Takahara J, Mori M, Ofuji N, Hashimoto K, Yamauchi J
Endocrinol Jpn. 1977 Feb;24(1):97-103. doi: 10.1507/endocrj1954.24.97.
The effects of prostaglandin E1 (PGE1) and indomethacin (IDM) on the release of several pituitary hormones from the rat pituitary were investigated in vitro. An addition of 2 microng/ml of PGE1 to the medium elicited the release of growth hormone (GH) and prolactin, but not of adrenocorticotropin (ACTH) and luteinizing hormone (LH). Although the addition of 1 microng/ml of IDM alone resulted in no effect on the basal release of these hormones, IDM diminished the release of ACTH induced by crude rat hypothalamic extracts (HE) or lysine-8-vasopressin (LVP), and LH induced by HE or luteinizing hormone-releasing hormone (LH-RH). These findings implicate that a part of PGE1 action might be a direct one on the pituitary gland and PGE1 might release GH and prolactin, whereas IDM might have a direct action on the pituitary gland, and that blunt the release of these pituitary hormones induced by several stimuli.
在体外研究了前列腺素E1(PGE1)和吲哚美辛(IDM)对大鼠垂体几种垂体激素释放的影响。向培养基中添加2微克/毫升的PGE1可引起生长激素(GH)和催乳素的释放,但不会引起促肾上腺皮质激素(ACTH)和黄体生成素(LH)的释放。虽然单独添加1微克/毫升的IDM对这些激素的基础释放没有影响,但IDM减少了粗制大鼠下丘脑提取物(HE)或赖氨酸-8-加压素(LVP)诱导的ACTH释放,以及HE或促黄体生成素释放激素(LH-RH)诱导的LH释放。这些发现表明,PGE1的部分作用可能是对垂体的直接作用,PGE1可能释放GH和催乳素,而IDM可能对垂体有直接作用,并减弱几种刺激诱导的这些垂体激素的释放。