Shin S H, Obonsawin M C, Bates L
Horm Res. 1984;19(1):33-42. doi: 10.1159/000179857.
Basal plasma prolactin concentration is controlled by tonic inhibition. The major prolactin-inhibiting factor (PIF) is believed to be dopamine. Factors other than dopamine have also been suggested as possible physiological PIF. One of the major candidates for the nondopaminergic PIF is considered to be gamma-aminobutyric acid (GABA). We have carefully examined the possible physiological role of GABA by monitoring, at every 2 min, the circulating prolactin concentration after GABA administration, in conscious freely moving rats. GABA (0.1 or 1 g/kg) had no significant direct effect on plasma prolactin in rats in which the dopaminergic receptors were completely blocked by pimozide, nor in hypophysectomized rats in which a pituitary had been grafted under the kidney capsule and was therefore removed from any hypothalamic influence. The effects of bicuculline, a GABA-receptor-blocking agent, was examined in order to find out whether a tonic inhibition is exerted by GABA after elimination of tonic dopaminergic inhibition on prolactin secretion. The pimozide-treated rat in which the dopaminergic tone is completely eliminated did not show any prominent elevation of plasma prolactin concentration after bicuculline (300 micrograms/kg) administration. However, GABA did have an inhibitory effect in a primary pituitary cell monolayer culture system. Therefore, we conclude that GABA does not play a significant role as a physiological PIF and that the inhibitory effect of GABA in vitro is of a pharmacological nature.
基础血浆催乳素浓度受紧张性抑制调控。主要的催乳素抑制因子(PIF)被认为是多巴胺。除多巴胺外,其他因素也被认为可能是生理性PIF。非多巴胺能PIF的主要候选因子之一被认为是γ-氨基丁酸(GABA)。我们通过在清醒自由活动的大鼠中,每隔2分钟监测给予GABA后循环催乳素浓度,仔细研究了GABA可能的生理作用。GABA(0.1或1 g/kg)对多巴胺能受体被匹莫齐特完全阻断的大鼠,以及对垂体被移植到肾包膜下从而脱离任何下丘脑影响的垂体切除大鼠的血浆催乳素,均无显著直接作用。为了弄清楚在消除对催乳素分泌的紧张性多巴胺能抑制后,GABA是否发挥紧张性抑制作用,我们研究了GABA受体阻断剂荷包牡丹碱的作用。在多巴胺能张力被完全消除的匹莫齐特处理大鼠中,给予荷包牡丹碱(300微克/千克)后,血浆催乳素浓度并未显著升高。然而,GABA在原代垂体细胞单层培养系统中确实具有抑制作用。因此,我们得出结论,GABA作为生理性PIF并不发挥重要作用,且GABA在体外的抑制作用具有药理学性质。