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花生四烯酸及其代谢产物在生长激素释放因子诱导的正中隆起生长抑素释放中的作用。

Role of arachidonic acid or its metabolites in growth-hormone-releasing factor-induced release of somatostatin from the median eminence.

作者信息

Aguila M C, Milenkovic L, McCann S M, Snyder G D

机构信息

Department of Physiology, University of Texas Southwestern Medical Center, Dallas.

出版信息

Neuroendocrinology. 1990 Sep;52(3):238-42. doi: 10.1159/000125592.

Abstract

The possible involvement of arachidonic acid (AA) release in growth-hormone-releasing factor (GRF)-induced somatostatin (SRIF) release from the median eminence (ME) of the hypothalamus was evaluated in adult male rats using an in vitro incubation system. The MEs were preincubated with [14C]-AA, then washed and incubated with vehicle or test agents, and the release of SRIF and [14C]-AA into the medium was measured. In the experiments designed only to determine SRIF release, the MEs were first preincubated for 30 min. The medium was then discarded and replaced with fresh buffer or test substances and incubated for 10, 20 and/or 30 min. GRF (10(-10) M) stimulated both AA and SRIF release significantly within 20 min, with maximum release occurring at 30 min. The stimulatory effect of GRF on AA release was coincident with the release of SRIF. A phospholipase A2 inhibitor (10(-6) M, quinacrine) completely abolished the stimulatory effect of GRF on both AA and SRIF release. The release of SRIF induced by GRF was also inhibited by both indomethacin (10(-6) M, a cyclooxygenase inhibitor) and metyrapone (10(-6) M, a cytochrome P-450 inhibitor). On the other hand, nordihydroguaiaretic acid (10(-6) M, a lipoxygenase inhibitor) had no effect on GRF-evoked SRIF release. The data presented here suggest that an important GRF-mediated event leading to SRIF secretion is an elevated release of AA from ME fragments in vitro. In conclusion, our data are suggestive that the stimulatory effect of GRF on SRIF release is due, in part, to the release and subsequent metabolism of AA to one or more metabolites.

摘要

利用体外孵育系统,在成年雄性大鼠中评估了花生四烯酸(AA)释放可能参与生长激素释放因子(GRF)诱导的下丘脑正中隆起(ME)中生长抑素(SRIF)释放的情况。将ME预先与[14C] - AA孵育,然后洗涤并与溶剂或测试剂一起孵育,测量SRIF和[14C] - AA释放到培养基中的量。在仅用于确定SRIF释放的实验中,ME首先预孵育30分钟。然后弃去培养基,用新鲜缓冲液或测试物质替换,并孵育10、20和/或30分钟。GRF(10^(-10) M)在20分钟内显著刺激了AA和SRIF的释放,最大释放发生在30分钟。GRF对AA释放的刺激作用与SRIF的释放同时发生。磷脂酶A2抑制剂(10^(-6) M,喹吖因)完全消除了GRF对AA和SRIF释放的刺激作用。GRF诱导的SRIF释放也受到吲哚美辛(10^(-6) M,一种环氧化酶抑制剂)和甲吡酮(10^(-6) M,一种细胞色素P - 450抑制剂)的抑制。另一方面,去甲二氢愈创木酸(10^(-6) M,一种脂氧合酶抑制剂)对GRF诱发的SRIF释放没有影响。此处呈现的数据表明,在体外,导致SRIF分泌的一个重要的GRF介导事件是ME片段中AA释放增加。总之,我们的数据表明GRF对SRIF释放的刺激作用部分归因于AA的释放及其随后代谢为一种或多种代谢产物。

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