Dh. Olster, IBOTENIC ACID-INDUCED LESIONS OF THE MEDIAL PREOPTIC AREA ANTERIOR HYPOTHALAMUS ENHANCE THE DISPLAY OF PROGESTERONE-FACILITATED LORDOSIS INMALE-RATS, Brain research, 626(1-2), 1993, pp. 99-105
Electrical lesions of the medial preoptic area/anterior hypothalamus (
MPOA/AH) have been reported to enhance the display of steroid-induced
lordosis in castrated male rats. This study employed the cell body-spe
cific neurotoxin, ibotenic acid, to ascertain whether neurons originat
ing in this region (as opposed to axons of passage) tonically inhibit
steroid-induced lordosis in adult male rats. Castrated, adult Long-Eva
ns males received bilateral electrical lesions or injections of iboten
ic acid or vehicle aimed at the MPOA/AH. Following administration of e
stradiol benzoate (EB) and progesterone, lordosis quotients (LQs) and
lordosis ratings (LRs) were significantly higher in groups of rats wit
h electrical lesions (LQ = 62.2 +/- 15.1; LR = 1.22 +/- 0.34) and ibot
enic acid-induced lesions (LQ = 58.1 +/- 12.2; LR = 0.99 +/- 0.24) tha
n in the control group (LQ = 12.8 +/- 7.3; LR = 0.22 +/- 0.13). To det
ermine whether this enhancement of receptive behavior in MPOA/AH-lesio
ned males was an effect on estradiol-induced, as compared to progester
one-facilitated lordosis, groups of castrated rats in a second experim
ent received bilateral injections of ibotenic acid or vehicle aimed at
the MPOA/AH and were tested for lordosis after administration of EB a
lone and again after injection of progesterone. Following treatment wi
th EB alone, rats with ibotenic acid-induced MPOA/AH lesions tended to
be slightly less receptive than control animals. However, following i
njections of progesterone, LQs and LRs were higher in the MPOA/AH-lesi
oned group than in the control animals, as had been observed in the fi
rst experiment. These data are consistent with the hypothesis that cel
l bodies, rather than axons of passage, originating in the MPOA/AH exe
rt tonic inhibitory control over the display of progesterone-facilitat
ed lordosis in adult male rats.