Ra. Mangels et al., EFFECT OF PHOTOPERIOD ON NEURAL ESTROGEN AND PROGESTIN RECEPTOR IMMUNOREACTIVITY IN FEMALE SYRIAN-HAMSTERS, Brain research, 796(1-2), 1998, pp. 63-74
This study explored the possibility that reduced behavioral responsive
ness to estradiol and progesterone in female Syrian hamsters exposed t
o a short photoperiod is associated with a reduction in the concentrat
ion of neural steroid receptors. The effects of long and short photope
riod (LP; SP) exposure on steroid receptor immunoreactivity were exami
ned in the ventromedial hypothalamus (VMH), medial tuberal region (mTu
), medial preoptic area (mPOA), medial nucleus of the amygdala (mAMYG)
, and the arcuate nucleus (ARC) of ovariectomized hamsters. In Experim
ent 1, exposure to SP for ten weeks attenuated the lordosis response f
ollowing sequential treatment with estradiol and progesterone. In a se
parate group of animals not given hormones, SP decreased the staining
intensity of estrogen receptor immunoreactive (ERIR) cells in the mPOA
while increasing the number of detectable ERIR cells in part of the m
AMYG. In Experiment 2, SP diminished the lordosis response as it did i
n Experiment 1. One week later, the same females were administered est
radiol systemically to induce progestin receptors (PR). Animals housed
in SP showed significantly reduced progestin receptor immunoreactivit
y (PRIR) in the VMH, mTu, mPOA, mAMYG, and ARC. Experiment 3 examined
whether the results of Experiment 2 might have been influenced by phot
operiodic effects on peripheral metabolism of estradiol, Among hamster
s housed in LP or SP, PRs were induced by estradiol implanted unilater
ally in the medial basal hypothalamus, thus bypassing possible photope
riodic effects on peripheral estradiol availability. This treatment re
sulted in significantly fewer cells with detectable PRIR in the VMH an
d mPOA of SP females, suggesting that the photoperiodic influences on
PR induction observed in Experiment 2 do not depend on alterations in
the peripheral availability of estradiol. (C) 1998 Elsevier Science B.
V. All rights reserved.