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游离脂肪酸在清醒家兔妊娠晚期肝脏胰岛素抵抗中的作用

Role of free fatty acids in hepatic insulin resistance during late pregnancy in conscious rabbits.

作者信息

Gilbert M, Pere M C, Baudelin A, Battaglia F C

机构信息

Laboratoire de Physiologie du Développement, Université Paris, France.

出版信息

Am J Physiol. 1991 Jun;260(6 Pt 1):E938-45. doi: 10.1152/ajpendo.1991.260.6.E938.

Abstract

This study addresses whether elevated free fatty acids (FFA) contribute to the hepatic insulin resistance of pregnancy. We applied a euglycemic hyperinsulinemic clamp with or without Intralipid plus heparin infusion in conscious virgin and pregnant rabbits after an 18-h fast coupled with chronic catheterization of the hepatic and portal veins and femoral artery. A primed constant infusion of [3-3H]glucose was used to determine glucose fluxes. Insulin was infused into a mesenteric vein for 140 min. In pregnant rabbits, basal net hepatic uptake of lactate was almost two times that of nonpregnant rabbits. During a euglycemic hyperinsulinemic clamp there was a decline of approximately 65% in hepatic lactate uptake in nonpregnant rabbits at 80 min, whereas a similar decrease was observed only at 140 min in pregnant rabbits. This effect was blocked by lipid infusion. In the basal state the hepatic uptake of FFA was greater in pregnant than in nonpregnant animals. During the hyperinsulinemic clamp the hepatic uptake dropped by approximately 70 and approximately 30% in nonpregnant and pregnant females, respectively. Lipid infusion did not prevent the hepatic FFA uptake and hepatic ketone body output from decreasing. Hepatic glucose production was totally suppressed in the control period in nonpregnant animals but not during lipid infusion (approximately 65%). Hepatic glucose production was not significantly different between pregnant and nonpregnant rabbits during lipid infusion. Glucose utilization was markedly reduced in nonpregnant animals during lipid infusion to levels comparable with that in pregnant animals.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究探讨游离脂肪酸(FFA)升高是否会导致妊娠期肝脏胰岛素抵抗。在18小时禁食并对清醒的未孕和孕兔进行肝门静脉和股动脉慢性插管后,我们对其施加了正常血糖高胰岛素钳夹,钳夹过程中分别进行或不进行脂肪乳剂加肝素输注。使用[3-³H]葡萄糖的首剂量持续输注来测定葡萄糖通量。胰岛素经肠系膜静脉输注140分钟。在孕兔中,基础状态下肝脏对乳酸的净摄取量几乎是非孕兔的两倍。在正常血糖高胰岛素钳夹期间,未孕兔在80分钟时肝脏对乳酸的摄取下降了约65%,而孕兔仅在140分钟时出现类似程度的下降。这种效应被脂质输注所阻断。在基础状态下,孕兔肝脏对FFA的摄取量高于未孕动物。在高胰岛素钳夹期间,未孕和孕兔肝脏对FFA的摄取分别下降了约70%和约30%。脂质输注并未阻止肝脏FFA摄取和肝脏酮体生成的减少。在对照期,未孕动物的肝脏葡萄糖生成完全受到抑制,但在脂质输注期间未完全抑制(约65%)。在脂质输注期间,孕兔和未孕兔的肝脏葡萄糖生成无显著差异。在脂质输注期间,未孕动物的葡萄糖利用率显著降低,降至与孕兔相当的水平。(摘要截断于250字)

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