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链脲佐菌素诱导的糖尿病和禁食对大鼠比目鱼肌细胞内钠及三磷酸腺苷的影响。

Effects of streptozotocin diabetes and fasting on intracellular sodium and adenosine triphosphate in rat soleus muscle.

作者信息

Moore R D, Munford J W, Pillsworth T J

出版信息

J Physiol. 1983 May;338:277-94. doi: 10.1113/jphysiol.1983.sp014673.

Abstract

The hypothesis that part of the insulin transduction system consists of a co-ordinated stimulation of the Na pump and of Na-H exchange by the hormone (Moore, 1981) requires that insulin plays a physiological role in the regulation of intracellular Na+. Moreover, this model predicts that in hypoinsulinaemic states, such as diabetes and fasting, intracellular pH and intracellular ATP levels would be depressed. The present study tests the hypothesis that in hypoinsulinaemic states intracellular Na+ is increased and intracellular ATP is decreased by measuring these parameters in soleus muscles removed from both diabetic and fasted rats. When rats were made diabetic by injection of streptozotocin (SZ) plasma insulin significantly decreased by 24 hr and plasma glucose and triglyceride levels increased. Intracellular Na+ was significantly elevated by 48 hr after injection of SZ. The elevation ranged from 18 to 48% and persisted for the duration of the experimental observation (up to 28 days). Intracellular ATP decreased significantly by the seventh day after SZ injection and remained depressed by about 24% for the duration (35 days) of the observation. In one series, a significant negative correlation was seen between plasma insulin levels and intracellular Na+ of both SZ-diabetic animals and their controls. Intracellular Na+ also significantly increased when hypoinsulinaemia was induced by fasting. Again, intracellular ATP did not decrease until after the elevation of intracellular Na+. After 72 hr of fasting, intracellular ATP was still decreased in spite of normal plasma glucose levels. Insulin therapy of SZ diabetic rats restored intracellular ATP and plasma glucose to normal, but did not restore intracellular Na+ to normal levels. The results confirm two predictions of the 'insulin transduction system model (Moore, 1981). Most strongly supported is that part of the model which indicates that the Na pump is regulated by physiological levels of insulin. This is especially convincing since hypoinsulinaemia produced by a non-pharmacological procedure, fasting, was associated with an increase in intracellular Na+.

摘要

胰岛素转导系统的一部分由激素对钠泵和钠-氢交换的协同刺激组成这一假说(Moore,1981),要求胰岛素在细胞内钠离子调节中发挥生理作用。此外,该模型预测,在低胰岛素血症状态下,如糖尿病和禁食时,细胞内pH值和细胞内ATP水平会降低。本研究通过测量从糖尿病和禁食大鼠分离的比目鱼肌中的这些参数,来检验低胰岛素血症状态下细胞内钠离子增加而细胞内ATP减少这一假说。当通过注射链脲佐菌素(SZ)使大鼠患糖尿病时,血浆胰岛素在24小时内显著降低,血浆葡萄糖和甘油三酯水平升高。注射SZ后48小时,细胞内钠离子显著升高。升高幅度在18%至48%之间,并在实验观察期(长达28天)内持续存在。注射SZ后第七天,细胞内ATP显著降低,并在观察期(35天)内持续降低约24%。在一个系列中,在SZ糖尿病动物及其对照的血浆胰岛素水平与细胞内钠离子之间观察到显著的负相关。禁食诱导低胰岛素血症时,细胞内钠离子也显著增加。同样,细胞内ATP直到细胞内钠离子升高后才降低。禁食72小时后,尽管血浆葡萄糖水平正常,但细胞内ATP仍降低。对SZ糖尿病大鼠进行胰岛素治疗可使细胞内ATP和血浆葡萄糖恢复正常,但不能使细胞内钠离子恢复到正常水平。结果证实了 “胰岛素转导系统模型”(Moore,1981)的两个预测。得到最有力支持的是该模型中表明钠泵受生理水平胰岛素调节的部分。这一点特别有说服力,因为由非药物程序禁食产生的低胰岛素血症与细胞内钠离子增加有关。

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