Key result
Baicalin at 20 or 50 mg/kg significantly decreased embryonic death rates in bromocriptine-treated mice by reducing IFN-gamma and elevating progesterone levels.
Why the study?
Does baicalin prevent abortion in bromocriptine-treated pregnant mice?
Does baicalin prevent abortion in bromocriptine-treated pregnant mice?
Baicalin exerts dose-dependent anti-abortive effects in a mouse model by reducing IFN-gamma and elevating progesterone levels.
Hypothesis-generating for baicalin in miscarriage prevention; clinical translation untested and should not change practice.
The Chinese herbal medicine Huang Qin (Radix Scutellariae) had been used for restless fetus for hundreds of years in China, however, little attention had been given to the components of the herb, specifically its ability to exert abortion-preventing effects at the maternal fatal interface. The present study was carried out to investigate the protective effects of baicalin and the possible mechanisms on pregnancies. Baicalin (at 10, 20, and 50 mg/kg BW respectively) was gavaged to bromocriptine-treated mice from gestation day (GD) 1 through GD 7. Abortion rates were calculated and the changes of interferon-gamma (IFN-gamma), interleukin-10 (IL-10) and progesterone were assayed on different gestation days. Results showed that the embryonic death rates were significantly decreased in groups supplemented with 20 or 50 mg/kg BW of baicalin, accompanied with reduced IFN-gamma and enhanced progesterone contents. Moreover, the highest levels of IFN-gamma appeared on GD 5 both in the control and in baicalin treated groups. It is concluded that baicalin can exert an anti-abortive effect by cutting down the production of IFN-gamma and elevating the levels of progesterone in a dose dependent manner and IFN-gamma is involved in an inflammatory reaction which is beneficial for a successful implantation.
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Ma et al. (2009) studied Bromocriptine-induced abortion. Baicalin vs. Control was evaluated on Embryonic death rates. Baicalin at 20 or 50 mg/kg significantly decreased embryonic death rates in bromocriptine-treated mice by reducing IFN-gamma and elevating progesterone levels.
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