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哺乳期大鼠过度喂养与短期心血管胰岛素抵抗有关。

Overfeeding During Lactation in Rats is Associated with Cardiovascular Insulin Resistance in the Short-Term.

机构信息

Departamento de Fisiología, Facultad de Medicina, Universidad Autónoma de Madrid, 28029 Madrid, Spain.

Departamento de Ciencias Médicas Básicas, Universidad San Pablo CEU, 28003 Madrid, Spain.

出版信息

Nutrients. 2020 Feb 20;12(2):549. doi: 10.3390/nu12020549.

Abstract

Childhood obesity is associated with metabolic and cardiovascular comorbidities. The development of these alterations may have its origin in early life stages such as the lactation period through metabolic programming. Insulin resistance is a common complication in obese patients and may be responsible for the cardiovascular alterations associated with this condition. This study analyzed the development of cardiovascular insulin resistance in a rat model of childhood overweight induced by overfeeding during the lactation period. On birth day, litters were divided into twelve (L12) or three pups per mother (L3). Overfed rats showed a lower increase in myocardial contractility in response to insulin perfusion and a reduced insulin-induced vasodilation, suggesting a state of cardiovascular insulin resistance. Vascular insulin resistance was due to decreased activation of phosphoinositide 3-kinase (PI3K)/Akt pathway, whereas cardiac insulin resistance was associated with mitogen-activated protein kinase (MAPK) hyperactivity. Early overfeeding was also associated with a proinflammatory and pro-oxidant state; endothelial dysfunction; decreased release of nitrites and nitrates; and decreased gene expression of insulin receptor (IR), glucose transporter-4 (GLUT-4), and endothelial nitric oxide synthase (eNOS) in response to insulin. In conclusion, overweight induced by lactational overnutrition in rat pups is associated with cardiovascular insulin resistance that could be related to the cardiovascular alterations associated with this condition.

摘要

儿童肥胖与代谢和心血管合并症有关。这些改变的发展可能起源于生命早期阶段,如哺乳期通过代谢编程。胰岛素抵抗是肥胖患者的常见并发症,可能是与该病症相关的心血管改变的原因。本研究通过在哺乳期过度喂养诱导的超重大鼠模型中分析了心血管胰岛素抵抗的发展。在出生日,将窝分为每只母鼠 12(L12)或 3 只幼崽(L3)。过度喂养的大鼠对胰岛素灌注的心肌收缩力增加较低,并且胰岛素诱导的血管舒张减少,表明存在心血管胰岛素抵抗。血管胰岛素抵抗是由于磷酸肌醇 3-激酶(PI3K)/ Akt 途径的激活减少所致,而心脏胰岛素抵抗与丝裂原激活蛋白激酶(MAPK)的过度活跃有关。早期过度喂养还与促炎和促氧化状态、内皮功能障碍、亚硝酸盐和硝酸盐释放减少以及胰岛素刺激下胰岛素受体(IR)、葡萄糖转运蛋白-4(GLUT-4)和内皮型一氧化氮合酶(eNOS)的基因表达减少有关。总之,哺乳期过度喂养诱导的幼鼠超重与心血管胰岛素抵抗有关,这可能与该病症相关的心血管改变有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/627a/7071409/4673243d89ac/nutrients-12-00549-g001.jpg

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