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大鼠肝细胞原代培养中氨基酸转运系统N的激素调节

Hormonal regulation of amino acid transport system N in primary cultures of rat hepatocytes.

作者信息

Gebhardt R, Kleemann E

出版信息

Eur J Biochem. 1987 Jul 15;166(2):339-44. doi: 10.1111/j.1432-1033.1987.tb13520.x.

Abstract

The transport of histidine and glutamine via system N in cultured hepatocytes was found to be subject to hormonal control. This long-term regulation showed the following characteristics. The transport capacity for histidine and glutamine (system N) increased slowly in response to the combination of dexamethasone and insulin to about 4-fold that of controls after 18-30 h. A similar time course was found for the stimulation of system N (2.5-fold) by dexamethasone and glucagon. In contrast the uptake of alpha-aminoisobutyric acid (system A) was rapidly stimulated 3-fold by dexamethasone and insulin and 5-fold by dexamethasone and glucagon within 3-6 h but decreased towards control rates after 24 h of cultivation in minimal essential medium. Dexamethasone, insulin and glucagon each stimulated glutamine uptake about 2-fold in cultures maintained in W/AB 77 medium, while the combination of dexamethasone with either glucagon or insulin resulted in a 3-4-fold increase. Dexamethasone was most effective at about 0.1 microM. Higher concentrations were less efficient. Insulin reached its optimal effect at concentrations above 1 microM. Kinetic analysis revealed that the increased capacity of glutamine transport in response to hormones was due to an increase in Vmax, while Km was essentially unchanged. The hormone-induced stimulation of system N was prevented by cycloheximide. The induced uptake of glutamine was inhibited by excess amounts of asparagine and histidine but not of alpha-methylaminoisobutyric acid or cysteine. These results clearly differentiate the hormonal regulation of system N from that of system A.

摘要

研究发现,培养的肝细胞中通过系统N转运组氨酸和谷氨酰胺的过程受激素控制。这种长期调节具有以下特点。组氨酸和谷氨酰胺(系统N)的转运能力在18 - 30小时后,对地塞米松和胰岛素的联合反应缓慢增加,达到对照的约4倍。地塞米松和胰高血糖素对系统N的刺激(2.5倍)也有类似的时间进程。相比之下,α-氨基异丁酸(系统A)的摄取在3 - 6小时内被地塞米松和胰岛素迅速刺激3倍,被地塞米松和胰高血糖素迅速刺激5倍,但在最低限度基本培养基中培养24小时后,摄取量降至对照水平。在地塞米松、胰岛素和胰高血糖素分别刺激在W/AB 77培养基中培养的细胞时,谷氨酰胺摄取增加约2倍,而地塞米松与胰高血糖素或胰岛素联合使用时,谷氨酰胺摄取增加3 - 4倍。地塞米松在约0.1微摩尔浓度时最有效,更高浓度时效果较差。胰岛素在浓度高于1微摩尔时达到最佳效果。动力学分析表明,激素作用下谷氨酰胺转运能力的增加是由于Vmax增加,而Km基本不变。放线菌酮可阻止激素对系统N的刺激。过量的天冬酰胺和组氨酸可抑制诱导的谷氨酰胺摄取,但α-甲基氨基异丁酸或半胱氨酸则不能。这些结果清楚地将系统N的激素调节与系统A的激素调节区分开来。

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