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生长激素释放因子刺激的生长抑素释放对钙调蛋白的依赖性

Calmodulin dependence of somatostatin release stimulated by growth hormone-releasing factor.

作者信息

Aguila M C, McCann S M

机构信息

Department of Physiology, University of Texas Health Science Center, Dallas 75235.

出版信息

Endocrinology. 1988 Jul;123(1):305-9. doi: 10.1210/endo-123-1-305.

Abstract

Experiments were performed in vitro to examine the possible role of calcium and calmodulin in GRF-induced somatostatin (SRIF) release from the median eminence. Adult male rats were used as tissue donors. The median eminences were first prestimulated in 0.4 ml Krebs Ringer bicarbonate glucose buffer (pH 7.4) containing bacitracin at 37C in an atmosphere of 95% O2, 5% CO2 with constant shaking for 30 min. When calcium was omitted, this medium was used during the prestimulation and stimulation periods. After prestimulation, the medium was discarded and replaced by medium containing the different substances to be tested (GRF, EGTA, calcium channel blockers, and calmodulin inhibitors). The stimulation of SRIF release induced by 10(-10) M GRF was not inhibited by omission of extracellular calcium or when the remaining CA+2 was chelated with 10(-4) M EGTA. The calcium channel blockers, nifendipine and verapamil (10(-6) M), failed to alter the increase of SRIF release induced by rGRF. Three calmodulin inhibitors were employed to examine the possible influence of calmodulin on GRF-induced SRIF release. Trifluoperazine (10(-6) M), triflupromazine (10(-6) M) and penfluridol (10(-7) M) had an inhibitory effect on the stimulation of SRIF release induced by GRF and failed to alter resting release. Thus, GRF can evoke SRIF release independently of extraterminal Ca+2 concentration and Ca+2 influx into the nerve terminals, but the releasing process involves translocation of Ca+2 from intracellular stores. The inhibitory effect of the calmodulin inhibitors on GRF-induced SRIF release, suggests that the translocated Ca+2 must bind to calmodulin in order to release SRIF.

摘要

进行了体外实验,以研究钙和钙调蛋白在生长激素释放因子(GRF)诱导的正中隆起生长抑素(SRIF)释放中可能发挥的作用。成年雄性大鼠用作组织供体。正中隆起首先在含有杆菌肽的0.4 ml Krebs-Ringer碳酸氢盐葡萄糖缓冲液(pH 7.4)中于37℃、95% O₂、5% CO₂的气氛中并持续振荡预刺激30分钟。当省略钙时,在预刺激和刺激期间使用该培养基。预刺激后,弃去培养基,并用含有不同待测物质(GRF、乙二醇双四乙酸(EGTA)、钙通道阻滞剂和钙调蛋白抑制剂)的培养基替换。10⁻¹⁰ M GRF诱导的SRIF释放刺激不受细胞外钙缺失的抑制,也不受用10⁻⁴ M EGTA螯合剩余Ca²⁺时的抑制。钙通道阻滞剂硝苯地平和维拉帕米(10⁻⁶ M)未能改变重组生长激素释放因子(rGRF)诱导的SRIF释放增加。使用三种钙调蛋白抑制剂来研究钙调蛋白对GRF诱导的SRIF释放的可能影响。三氟拉嗪(10⁻⁶ M)、三氟丙嗪(10⁻⁶ M)和五氟利多(10⁻⁷ M)对GRF诱导的SRIF释放刺激有抑制作用,且未改变基础释放。因此,GRF可独立于终末外Ca²⁺浓度和Ca²⁺流入神经末梢而引起SRIF释放,但释放过程涉及Ca²⁺从细胞内储存库的转运。钙调蛋白抑制剂对GRF诱导的SRIF释放的抑制作用表明,转运的Ca²⁺必须与钙调蛋白结合才能释放SRIF。

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