Literature DB >> 15734724

A nonspecific phosphotyrosine phosphatase inhibitor, bis(maltolato)oxovanadium(IV), improves glucose tolerance and prevents diabetes in Zucker diabetic fatty rats.

Carol L Winter1, Jana S Lange, Michael G Davis, Gina S Gerwe, Thomas R Downs, Kevin G Peters, Bhavani Kasibhatla.   

Abstract

The molecular basis of insulin resistance, a major risk factor for development of Type II diabetes, involves defective insulin signaling. Insulin-mediated signal transduction is negatively regulated by the phosphotyrosine phosphatase, PTP1B, and numerous studies have demonstrated that organo-vanadium compounds, which are nonselective phosphotyrosine phosphatase inhibitors, have insulin-mimetic properties. However, whether or not vanadium compounds can prevent the transition from insulin resistance to overt diabetes is unknown. We compared the ability of bis(maltolato)oxovanadium(IV) (BMOV), an orally bioavailable organo-vanadium compound, and rosiglitazone maleate (RSG), a known insulin sensitizer, to prevent development of diabetes in Zucker diabetic fatty (ZDF) rats. Treatment began at 6 weeks of age when animals are insulin resistant and hyperinsulinemic, but not yet hyperglycemic, and ended at 12 weeks of age, which is 4 weeks after ZDF rats typically develop overt diabetes. BMOV-treated ZDF rats did not develop hyperglycemia, showed significant improvement in insulin sensitivity, and retained normal pancreatic islet morphology and endocrine cell distribution, similar to RSG-treated animals. BMOV and RSG treatment also prevented the hyper-phagia and polydipsia present in untreated ZDF rats; however, BMOV-treated ZDF rats gained much less weight than did RSG-treated animals. Circulating levels of adiponectin decreased in untreated ZDF rats compared to lean controls, but these levels remained normal in BMOV-treated ZDF rats. In contrast, in RSG-treated ZDF rats, plasma adiponectin levels were nearly 4-fold higher than in lean control rats, primarily as a result of a large increase in the amount of low-molecular weight forms of adiponectin in circulation. These data demonstrate that phosphatase inhibition offers a new approach to diabetes prevention, one that may have advantages over current approaches.

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Year:  2005        PMID: 15734724     DOI: 10.1177/153537020523000307

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


  11 in total

Review 1.  Protein phosphatases in pancreatic islets.

Authors:  Henrik Ortsäter; Nina Grankvist; Richard E Honkanen; Åke Sjöholm
Journal:  J Endocrinol       Date:  2014-03-28       Impact factor: 4.286

2.  Inhibition of protein tyrosine phosphatases enhances cerebral collateral growth in rats.

Authors:  Ivo Buschmann; Daniel Hackbusch; Nora Gatzke; André Dülsner; Manuela Trappiel; Markus Dagnell; Arne Ostman; Rob Hooft van Huijsduijnen; Kai Kappert
Journal:  J Mol Med (Berl)       Date:  2014-05-27       Impact factor: 4.599

3.  Effect of vanadate on gene expression of the insulin signaling pathway in skeletal muscle of streptozotocin-induced diabetic rats.

Authors:  Dan Wei; Ming Li; Wenjun Ding
Journal:  J Biol Inorg Chem       Date:  2007-09-14       Impact factor: 3.358

4.  Ternary oxovanadium(IV) complexes of ONO-donor Schiff base and polypyridyl derivatives as protein tyrosine phosphatase inhibitors: synthesis, characterization, and biological activities.

Authors:  Caixia Yuan; Liping Lu; Xiaoli Gao; Yanbo Wu; Maolin Guo; Ying Li; Xueqi Fu; Miaoli Zhu
Journal:  J Biol Inorg Chem       Date:  2009-03-17       Impact factor: 3.358

5.  Deletion of protein tyrosine phosphatase 1b improves peripheral insulin resistance and vascular function in obese, leptin-resistant mice via reduced oxidant tone.

Authors:  M Irfan Ali; Pimonrat Ketsawatsomkron; Eric J Belin de Chantemele; James D Mintz; Kenjiro Muta; Christina Salet; Stephen M Black; Michel L Tremblay; David J Fulton; Mario B Marrero; David W Stepp
Journal:  Circ Res       Date:  2009-09-24       Impact factor: 17.367

6.  Inhibition of protein tyrosine phosphatase-1B with antisense oligonucleotides improves insulin sensitivity and increases adiponectin concentrations in monkeys.

Authors:  Michael M Swarbrick; Peter J Havel; Arthur A Levin; Andrew A Bremer; Kimber L Stanhope; Madeline Butler; Sheri L Booten; James L Graham; Robert A McKay; Susan F Murray; Lynnetta M Watts; Brett P Monia; Sanjay Bhanot
Journal:  Endocrinology       Date:  2009-01-22       Impact factor: 4.736

7.  Inhibition of protein tyrosine phosphatase improves angiogenesis via enhancing Ang-1/Tie-2 signaling in diabetes.

Authors:  Jian-Xiong Chen; Qinhui Tuo; Duan-Fang Liao; Heng Zeng
Journal:  Exp Diabetes Res       Date:  2012-02-12

8.  Bis(maltolato)oxovanadium(IV) Induces Angiogenesis via Phosphorylation of VEGFR2.

Authors:  Laura Parma; Hendrika A B Peters; Maria E Johansson; Saray Gutiérrez; Henk Meijerink; Sjef de Kimpe; Margreet R de Vries; Paul H A Quax
Journal:  Int J Mol Sci       Date:  2020-06-30       Impact factor: 5.923

9.  Inhibition of Src homology 2 domain-containing phosphatase 1 increases insulin sensitivity in high-fat diet-induced insulin-resistant mice.

Authors:  Janine Krüger; Ernst Wellnhofer; Heike Meyborg; Philipp Stawowy; Arne Östman; Ulrich Kintscher; Kai Kappert
Journal:  FEBS Open Bio       Date:  2016-01-04       Impact factor: 2.693

10.  High T3 Induces β-Cell Insulin Resistance via Endoplasmic Reticulum Stress.

Authors:  Bo Liang; Liyun Liu; Huibin Huang; Liangyi Li; Jingxiong Zhou
Journal:  Mediators Inflamm       Date:  2020-07-22       Impact factor: 4.711

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