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胃泌素释放肽对人胰腺生长激素释放因子诱导的大鼠生长激素(GH)分泌的抑制作用。

Inhibition by gastrin-releasing peptide of growth hormone (GH) secretion induced by human pancreatic GH-releasing factor in rats.

作者信息

Kabayama Y, Kato Y, Shimatsu A, Ohta H, Yanaihara N, Imura H

出版信息

Endocrinology. 1984 Aug;115(2):649-53. doi: 10.1210/endo-115-2-649.

Abstract

Intravenous injection of synthetic human pancreatic GH-releasing factor (1-44) [hpGRF(1-44)] (50 ng-1 micrograms/100 g BW) resulted in a dose-related increase in plasma GH levels in urethane-anesthetized male rats. Pretreatment with cysteamine (30 mg/100 g BW, sc, 4 h previously) or anti-SRIF rabbit serum (0.5 ml/rat, iv, 1 h previously) raised basal plasma GH levels and markedly exaggerated the plasma GH response to hpGRF (1-44) (80 ng/100 g BW, iv). The intraventricular injection of gastrin-releasing peptide (GRP) (1 micrograms/rat) completely inhibited the increase of plasma GH induced by hpGRF (80 ng/100 g BW, iv) in control rats. However, in the rats treated with cysteamine or anti-SRIF rabbit serum, the inhibitory effect of GRP on hpGRF-induced GH release was significantly attenuated. hpGRF (10(-11)-10(-8) M) stimulated in a dose-related manner GH release from rat anterior pituitary cells superfused in vitro. GRP (10(-5) M) did not affect pituitary GH release induced by hpGRF (10(-9) M) in vitro. These results indicate that hpGRF stimulates rat GH secretion by acting at the pituitary level and the hypothalamic SRIF interacts with the action of GRF, and that GRP inhibits GH secretion, at least in part, by stimulating SRIF release from the hypothalamus.

摘要

给氨基甲酸乙酯麻醉的雄性大鼠静脉注射合成的人胰腺生长激素释放因子(1 - 44)[hpGRF(1 - 44)](50纳克 - 1微克/100克体重)可导致血浆生长激素水平呈剂量依赖性升高。预先用半胱胺(30毫克/100克体重,皮下注射,提前4小时)或抗生长抑素兔血清(0.5毫升/大鼠,静脉注射,提前1小时)处理可提高基础血浆生长激素水平,并显著增强血浆生长激素对hpGRF(1 - 44)(80纳克/100克体重,静脉注射)的反应。向脑室注射胃泌素释放肽(GRP)(1微克/大鼠)可完全抑制对照大鼠中由hpGRF(80纳克/100克体重,静脉注射)诱导的血浆生长激素升高。然而,在经半胱胺或抗生长抑素兔血清处理的大鼠中,GRP对hpGRF诱导的生长激素释放的抑制作用明显减弱。hpGRF(10⁻¹¹ - 10⁻⁸摩尔/升)以剂量依赖性方式刺激体外灌流的大鼠垂体前叶细胞释放生长激素。GRP(10⁻⁵摩尔/升)在体外不影响由hpGRF(10⁻⁹摩尔/升)诱导的垂体生长激素释放。这些结果表明,hpGRF通过作用于垂体水平刺激大鼠生长激素分泌,下丘脑生长抑素与GRF的作用相互影响,并且GRP至少部分地通过刺激下丘脑释放生长抑素抑制生长激素分泌。

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