Smock T, Arnold S, Albeck D, Emerson P, Garritano J, Burrows K, Derber W, Sanson C, Marrs K, Weatherly H
Howard Hughes Undergraduate Research Laboratory, Department of Psychology, University of Colorado, Boulder 80309.
Brain Res. 1992 Dec 11;598(1-2):138-42. doi: 10.1016/0006-8993(92)90177-b.
A projection from the medial amygdaloid nucleus to the hippocampus and septum probably uses vasopressin as a transmitter. The nucleus synthesizes vasopressin and activation of the nucleus has a hippocampal effect that is completely blocked by a vasopressin antagonist. The afferent and efferent projections of this peptidergic nucleus suggest a possible role for the system in sexual behavior. Stimulation of the nucleus inhibits the output of the hippocampus in both genders and reorganizes behavior for a period of 15-20 min. In males, the effect of peptidergic activation is to produce a behavior that resembles the post-ejaculatory interval in coitus. This state is characterized by an EEG that resembles slow-wave sleep and by ultrasonic vocalizations at a characteristic frequency of 22 kHz. Castration in either gender causes depletion of the peptide from the target fields and eliminates the peptidergic signal in the hippocampus after about 15 weeks. The effects of castration in males can be reversed by testosterone replacement. The fluctuation of estrogen levels in rat plasma during the estrus cycle happens too quickly to impact the peptidergic system, and thus there is no significant change in the strength of the peptidergic signal among the proestrus, estrus, metestrus and diestrus stages. This fact permits study of the physiology of the system without concern for stage of estrus but does not permit conclusions regarding its function in females.
从内侧杏仁核到海马体和隔区的投射可能以血管加压素作为递质。该核团合成血管加压素,且其激活对海马体产生的效应会被血管加压素拮抗剂完全阻断。这个肽能核团的传入和传出投射表明该系统在性行为中可能发挥作用。刺激该核团会抑制两性海马体的输出,并在15 - 20分钟内重新组织行为。在雄性中,肽能激活的作用是产生一种类似于性交后射精间期的行为。这种状态的特征是脑电图类似于慢波睡眠,以及发出频率为22千赫的特征性超声波叫声。无论雄性还是雌性,阉割都会导致靶区肽的消耗,并在大约15周后消除海马体中的肽能信号。雄性阉割的影响可以通过睾酮替代来逆转。大鼠血浆中雌激素水平在发情周期中的波动太快,无法影响肽能系统,因此在发情前期、发情期、发情后期和间情期阶段,肽能信号的强度没有显著变化。这一事实使得可以在不考虑发情阶段的情况下研究该系统的生理学,但无法得出关于其在雌性中功能的结论。