Arisawa M, Snyder G D, Yu W H, De Palatis L R, Ho R H, McCann S M
Department of Obstetrics and Gynecology, Tachikawa Kyosai Hospital, Tokyo, Japan.
Neuroendocrinology. 1990 Jul;52(1):22-7. doi: 10.1159/000125533.
To evaluate a possible physiological role of endogenous substance P (SP) in the control of prolactin (PRL) release, conscious adult male rats were given injections of a specific antiserum against SP (anti-SP) into the third ventricle (3 microliters) or intravenously (0.5 ml). Third-ventricular injection of anti-SP induced a significant increase in plasma PRL levels when compared to values in control animals injected with normal rabbit serum (p less than 0.02). Plasma PRL concentrations were significantly elevated within 2 h after injection of antiserum and remained elevated for the 4-hour duration of the experiment. In contrast, injections of large doses of anti-SP intravenously had no effect on plasma PRL levels. In order to confirm the effect of SP itself, synthetic SP was injected intravenously and intraventricularly. Opposite effects of SP on PRL release were observed after intravenous and intraventricular injections of low or high doses of the peptide. A lower dose of SP (10 ng, 7.42 pmol) injected into the third ventricle suppressed the release of PRL (p less than 0.01), whereas higher doses (1 microgram, 0.74 nmol, or 5 micrograms, 3.71 nmol) had a stimulatory effect on PRL release (p less than 0.01). Similarly, a low dose of SP (0.1 microgram, 0.07 nmol) injected intravenously lowered plasma PRL (p less than 0.05). Large doses of intravenous SP (50 micrograms, 37.1 nmol) dramatically stimulated PRL release (p less than 0.001). To evaluate a possible direct action of SP on PRL release from the anterior pituitary, the peptide was incubated with dispersed anterior pituitary cells for 1 h.(ABSTRACT TRUNCATED AT 250 WORDS)
为评估内源性P物质(SP)在催乳素(PRL)释放调控中可能的生理作用,将抗SP特异性抗血清注射到成年雄性清醒大鼠的第三脑室(3微升)或静脉内(0.5毫升)。与注射正常兔血清的对照动物相比,第三脑室注射抗SP导致血浆PRL水平显著升高(p<0.02)。注射抗血清后2小时内血浆PRL浓度显著升高,并在实验的4小时内持续升高。相比之下,静脉注射大剂量抗SP对血浆PRL水平无影响。为证实SP本身的作用,将合成SP静脉内和脑室内注射。静脉内和脑室内注射低剂量或高剂量该肽后,观察到SP对PRL释放的相反作用。第三脑室内注射较低剂量的SP(10纳克,7.42皮摩尔)可抑制PRL释放(p<0.01),而较高剂量(1微克,0.74纳摩尔,或5微克,3.71纳摩尔)对PRL释放有刺激作用(p<0.01)。同样,静脉注射低剂量的SP(0.1微克,0.07纳摩尔)可降低血浆PRL(p<0.05)。大剂量静脉注射SP(50微克,37.1纳摩尔)显著刺激PRL释放(p<0.001)。为评估SP对垂体前叶PRL释放的可能直接作用,将该肽与分散的垂体前叶细胞孵育1小时。(摘要截短于250字)