Mikines K J, Sonne B, Richter E A, Christensen N J, Galbo H
Am J Physiol. 1985 Mar;248(3 Pt 1):E327-32. doi: 10.1152/ajpendo.1985.248.3.E327.
The role of hepatic autonomic nerves in glucose production during hypoglycemia was studied. Selective, surgical denervation of the liver was performed in rats, which reduced hepatic norepinephrine concentrations by 96%. Hypoglycemia was induced by 250 mU of insulin intra-arterially in anesthetized as well as in chronically catheterized, awake rats. Half of the anesthetized denervated or sham-operated rats had previously been adrenodemedullated. Glucose turnover was measured by primed, constant intravenous infusion of [3-3H]glucose. Before as well as during hypoglycemia the arterial glucose concentration and rates of production and utilization of glucose were similar in denervated rats and control rats. Also hepatic glycogen depletion was similar in the groups. The lack of effect of denervation could not be ascribed to compensating changes in hormone or substrate levels. In adrenodemedullated rats lack of glucose recovery from hypoglycemia was accompanied by delayed normalization of glucose clearance. In fed rats, activity in hepatic autonomic nerves is not a primary mechanism increasing glucose production during acute hypoglycemia. Epinephrine enhances glucose recovery by decreasing glucose clearance rather than by increasing glucose production, at least when glucagon is present.
研究了肝脏自主神经在低血糖期间葡萄糖生成中的作用。对大鼠进行了选择性肝手术去神经支配,使肝脏去甲肾上腺素浓度降低了96%。在麻醉的以及长期插管的清醒大鼠中,通过动脉内注射250 mU胰岛素诱导低血糖。一半麻醉的去神经支配大鼠或假手术大鼠先前已进行肾上腺髓质切除。通过静脉内给予[3-³H]葡萄糖的初始负荷和持续输注来测量葡萄糖周转率。在低血糖之前和期间,去神经支配大鼠和对照大鼠的动脉葡萄糖浓度以及葡萄糖的生成和利用速率相似。各组之间肝糖原耗竭情况也相似。去神经支配无作用不能归因于激素或底物水平的代偿性变化。在肾上腺髓质切除的大鼠中,低血糖时葡萄糖恢复缺乏伴有葡萄糖清除率延迟恢复正常。在喂食的大鼠中,至少在存在胰高血糖素时,肝脏自主神经活动不是急性低血糖期间增加葡萄糖生成的主要机制。肾上腺素通过降低葡萄糖清除率而非增加葡萄糖生成来促进葡萄糖恢复。