Black cohosh
StarActaea racemosa
Synonyms: Megotrys serpentaria, Macrotrys racemosa, Cimicifuga serpentaria, Thalictrodes racemosa, Cimicifuga racemosa, Botrophis serpentaria
Western Herbalism Properties
Traditional Uses
Black cohosh has an extensive ethnobotanical and Western herbal record. The Cherokee used a root decoction or infusion as a tonic, a remedy for rheumatism, colds, coughs, kidney trouble, and as a sedative, stimulant, and aid for menstrual and uterine complaints; the Iroquois employed it as an analgesic for rheumatism and as a kidney aid; the Penobscot, Delaware, and Micmac also used the rhizome for pain, kidney conditions, and tuberculosis (Hamel and Chiltoskey 1975; Herrick 1977; Tantaquidgeon 1942). In nineteenth-century Eclectic American practice, Lloyd, King, and Scudder employed black cohosh rhizome as a leading remedy for rheumatic and muscular pain, chorea, and ovarian, uterine, and menopausal complaints (King's American Dispensatory, Felter and Lloyd 1898). It remains an officially recognized herbal medicine in Europe (ESCOP, German Commission E) for menopausal symptoms.
Gallery
Botanical Description
Actaea racemosa (formerly Cimicifuga racemosa), known as black cohosh, black snakeroot, or fairy candle, is a tall perennial herb of the Ranunculaceae native to rich, moist deciduous woodlands of eastern North America, from Ontario and Maine south to Georgia. Plants arise from a stout, knotty, blackish rhizome bearing many fibrous roots and produce one or more erect flowering stems 1 to 2.5 m tall. The leaves are large, alternate, and two- to three-times ternately compound, with broadly ovate leaflets bearing sharply toothed and irregularly lobed margins. Inflorescences are tall, slender, wand-like racemes (sometimes branched) of small, pungent-scented flowers; each flower has four to five quickly deciduous sepals and numerous showy white stamens, the petals being reduced or absent. The fruit is a dry follicle containing several seeds.
Active Constituents
Actein
9,19-cycloartane (cycloartenol-type) triterpene glycosideConcentration: Major triterpene glycoside of the rhizome/root
One of the principal cycloartanol-type triterpene glycosides regarded as a marker for black cohosh activity. It has been associated with vasoactive (hypotensive, peripheral vasodilatory) effects and, in vitro, with modulation of cell signalling; it does not bind classical estrogen receptors, consistent with the herb's largely non-estrogenic mechanism.
23-epi-26-deoxyactein (formerly 27-deoxyactein)
Cycloartane triterpene glycosideConcentration: Major glycoside; commonly used analytical marker for standardisation
A dominant, chemically stable triterpene glycoside widely used to standardise commercial extracts. Contributes to the triterpene fraction credited with the extract's climacteric-symptom activity.
Cimicifugoside (cimigoside) / cimiracemoside A
Cycloartane triterpene glycosidesConcentration: Present as characteristic glycosides of the root
Members of the cimicifugoside/cimiracemoside series of cycloartane glycosides characteristic of the genus. Part of the triterpene complex implicated in the herb's central and vasomotor effects rather than direct estrogenic stimulation.
Cimigenol glycosides (cimigenol-3-O-xyloside / -arabinoside)
Cycloartane triterpene glycosides (cimigenol aglycone)Concentration: Minor to moderate constituents of the triterpene fraction
Cimigenol-based glycosides form part of the diverse triterpene glycoside pool. They are of interest chiefly as chemotaxonomic and quality-control markers and contribute to the overall bioactive triterpene content.
Fukinolic acid and cimicifugic acids A/B
Phenylpropanoid / hydroxycinnamic acid estersConcentration: Characteristic phenolic constituents
Caffeic/ferulic-acid-derived esters unique to Cimicifuga. They show antioxidant activity and mild weak-estrogenic/serotonergic-related activity in vitro and serve as authentication markers distinguishing genuine Actaea racemosa from Asian adulterant species.
Caffeic and isoferulic acid
Hydroxycinnamic (phenolic) acidsConcentration: Minor phenolic constituents
Simple phenolic acids contributing antioxidant and anti-inflammatory activity to the whole extract.
N-methylserotonin and related serotonergic amides
Indole alkaloid / biogenic amineConcentration: Trace nitrogen-containing constituents
Serotonin-like constituents that bind and act as partial agonists at 5-HT7 (and 5-HT1A) receptors in vitro, providing a mechanistic basis for the proposed serotonergic contribution to relief of hot flushes and mood/sleep symptoms.
Formononetin (historically reported)
IsoflavoneConcentration: Not reliably detectable in authenticated A. racemosa
Early reports described the isoflavone formononetin, but subsequent analyses of authenticated material have generally failed to confirm its presence; its absence supports the view that black cohosh is not meaningfully phytoestrogenic.
⚠ Drug Interactions
Tamoxifen
Black cohosh extract inhibits cytochrome P450 2D6 and 3A4 in vitro, enzymes involved in converting tamoxifen to its active metabolite endoxifen; both agents also carry rare hepatotoxicity, so concurrent use may raise additive liver risk.
Clinical note: Clinical significance is unproven, but caution and monitoring of liver enzymes are advised when combined; discuss with oncologist before use in breast-cancer patients.
Atorvastatin and other statins / hepatotoxic drugs
A published case report linked concurrent atorvastatin and black cohosh to elevated liver enzymes, and actein shows synergistic effects with simvastatin in vitro. Rare idiosyncratic hepatotoxicity attributed to black cohosh may compound the risk of other hepatotoxic agents.
Clinical note: Avoid or monitor transaminases when used with statins or other potentially hepatotoxic medications; discontinue if signs of liver injury (jaundice, dark urine, right-upper-quadrant pain) occur.
Cisplatin
In vitro breast-cancer cell studies found black cohosh extract decreased the cytotoxicity of cisplatin (while enhancing that of some other chemotherapeutics), suggesting a potential antagonistic interaction.
Clinical note: Patients receiving cisplatin-based chemotherapy should avoid concurrent black cohosh unless supervised by their oncology team.
Preparation Methods
Standardised dried-extract tablet/capsule
Parts: rhizome, root
Commercial products are typically standardised isopropanolic or ethanolic dry extracts delivering roughly 20-40 mg extract (about 1 mg triterpene glycosides as 23-epi-26-deoxyactein) once or twice daily. Because rare idiosyncratic liver injury has been reported, use is generally limited to 6 months, liver-related symptoms should prompt discontinuation, and use is discouraged in existing liver disease or during pregnancy.
Decoction / tincture of the dried root
Parts: rhizome, root
Traditionally the dried root was simmered as a decoction or prepared as an ethanolic tincture. The fresh root and overdoses can cause frontal headache, nausea, dizziness and slowed heart rate, so only modest amounts of well-identified dried material were used. Should not be confused with toxic 'blue cohosh' (Caulophyllum thalictroides), a different plant.
Clinical Studies
Efficacy of black cohosh (Cimicifuga racemosa L.) in treating early symptoms of menopause: a randomized clinical trial
Eighty-four early post-menopausal women received 6.5 mg/day of dried black cohosh root extract or placebo for 8 weeks. Greene Climacteric Scale total scores fell significantly more with black cohosh at weeks 4 and 8 (about 12.9 points greater reduction at week 8), with improvement across vasomotor, psychological and somatic subscales and no reported side effects.
Phase III double-blind, randomized, placebo-controlled crossover trial of black cohosh in the management of hot flashes: NCCTG trial N01CC1
In women (many with a history of breast cancer) black cohosh 20 mg twice daily produced a mean 20% reduction in hot-flash score versus 27% for placebo, a non-significant difference. The trial found no evidence that black cohosh reduced hot flashes more than placebo, illustrating the mixed efficacy data for this indication.
Black cohosh (Cimicifuga spp.) for menopausal symptoms
This Cochrane review of 16 trials (>2000 women) concluded there was insufficient evidence to support the use of black cohosh for menopausal symptoms, citing heterogeneity and methodological limitations while noting the herb was generally well tolerated in the short term.
Historical Texts
Eastern North American Indigenous ethnobotany (Cherokee, Delaware/Lenape, Iroquois and others)
Pre-1800 traditional useKing's American Dispensatory (Eclectic medicine); John King's writings
19th century (King introduced it for acute rheumatism c.1844)German Commission E monograph
1989 (20th-century regulatory phytotherapy)References
- Leach MJ, Moore V. Black cohosh (Cimicifuga spp.) for menopausal symptoms . Cochrane Database of Systematic Reviews (2012) [DOI]
- Pockaj BA, Gallagher JG, Loprinzi CL, et al.. Phase III double-blind, randomized, placebo-controlled crossover trial of black cohosh in the management of hot flashes: NCCTG trial N01CC1 . Journal of Clinical Oncology (2006) [DOI]
- Memorial Sloan Kettering Cancer Center, Integrative Medicine. Black Cohosh — About Herbs monograph . MSKCC About Herbs, Botanicals & Other Products (mskcc.org) (2024) [DOI]
- National Cancer Institute. Black Cohosh (PDQ) — Health Professional Version . NCI PDQ Integrative, Alternative, and Complementary Therapies (2023) [DOI]
This information is for educational purposes only and is not intended to replace professional medical advice. Always consult a qualified healthcare provider before using any herbal remedy, especially if you are pregnant, nursing, or taking medications.
📝 Notes
Public notes from the community and your own private notes on Black cohosh.
No notes yet.