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内毒素作用后骨骼肌葡萄糖摄取增加的神经调节

Neural regulation of the enhanced uptake of glucose in skeletal muscle after endotoxin.

作者信息

Lang C H

机构信息

Department of Surgery, State University of New York, Stony Brook 11794-8191, USA.

出版信息

Am J Physiol. 1995 Aug;269(2 Pt 2):R437-44. doi: 10.1152/ajpregu.1995.269.2.R437.

Abstract

Previous studies have demonstrated that in vivo injection of lipopolysaccharide (LPS) acutely stimulates glucose uptake (GU) in skeletal muscle. The purpose of the present study was to determine whether this enhanced GU is neurally mediated. In the first group of rats, a unilateral sciatic nerve transection was performed 3 h before injection of LPS, and in vivo GU was assessed using 2-[14C]deoxy-D-glucose 40 min after LPS injection. At this time, LPS-treated rats were hyperglycemic (12 mM), and insulin levels were not different from control rats. In the innervated leg, LPS increased GU 43-228%, depending on the muscle type. In contrast, LPS failed to increase GU in muscles from the denervated limb. In other experiments, somatostatin was infused to produce an insulinopenic condition before the injection of LPS. Despite insulinopenia, muscle GU was still increased by LPS. In control rats, in which the euglycemic hyperinsulinemic clamp technique was used, acute muscle denervation was shown to impair insulin-mediated GU in the presence of pharmacological, but not physiological, insulin levels. Non-insulin-mediated GU (NIMGU) was assessed in rats that were insulinopenic and hyperglycemic. In innervated muscle, NIMGU was increased 56-126 and 118-145% when the plasma glucose was elevated to 9 and 12 mM, respectively. In contrast, hyperglycemia-induced increases in NIMGU were attenuated in denervated muscle. These data demonstrate that 1) the early LPS-induced stimulation of muscle GU is mediated via a non-insulin-mediated pathway and 2) the LPS-induced increase in NIMGU in muscle is neurally mediated.

摘要

先前的研究表明,体内注射脂多糖(LPS)可急性刺激骨骼肌中的葡萄糖摄取(GU)。本研究的目的是确定这种增强的GU是否由神经介导。在第一组大鼠中,在注射LPS前3小时进行单侧坐骨神经横断,并在注射LPS后40分钟使用2-[14C]脱氧-D-葡萄糖评估体内GU。此时,LPS处理的大鼠血糖过高(12 mM),胰岛素水平与对照大鼠无差异。在神经支配的腿部,LPS使GU增加了43%-228%,具体取决于肌肉类型。相比之下,LPS未能增加去神经支配肢体肌肉中的GU。在其他实验中,在注射LPS前输注生长抑素以产生胰岛素缺乏状态。尽管存在胰岛素缺乏,但LPS仍可增加肌肉GU。在使用正常血糖高胰岛素钳夹技术的对照大鼠中,急性肌肉去神经支配显示在药理学而非生理学胰岛素水平存在时会损害胰岛素介导的GU。在胰岛素缺乏和血糖过高的大鼠中评估了非胰岛素介导的GU(NIMGU)。在神经支配的肌肉中,当血浆葡萄糖分别升高至9 mM和12 mM时,NIMGU分别增加56%-126%和118%-145%。相比之下,去神经支配的肌肉中高血糖诱导的NIMGU增加减弱。这些数据表明:1)早期LPS诱导的肌肉GU刺激是通过非胰岛素介导的途径介导的;2)LPS诱导的肌肉中NIMGU增加是由神经介导的。

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