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Abstract
Steroid feedback regulates GnRH secretion and previous
work has implicated GABAergic neurons as a mediator of
these effects. We examined GABAergic postsynaptic
currents (PSCs) in GFP-identified GnRH neurons from mice
exposed to different steroid milieux in vivo. Adult
mice were ovariectomized and treated with estradiol
(OVX+E, controls) or E plus progesterone (P, OVX+E+P).
P decreased PSC frequency, a presynaptic effect, and PSC
size, which could be via pre- and/or postsynaptic
mechanisms. In contrast, dihydrotestosterone (DHT,
OVX+E+DHT) increased both GABAergic PSC frequency and
size in GnRH neurons. Tetrodotoxin (TTX), which
eliminates action potential-dependent presynaptic
effects, did not alter frequency, suggesting DHT may
have increased PSC frequency by increasing connectivity
between GABAergic and GnRH neurons. TTX reduced PSC
size below control values, indicating DHT may augment
presynaptic GABA release but inhibits the postsynaptic
GnRH neuron response. In mice treated with both P and
DHT (OVX+E+P+DHT), PSC frequency and size were similar
to controls, suggesting these steroids counteract one
another. These results demonstrate GABAergic neurons
participate in integrating and conveying steroid
feedback to GnRH neurons, defining a potential central
mechanism for steroid regulation of GnRH neurons during
the reproductive cycle, and providing one possible
mechanism for increased activity of these cells in
hyperandrogenic females.
Key words:
Gonadotropin-releasing hormone
Neurotransmitters
Progesterone
Testosterone
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