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离子载体A23187对灌注大鼠肝脏中钙离子通量及α-肾上腺素能激动剂作用的影响

The effect of ionophore A23187 on calcium ion fluxes and alpha-adrenergic-agonist action in perfused rat liver.

作者信息

Reinhart P H, Taylor W M, Bygrave F L

出版信息

Biochem J. 1983 Aug 15;214(2):405-12. doi: 10.1042/bj2140405.

Abstract

The effect of ionophore A23187 on cellular Ca2+ fluxes, glycogenolysis and respiration was examined in perfused liver. At low extracellular Ca2+ concentrations (less than 4 microM), A23187 induced the mobilization of intracellular Ca2+ and stimulated the rate of glycogenolysis and respiration. As the extracellular Ca2+ concentration was elevated, biphasic cellular Ca2+ fluxes were observed, with Ca2+ uptake preceding Ca2+ efflux. Under these conditions, both the glycogenolytic response and the respiratory response also became biphasic, allowing the differentiation between the effects of extracellular and intracellular Ca2+. Under all conditions examined the rate of Ca2+ efflux induced by A23187 was much slower than the rate of phenylephrine-induced Ca2+ efflux, although the net amounts of Ca2+ effluxed were similar for both agents. The effect of A23187 on phenylephrine-induced Ca2+ fluxes, glycogenolysis and respiration is dependent on the extracellular Ca2+ concentration. At concentrations of less than 50 microM-Ca2+, A23187 only partially inhibited alpha-agonist action, whereas at 1.3 mM-Ca2+ almost total inhibition was observed. The action of A23187 at the cellular level is complex, dependent on the experimental conditions used, and shows both differences from and similarities to the hepatic action of alpha-adrenergic agonists.

摘要

在灌注肝脏中研究了离子载体A23187对细胞Ca2+通量、糖原分解和呼吸作用的影响。在低细胞外Ca2+浓度(小于4 microM)时,A23187诱导细胞内Ca2+的动员,并刺激糖原分解和呼吸作用的速率。随着细胞外Ca2+浓度升高,观察到双相性细胞Ca2+通量,Ca2+摄取先于Ca2+外流。在这些条件下,糖原分解反应和呼吸反应也变为双相性,从而能够区分细胞外和细胞内Ca2+的作用。在所有检测条件下,A23187诱导的Ca2+外流速率比去氧肾上腺素诱导的Ca2+外流速率慢得多,尽管两种药物的Ca2+净外流量相似。A23187对去氧肾上腺素诱导的Ca2+通量、糖原分解和呼吸作用的影响取决于细胞外Ca2+浓度。在浓度小于50 microM-Ca2+时,A23187仅部分抑制α-激动剂作用,而在1.3 mM-Ca2+时观察到几乎完全抑制。A23187在细胞水平的作用是复杂的,取决于所使用的实验条件,并且与α-肾上腺素能激动剂的肝脏作用既有差异又有相似之处。

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