期刊
INTERNATIONAL JOURNAL OF OBESITY
卷 27, 期 -, 页码 S49-S52出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.ijo.0802501
关键词
salicylates; diabetes; kinases
资金
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK051729, R01DK045943] Funding Source: NIH RePORTER
- NIDDK NIH HHS [R01 DK45943, R01 DK51729] Funding Source: Medline
Antidiabetic effects associated with salicylates have been known for years, although the underlying mechanisms were not understood. We have been reinvestigating these effects in the light of recent discoveries in the areas of signal transduction and insulin resistance. Our findings showed that signaling pathways leading to IkappaB kinase beta (IKKbeta) and NF-kappaB are activated in insulin-responsive tissues of obese and high-fat-fed animals. Since activation correlates with the development of insulin resistance, we asked whether signaling through this might be involved in the pathogenesis of insulin resistance. Heterozygous gene deletion (Ikkbeta+/-) or salicylates, working as IKKbeta inhibitors, improved insulin sensitivity in insulin-resistant rodent models. Furthermore, high doses of salicylates ( aspirin or salicylate) improved insulin sensitivity in patients with type II diabetes. Our studies implicate an inflammatory process in the pathogenesis of insulin resistance in obesity and type II diabetes mellitus and identify the IKKbeta/ NF-kappaB pathway as a molecular mediator of insulin resistance and pharmacological target for insulin sensitization.
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