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INVIVO 5-HIAA RELEASE FROM THE ANTERIOR HYPOTHALAMUS IN THE OVARIECTOMIZED AND ESTRADIOL TREATED RAT FOLLOWING PERFUSION WITH PROGESTERONE
被引:5
|作者:
MEYER, DC
HOLMAN, M
CONNEL, R
MCREE, C
JACOBS, M
机构:
[1] Department of Physiology Eastern Virginia Medical School, Norfolk, 23501, Virginia
关键词:
5-HIAA;
anterior hypothalamus;
estradiol;
in vivo release;
progesterone;
D O I:
10.1007/BF00968558
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In the present study the frequency and magnitude of the release of 5-Hydroxyindoleacetic Acid (5-HIAA) was measured from the anterior hypothalamus of ovariectomized (OVX) and OVX rats treated with estradiol (E2). Female, Holtzman strain rats were maintained on a photoperiod of 14 H light from 0100 to 1500 H and experiments performed from 0900 to 1700 H. Animals exhibiting four-day estrous cycles (250-300 gms) were OVX (20 days recovery) and a push-pull-cannula (PPC) implanted and stereotaxically aimed at the SCN region in the anterior hypothalamus. Following a 7-10 day recovery push-pull-perfusion (PPP) experiments were performed on either OVX females or on OVX females in which a silastic E2 implant (150 μg E2/ml. sesame oil), was placed sc 48 H prior to PPP. In other experiments progesterone (P4) was perfused in a pulsatile manner over the SCN region of the anterior hypothalamus. The overall average 5-HIAA release in the OVX treated rats (548±358 pg/10 min.) was similar to that in the OVX E2 group (694±148 pg/10 min). The average period of 5-HIAA release was (48.2±5.5 min) in the OVX group and (56.0±9.8 min) in the OVX E2 group. These results indicate that exposure of long term OVX rats (20 days) to E2 has no effect on the release or period of 5-HIAA release from serotonergic terminals concentrated in the SCN of the anterior hypothalamus. Pulsatile perfusions of P4 over the SCN region in the OVX E2 treated rat significantly decreased 5-HIAA release but had no effect on the frequency of 5-HIAA release. This suggests that the pulsatile perfusion of P4 can modulate serotonergic activity and potentially affect serotonergic dependent neuroendocrine systems. © 1990 Plenum Publishing Corporation.
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页码:805 / 813
页数:9
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