Literature DB >> 11281851

Current therapies and emerging targets for the treatment of diabetes.

A S Wagman1, J M Nuss.   

Abstract

Concurrent with the spread of the western lifestyle, the prevalence of all types of diabetes is on the rise in the world's population. The number of diabetics is increasing by 4-5% per year with an estimated 40-45% of individual's over the age of 65 years having either type II diabetes or impaired glucose tolerance. Since the signs of diabetes are not immediately obvious, diagnosis can be preceded by an extended period of impaired glucose tolerance resulting in the prevalence of beta-cell dysfunction and macrovascular complications. In addition to increased medical vigilance, diabetes is being combatted through aggressive treatment directed at lowering circulating blood glucose and inhibiting postprandial hyperglycemic spikes. Current strategies to treat diabetes include reducing insulin resistance using glitazones, supplementing insulin supplies with exogenous insulin, increasing endogenous insulin production with sulfonylureas and meglitinides, reducing hepatic glucose production through biguanides, and limiting postprandial glucose absorption with alpha-glucosidase inhibitors. In all of these areas, new generations of small molecules are being investigated which exhibit improved efficacy and safety profiles. Promising biological targets are also emerging such as (1) insulin sensitizers including protein tyrosine phosphatase-1B (PTP-1B) and glycogen synthase kinase 3 (GSK3), (2) inhibitors of gluconeogenesis like pyruvate dehydrogenase kinase (PDH) inhibitors, (3) lipolysis inhibitors, (4) fat oxidation including carnitine palmitoyltransferase (CPT) I and II inhibitors, and (5) energy expenditure by means of beta 3-adrenoceptor agonists. Also important are alternative routes of glucose disposal such as Na+-glucose cotransporter (SGLT) inhibitors, combination therapies, and the treatment of diabetic complications (eg. retinopathy, nephropathy, and neuropathy). With may new opportunities for drug discovery, the prospects are excellent for development of innovative therapies to effectively manage diabetes and prevent its long term complications. This review highlights recent (1997-2000) advances in diabetes therapy and research with an emphasis on small molecule drug design (275 references).

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Year:  2001        PMID: 11281851     DOI: 10.2174/1381612013397915

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  27 in total

1.  Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation.

Authors:  Mario O Salazar; Oscar Micheloni; Andrea M Escalante; Ricardo L E Furlan
Journal:  Mol Divers       Date:  2011-01-06       Impact factor: 2.943

Review 2.  Structural insight into function and regulation of carnitine palmitoyltransferase.

Authors:  Arne C Rufer; Ralf Thoma; Michael Hennig
Journal:  Cell Mol Life Sci       Date:  2009-05-09       Impact factor: 9.261

3.  Tissue-specific kinase expression and activity regulate flux through the pyruvate dehydrogenase complex.

Authors:  Alla Klyuyeva; Alina Tuganova; Natalia Kedishvili; Kirill M Popov
Journal:  J Biol Chem       Date:  2018-11-27       Impact factor: 5.157

4.  Radiosynthesis and in Vivo Evaluation of [11C]A1070722, a High Affinity GSK-3 PET Tracer in Primate Brain.

Authors:  Jaya Prabhakaran; Francesca Zanderigo; Kiran Kumar Solingapuram Sai; Harry Rubin-Falcone; Matthew J Jorgensen; Jay R Kaplan; Akiva Mintz; J John Mann; J S Dileep Kumar
Journal:  ACS Chem Neurosci       Date:  2017-05-17       Impact factor: 4.418

Review 5.  Turning glucosuria into a therapy: Efficacy and safety with SGLT2 inhibitors.

Authors:  Anupa K Patel; Vivian Fonseca
Journal:  Curr Diab Rep       Date:  2010-04       Impact factor: 4.810

6.  Molecular dynamic simulations reveal the mechanism of binding between xanthine inhibitors and DPP-4.

Authors:  Yongliang Gu; Wei Wang; Xiaolei Zhu; Keke Dong
Journal:  J Mol Model       Date:  2014-01-31       Impact factor: 1.810

7.  Comparative docking assessment of glucokinase interactions with its allosteric activators.

Authors:  Vandana Kumari; Chenglong Li
Journal:  Curr Chem Genomics       Date:  2008-12-30

8.  Evaluation of the utility of homology models in high throughput docking.

Authors:  Philippe Ferrara; Edgar Jacoby
Journal:  J Mol Model       Date:  2007-05-09       Impact factor: 1.810

9.  Discovery and functional characterization of a novel small molecule inhibitor of the intracellular phosphatase, SHIP2.

Authors:  A Suwa; T Yamamoto; A Sawada; K Minoura; N Hosogai; A Tahara; T Kurama; T Shimokawa; I Aramori
Journal:  Br J Pharmacol       Date:  2009-08-19       Impact factor: 8.739

Review 10.  Inhibition of the insulin-like growth factor-1 receptor (IGF1R) tyrosine kinase as a novel cancer therapy approach.

Authors:  Rongshi Li; Alan Pourpak; Stephan W Morris
Journal:  J Med Chem       Date:  2009-08-27       Impact factor: 7.446

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