Medical Attributes of Coriandrum sativum - Coriander

by Victoria Ditchkus
Wilkes University
Wilkes-Barre, PA

July 2015

Coriandrum sativum (coriander) is an annual herbaceous plant belonging to the Apiaceae (parsnip family) (Singh et al. 2012). The plant has both compound and simple leaves that are alternate on an erect stem. The flowers are bisexual, with blue/purple, pink/red, and white corollas (Go Botany 2011). The fruits are dry schizocarps. Flowers occur in flat, round umbels. Coriander is native to the Mediterranean but is grown worldwide. It is mostly seen growing in meadows and fields (Go Botany 2011).

Coriander enjoys a wide range of herbal uses. These include: a digestive, an anti-microbial, anti-oxidant, anti-diabetic, anxiolytic, anti-epileptic, anti-depressant, anti-mutagenic, anti-inflammatory, anti-dyslipidemic, anti-hypertensive, neuro-protective, diuretic, hypoglycemic, analgesic, anti-convulsant, and anti-cancer (Laribi et al.2015). It has also been shown to have lead-detoxifying potential (Velaga et al. 2014). More recently the bioactive constituents are used in combination with conventional drugs to enhance the treatment of diseases such as Alzheimer’s and cancer and has been used to treat diabetes, hyperlipidemia, liver disease, and cancer (Hwang et al. 2014). It has also been known to treat malaria, stomach offset and nausea (Balasubramanian et al. 2015). The plant is a good source of lipids and the essential oil linalool found in the seeds (Sahib et al. 2012).  All parts of the plant are used for flavoring and for the medicinal uses in various cultures (Sahib et al. 2012). The main cultures that use the herb are those of India but many European cultures as well as Russians have used them (Pieroni & Gray. 2008).

Many chemical constituents have been found in coriander but a few are especially noteworthy. Decyl (10) and nonyl (9) aldehydes comprise the main part of the leaves, giving them their distinctive aroma. Other major components of the leaves include 2-decenoic acid, decanoic acid (capric acid) and tetradecenoic acid. The seeds of the coriander contain linalool, which is a ten-carbon, terpene alcohol. Aldehydes in the leaves give the plant a soapy taste (Compound Interest 2014). Coriander oil is the most common part of the plant used and is comprised of several compounds. These include borneol, linalool, cineole, cymene, terpineol, dipentene, phellandrene, pinene and terpinolene (Esoteric Oils 2015). The oil is extracted from the seeds of the plant and is claimed to have many uses including to refresh and to uplift the mind, to help with mental fatigue, migraine, tension and nervous weakness, has a warming effect on the stomach and relieve gas and cramps while revitalizing the glandular system, is helpful for alleviating rheumatism and arthritis pain, as well as muscle spasms and is useful with colds and flu. It also acts as a general cleanser of the body, to rid it of toxins and fluid wastes (Esoteric Oils 2015). The essential oils from leaves and fruits of Coriandrum sativum were analyzed by gas chromatography and found to contain 44 compounds mostly of aromatic acids containing 2-decenoic acid (30.8%), E-11-tetradecenoic acid (13.4%), capric acid (12.7%), undecyl alcohol (6.4%), tridecanoic acid (5.5%) and undecanoic acid (7.1%) as major constituents. The seed oil was found to contain 53 compounds where the major compounds are linalool (37.7%), geranyl acetate (17.6%) and γ-terpinene(14.4%) (Bhuiyan et al. 2009).

Much research has been conducted to test the medical effectiveness of coriander. Some studies have shown that coriander can help prevent dental caries via anti-bacterial activity when the coriander essential oils were incorporated into a mouthwash (Freires et al. 2015). Clinical trials showed the coriander oil has good anti-bacterial activity towards Streptococcus pyogenes and methicillin resistant Staphylococcus aureus (MRSA) (Casetti et al. 2012). These clinical trials tested the tolerance of a cream and lotion containing the essential oil of coriander. No skin irritation was observed. Thus, essential coriander oil might be a useful antiseptic for the prevention and treatment of skin infections with Gram-positive bacteria.

Some in vitro and in vivo studies have found that coriander has the potential to prevent skin photo-aging (Hwang et al. 2014). Additional in vitro and in vivo studies show that coriander fruit exhibits gut stimulatory, inhibitory, and hypotensive effects, as well as diuretic activity (Jabeen et al. 2009).

One in vivo study showed that coriander reduced hyperglycemia in mice with diabetes when incorporated into the diet and drinking water. Also an aqueous extract of coriander increased 2-deoxyglucose transport, glucose oxidation, and incorporation of glucose into glycogen of isolated murine abdominal muscle comparable with m-insulin (Gray & Flatt 1999). Tests with aqueous extract of coriander evoked a stimulation of insulin secretion from a clonal B-cell line (Gray & Flatt 1999). The activity of the extract was heat stable, acetone soluble, and unaltered by acid or dialysis. Reduced activity was seen with exposure to alkali. Insulin-releasing activity was seen in hexane and in water. These results show that coriander has antihyperglycaemic, insulin-releasing, and insulin-like activity (Gray & Flatt 1999). A rat model also showed that an aqueous extract from the leaves and stems of coriander showed significant antihyperglycaemic activity.  The in vitro experiments with alpha-glucosidase revealed a competitive-type inhibition of the α-glucosidase in the gastrointestinal tract. Both of these results confirm anti-diabetic properties of coriander extract (Brindis et al. 2014).

A study using rats showed that treatment with hydroalcoholic seed extract of coriander resulted in a tissue-specific amelioration of oxidative stress produced by lead (Velaga et al. 2014).      

Coriander does not have many adverse side effects when taken. A few include allergic reactions, sensitivity to sun light, stomach pain, diarrhea, and skin darkening (WebMD 2009). One should be cautious if using coriander while breast-feeding and while pregnant. Also those allergic to mugwort, aniseed, caraway, fennel, dill, or similar plants may be allergic to coriander (WebMD 2009).

Many studies have been done on coriander to test coriander's medicinal uses. All of the tests and trials have shown coriander to be effective in treating certain conditions such as diabetes (Brindis et al. 2014 and Gray & Flatt 1999). Use of coriander is not accompanied by too many side effects, but caution should always be taken. More scientific evidence is needed to more precisely determine coriander’s level of safety and to determine correct dosing (WebMD 2009).

LITERATURE CITED

Balasubramanian S, P. Roselin, K.K. Singh, J. Zachariah, & S.N.Saxena. 2015 Post harvest processing and benefits of black pepper, coriander, cinnamon, fenugreek and turmeric spices. Crit Rev Food Sci Nutr. 2015 Mar 6:0. [Epub ahead of print]

Bhuiyan, M., J. Begum, & M. Sultana. 2009. Chemical composition of leaf and seed essential oil of Coriandrum sativum L. from Bangladesh. Bangladesh Journal Of Pharmacology. 4(2), 150-153.

Brindis F, M. González-Andrade, M.E. González-Trujano, S. Estrada-Soto, & R. Villalobos-Molina. 2014. Postprandial glycaemia and inhibition of α-glucosidase activity by aqueous extract from Coriandrum sativum. Nat Prod Res. 28(22):2021-5.

Casetti F., S. Bartelke, K. Biehler, M. Augustin, C.M. Schempp, & U. Frank. 2012. Antimicrobial activity against bacteria and dermatological relevance and skin tolerance of the essential oil from Coriandrum sativum L. fruits. Phytother Res. 26(3):420-4.

Compound Interest. 2014. Chemistry of Coriander. http://www.compoundchem.com/wp-content/uploads/2014/02/The-Chemistry-of-Coriander.pdf

Esoteric Oils. 2015. Coriander essential oil information. Sallamander Concepts (Pty) Ltd. http://www.essentialoils.co.za/essential-oils/coriander.htm

Freires, I.A., C. Denny, B. Benso, S.M. de Alencar, & P.L. Rosalen. 2015. Antibacterial activity of essential oils and their isolated constituents against carcinogenic bacteria: A systematic review. Molecules. 20(4):7329-58.

Go Botany. 2011. Coriandrum sativum. New England Wild Flower Society. https://gobotany.newenglandwild.org/species/coriandrum/sativum/

Gray, A.M., & P.R. Flatt. 1999. Insulin-releasing and insulin-like activity of the traditional anti-diabetic plant Coriandrum sativum (coriander). Br J Nutr. 81(3):203-9.

Hwang E, D.G. Lee, S.H. Park, M.S. Oh, & S.Y. Kim. 2014. Coriander leaf extract exerts antioxidant activity and protects against UVB-induced photoaging of skin by regulation of procollagen type I and MMP-1 expression. J Med Food. 17(9):985-95.

Jabeen, Q., S. Bashir, B. Lyoussi, & A.H. Gilani. 2009. Coriander fruit exhibits gut modulatory, blood pressure lowering and diuretic activities. J Ethnopharmacol. 122(1):123-30.

Laribi, B., K. Kouki, M. M'Hamdi, & T. Bettaieb. 2015. Coriander (Coriandrum sativum L.) and its bioactive constituents. Fitoterapia. 103:9-26.

Pieroni A, & C. Gray. 2008. Herbal and food folk medicines of the Russlanddeutschen living in Kunzelsau/Talacker, South-Western Germany. Phytother Res. 22(7):889-901.
 
Sahib N.G., F. Anwar, A.H. Gilani, A.A. Hamid, N. Saari, & K.M. Alkharfy. 2012. Coriander (Coriandrum sativum L.): a potential source of high-value components for functional foods and nutraceuticals— a review. Phytother Res. 27(10):1439-56.

Singh S.K., R.K. Kakani, R.S. Meena, A. Pancholy, R. Pathak, & A. Raturi. 2012. Studies on genetic divergence among Indian varieties of a spice herb, Coriandrum sativum. J Environ Biol. 33(4):781-9.

Velaga M.K., P.R. Yallapragada, D. Williams, S. Rajanna, & R. Bettaiya. 2014. Hydroalcoholic seed extract of Coriandrum sativum (Coriander) alleviates lead-induced oxidative stress in different regions of rat brain.  Biol Trace Elem Res. 159(1-3):351-63.

WebMD. 2009. Coriander. http://www.webmd.com/vitamins-supplements/ingredientmono-117-CORIANDER.aspx?activeIngredientId=117&activeIngredientName=CORIANDER


This paper was developed as part of the BIO 368 - Medical Botany course offered at Wilkes University during the summer of 2015. Course instructor was Kenneth M. Klemow, Ph.D. (kenneth.klemow@wilkes.edu). The information contained herein is based on published sources, and is made available for academic purposes only. No warrantees, expressed or implied, are made about the medical usefulness or dangers associated with the plant species in question.

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This page posted and maintained by Kenneth M. Klemow, Ph.D., Biology Department, Wilkes University, Wilkes-Barre, PA 18766. (570) 408-4758, kenneth.klemow@wilkes.edu.