How It Works
Bottom Line: Bitter melon might be able to lower blood glucose levels, but it should not be used to treat diabetes because it is not known how it interacts with insulin or other medications.
Several active substances in bitter melon have been studied in both animals and humans. These experiments show that these substances act in the same way as insulin, by increasing the entry of glucose into cells and promoting its processing and storage in the liver, muscle, and fat. Bitter melon also prevents the conversion of stored nutrients to glucose and the release of this glucose into the blood. However, researchers have not established the correct dosage of bitter melon for effectively treating the high blood glucose levels in diabetes, and therefore it cannot be recommended as a replacement therapy for insulin or hypoglycemic drugs.
Bitter melon extracts are able to kill leukemia cells in the laboratory and slow the growth of breast cancer in mice, but it is unknown whether these effects occur in humans. A study in humans showed bitter melon had little effect on the immune system of cervical cancer patients. In laboratory tests, bitter melon extracts also inhibit the ability of HIV to insert its DNA into the chromosomes of human cells, but it is also not known whether this effect would occur in humans.
Purported Uses
To prevent cancer
A few laboratory studies show that bitter melon extracts can kill certain cancer cells, but there is no proof from clinical trials that bitter melon can prevent cancer.
To treat diabetes
A handful of small and poorly-designed clinical trials show that bitter melon extracts can lower blood glucose levels, but larger and better-designed clinical trials are needed to fully support this use.
To reduce fever
No scientific evidence supports this use.
To treat HIV and AIDS
Preliminary laboratory studies show that bitter melon can slow the ability of HIV to insert its genes into human chromosomes, but there is no proof from clinical trials that bitter melon can treat HIV or AIDS.
To treat infections
Bitter melon extracts can kill certain viruses on contact in the laboratory, but there is no proof from clinical trials that this herb can treat infections.
To relieve menstrual problems
No scientific evidence supports this use.
Warnings
The covering on bitter melon seeds (called red arils) are toxic in children, causing vomiting, diarrhea, and death.
This product is regulated by the F.D.A. as a dietary supplement. Unlike approved drugs, supplements are not required to be manufactured under specific standardized conditions. This product may not contain the labeled amount or may be contaminated. In addition, it may not have been tested for safety or effectiveness.
Do Not Take If
You are pregnant (Bitter melon can cause vaginal bleeding, premature contractions, and abortion).
You are taking insulin (Bitter melon may have additive effects).
You are taking hypoglycemic medication for diabetes (Bitter melon may have additive effects).
Side Effects
Low blood sugar
Liver damage (this has been shown in animals, but not in humans)
Ingestion of the seeds of bitter melon can cause toxicity to red blood cells, which includes headache, fever, abdominal pain, and coma.
Special Point
Researchers have not established the correct dosage or long-term effects of bitter melon for treating the high blood glucose levels in diabetes, and therefore it cannot be recommended as a replacement therapy for insulin or hypoglycemic drugs.
Scientific Name
Momordica charantia
Common Name
Bitter gourd, bitter apple, wild cucumber, bitter cucumber, balsam apple, balsam pear, margose, la-kwa, leprosy gourd, karela
Clinical Summary
Derived from the fruit and seed of the tree. Bitter melon has been used to treat diabetes, cancer, viral infections, and immune disorders. In vitro and animal studies indicate anticancer
(3) (7) (8), antiviral
(9) (10), and lipid lowering
(11) effects. Bitter melon exerted significant hypoglycemic effects in both healthy and diabetic patients
(1) (2), but had no effect on natural killer cell activity in a study of cervical cancer patients
(6).
Children and pregnant women should not use bitter melon because of its potential toxicity.
There is a potential for additive effect when bitter melon is combined with insulin or oral hypoglycemic agents.
Purported uses
Cancer prevention
Diabetes
Fever
HIV and AIDS
Infections
Menstrual disorder
Constituents
Fruit:
Glycosides: momordin, charantin
Alkaloids: momordicin
Others: polypeptide-P
Oils (seed only): stearic, linoleic, oleic acids
Glycoproteins: alpha-momorcharin, beta-momorcharin, lectins
Others: vicine (pyrimidine nucleoside), protein MAP30
(1)
Mechanism of Action
The compounds present in bitter melon including vicine, charantin, and polypeptide-P increase glucose uptake and glycogen synthesis in the liver, muscle, and adipose tissue, and improve glucose tolerance. Studies with hepatic enzymes in mice revealed reduction in glucose-6-phosphatase and fructose-1,6-bisphosphatase activity, and increased glucose oxidation by G6PDH pathway. Bitter melon displays cytotoxic activity against leukemic cells in vitro (guanylate cyclase inhibitor) and has a cytostatic effect on MDA-MB-231 human breast cancer cells xenografted into mice. MAP30 also demonstrates dose-dependent inhibition of HIV-1 integrase leading to poor viral DNA integration, thus inhibiting T lymphocyte and monocytes.
(1) (2) (3). Bitter melon also inhibits P-glycoprotein and can alter the pharmacokinetics of drugs by inhibiting the P-glycoprotein-mediated efflux
(12).
Warnings
Red arils (covering on seed) are reportedly toxic in children, causing vomiting, diarrhea, and death.
(1)
Contraindications
Bitter melon is contraindicated in pregnant women as it can induce bleeding, contractions, and abortion.
Adverse Reactions
Hypoglycemia and hepatotoxicity were reported in animal studies.
Toxicity: Ingestion of vicine (seed) may cause favism characterized by headache, fever, abdominal pain, and coma.
(4)
Herb-Drug Interactions
Insulin: Bitter melon may have an additive effect when used concomitantly.
Hypoglycemics: Bitter melon may have additive effect when used concomitantly.
(4) (5)
References
- DerMarderosian A, editor. The Review of Natural Products. St. Louis: Facts and Comparisons; 1999.
- Huang KC. The Pharmacology of Chinese Herbs, 2nd ed. New York: CRC Press; 1999.
- Lee-Huang S, et al. Inhibition of MDA-MD-231 human breast tumor xenografts and HER2 expression by anti-tumor agents GAP31 and MAP30. Anticancer Res 2000;20:653-9.
- Brinker F. Herb Contraindications and Drug Interactions, 3rd ed. Sandy (OR): Eclectic Medical Publications; 2001.
- Srivastava Y, et al. Antidiabetic and adaptogenic properties of momordica charantia extract: an experimental and clinical evaluation. Phytotherapy Res 1993;7:285-9.
- Pongnikorn S, Fongmoon D, Kasinrerk W, Limtrakul PN. Effect of bitter melon (Momordica charantia Linn) on level and function of natural killer cells in cervical cancer patients with radiotherapy. J Med Assoc Thai. 2003 Jan;86(1):61-8.
- Deep G, Dasgupta T, Rao AR, Kale RK. Cancer preventive potential of Momordica charantia L. against benzo(a)pyrene induced fore-stomach tumourigenesis in murine model system. Indian J Exp Biol. 2004 Mar;42(3):319-22.
- Xiong SD, Yu K, Liu XH, et al. Ribosome-inactivating proteins isolated from dietary bitter melon induce apoptosis and inhibit histone deacetylase-1 selectively in premalignant and malignant prostate cancer cells. Int J Cancer. 2009 Aug 15;125(4):774-82.
- Lee-Huang S, Huang PL, Chen HC, et al. Anti-HIV and anti-tumor activities of recombinant MAP30 from bitter melon. Gene. 1995 Aug 19;161(2):151-6.
- Fan JM, Zhang Q, Xu J, et al. Inhibition on Hepatitis B virus in vitro of recombinant MAP30 from bitter melon. Mol Bio Rep 2009 Feb;36(2):381-8.
- Nerurkar PV, Lee YK, Linden EH, et al. Lipid lowering effects of Momordica charantia (Bitter Melon) in HIV-1-protease inhibitor-treated human hepatoma cells, HepG2. Br J Pharmacol. 2006 Aug;148(8):1156-64.
- Konishi T, Satsu H, Hatsugai Y, et al. Inhibitory effect of a bitter melon extract on the P-glycoprotein activity in intestinal Caco-2 cells. Br J Pharmacol. 2004 Oct;143(3):379-87.