Literature DB >> 6345240

Insulin binding and removal by livers of genetically obese rats.

C Karakash, B Jeanrenaud.   

Abstract

Livers from 9-10-wk-old genetically obese and hyperinsulinemic (fa/fa) rats contained more DNA, proteins, and lipids than livers of age-matched controls. Actually, the increase in liver mass of fa/fa rats was mainly due to an increased cell number. On perfusion with insulin (1.75-16 nM), livers of obese fa/fa rats removed 35-40% less insulin per gram tissue than control livers. When calculated on a per organ basis, removal capacity was, however, similar in livers of control and obese fa/fa rats. The binding of 125I-insulin to as well as the insulin removal by isolated hepatocytes was also assessed. Contrary to previous unexpected data in which the downregulation of insulin receptors by hyperinsulinemia was reported not to prevail in hepatocytes from obese fa/fa rats, it was found that the binding capacity of hepatocytes from fa/fa rats was decreased by 45% without alteration of the binding affinity. Moreover, in hepatocytes from obese fa/fa rats, both binding and removal of insulin were lowered to an analogous extent. It is concluded that livers of obese fa/fa rats behave, with regard to insulin binding and removal, as those of other hyperinsulinemic obese animals.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6345240     DOI: 10.2337/diab.32.7.605

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  4 in total

1.  Insulin-dependent changes in subcellular distribution of liver insulin receptors in obese Zucker rats.

Authors:  S López; B Desbuquois; M C Postel-Vinay; C Benelli; M Lavau
Journal:  Diabetologia       Date:  1988-12       Impact factor: 10.122

Review 2.  An hypothesis on the aetiology of obesity: dysfunction of the central nervous system as a primary cause.

Authors:  B Jeanrenaud
Journal:  Diabetologia       Date:  1985-08       Impact factor: 10.122

3.  Identification of radioactive insulin fragments liberated by insulin proteinase during the degradation of semisynthetic [3H]GlyA1]insulin and [3H]PheB1]insulin.

Authors:  J G Davies; A V Muir; K Rose; R E Offord
Journal:  Biochem J       Date:  1988-01-01       Impact factor: 3.857

4.  Class III PI3K regulates organismal glucose homeostasis by providing negative feedback on hepatic insulin signalling.

Authors:  Ivan Nemazanyy; Guillaume Montagnac; Ryan C Russell; Lucille Morzyglod; Anne-Françoise Burnol; Kun-Liang Guan; Mario Pende; Ganna Panasyuk
Journal:  Nat Commun       Date:  2015-09-21       Impact factor: 14.919

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.