AllNutritionals.com provides facts about all Nutritional supplements, Food calorie and nutrient counter, and nutritional calculators.  

Black Cohosh (Cimicifuga racemosa [L.] Nutt.)


Table Of ContentsPrevious PageNext Page

Black Cohosh (Cimicifuga racemosa [L.] Nutt.)

Background

Black cohosh is popular as an alternative to hormonal therapy in the treatment of menopausal (climacteric) symptoms such as hot flashes, mood disturbances, diaphoresis, palpitations, and vaginal dryness. Several controlled trials and case series have reported black cohosh to improve menopausal symptoms for up to six months. Although these initial studies are suggestive, they have been few in number and have universally suffered from methodological weaknesses.

The mechanism of action of black cohosh remains unclear, and the effects on estrogen receptors or hormonal levels (if any) have not been fully elucidated. Recent publications suggest that there may be no direct effects on estrogen receptors, although this is an area of active controversy (1-8). Safety and efficacy data beyond six months are not available, although recent reports suggest safety of short-term use, including in women experiencing menopausal symptoms for whom estrogen replacement therapy is contraindicated (9;10). Nonetheless, due to a lack of long-term follow-up, caution is advisable until better-quality safety data are available. Use of black cohosh in high-risk populations (such as in women with a history of breast cancer) should be under the supervision of a licensed healthcare professional.

Synonyms

Actaea macrotys, Actaea racemosa L., actee a grappes, Amerikanisches wanzenkraut, baneberry, black snakeroot, botrophis serpentaria, bugwort, cohosh bugbane, Cimicifuga, Cimicifugae racemosae rhizoma, cimicifugawurzelstock, herbe au punaise, macrotys, Macrotys actaeoides, rich weed, rattle root, rattle snakeroot, rattle top, rattle weed, richweed, schwarze schlangenwurzel, solvlys, squaw root, Thalictrodes racemosa , Traubensilberkerze, Wanzwnkraut.

Note : Do not confuse black cohosh with blue cohosh ( Caulophyllum thalictroides ), which contains chemicals that may damage the heart and raise blood pressure. Do not confuse black cohosh ( Cimicifuga racemosa ) with cimicifuga foetida , bugbane, fairy candles, or sheng ma; these are species from the same family ( Ranunculaceae ) with different effects.

Evidence

These uses have been tested in humans or animals. Safety and effectiveness have not always been proven. Some of these conditions are potentially serious, and should be evaluated by a qualified healthcare provider.

Uses based on scientific evidenceGrade*Menopausal symptoms
Black cohosh is a popular alternative to prescription hormonal therapy for treatment of menopausal symptoms such as hot flashes, mood problems, perspiration, heart palpitations, and vaginal dryness. Initial human research suggests that black cohosh may improve some of these symptoms for up to six months. However, most studies are not well designed and results are not conclusive. Most research has used a specially designed questionnaire to measure menopausal symptoms which does not consider some of the important symptoms of menopause such as vaginal dryness, but does measure other symptoms which are not commonly associated with menopause, such as tingling sensations and dizziness. Well-designed studies are needed using black cohosh for longer than six months.

B

Joint pain
There is not enough human research to make a clear recommendation about the use of black cohosh for painful joints in rheumatoid arthritis or osteoarthritis.

C

* Key to grades
A:
Strong scientific evidence for this use;
B:
Good scientific evidence for this use;
C:
Unclear scientific evidence for this use;
D:
Fair scientific evidence against this use (it may not work);
F:
Strong scientific evidence against this use (it likely does not work).

Uses based on tradition or theory
The below uses are based on tradition or scientific theories. They often have not been thoroughly tested in humans, and safety and effectiveness have not always been proven. Some of these conditions are potentially serious, and should be evaluated by a qualified healthcare provider.

Anxiety, aphrodisiac, appetite stimulant, asthma, back pain, breast disease, breast pain/inflammation (mastitis), bone diseases, bronchitis, cervical dysplasia (abnormal pap smear), child birth (labor induction), cough remedy, decreased blood platelets, depression, diarrhea, dizziness, edema, endometriosis, fever, gall bladder disorders, headache, heart disease/palpitations, high blood pressure, infertility, inflammation, insect repellent, itchiness, kidney inflammation, liver disease, malaria, menstrual period problems, miscarriage, muscle pain, muscle spasms, ovarian cysts, pancreatitis, perspiration, pertussis (whooping cough), polycystic breast disease, polycystic ovarian syndrome, premenstrual syndrome (PMS), ringing in the ears, sleep disorders, snakebites, sore throat, tamoxifen-related hot flashes, uterine diseases and bleeding, vaginal discharge, yellow fever.

Dosing

The below doses are based on scientific research, publications, traditional use, or expert opinion. Many herbs and supplements have not been thoroughly tested, and safety and effectiveness may not be proven. Brands may be made differently, with variable ingredients, even within the same brand. The below doses may not apply to all products. You should read product labels, and discuss doses with a qualified healthcare provider before starting therapy.

Standardization

Standardization involves measuring the amount of certain chemicals in products to try to make different preparations similar to each other. It is not always known if the chemicals being measured are the "active" ingredients. The dose of black cohosh is often based on the amount of the chemical 27-deoxyactein. The German product, Remifemin®, used in most human studies, contains an alcoholic extract of black cohosh standardized to contain 1 milligram of 27-deoxyactein in each 20 milligram tablet. The manufacturing process and dosing recommendations for Remifemin® have changed over the past 20 years, and doses used in different studies are not always the same. A standardized liquid formulation of Remifemin® has also been used in some studies.

Adults (18 years and older)

Tablets : For menopausal symptoms, studies have used 20 milligram or 40 milligram Remifemin® tablets (containing 1 or 2 milligrams of 27-deoxyactein) twice daily or 40 drops of a liquid extract. Some clinical studies have used 20 milligrams taken twice daily.

Dried rhizome (root) : The British Herbal Compendium recommends 40 to 200 milligrams of dried rhizome daily in divided doses, although traditional doses have been as high as 1 gram three times daily.

Tincture/Liquid : The British Herbal Compendium recommends 0.4 to 2 milliliters of a (1:10) 60% ethanol tincture daily.

Children (younger than 18 years)

There is not enough scientific information to recommend black cohosh in children.

Safety

The U.S. Food and Drug Administration does not strictly regulate herbs and supplements. There is no guarantee of strength, purity or safety of products, and effects may vary. You should always read product labels. If you have a medical condition, or are taking other drugs, herbs, or supplements, you should speak with a qualified healthcare provider before starting a new therapy. Consult a healthcare provider immediately if you experience side effects.

Allergies

Avoid if allergic to black cohosh or other members of the Ranunculaceae (buttercup or crowfoot) family. In nature, black cohosh contains small amounts of salicylic acid (which is found in aspirin), but it is not clear how much (if any) is present in commercially available products. Black cohosh should be used cautiously in people allergic to aspirin or to other salicylates.

Side Effects and Warnings

Black cohosh is generally well tolerated in recommended doses and has been studied for up to six months. High doses of black cohosh may cause frontal headache, dizziness, perspiration, or visual disturbances. Several side effects have been noted in studies, including constipation, intestinal discomfort, loss of bone mass (leading to osteoporosis), irregular or slow heart beat, low blood pressure, nausea and vomiting.

It is not clear if black cohosh is safe in individuals with hormone-sensitive conditions such as breast cancer, uterine cancer, or endometriosis. There is controversy as to whether black cohosh is similar to estrogen in its mechanism, although recent studies suggest that it may not be. The influence of black cohosh on anti-estrogen drugs (like tamoxifen) or hormone replacement therapy is not clear. It is not known if black cohosh possesses the beneficial effects that estrogen is believed to have on bone mass, or the potential harmful effects such as increased risk of stroke or hormone-sensitive cancers.

There are three cases reported in Australia of hepatitis (liver damage) in individuals who used combination herbal products containing black cohosh, requiring liver transplantation for severe liver failure in two of these patients. These reports are concerning, although the cases have been criticized by some as not being adequately substantiated. Nonetheless, patients with liver disease should consult a licensed healthcare professional before using black cohosh.

Black cohosh should be used cautiously in patients with a history of blood clots or stroke, seizure disorder, taking medications for high blood pressure, known allergy to aspirin/salicylates, liver disease, or hormone-sensitive cancers.

Pregnancy and Breastfeeding

Safety during pregnancy and breastfeeding has not been established. Black cohosh may relax the muscular wall of the uterus, and some nurse-midwives in the United States use black cohosh to stimulate labor. There is one report of severe multi-organ damage in a child delivered with the aid of both black cohosh and blue cohosh ( Caulophyllum thalictroides ), who was not breathing at the time of birth. The child survived with permanent brain damage. However, blue cohosh is known to have effects on the heart and blood vessels and may have been responsible for these effects.

Tinctures may be ill-advised during pregnancy due to potentially high alcohol content.

References

1. Anderson IB, Mullen WH, Meeker JE, et al. Pennyroyal toxicity: measurement of toxic metabolite levels in two cases and review of the literature. Ann Intern Med 1996;124(8):726-734.

2. Anon. Cimicifuga racemosa - Monograph. Altern Med Rev 2003;8(2):186-189.

3. Baillie N, Rasmussen P. Black and blue cohosh in labour. N Z Med J 1997;110 (1036) :20-21.

4. Beuscher N, Reichert R. Cimicifuga racemosa L. - black cohosh. Zeit Phytother 1995;16:301-310.

5. Boblitz N, Schrader E, Henneicke-von Zepelin HH, et al. Benefit of a fixed drug combination containing St. John's wort and black cohosh for climacteric patients -- results of a randomised clinical trial (poster presentaion from 6th Annual Symposium on Complementary Health Care, Exeter, England, December 2-4, 1999). Focus Alt Comp Ther (FACT) 2000;5(1):85-86.

6. Bodinet C, Freudenstein J. Influence of Cimicifuga racemosa on the proliferation of estrogen receptor-positive human breast cancer cells. Breast Cancer Res Treat 2002;76(1):1-10.

7. Borrelli F, Ernst E. Cimicifuga racemosa: a systematic review of its clinical efficacy. Eur J Clin Pharmacol 2002;58(4):235-241.

8. Borrelli F, Izzo AA, Ernst E. Pharmacological effects of Cimicifuga racemosa. Life Sci 2003;73(10):1215-1229.

9. Burdette JE, Liu J, Chen SN, et al. Black cohosh acts as a mixed competitive ligand and partial agonist of the serotonin receptor. J Agric Food Chem 2003;51(19):5661-5670.

10. Daiber W. Menopause symptoms: success without hormones. Arztl Praxis 1983;35:1946-1947.

11. Dixon-Shanies D, Shaikh N. Growth inhibition of human breast cancer cells by herbs and phytoestrogens. Oncol Rep 1999;6(6):1383-1387.

12. Dog TL, Powell KL, Weisman SM. Critical evaluation of the safety of Cimicifuga racemosa in menopause symptom relief. Menopause 2003;10(4):299-313.

13. Duker EM, Kopanski L, Jarry H, et al. Effects of extracts from Cimicifuga racemosa on gonadotropin release in menopausal women and ovariectomized rats. Planta Med 1991;57(5):420-424.

14. Einer-Jensen N, Zhao J, Andersen KP, et al. Cimicifuga and Melbrosia lack oestrogenic effects in mice and rats. Maturitas 1996;25(2):149-153.

15. Freudenstein J, Bodinet C. Influence of an isopropanolic aqueous extract of Cimicifuga racemosae rhizoma on the proliferation of MCF-7 cells. 23rd International LOF-Symposium on Phytoestrogens, University of Ghent, Belgium (January 15, 1999).

16. Genazzani E, Sorrentino L. Vascular action of acteina: active constituent of Actaea racemosa L. Nature 1962;194(4828):544-545.

17. Gunn TR, Wright IM. The use of black and blue cohosh in labour. N Z Med J 1996;109(1032):410-411.

18. Hailemeskel B, Lee HJ, Thomhe H. Incidence of potential herb-drug interactions among herbal users. ASHP Midyear Clinical Meeting 2000;35:p-267e.

19. Hemmi H, Kitame F, Ishida N, et al. Inhibition of thymidine transport into phytohemagglutinin-stimulated lymphocytes by triterpenoids from species. J Pharm Dyn 1979;2:339-349.

20. Hemmi H, Kusano G, Ishida N. Selective inhibition of nucleoside transport into mouse lymphoma L- 5178Y cells by cimicfugoside. J Pharmacobiodyn 1980;3(12):636-642.

21. Hernandez MG, Pluchino S. Cimicifuga racemosa for the treatment of hot flushes in women surviving breast cancer. Maturitas 2003;44 Suppl 1:S59-S65.

22. Hunter A. Cimicifuga racemosa: pharmacology, clinical trials and clinical use. Eur J Herbal Med 1999;5(1):19-25.

23. Huntley A, Ernst E. A systematic review of the safety of black cohosh. Menopause 2003;10(1):58-64.

24. Jacobson JS, Troxel AB, Evans J, et al. Randomized trial of black cohosh for the treatment of hot flashes among women with a history of breast cancer. J Clin Oncol 2001;19(10):2739-2745.

25. Jarry H, Harnischfeger G, Duker E. [The endocrine effects of constituents of Cimicifuga racemosa. 2. In vitro binding of constituents to estrogen receptors]. Planta Med 1985;51(4):316-319.

26. Jarry H, Harnischfeger G. [Endocrine effects of constituents of Cimicifuga racemosa. 1. The effect on serum levels of pituitary hormones in ovariectomized rats]. Planta Med 1985;51(1):46-49.

27. Jarry H, Metten M, Spengler B, et al. In vitro effects of the Cimicifuga racemosa extract BNO 1055. Maturitas 2003;44 Suppl 1:S31-S38.

28. Johnson BM, van Breemen RB. In vitro formation of quinoid metabolites of the dietary supplement Cimicifuga racemosa (black cohosh). Chem Res Toxicol 2003;16(7):838-846.

29. Kligler B. Black cohosh. Am Fam Physician 2003;68(1):114-116.

30. Koeda M, Aoki Y, Sakurai N, et al. Studies on the Chinese crude drug "shoma." IX. Three novel cyclolanostanol xylosides, cimicifugosides H-1, H-2 and H-5, from cimicifuga rhizome. Chem Pharm Bull (Tokyo) 1995;43(5):771-776.

31. Korn WD. Six month oral toxicity study with remifemin-granulate in rats followed by an 8-week recovery period. International Bioresearch, Hannover, Germany 1991;1.

32. Lehmann-Willenbrock E, Riedel HH. [Clinical and endocrinologic studies of the treatment of ovarian insufficiency manifestations following hysterectomy with intact adnexa]. Zentralbl Gynakol 1988;110(10):611-618.

33. Li W, Sun Y, Liang W, et al. Identification of caffeic acid derivatives in Actea racemosa (Cimicifuga racemosa, black cohosh) by liquid chromatography/tandem mass spectrometry. Rapid Commun Mass Spectrom 2003;17(9):978-982.

34. Lieberman S. A review of the effectiveness of Cimicifuga racemosa (black cohosh) for the symptoms of menopause. J Womens Health 1998;7(5):525-529.

35. Liske E, Hanggi W, Henneicke-von Zepelin HH, et al. Physiological investigation of a unique extract of black cohosh (Cimicifugae racemosae rhizoma): a 6-month clinical study demonstrates no systemic estrogenic effect. J Womens Health Gend Based Med 2002;11(2):163-174.

36. Liske E, Wüstenberg P, Boblitz N. Human-pharmacological investigations during treatment of climacteric complaints with Cimicifuga racemosa (Remifemin): No estrogen-like effects. ESCOP 2001;1:1.

37. Liske E, Wustenberg P. Efficacy and safety of phytomedicines with particular references to Cimicifuga racemosa. J Med Assoc Thai 1998;Jan:s108.

38. Liske E, Wüstenberg P. Therapy of climacteric complaints with Cimicifuga racemosa: herbal medicine with clinically proven evidence [poster presentation]. Menopause 1998;5(4):250.

39. Liske E. Therapeutic efficacy and safety of Cimicifuga racemosa for gynecologic disorders. Adv Ther 1998;15(1):45-53.

40. Liu J, Burdette JE, Xu H, et al. Evaluation of estrogenic activity of plant extracts for the potential treatment of menopausal symptoms. J Agric Food Chem 2001;49(5):2472-2479.

41. Liu Z, Yang Z, Zhu M, et al. [Estrogenicity of black cohosh (Cimicifuga racemosa) and its effect on estrogen receptor level in human breast cancer MCF-7 cells]. Wei Sheng Yan Jiu 2001;30(2):77-80.

42. Lontos S, Jones RM, Angus PW, et al. Acute liver failure associated with the use of herbal preparations containing black cohosh. Med J Aust 2003;179(7):390-391.

43. Lupu R, Mehmi I, Atlas E, et al. Black cohosh, a menopausal remedy, does not have estrogenic activity and does not promote breast cancer cell growth. Int J Oncol 2003;23(5):1407-1412.

44. Mahady GB. Is black cohosh estrogenic? Nutr Rev 2003;61(5 Pt 1):183-186.

45. McFarlin BL, Gibson MH, O'Rear J, et al. A national survey of herbal preparation use by nurse-midwives for labor stimulation. Review of the literature and recommendations for practice. J Nurse Midwifery 1999;44(3):205-216.

46. McKenna DJ, Jones K, Humphrey S, et al. Black cohosh: efficacy, safety, and use in clinical and preclinical applications. Altern Ther Health Med 2001;7(3):93-100.

47. Mills SY, Jacoby RK, Chacksfield M, et al. Effect of a proprietary herbal medicine on the relief of chronic arthritic pain: a double-blind study. Br J Rheumatol 1996;35(9):874-878.

48. Nesselhut T, Schellhase C, Dietrich R, et al. [Investigations into the growth-inhibitive efficacy of phytopharmacopia with estrogen-like influences on mammary gland carcinoma cells] (translated from German). Arch Gynecol Obstet 1993;254:817-818.

49. Pepping J. Black cohosh: Cimicifuga racemosa. Am J Health Syst Pharm 1999;56(14):1400-1402.

50. Popp M, Schenk R, Abel G. Cultivation of Cimicifuga racemosa (L.) nuttal and quality of CR extract BNO 1055. Maturitas 2003;44 Suppl 1:S1-S7.

51. Pritchard JB, French JE, Davis BJ, Haseman JK. The role of transgenic mouse models in carcinogen identification. Environmental Health Perspectives 2003;111(4):444-454

52. Seidlova-Wuttke D, Hesse O, Jarry H, et al. Evidence for selective estrogen receptor modulator activity in a black cohosh (Cimicifuga racemosa) extract: comparison with estradiol-17beta. Eur J Endocrinol 2003;149(4):351-362.

53. Seidlova-Wuttke D, Jarry H, Becker T, et al. Pharmacology of Cimicifuga racemosa extract BNO 1055 in rats: bone, fat and uterus. Maturitas 2003;44 Suppl 1:S39-S50.

54. Shuster J. Heparin and thrombocytopenia. Black Cohosh root? Chasteberry tree? Seizures! Hosp Pharm 1996;31:1553-1554.

55. Siess VM, Seybold G. [Studies on the effects of Pulsatilla pratensis, Cimicifuga racemosa and Aristolochia clematitis on the estrus in infantile and castrated white mice]. Arzneimittelforschung 1960;10:514-520.

56. Stoll W. Phytotherapeutikum beeinflusst atrophisches Vaginal epithel. Doppelblindversuch Cimicifuga vs. Oestrogenpraeparat [Phytopharmaceutical influences on atrophic vaginal epithelium. Double-blind study on Cimicifuga vs. an estrogen preparation]. Therapeutickon 1987;1:23-32.

57. Stolze H. [An alternative to treat menopausal complaints]. Gynecologie 1982;1:14-16.

58. Struck D, Tegtmeier M, Harnischfeger G. Flavones in extracts of . Planta Med 1997;63:289-290.

59. Takahira M, Kusano A, Shibano M, et al. Antimalarial activity and nucleoside transport inhibitory activity of the triterpenic constituents of Cimicifuga spp. Biol Pharm Bull 1998;21(8):823-828.

60. Thomsen M, Schmidt M. Hepatotoxicity from Cimicifuga Racemosa? Recent Australian Case Report not Sufficiently Substantiated. J Altern Complement Med 2003;9(3):337-340.

61. Vitetta L, Thomsen M, Sali A. Black cohosh and other herbal remedies associated with acute hepatitis. Med J Aust 2003;178(8):411-412.

62. Vorberg G. Treatment of menopause symptoms. ZFA 1984;60:626-629.

63. Warnecke G. Using phyto-treatment to influence menopause symptoms. Med Welt 1985;36:871-874.

64. Whiting PW, Clouston A, Kerlin P. Black cohosh and other herbal remedies associated with acute hepatitis. Med J Aust 2002;177(8):440-443.

65. Zava DT, Dollbaum CM, Blen M. Estrogen and progestin bioactivity of foods, herbs, and spices. Proc Soc Exp Biol Med 1998;217(3):369-378.

66. Zierau O, Bodinet C, Kolba S, et al. Antiestrogenic activities of Cimicifuga racemosa extracts. J Steroid Biochem Mol Biol 2002;80(1):125-130.

January 01, 2004

Top Of PageTable Of ContentsPrevious PageNext Page

 
Copyright © 2004 AllNutritionals.com All Rights reserved.
Last updated: January 2004.

Disclaimer:All the information in AllNutritionals.com is provided by medical professionals & is meant only for informational purpose. The site does not guarantee the accuracy or authenticity of the information. Use of any information is solely at the user's own risk.

Partners
  Our partner sites ...
Nutritional Analysis and Tools| Forex tutorials