Arisawa M, De Palatis L, Ho R, Snyder G D, Yu W H, Pan G, McCann S M
Department of Obstetrics and Gynecology, School of Medicine, Keio University, Tokyo, Japan.
Neuroendocrinology. 1990 May;51(5):523-9. doi: 10.1159/000125386.
Substance P (SP) has been shown to be present in the hypothalamus and anterior pituitary. To evaluate a possible physiological role of endogenous SP in the control of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) release, specific antiserum against SP (anti-SP) was injected intraventricularly (3 microliters into the third ventricle) or intravenously (50 or 200 microliters) into conscious, ovariectomized (OVX) rats. Third ventricular injection of the antiserum induced a significant decrease in both plasma LH and FSH levels when compared to values in control animals injected with normal rabbit serum (p less than 0.01 and p less than 0.025, respectively). The effect was observed within 10 mi and levels remained suppressed for 60 min. In contrast, intravenous injection of large doses of anti-SP had no effect on the release of both hormones. In order to confirm the stimulatory effect of SP itself, synthetic SP was injected intravenously and intraventricularly into estrogen-primed (E-primed), OVX rats. Synthetic SP dramatically stimulated LH release, but not FSH release when injected either intravenously or intraventricularly at doses of 10 and 50 micrograms (p less than 0.001, p less than 0.005 vs. control, respectively). To investigate any direct action of SP on gonadotropin release from the anterior pituitary gland, synthetic SP was incubated with dispersed anterior pituitary cells harvested from E-primed OVX rats. SP did not affect the release of gonadotropins in vitro. These results indicate that endogenous hypothalamic SP exerts a tonic stimulatory hypothalamic control of basal gonadotropin release in OVX rats.
P物质(SP)已被证明存在于下丘脑和垂体前叶。为了评估内源性SP在促黄体生成素(LH)和促卵泡激素(FSH)释放控制中的可能生理作用,将抗SP的特异性抗血清经脑室注射(3微升注入第三脑室)或静脉注射(50或200微升)到清醒的去卵巢(OVX)大鼠体内。与注射正常兔血清的对照动物相比,经第三脑室注射抗血清可使血浆LH和FSH水平显著降低(分别为p<0.01和p<0.025)。在10分钟内观察到该效应,且水平在60分钟内持续受到抑制。相比之下,静脉注射大剂量抗SP对这两种激素的释放没有影响。为了证实SP本身的刺激作用,将合成SP经静脉和脑室注射到雌激素预处理(E预处理)的OVX大鼠体内。当以10和50微克的剂量经静脉或脑室注射时,合成SP显著刺激LH释放,但不刺激FSH释放(分别与对照相比,p<0.001,p<0.005)。为了研究SP对垂体前叶促性腺激素释放的任何直接作用,将合成SP与从E预处理的OVX大鼠收获并分散的垂体前叶细胞一起孵育。SP在体外不影响促性腺激素的释放。这些结果表明,内源性下丘脑SP对OVX大鼠基础促性腺激素释放发挥着紧张性刺激的下丘脑控制作用。