Menoprogen, a TCM Herbal Formula for Menopause, Increases Endogenous E-2 in an Aged Rat Model of Menopause by Reducing Ovarian Granulosa Cell Apoptosis.
posted on 2016-08-08, 00:00authored byY Li, H Ma, Y Lu, BJ Tan, L Xu, TO Lawal, GB Mahady, D Liu
The effect of Menoprogen (MPG) on ovarian granulosa cell (GC) apoptosis was investigated in vitro and in vivo in an aged rat model
of menopause. Intragastric administration of Menoprogen or estradiol valerate to 14-month-old senile female rats for eight weeks
increased plasma E2 levels, as well as the weight of both ovarian and uterine tissues. Flow cytometric (FCM) analysis of isolated GCs
from MPG-treated aged rats showed reductions in the G0/G1 ratio and apoptotic peaks. Isolated GCs also exhibited an increase
in cell size and the number of cytoplastic organelles and intracellular gap junctions, the reappearance of secretory granules, and a
lack of apoptotic bodies as determined by TEM. Results from a TdT-mediated dUTP nick end-labeling (TUNEL) assay revealed a
reduction in TUNEL-positive GCs after MPG treatment. Immunohistochemical analysis showed a downregulation of proapoptotic
Bax proteins and an upregulation of antiapoptotic Bcl-2 proteins. The addition of MPG-medicated serum to the media of cultured
GCs also reduced cadmium chloride-induced apoptosis and downregulated caspase-3 protein expression. This work demonstrates
that Menoprogen inhibits GC apoptosis in aged female rats and thereby increases E2 production.This represents a novel mechanism
of action for this herbal medicine in the treatment of menopausal symptoms.
Funding
This study was supported by a project funded by the Priority
Academic Program Development (PAPD) of Jiangsu Higher
Education Institutions, supported by the Open Project
Program of Traditional Chinese Medicine Department of
Nanjing University of Chinese Medicine, Nanjing 210046,
China (YS2012ZYX304), supported by the Fund of Ministry
of Science Technology of China for Special Project before
Major Basic Research (no. 2003CCA01700). This publication
was supported in part by Grant no. R21-AT02381 from the
National Center for Complementary and Integrative Health
(previously NCCAM) at NIH.