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通过胰岛素受体底物蛋白调节胰岛素信号传导和β细胞功能。

Regulating insulin signaling and beta-cell function through IRS proteins.

作者信息

White Morris F

机构信息

Howard Hughes Medical Institute, Division of Endocrinology, Children's Hospital Boston, Harvard Medical School, Karp Family Research Laboratories, Room 4210, 300 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Can J Physiol Pharmacol. 2006 Jul;84(7):725-37. doi: 10.1139/y06-008.

Abstract

Diabetes mellitus is a complex disorder that arises from various causes, including dysregulated glucose sensing and impaired insulin secretion (maturity onset diabetes of youth, MODY), autoimmune-mediated beta-cell destruction (type 1), or insufficient compensation for peripheral insulin resistance (type 2). Type 2 diabetes is the most prevalent form that usually occurs at middle age; it afflicts more than 30 million people over the age of 65, but is appearing with greater frequency in children and adolescents. Dysregulated insulin signaling exacerbated by chronic hyperglycemia promotes a cohort of systemic disorders--including dyslipidemia, hypertension, cardiovascular disease, and female infertility. Understanding the molecular basis of insulin resistance can prevent these disorders and their inevitable progression to type 2 diabetes.

摘要

糖尿病是一种由多种原因引起的复杂疾病,这些原因包括葡萄糖感知失调和胰岛素分泌受损(青年发病的成年型糖尿病,MODY)、自身免疫介导的β细胞破坏(1型糖尿病),或对周围胰岛素抵抗的代偿不足(2型糖尿病)。2型糖尿病是最常见的形式,通常发生在中年;65岁以上的人群中有超过3000万人患有此病,但在儿童和青少年中的发病率也越来越高。慢性高血糖加剧的胰岛素信号失调会引发一系列全身性疾病,包括血脂异常、高血压、心血管疾病和女性不孕。了解胰岛素抵抗的分子基础可以预防这些疾病及其不可避免地发展为2型糖尿病。

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