
. In Indian Medicinal Plants a compendium of 500 species. Orient Longman Private Limited, Chennai; 1994. p. 74.
Kim M, Shin HK. The water-soluble extract of chicory reduces glucose uptake from the perfused jejunum in rats. J Nutr 1996;126:2236-42.
Wilson RS. Chicory root yield and carbohydrate composition is influenced by cultivar selection, planting, and harvest date. Crop Sci 2004;44:748-52.
Madrigal L, Sangronis E. Inulin and derivates as key ingredients in functional foods. Arch Latinoam Nutr 2007;57:387-96.
Douglas JA, Poll JT. A preliminary assessment of chicory (Cichorium intybus
) as an energy crop. N Z J Exp Agric 1986;14:223-5.
Niness KR. Inulin and oligofructose: What are they? J Nutr 1999;129 7 Suppl: 1402S-6S.
Nandagopal S, Kumari BD. Phytochemical and antibacterial studies of chicory (Cichorium intybus
L. ) – A multipurpose medicinal plant. Adv Biol Res 2007;1:17-21.
Carpita NC, Kanabus J, Housley TL. Linkage structure of fructans and fructan oligomers from Triticum aestivum
and Festuca arundinacea
leaves. J Plant Physiol 1989;134:162-8.
van Loo J, Coussement P, de Leenheer L, Hoebregs H, Smits G. On the presence of inulin and oligofructose as natural ingredients in the western diet. Crit Rev Food Sci Nutr 1995;35:525-52.
Phelps CF. The physical properties of inulin solutions. Biochem J 1965;95:41-7.
Finke B, Stahl B, Pritschet M, Facius D, Wolfgang J, Boehm G. Preparative continuous annular chromatography (P-CAC) enables the large-scale fractionation of fructans. J Agric Food Chem 2002;50:4743-8.
Fiordaliso M, Kok N, Desager JP, Goethals F, Deboyser D, Roberfroid M, et al.
Dietary oligofructose lowers triglycerides, phospholipids and cholesterol in serum and very low density lipoproteins of rats. Lipids 1995;30:163-7.
Custic M, Poljak M, Toth N. Effects of nitrogen upon the quality and yield of head chicory (Cichorium intybus
). Acta Hortic 2000;533:401-10.
Baek HH, Cadwallader KR. Roasted chicory aroma evaluation by gas chromatography mass spectrometry olfactometry. J Food Sci 1998;63:234-7.
Mares D, Romagnoli C, Tosi B, Andreotti E, Chillemi G, Poli F. Chicory extracts from Cichorium intybus
L. as potential antifungals. Mycopathologia 2005;160:85-91.
Peters AM, Van Amerongen A. Sesquiterpene lactones in chicory (Cichorium intybus
L) – Distribution in chicons and effect of storage. Food Res Int 1996;29:439-44.
Poli F, Sacchetti G, Tosi B, Fogagnolo M, Chillemi G, Lazzarin R, et al
. Variation in the content of the main guaianolides and sugars in Cichorium intybus
var. “Rosso di Chioggia” selections during cultivation. Food Chem 2002;76:139-47.
Picman A. Biological activities of sesquiterpene lactones. Biochem Syst Ecol 1986;14:255-81.
Peters AM, Van AA. Relationship between levels of sesquiterpene lactones in chicory and sensory evaluation. J Am Soc Hortic Sci 1998;123:326-9.
Hussain H, Hussain J, Saleem M, Miana GA, Riaz M, Krohn K, et al.
Cichorin A: A new benzo-isochromene from Cichorium intybus
. J Asian Nat Prod Res 2011;13:566-9.
Hussain H, Hussain J, Ali S, Al-Harrasi A, Saleem M, Miana GA, et al.
Cichorins B and C: Two new benzo-isochromenes from Cichorium intybus
. J Asian Nat Prod Res 2012;14:297-300.
Bais HP, Ravishankar GA. Cichorium intybus
L – Cultivation, processing, utility, value addition and biotechnology with an emphasis on current status and future prospects. J Sci Food Agric 2001;81:467-84.
de Kraker JW, Franssen MC, de Groot A, Konig WA, Bouwmeester HJ. (+)-Germacrene A biosynthesis. The committed step in the biosynthesis of bitter sesquiterpene lactones in chicory Plant Physiol 1998;117:1381-92.
Du H, Yuan S, Jiang P. Chemical constituents of Cichorium intybus
L. Zhongguo Zhong Yao Za Zhi 1998;23:682-3, 704.
Cho YJ, Sinha J, Park JP, Yun JW. Production of inulooligosaccharides from chicory extract by endoinulinase from Xanthomonas oryzae No 5. Enzyme Microb Technol 2001;28:439-445.
He Y, Guo YJ, Gao YY. Studies on chemical constituents of root of Cichorium intybus
. Zhongguo Zhong Yao Za Zhi 2002;27:209-10.
Ying GW, Gui LJ. Chicory seeds: A potential source of nutrition for food and feed. J Anim Plant Sci2012;13:1736-46.
Patil G, Vishwkarma U. Flavone and flavone glycoside from Cichorium intybus
L. IJPSR 2012;3:801-5.
Innocenti M, Gallori S, Giaccherini C, Ieri F, Vincieri FF, Mulinacci N. Evaluation of the phenolic content in the aerial parts of different varieties of Cichorium intybus
L. J Agric Food Chem 2005;53:6497-502.
Malarz J, Stojakowska A, Kisiel W. Sesquiterpene lactones in a hairy root culture of Cichorium intybus
. Z Naturforsch C 2002;57:994-7.
Roberfroid MB, Cumps J, Devogelaer JP. Dietary chicory inulin increases whole-body bone mineral density in growing male rats. J Nutr 2002;132:3599-602.
Roberfroid MB. Inulin-type fructans: Functional food ingredients. J Nutr 2007;137 11 Suppl: 2493S-502S.
Cani PD, Dewever C, Delzenne NM. Inulin-type fructans modulate gastrointestinal peptides involved in appetite regulation (glucagon-like peptide-1 and ghrelin) in rats. Br J Nutr 2004;92:521-6.
Nayeemunnisa A. Alloxan diabetes-induced oxidative stress and impairment of oxidative defense system in rat brain: Neuroprotective effects of Cichorium intybus
. Int J Diabetes Metab 2009;17:105-9.
Jamshidzadeha A, Khoshnooda J, Dehghanib Z, Niknaha H. Hepatoprotective activity of Cichorium intybus
L. leaves extract against carbon tetrachloride induced toxicity. Iran J Pharm Res 2006;5:41-6.
Hassan HA. The prophylactic role of some edible wild plants against nitrosamine precursors experimentally-induced testicular toxicity in male albino rats. J Egypt Soc Toxicol 2008;38:1-11.
Nishimura H, Kondo Y, Nagasaka T, Satoh A. Allelochemicals in chicory and utilization in processed foods. J Chem Ecol 2000;26:2233-41.
Heckendorn F, Häring DA, Maurer V, Senn M, Hertzberg H. Individual administration of three tanniferous forage plants to lambs artificially infected with Haemonchus contortus
and Cooperia curticei
. Vet Parasitol 2007;146:123-34.
Athanasiadou S, Gray D, Younie D, Tzamaloukas O, Jackson F, Kyriazakis I. The use of chicory for parasite control in organic ewes and their lambs. Parasitology 2007;134(Pt 2):299-307.
Tzamaloukas O, Athanasiadou S, Kyriazakis I, Huntley JF, Jackson F. The effect of chicory (Cichorium intybus
) and sulla (Hedysarum coronarium
) on larval development and mucosal cell responses of growing lambs challenged with Teladorsagia circumcincta
. Parasitology 2006;132(Pt 3):419-26.
Tabassum N, Qazi MA, Shah A, Shah MY. Curative potential of Kashni (Cichorium intybus
L.) extract against carbon tetrachloride induced hepatocellular damage in rats. Pharmacologyonline 2010;2:971-8.
Hassan HA, Yousef MI. Ameliorating effect of chicory (Cichorium intybus
L.)-supplemented diet against nitrosamine precursors-induced liver injury and oxidative stress in male rats. Food Chem Toxicol 2010;48:2163-9.
Ahmed B, Khan S, Masood MH, Siddique AH. Anti-hepatotoxic activity of cichotyboside, a sesquiterpene glycoside from the seeds of Cichorium intybus
. J Asian Nat Prod Res 2008;10:223-31.
Naseem N, Latif MS, Tahir M, Naveed AK, Hassan M, Malik SA. Hepatoprotective effect of Cichorium intybus
L. (Kasani) extracts against Carbon tetrachloride induced liver damage. JRMC 2009;13:53-5.
Naseem N, Khurshid R, Qamar T, Tahir M, Naveed AK, Hussaini SF, et al
. Effects of the aqueous and alcoholic extracts of seeds of Cichorium intybus
Linn (Kasni) in the treatment of liver damaged by carbon tetrachloride (CCl4
). Ann Pak Inst Med Sci 2011;7:200-3.
Akram J, Mohammad JK, Zahra D, Hossein N. Hepatoprotective activity of Cichorium intybus
L. leaves extract against carbon tetrachloride induced toxicity. Iran J Pharm Res 2006;1:41-6.
Ahmed B, Al-Howiriny TA, Siddiqui AB. Antihepatotoxic activity of seeds of Cichorium intybus
. J Ethnopharmacol 2003;87:237-40.
Atta AH, Elkoly TA, Mouneir SM, Kamel G, Alwabel NA, Zaher S. Hepatoprotective effect of methanol extracts of Zingiber officinale
and Cichorium intybus
. Indian J Pharm Sci 2010;72:564-70.
Delzenne NM, Cani PD, Daubioul C, Neyrinck AM. Impact of inulin and oligofructose on gastrointestinal peptides. Br J Nutr 2005;93 Suppl 1:S157-61.
Kaskoos RA. Antidiabetic activity of Cichorium intybus
L. seeds on STZ – Induced diabetic rats. IRJP 2012;3:161-4.
Pushparaj PN, Low HK, Manikandan J, Tan BK, Tan CH. Anti-diabetic effects of Cichorium intybus
in streptozotocin-induced diabetic rats. J Ethnopharmacol 2007;111:430-4.
Kim HM, Kim HW, Lyu YS, Won JH, Kim DK, Lee YM, et al.
Inhibitory effect of mast cell-mediated immediate-type allergic reactions by Cichorium intybus
. Pharmacol Res 1999;40:61-5.
Williams CM. Effects of inulin on lipid parameters in humans. J Nutr 1999;129 7 Suppl: 1471S-3S.
Kim M. The water-soluble extract of chicory reduces cholesterol uptake in gut-perfused rats. Nutr Res 2000;20:1017-26.
Cavin C, Delannoy M, Malnoe A, Debefve E, Touché A, Courtois D, et al.
Inhibition of the expression and activity of cyclooxygenase-2 by chicory extract. Biochem Biophys Res Commun 2005;327:742-9.
Ripoll C, Schmidt B, Ilic N, Poulev A, Dey M, Kurmukov AG. Antiinflammatory effects of a sesquiterpene lactone extract from chicory (Cichorium intybus
L.) roots. Nat Prod Commun 2007;2:717-22.
Jindal MN, Patel VR, Patel NB. Pharmacological actions of aqueous and alcoholic extracts of roots of Cichorium intybus
L. Indian J Pharmacol 1975;7:24-33.
Hughes R, Rowland IR. Stimulation of apoptosis by two prebiotic chicory fructans in the rat colon. Carcinogenesis 2001;22:43-7.
Reddy BS, Hamid R, Rao CV. Effect of dietary oligofructose and inulin on colonic preneoplastic aberrant crypt foci inhibition. Carcinogenesis 1997;18:1371-4.
Quintero A, Pelcastre A, Solano JD. Antitumoral activity of new pyrimidine derivatives of sesquiterpene lactones. J Pharm Pharm Sci 1999;2:108-12.
Bischoff TA, Kelley CJ, Karchesy Y, Laurantos M, Nguyen-Dinh P, Arefi AG. Antimalarial activity of lactucin and lactucopicrin: Sesquiterpene lactones isolated from Cichorium intybus
L. J Ethnopharmacol 2004;95:455-7.
Debarbieux-Deleporte M, Delbreil B, Collin T, Delcourt P, Vasseur J, Prevarskaya N, et al.
InsP(3)-mediated calcium release induced by heterologous expression of total chicory Leaf RNA. Biol Cell 2002;94:545-52.
Debarbieux M, Ouadid-Ahidouch H, Delpierre N, Vasseur J, Prevarskaya N. A calcium homeostasis mechanism induced by heterologous expression of total RNA from chicory leaves in Xenopus oocytes
. J Membr Biol 1999;167:25-33.
Abrams SA, Griffin IJ, Hawthorne KM, Liang L, Gunn SK, Darlington G, et al.
A combination of prebiotic short- and long-chain inulin-type fructans enhances calcium absorption and bone mineralization in young adolescents. Am J Clin Nutr 2005;82:471-6.
Coudray C, Bellanger J, Castiglia-Delavaud C, Rémésy C, Vermorel M, Rayssignuier Y. Effect of soluble or partly soluble dietary fibres supplementation on absorption and balance of calcium, magnesium, iron and zinc in healthy young men. Eur J Clin Nutr 1997;51:375-80.
van den Heuvel EG, Schaafsma G, Muys T, van Dokkum W. Nondigestible oligosaccharides do not interfere with calcium and nonheme-iron absorption in young, healthy men. Am J Clin Nutr 1998;67:445-51.
de Kraker JW, Franssen MC, Dalm MC, de Groot A, Bouwmeester HJ. Biosynthesis of germacrene A carboxylic acid in chicory roots. Demonstration of a cytochrome P450 (+)-germacrene a hydroxylase and NADP -dependent sesquiterpenoid dehydrogenase (s) involved in sesquiterpene lactone biosynthesis. Plant Physiol 2001;125:1930-40.
de Kraker JW, Franssen MC, Joerink M, de Groot A, Bouwmeester HJ. Biosynthesis of costunolide, dihydrocostunolide, and leucodin. Demonstration of cytochrome p450-catalyzed formation of the lactone ring present in sesquiterpene lactones of chicory. Plant Physiol 2002;129:257-68.
Flamm G, Glinsmann W, Kritchevsky D, Prosky L, Roberfroid M. Inulin and oligofructose as dietary fiber: A review of the evidence. Crit Rev Food Sci Nutr 2001;41:353-62.
Roberfroid MB, Van Loo JA, Gibson GR. The bifidogenic nature of chicory inulin and its hydrolysis products. J Nutr 1998;128:11-9.
Chow J. Probiotics and prebiotics: A brief overview. J Ren Nutr 2002;12:76-86.
Reddy BS. Prevention of colon cancer by pre- and probiotics: Evidence from laboratory studies. Br J Nutr 1998;80:S219-23.
Reddy BS. Possible mechanisms by which pro- and prebiotics influence colon carcinogenesis and tumor growth. J Nutr 1999;129 7 Suppl: 1478S-82S.
Grieshop CM, Flickinger EA, Bruce KJ, Patil AR, Czarnecki-Maulden GL, Fahey GC Jr. Gastrointestinal and immunological responses of senior dogs to chicory and mannan-oligosaccharides. Arch Anim Nutr 2004;58:483-93.
Menne E, Guggenbuhl N, Roberfroid M. Fn-type chicory inulin hydrolysate has a prebiotic effect in humans. J Nutr 2000;130:1197-9.
Minaiyan M, Ghannadi AR, Mahzouni P, Abed AR. Preventive effect of Cichorium Intybus
L. two extracts on cerulein-induced acute pancreatitis in mice. Int J Prev Med 2012;3:351-7.
Kocsis I, Hagymasi K, Kery A, Szoke E, Blazovics A. Effects of chicory on pancreas status of rats in experimental dislipidemia. Acta Biol Szeged 2003;47:143-6.
Bezic N, Skocibusic M, Dunkic V, Radonic A. Composition and antimicrobial activity of Achillea clavennae
L. essential oil. Phytother Res 2003;17:1037-40.
Mehmood N, Zubair M, Rizwan K, Rasool N, Shahid M, Uddin Ahmad V. Antioxidant, antimicrobial and phytochemical analysis of Cichorium intybus
seeds extract and various organic fractions. Iran J Pharm Res 2012;11:1145-51.
Kilani S, Ben Sghaier M, Limem I, Bouhlel I, Boubaker J, Bhouri W, et al. In vitro
evaluation of antibacterial, antioxidant, cytotoxic and apoptotic activities of the tubers infusion and extracts of Cyperus rotundus
. Bioresour Technol 2008;99:9004-8.
Allahghadri T, Rasooli I, Owlia P, Nadooshan MJ, Ghazanfari T, Taghizadeh M, et al.
Antimicrobial property, antioxidant capacity, and cytotoxicity of essential oil from cumin produced in Iran. J Food Sci 2010;75:H54-61.
Ayala-Zavala JF, Rosas-Domínguez C, Vega-Vega V, González-Aguilar GA. Antioxidant enrichment and antimicrobial protection of fresh-cut fruits using their own byproducts: Looking for integral exploitation. J Food Sci 2010;75:R175-81.
Petrovic J, Stanojkovic A, Comic LJ, Curcic S. Antibacterial activity of Cichorium intybus
. Fitoterapia 2004;75:737-9.
Bajpai VK, Al-Reza SM, Choi UK, Lee JH, Kang SC. Chemical composition, antibacterial and antioxidant activities of leaf essential oil and extracts of Metasequioa glyptostroboides
Miki ex Hu. Food Chem Toxicol 2009;47:1876-83.
Signoretto C, Marchi A, Bertoncelli A, Burlacchini G, Tessarolo F, Caola I, et al.
Effects of mushroom and chicory extracts on the physiology and shape of Prevotella intermedia
, a periodontopathogenic bacterium. J Biomed Biotechnol 2011;2011:635348.
Gazzani G, Daglia M, Papetti A, Gregotti C.In vitro
and ex vivo
anti- and prooxidant components of Cichorium intybus
. J Pharm Biomed Anal 2000;23:127-33.
Cevallos-Casals BA, Byrne D, Okie WR, Cisneros-Zevallos L. Selecting new peach and plum genotypes rich in phenolic compounds and enhanced functional properties. Food Chem 2006;96:273-80.
Lavelli V. Antioxidant activity of minimally processed red chicory (Cichorium intybus
L.) evaluated in xanthine oxidase-, myeloperoxidase-, and diaphorase-catalyzed reactions. J Agric Food Chem 2008;56:7194-200.
Liu H, Wang Q, Liu Y, Chen G, Cui J. Antimicrobial and antioxidant activities of Cichorium intybus
root extract using orthogonal matrix design. J Food Sci 2013;78:M258-63.
Roy-Choudhury A, Venkatakrishna-Bhatt H. Spermatogenic inhibition by Cichorium intybus
L. aqueous root suspension in mice. Naturwissenschaften 1983;70:365-6.
Keshri G, Lakshmi V, Singh MM. Postcoital contraceptive activity of some indigenous plants in rats. Contraception 1998;57:357-60.
Willi R, Pfab F, Huss-Marp J, Buters JT, Zilker T, Behrendt H, et al.
Contact anaphylaxis and protein contact dermatitis in a cook handling chicory leaves. Contact Dermatitis 2009;60:226-7.
Escudero A, Bartolomé B, Sánchez-Guerrero IM, Palacios R. Lettuce and chicory sensitization. Allergy 1999;54:183-4.
Nemery B, Demedts M. Occupational asthma in a chicory grower. Lancet 1989;1:672-3.
[Figure 1], [Figure 2]
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| ||International Journal of Molecular Sciences. 2019; 20(5): 1155 |
|[Pubmed] | [DOI]|
||Environmental factorsí effect on seed germination and seedling growth of chicory (Cichorium intybus L.) as an important medicinal plant
| ||Fatemeh Vahabinia,Hemmatollah Pirdashti,Esmaeil Bakhshandeh |
| ||Acta Physiologiae Plantarum. 2019; 41(2) |
|[Pubmed] | [DOI]|
||Asteraceae species as potential environmental factors of allergy
| ||Marta Denisow-Pietrzyk,Lukasz Pietrzyk,Bozena Denisow |
| ||Environmental Science and Pollution Research. 2019; |
|[Pubmed] | [DOI]|
||Experimental optimization of chicory root (Cichorium intybus
L.) aqueous extracts formulation by novel approach of ongoing ultrasonic vacuum spray drying using response surface methodology
| ||Samaneh Sadeghzadeh Namavar,Reza Amiri Chayjan,Jafar Amiri Parian,Mohammad Ali Zolfigol |
| ||Journal of Food Process Engineering. 2018; : e12830 |
|[Pubmed] | [DOI]|
||Chicory (Cichorium intybus) Herb: Chemical Composition, Pharmacology, Nutritional and Healthical Applications
| ||Muhammad Saeed,Mohamed E. Abd El-Hac,Mahmoud Alagawany,Muhammad A. Arain,Muhammad Arif,Muhammad A. Mirza,Muhammad Naveed,Sun Chao,Muhammad Sarwar,Maryam Sayab,Kuldeep Dhama |
| ||International Journal of Pharmacology. 2017; 13(4): 351 |
|[Pubmed] | [DOI]|
||Chemical Composition and Nutritive Benefits of Chicory (Cichorium intybus) as an Ideal Complementary and/or Alternative Livestock Feed Supplement
| ||Ifeoma Chinyelu Nwafor,Karabo Shale,Matthew Chilaka Achilonu |
| ||The Scientific World Journal. 2017; 2017: 1 |
|[Pubmed] | [DOI]|
||Variability of Secondary Metabolites of the Species Cichorium intybus L. from Different Habitats
| || |
| ||Plants. 2017; 6(3): 38 |
|[Pubmed] | [DOI]|
||Fiber Compounds and Human Health
| ||Montana Camara,Virginia Fernandez-Ruiz,Patricia Morales,Maria Cortes Sanchez-Mata |
| ||Current Pharmaceutical Design. 2017; 23(19): 2835 |
|[Pubmed] | [DOI]|