胰岛素输注引起的暂时性和持续性低血糖鸡的碳水化合物代谢

Yumi Chida, Haruhiko Ohtsu, Kazuaki Takahashi, Kan Sato, Masaaki Toyomizu, Yukio Akiba
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引用次数: 22

摘要

为了阐明鸡对血糖浓度的特异性调节机制,研究了急性和持续性低血糖鸡的肝脏、肌肉和肾脏的碳水化合物代谢以及血液中代谢物的浓度。实验采用单次注射胰岛素(8u /kg BW)或连续注射胰岛素(22.5 U/kg BW/天)4 d诱导急性和持续性低血糖。急性低血糖时血浆非酯化脂肪酸(NEFA)浓度和肝脏、肌肉d-3-羟基丁酸(3HB)浓度升高。持续低血糖第3天,血浆NEFA浓度、血液和肝脏中3HB浓度没有变化,而肌肉中3HB浓度下降。急性低血糖时肝脏中磷酸果糖激酶(PFK)活性有升高的趋势,但PFK和丙酮酸激酶(PK)活性没有变化。在持续低血糖时,肝脏PFK活性在第1天升高,在第3天逆转,肌肉PK活性小幅升高,而肝脏和肾脏的PK和磷酸烯醇丙酮酸羧激酶(PEPCK)活性无显著变化。结果表明,持续低血糖鸡肝糖酵解量先短暂升高,后小幅下降,而肌肉糖酵解量和肝肾糖异生量变化不显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carbohydrate metabolism in temporal and persistent hypoglycemic chickens induced by insulin infusion

In order to elucidate the regulatory mechanism of blood glucose concentrations specific to chickens, carbohydrate metabolism in the liver, muscle and kidney and metabolite concentrations in the blood were investigated in chickens with acute and persistent hypoglycemia. Acute and persistent hypoglycemia were experimentally induced by a single injection of insulin (8 U/kg BW) or by continuous infusion of insulin (22.5 U/kg BW/day) for 4 days. Non-esterified fatty acid (NEFA) concentration in plasma and d-3-hydroxybutyrate (3HB) concentrations in liver and muscle increased in the acute hypoglycemia. Plasma NEFA concentration and 3HB concentration in the blood and liver were not changed at day 3 of persistent hypoglycemia, while 3HB concentration in the muscle was decreased. Phosphofructokinase (PFK) activity in the liver tended to increase but PFK and pyruvate kinase (PK) activities were unchanged in acute hypoglycemia. In persistent hypoglycemia, increase of hepatic PFK activity at day 1 in which it was reversed at day 3, and a small increase of muscle PK activity were observed, while PK and phosphoenolpyruvate carboxykinase (PEPCK) activities in the liver and kidney were not significantly changed. These results show that in the persistent hypoglycemic chickens, hepatic glycolysis transiently increases, which is followed by a small decrease, while glycolysis in muscles and gluconeogenesis in the liver and kidney are not significantly changed.

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