Activation-dependent regulation of galanin gene expression in gonadotropin-releasing hormone neurons in the female rat [see comments]
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Clifton, Donald K.
Rossmanith, Winfried G.
Steiner, Robert A.
Marks, Daniel L.
Lent, Karin L.
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Endocrine Society
Abstract
In rats, galanin is colocalized in GnRH neurons, and galanin mRNA in GnRH
neurons is increased coincidentally with the preovulatory gonadotropin
surge. Whether the induction of galanin mRNA in GnRH neurons at proestrus
reflects the action of sex steroids is unknown. We tested this hypothesis
by challenging ovariectomized rats (n = 7) with estrogen and progesterone
(E/P) to induce a LH surge and measuring galanin mRNA in GnRH neurons to
determine whether there was an associated induction of galanin message in
these cells. We used single and double label in situ hybridization and
image analysis to compare among groups the levels of both galanin mRNA and
GnRH mRNA in GnRH neurons. We found that steroid-primed animals showed an
approximately 400% induction of galanin mRNA signal in GnRH neurons over
that in vehicle-treated animals. Second, we hypothesized that
steroid-dependent events which induce the expression of galanin mRNA in
GnRH neurons depend on transsynaptic input to GnRH neurons. We tested this
hypothesis by examining the effect of a pharmacological blockade of the
steroid-induced activation of GnRH neurons on levels of galanin mRNA in
these cells. We killed groups of ovariectomized adult female rats at the
peak of a E/P-primed LH surge (n = 7) and after steroid priming followed
by blockade of the LH surge with either the general anesthetic
pentobarbital (n = 7) or the specific alpha-adrenergic receptor blocker
phenoxybenzamine (n = 7). When we examined signal levels representing
galanin mRNA content in GnRH neurons, we observed a 4-fold increase in
signal for galanin mRNA in the GnRH neurons of steroid-primed (E/P surge)
animals compared with that in oil-treated controls (P < 0.0004). This
increase in galanin mRNA was prevented when the LH surge was blocked by
treatment with either pentobarbital or phenoxybenzamine (P < 0.03 and P <
0.0001 vs. E/P surge controls, respectively). Cellular levels of GnRH mRNA
were not different among control, E/P, and E/P plus pentobarbital groups
(P > 0.2). These observations suggest that an increase in galanin mRNA
levels in GnRH neurons is tightly coupled to the occurrence of a LH surge.
By inference, induction of galanin mRNA in GnRH neurons reflects their
activation, possibly via afferent neurons that transduce the steroid
signal to GnRH neurons.
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Citation
Endocrinology. 1994 May;134(5):1991-8
