Literature DB >> 11684411

Insulin resistance: a phosphorylation-based uncoupling of insulin signaling.

Y Zick.   

Abstract

Insulin resistance refers to a decreased capacity of circulating insulin to regulate nutrient metabolism. It is associated with the development of type 2 diabetes--an ever-increasing epidemic of the 21st century. Recent studies reveal that agents that induce insulin resistance exploit phosphorylation-based negative-feedback control mechanisms, otherwise utilized by insulin itself, to uncouple the insulin receptor from its downstream effectors and thereby terminate insulin signal transduction. This article describes recent findings that present novel viewpoints of the molecular basis of insulin resistance, focusing on the cardinal role of Ser/Thr protein kinases as emerging key players in this arena.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11684411     DOI: 10.1016/s0962-8924(01)02129-8

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  79 in total

1.  IRS1 degradation and increased serine phosphorylation cannot predict the degree of metabolic insulin resistance induced by oxidative stress.

Authors:  R Potashnik; A Bloch-Damti; N Bashan; A Rudich
Journal:  Diabetologia       Date:  2003-05-15       Impact factor: 10.122

Review 2.  Molecular mechanism of insulin resistance.

Authors:  Samir Bhattacharya; Debleena Dey; Sib Sankar Roy
Journal:  J Biosci       Date:  2007-03       Impact factor: 1.826

3.  Physical exercise reduces pyruvate carboxylase (PCB) and contributes to hyperglycemia reduction in obese mice.

Authors:  Vitor Rosetto Muñoz; Rafael Calais Gaspar; Barbara Moreira Crisol; Guilherme Pedron Formigari; Marcella Ramos Sant'Ana; José Diego Botezelli; Rodrigo Stellzer Gaspar; Adelino S R da Silva; Dennys Esper Cintra; Leandro Pereira de Moura; Eduardo Rochete Ropelle; José Rodrigo Pauli
Journal:  J Physiol Sci       Date:  2017-07-14       Impact factor: 2.781

4.  Mechanism of feedback regulation of insulin receptor substrate-1 phosphorylation in primary adipocytes.

Authors:  Ingeborg Hers; Jeremy M Tavaré
Journal:  Biochem J       Date:  2005-06-01       Impact factor: 3.857

5.  Phosphoinositide 3-kinase catalytic subunit deletion and regulatory subunit deletion have opposite effects on insulin sensitivity in mice.

Authors:  Saskia M Brachmann; Kohjiro Ueki; Jeffrey A Engelman; Ronald C Kahn; Lewis C Cantley
Journal:  Mol Cell Biol       Date:  2005-03       Impact factor: 4.272

6.  Burn injury-induced IRS-1 degradation in mouse skeletal muscle.

Authors:  X-M Lu; Rg Tompkins; Aj Fischman
Journal:  Int J Burns Trauma       Date:  2013-01-24

7.  Serine phosphorylation proximal to its phosphotyrosine binding domain inhibits insulin receptor substrate 1 function and promotes insulin resistance.

Authors:  Yan-Fang Liu; Avia Herschkovitz; Sigalit Boura-Halfon; Denise Ronen; Keren Paz; Derek Leroith; Yehiel Zick
Journal:  Mol Cell Biol       Date:  2004-11       Impact factor: 4.272

8.  Brain-derived neurotrophic factor-dependent synaptic plasticity is suppressed by interleukin-1β via p38 mitogen-activated protein kinase.

Authors:  Liqi Tong; G Aleph Prieto; Enikö A Kramár; Erica D Smith; David H Cribbs; Gary Lynch; Carl W Cotman
Journal:  J Neurosci       Date:  2012-12-05       Impact factor: 6.167

Review 9.  Metabolic implications of severe burn injuries and their management: a systematic review of the literature.

Authors:  Bishara S Atiyeh; S William A Gunn; Saad A Dibo
Journal:  World J Surg       Date:  2008-08       Impact factor: 3.352

10.  Protein kinase C-zeta phosphorylates insulin receptor substrate-1, -3, and -4 but not -2: isoform specific determinants of specificity in insulin signaling.

Authors:  Sihoon Lee; Edward G Lynn; Jeong-A Kim; Michael J Quon
Journal:  Endocrinology       Date:  2008-01-17       Impact factor: 4.736

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.