TY - JOUR
T1 - Inhibitory effect of neural transections of dorsal raphe nucleus on induction of nocturnal prolactin surge by vaginal stimulation in ovariectomized rats
AU - Maekawa, Fumihiko
AU - Tsukahara, Shinji
AU - Tsukamura, Hiroko
AU - Maeda, Kei Ichiro
AU - Yamanouchi, Korehito
PY - 1998/11/30
Y1 - 1998/11/30
N2 - The effect of complete (CC), anterior (AC) or posterior (PC) cut of the dorsal raphe nucleus (DRn) on induction of the nocturnal prolactin (PRL) surge by electrical vaginal stimulation (VS) was investigated in ovariectomized rats. Plasma level of PRL was measured by radioimmunoassay before and after VS. The data revealed that PRL levels increased in early morning on the day following VS in the rats without brain surgery or with sham-operation. In contrast, the nocturnal PRL surge did not occur in the CC, AC, or PC rats. These results suggest that both the anterior and the posterior fibers of the DRn plays an important role in induction of nocturnal PRL surge by VS in ovariectomized rats.
AB - The effect of complete (CC), anterior (AC) or posterior (PC) cut of the dorsal raphe nucleus (DRn) on induction of the nocturnal prolactin (PRL) surge by electrical vaginal stimulation (VS) was investigated in ovariectomized rats. Plasma level of PRL was measured by radioimmunoassay before and after VS. The data revealed that PRL levels increased in early morning on the day following VS in the rats without brain surgery or with sham-operation. In contrast, the nocturnal PRL surge did not occur in the CC, AC, or PC rats. These results suggest that both the anterior and the posterior fibers of the DRn plays an important role in induction of nocturnal PRL surge by VS in ovariectomized rats.
KW - Dorsal raphe nucleus
KW - Neural transection
KW - Prolactin
KW - Pseudopregnancy
KW - Radioimmunoassay
KW - Rat
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U2 - 10.1016/S0006-8993(98)01019-1
DO - 10.1016/S0006-8993(98)01019-1
M3 - Article
C2 - 9824697
AN - SCOPUS:0032583267
SN - 0006-8993
VL - 813
SP - 195
EP - 199
JO - Brain Research Protocols
JF - Brain Research Protocols
IS - 1
ER -