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  2. Effects of N-adamantyl-4-methylthiazol-2-amine on hyperglycemia, hyperlipidemia and oxidative stress in streptozotocin-induced diabetic rats

Effects of N-adamantyl-4-methylthiazol-2-amine on hyperglycemia, hyperlipidemia and oxidative stress in streptozotocin-induced diabetic rats

  • Eur J Pharmacol. 2014 Aug 5:736:26-34. doi: 10.1016/j.ejphar.2014.04.031.
Seung-Ju Yang 1 Woo Je Lee 2 Eun-A Kim 3 Kee Dal Nam 4 Hoh-Gyu Hahn 4 Soo Young Choi 5 Sung-Woo Cho 6
Affiliations

Affiliations

  • 1 Department of Biomedical Laboratory Science, Konyang University, Daejeon 302-718, Republic of Korea.
  • 2 Department of Internal Medicine, University of Ulsan College of Medicine, Seoul 138-736, Republic of Korea.
  • 3 Department of Biochemistry and Molecular Biology, University of Ulsan College of Medicine, 88 Olympic-Ro 43-Gil, Songpa-gu, Seoul 138-736, Republic of Korea.
  • 4 Chemical Kinomics Research Center, Korea Institute of Science and Technology, Seoul 136-791, Korea.
  • 5 Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University, Chuncheon 200-702, Republic of Korea.
  • 6 Department of Biochemistry and Molecular Biology, University of Ulsan College of Medicine, 88 Olympic-Ro 43-Gil, Songpa-gu, Seoul 138-736, Republic of Korea. Electronic address: swcho@amc.seoul.kr.
Abstract

Thiazole derivatives are attractive candidates for drug development because they can be efficiently synthesized and are active against a number of diseases and conditions, including diabetes. In our present study, we investigated the anti-inflammatory and antioxidant properties of N-adamantyl-4-methylthiazol-2-amine (KHG26693), a new thiazole derivative, in a streptozotocin (STZ)-induced model of diabetes mellitus. STZ-induced diabetic rats were intraperitoneally administered KHG26693 (3mg/kg-body weight/day) for 4 weeks. KHG26693 administration significantly decreased blood glucose, triglycerides, and Cholesterol and increased Insulin. KHG26693 also suppressed several inflammatory responses in STZ-induced diabetic rats, as evidenced by decreased levels of serum tumor necrosis factor-α, interleukin-1β, and nitric oxide. Additionally, KHG26693 significantly modulated hepatic lipid peroxidation, catalase and superoxide dismutase activity, and the nonenzymatic antioxidant status (e.g., Vitamins C and E), and reduced the glutathione content. These anti-inflammatory/antioxidative actions occurred as a result of the downregulation of inducible nitric oxide synthase and nuclear factor-kappa B. Taken together, our results suggest that KHG26693 successfully reduces the production of oxidative stress in STZ-induced diabetic rats by regulating the oxidation-reduction system, specifically increasing antioxidant capacity. Furthermore, KHG26693 treatment significantly reverted the key Enzymes of glucose metabolism, such as Glucokinase, glucose-6-phosphatase, glycogen synthase, glycogen phosphorylase, and fructose-1,6-bisphosphatase, to near-normal levels in liver tissues. These results indicate that KHG26693 normalizes disturbed glucose metabolism by enhancing glucose utilization and decreasing liver glucose production via Insulin release, suggesting the possibility of future diabetes treatments.

Keywords

Antioxidant; Diabetes; Inflammation; Oxidative stress; Thiazole derivative.

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