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葡萄糖依赖性生长激素释放因子和生长抑素从体外灌流大鼠下丘脑释放的特性研究

Characterization of the glucose-dependent release of growth hormone-releasing factor and somatostatin from superfused rat hypothalami.

作者信息

Baes M, Vale W W

机构信息

Clayton Foundation Laboratories for Peptide Biology, Salk Institute, San Diego, Calif.

出版信息

Neuroendocrinology. 1990 Feb;51(2):202-7. doi: 10.1159/000125338.

Abstract

The glucose-dependent secretion of the neuropeptides, growth hormone-releasing factor (GRF) and somatostatin (SRIF), by hypothalamic fragments was studied in vitro using a superfusion system. After equilibration of mediobasal hypothalami in HEPES-buffered Krebs-Ringer solution containing 5.5 mM glucose, glucose levels in the superfusion medium were altered. Lowering the glucose concentration in the medium from 5.5 to 2.7 or 1.1 mM provoked a rapid increase in GRF and SRIF release in a concentration and Ca2+-dependent manner. At 1.1 mM glucose, neuropeptide secretion was elevated 3- to 4-fold. The increase of GRF and SRIF release induced by low glucose was transient since stimulated neuropeptide secretion declined to basal levels in the continued presence of low glucose. Furthermore, after reequilibration in 5.5 mM glucose, no second stimulation of neuropeptide release could be induced by reduced glucose. Intracellular glucopenia induced by addition of 2-deoxy-D-glucose (16.5 mM) to the superfusion medium containing 5.5 mM glucose, also evoked increases in GRF and SRIF release. The sensitivity of GRF and SRIF neurons to glucose was absent in the postnatal period until day 9 after birth and then gradually increased. The parallel increases of GRF and SRIF release in response to low glucose observed in the present in vitro study, together with the suppression of plasma GH levels occurring in hypoglycemia in the rat, suggest that, in this condition, the inhibition of GH release induced by elevated SRIF levels predominates whereas the increase of GRF release might serve to attenuate this effect of SRIF.

摘要

利用超灌注系统在体外研究了下丘脑片段对神经肽、生长激素释放因子(GRF)和生长抑素(SRIF)的葡萄糖依赖性分泌。在含有5.5 mM葡萄糖的HEPES缓冲的 Krebs-Ringer溶液中使中基底下丘脑平衡后,改变超灌注培养基中的葡萄糖水平。将培养基中的葡萄糖浓度从5.5 mM降至2.7 mM或1.1 mM会以浓度和Ca2+依赖性方式迅速增加GRF和SRIF的释放。在1.1 mM葡萄糖时,神经肽分泌升高3至4倍。低葡萄糖诱导的GRF和SRIF释放增加是短暂的,因为在持续存在低葡萄糖的情况下,刺激的神经肽分泌会降至基础水平。此外,在重新平衡至5.5 mM葡萄糖后,降低葡萄糖不能诱导神经肽释放的第二次刺激。向含有5.5 mM葡萄糖的超灌注培养基中添加2-脱氧-D-葡萄糖(16.5 mM)诱导的细胞内葡萄糖缺乏也会引起GRF和SRIF释放增加。GRF和SRIF神经元对葡萄糖的敏感性在出生后直到出生后第9天才出现,然后逐渐增加。在本体外研究中观察到的GRF和SRIF释放对低葡萄糖的平行增加,以及大鼠低血糖时血浆GH水平的抑制,表明在这种情况下,SRIF水平升高诱导的GH释放抑制占主导,而GRF释放的增加可能有助于减弱SRIF的这种作用。

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