Scacchi P, Carbone S, Szwarcfarb B, Rondina D, Wuttke W, Moguilevsky J A
Departamento de Fisiología, Facultad de Medicina, Universidad de Buenos Aires, Argentina.
Brain Res Dev Brain Res. 1998 Jan 14;105(1):51-8.
The present studies were designed to study the interrelationships between GABAergic, serotoninergic and excitatory amino acids systems (EAAs) in the control of gonadotropin secretion in prepubertal female rats. For this purpose we determined the effects of N-methyl-D-aspartate (NMDA), an exogenous agonist of EAAs receptors, on LH and FSH secretion in 16-day-old female rats in which the GABA-A and GABA-B receptors were blocked by bicuculline and baclofen or serotonin (5-HT) depleted by p-choloroamphetamine (PCA). In addition the effects of the GABAergic and serotoninergic systems on LH and FSH secretion were evaluated in animals treated with dibenzocycloalkenimine (diocilpine MK-801), an antagonist of NMDA neurotransmission. While muscimol, a GABA-A agonist, induced a significant increase in LH and FSH levels (P < 0.01), baclofen, a GABA-B agonist, had an inhibitory effect on these hormones (P < 0.01). MK 801, a NMDA receptor antagonist, not only suppressed the stimulatory effect of NMDA on LH and FSH but also blocked the stimulatory effect of muscimol without modifying the inhibitory action of baclofen on both gonadotropins. Bicuculline, a GABA-A receptor antagonist, did not modify the release effect of NMDA on LH and FSH. 5-HTP, a precursor of 5-HT that increases the levels of this neurotransmitter in the central nervous system significantly increased (P < 0.01) the plasma levels of LH and FSH, and this effect was blocked by the NMDA receptor antagonist MK-801. We conclude that the stimulatory effects of GABAergic and serotoninergic systems in prepubertal female rats are connected with the activation of EAA neurotransmission, while the stimulatory effects of NMDA appear to be independent of serotoninergic and GABAergic actions on LH and FSH secretion. Since both GABA and serotonin systems change their effects on LH and FSH during sexual maturation from a stimulatory action in prepubertal to an inhibitory action in adult rats and since NMDA neurotransmission has a stimulatory effect on gonadotropin secretion both in prepubertal and adult rats, it is clear that the interrelationships between GABAergic and serotoninergic systems with EAAs in the gonadotropin control are different in prepubertal and in adult rats.
本研究旨在探讨γ-氨基丁酸能(GABAergic)、5-羟色胺能(serotoninergic)和兴奋性氨基酸系统(EAAs)在控制青春期前雌性大鼠促性腺激素分泌中的相互关系。为此,我们测定了EAA受体的外源性激动剂N-甲基-D-天冬氨酸(NMDA)对16日龄雌性大鼠促黄体生成素(LH)和促卵泡生成素(FSH)分泌的影响,这些大鼠的GABA-A和GABA-B受体被荷包牡丹碱和巴氯芬阻断,或者5-羟色胺(5-HT)被对氯苯丙胺(PCA)耗竭。此外,在使用二苯并环烯亚胺(地卓西平MK-801)(一种NMDA神经传递拮抗剂)处理的动物中,评估了GABA能和5-羟色胺能系统对LH和FSH分泌的影响。GABA-A激动剂蝇蕈醇可使LH和FSH水平显著升高(P<0.01),而GABA-B激动剂巴氯芬对这些激素有抑制作用(P<0.01)。NMDA受体拮抗剂MK 801不仅抑制了NMDA对LH和FSH的刺激作用,还阻断了蝇蕈醇的刺激作用,而未改变巴氯芬对两种促性腺激素的抑制作用。GABA-A受体拮抗剂荷包牡丹碱未改变NMDA对LH和FSH的释放作用。5-HT的前体5-羟色氨酸(5-HTP)可显著提高中枢神经系统中这种神经递质的水平,从而使LH和FSH的血浆水平显著升高(P<0.01),而这种作用被NMDA受体拮抗剂MK-801阻断。我们得出结论,青春期前雌性大鼠中GABA能和5-羟色胺能系统的刺激作用与EAA神经传递的激活有关,而NMDA的刺激作用似乎独立于其对LH和FSH分泌的5-羟色胺能和GABA能作用。由于GABA和5-羟色胺系统在性成熟过程中对LH和FSH的作用从青春期前的刺激作用转变为成年大鼠的抑制作用,并且由于NMDA神经传递在青春期前和成年大鼠中均对促性腺激素分泌有刺激作用,显然青春期前和成年大鼠中GABA能和5-羟色胺能系统与EAA在促性腺激素控制中的相互关系是不同的。