Ottlecz A, Samson W K, McCann S M
Endocrinology. 1984 Feb;114(2):359-63. doi: 10.1210/endo-114-2-359.
Prostacyclin (PGI2) (1-5 micrograms in 3 microliters 0.05 M Tris/HCl buffer, pH 7.5) and its stable metabolite, 6-oxo-PGF1 alpha, were microinjected into the third ventricle of ovariectomized rats, and plasma FSH, GH, PRL, and TSH levels were measured by RIA. Control animals received 3 microliters buffer. Injection of 5 micrograms PGI2 dramatically elevated plasma PRL values (4- to 5-fold) at 5 and 15 min, whereas the same dose of 6-oxo-PGF1 alpha produced a significant but smaller (2-fold) stimulatory effect. A delayed increase (1.5-fold) in plasma GH occurred after intraventricular PGI2 at 30 and 60 min. 6-Oxo-PGF1 alpha failed to alter GH levels. There were no alterations in plasma FSH and TSH after intraventricular injection of PGI2. Dispersed, overnight cultured cells from anterior pituitaries of ovariectomized rats were tested with 10(-4)-10(-7) M PGI2 and its metabolite. After 15 min of incubation, 3 X 10(-5) PGI2 produced a highly significant elevation in GH release (P less than 0.001), whereas there was no alteration in PRL levels. Only pharmacological doses of 6-oxo-PGF1 alpha (10(-4) M) stimulated GH release. There was no alteration in PRL release by the cultured cells even in the presence of 10(-4) PGI2. These results suggest that PGI2 stimulates PRL release by a hypothalamic action either to increase the release of PRL-releasing factor, or to decrease release of PRL-inhibiting factor, or by both mechanisms. The delayed stimulatory effect of PGI2 on the release of GH may be exerted via an effect on the anterior lobe itself, since PGI2 was effective in stimulating GH release by the incubated pituitary cells.
将前列环素(PGI2)(1 - 5微克溶于3微升0.05 M Tris/HCl缓冲液,pH 7.5)及其稳定代谢产物6 - 氧代 - PGF1α微量注射到去卵巢大鼠的第三脑室,并通过放射免疫分析法测定血浆促卵泡激素(FSH)、生长激素(GH)、催乳素(PRL)和促甲状腺激素(TSH)水平。对照动物注射3微升缓冲液。注射5微克PGI2后,在5分钟和15分钟时血浆PRL值显著升高(4至5倍),而相同剂量的6 - 氧代 - PGF1α产生显著但较小(2倍)的刺激作用。脑室内注射PGI2后,在30分钟和60分钟时血浆GH出现延迟升高(1.5倍)。6 - 氧代 - PGF1α未能改变GH水平。脑室内注射PGI2后,血浆FSH和TSH无变化。用10^(-4) - 10^(-7) M PGI2及其代谢产物对去卵巢大鼠垂体前叶分散培养过夜的细胞进行测试。孵育15分钟后,3×10^(-5) PGI2使GH释放显著升高(P < 0.001),而PRL水平无变化。只有药理剂量的6 - 氧代 - PGF1α(10^(-4) M)刺激GH释放。即使存在10^(-4) PGI2,培养细胞的PRL释放也无变化。这些结果表明,PGI2通过下丘脑作用刺激PRL释放,可能是增加催乳素释放因子的释放,或减少催乳素抑制因子的释放,或通过两种机制共同作用。PGI2对GH释放的延迟刺激作用可能是通过对垂体前叶本身的作用实现的,因为PGI2能有效刺激孵育的垂体细胞释放GH。