Literature DB >> 15948674

Kv1.3 potassium channel blockade as an approach to insulin resistance.

Gary V Desir1.   

Abstract

Diabetes mellitus is a devastating metabolic disease caused by either insulin deficiency or resistance and characterised by abnormal glucose, protein and lipid metabolism. It affects > 150 million people worldwide, 14 million in the US alone (90% Type II and 10% Type I) where it accounts for approximately 15% of healthcare expenditure. Insulin resistance is a cardinal feature of Type II diabetes. The molecular mechanisms that mediate insulin resistance are under intense scrutiny, and a major goal of this effort is to uncover potential therapeutic targets. Recent data indicate that the voltage-gated potassium channel, Kv1.3, is an important regulator of peripheral insulin sensitivity and glucose metabolism. Indeed, Kv1.3 channel inhibition increases insulin sensitivity by decreasing inflammatory cytokines and by facilitating the translocation of GLUT4 to the plasma membrane. In light of these novel findings, the author believes that Kv1.3 is a promising target for the development of drugs useful in the management of insulin resistance and diabetes.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15948674     DOI: 10.1517/14728222.9.3.571

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  8 in total

1.  Targeting the ion channel Kv1.3 with scorpion venom peptides engineered for potency, selectivity, and half-life.

Authors:  Wilson Edwards; Wai-Ping Fung-Leung; Chichi Huang; Ellen Chi; Nancy Wu; Yi Liu; Michael P Maher; Rachelle Bonesteel; Judith Connor; Ross Fellows; Elena Garcia; Jerry Lee; Lu Lu; Karen Ngo; Brian Scott; Hong Zhou; Ronald V Swanson; Alan D Wickenden
Journal:  J Biol Chem       Date:  2014-06-17       Impact factor: 5.157

Review 2.  Analogs of the sea anemone potassium channel blocker ShK for the treatment of autoimmune diseases.

Authors:  Christine Beeton; Michael W Pennington; Raymond S Norton
Journal:  Inflamm Allergy Drug Targets       Date:  2011-10

Review 3.  Kv1.3: a potential pharmacological target for diabetes.

Authors:  Bok Hee Choi; Sang June Hahn
Journal:  Acta Pharmacol Sin       Date:  2010-08-16       Impact factor: 6.150

4.  Specific Kv1.3 blockade modulates key cholesterol-metabolism-associated molecules in human macrophages exposed to ox-LDL.

Authors:  Yong Yang; Yan-Fu Wang; Xiao-Fang Yang; Zhao-Hui Wang; Yi-Tian Lian; Ying Yang; Xiao-Wei Li; Xiang Gao; Jian Chen; Yan-Wen Shu; Long-Xian Cheng; Yu-Hua Liao; Kun Liu
Journal:  J Lipid Res       Date:  2012-10-24       Impact factor: 5.922

Review 5.  HIV-associated neurocognitive disorder: pathogenesis and therapeutic opportunities.

Authors:  Kathryn A Lindl; David R Marks; Dennis L Kolson; Kelly L Jordan-Sciutto
Journal:  J Neuroimmune Pharmacol       Date:  2010-04-16       Impact factor: 4.147

6.  A small-molecule Psora-4 acts as a caloric restriction mimetic to promote longevity in C. elegans.

Authors:  Tesfahun Dessale Admasu; Diogo Barardo; Li Fang Ng; Krishna Chaithanya Batchu; Amaury Cazenave-Gassiot; Markus R Wenk; Jan Gruber
Journal:  Geroscience       Date:  2021-05-14       Impact factor: 7.581

7.  Mitochondrial Ultrastructure and Glucose Signaling Pathways Attributed to the Kv1.3 Ion Channel.

Authors:  Christopher P Kovach; Dolly Al Koborssy; Zhenbo Huang; Brandon M Chelette; James M Fadool; Debra A Fadool
Journal:  Front Physiol       Date:  2016-05-19       Impact factor: 4.566

8.  Serum level of Interleukin-8 in subjects with diabetes, diabetes plus oral lichen planus, and oral lichen planus: A biochemical study.

Authors:  Atefeh Tavangar; Faezeh Khozeimeh; Fereshtehossadat Ghoreishian; Mahsa Abbasi Boroujeni
Journal:  Dent Res J (Isfahan)       Date:  2016-09
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.