Article
Isopropanolic extract of black cohosh stimulates osteoprotegerin production by human osteoblasts.
Department of Obstetrics and Gynecology, Georg-August-University of Göttingen, Göttingen, Germany.
Journal of Bone and Mineral Research (impact factor:
6.37).
11/2005;
20(11):2036-43.
DOI:10.1359/JBMR.050716
pp.2036-43
Source: PubMed
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Citations (0)
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Article: Estrogen-like effect of a Cimicifuga racemosa extract sub-fraction as assessed by in vivo, ex vivo and in vitro assays.
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ABSTRACT: Black cohosh (Cimicifuga racemosa) is used in the treatment of painful menstruation and menopausal symptoms. Data about the nature of the active compounds and mechanism(s) of action are still controversial, chiefly with respect to its estrogenic activity. This work aimed to assess the possible estrogenic activity of a commercial dry hydro-alcoholic extract of C. racemosa and its hydrophilic and lipophilic sub-fractions on in vivo, ex vivo, and in vitro assays. In a yeast estrogen screen, only the lipophilic sub-fraction was able to activate the human estrogen receptor alpha, with a lower potency but comparable efficacy to that of 17 beta-estradiol. Neither the total extract nor the lipophilic sub-fraction showed an in vivo uterotrophic effect in 21-day-old rats. Uterine tissues obtained ex vivo from C. racemosa treated animals were generally much less sensitive to oxytocin, prostaglandin F(2alpha,) and bradykinin than tissues obtained from estradiol valerate treated rats. The lipophilic sub-fraction, instead, induced a dose-dependent inhibitory activity on the in vitro response to oxytocin, prostaglandin F(2alpha,) and bradykinin of uterine horns from naïve 28-day-old rats, with a potency rate close to 1:30 of that of 17 beta-estradiol. Reported results confirm the effectiveness of C. racemosa in menstrual distress and further emphasize the possibility that lipophilic constituents bind to an as yet not identified estrogen receptor, likely inversely involved in inflammation.The Journal of Steroid Biochemistry and Molecular Biology 107(3-5):262-9. · 3.05 Impact Factor
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Keywords
24-48 h. Time-course experiments
ALP activity
bone-specific alkaline phosphatase activity
ELISA system
estrogen replacement therapy
iCR effect
iCR enhances differentiation
maximum effect
menopausal symptoms
OPG mRNA levels
OPG-to-RANKL ratio
osteoblastic differentiation markers
osteoblastic OPG protein secretion
osteocalcin expression
protein secretion
RANKL expression
RANKL mRNA steady-state levels
semiquantitative RT-PCR
serum-free conditions
stimulatory effect