alpha 7-Nicotinic Acetylcholine Receptor Agonist Ameliorates Nicotine Plus High-Fat Diet-Induced Hepatic Steatosis in Male Mice by Inhibiting Oxidative Stress and Stimulating AMPK Signaling

التفاصيل البيبلوغرافية
العنوان: alpha 7-Nicotinic Acetylcholine Receptor Agonist Ameliorates Nicotine Plus High-Fat Diet-Induced Hepatic Steatosis in Male Mice by Inhibiting Oxidative Stress and Stimulating AMPK Signaling
المؤلفون: Hasan, MK, Friedman, TC, Sims, C, Lee, DL, Espinoza-Derout, J, Ume, A, Chalfant, V, Lee, ML, Sinha-Hikim, I, Lutfy, K, Liu, Y, Mahata, SK, Sinha-Hikim, AP
المصدر: Hasan, MK; Friedman, TC; Sims, C; Lee, DL; Espinoza-Derout, J; Ume, A; et al.(2018). alpha 7-Nicotinic Acetylcholine Receptor Agonist Ameliorates Nicotine Plus High-Fat Diet-Induced Hepatic Steatosis in Male Mice by Inhibiting Oxidative Stress and Stimulating AMPK Signaling. ENDOCRINOLOGY, 159(2), 931-944. doi: 10.1210/en.2017-00594. UC Office of the President: Tobacco-Related Disease Research Program. Retrieved from: http://www.escholarship.org/uc/item/9qc962kh
بيانات النشر: eScholarship, University of California, 2018.
سنة النشر: 2018
مصطلحات موضوعية: Male, Nicotine, alpha7 Nicotinic Acetylcholine Receptor, Mice, Obese, AMP-Activated Protein Kinases, Diet, High-Fat, Mice, Inbred C57BL, Fatty Liver, Mice, Oxidative Stress, Bridged Bicyclo Compounds, Benzamides, Animals, Signal Transduction
الوصف: α7-Nicotinic acetylcholine receptor (α7nAChR) agonists confer protection against a wide variety of cytotoxic insults and suppress oxidative stress and apoptosis in various cell systems, including hepatocytes. We recently demonstrated that nicotine, when combined with a high-fat diet (HFD), triggers oxidative stress, activates hepatocyte apoptosis, and exacerbates HFD-induced hepatic steatosis in male mice. This study evaluates whether PNU-282987 (PNU), a specific α7nAChR agonist, is effective in preventing nicotine plus HFD-induced hepatic steatosis. Adult C57BL6 male mice were fed a normal chow diet or HFD with 60% of calories derived from fat and received twice-daily intraperitoneal injections of 0.75 mg/kg body weight (BW) of nicotine, PNU (0.26 mg/kg BW), PNU plus nicotine, or saline for 10 weeks. PNU treatment was effective in attenuating nicotine plus HFD-induced increase in hepatic triglyceride levels, hepatocyte apoptosis, and hepatic steatosis. The preventive effects of PNU on nicotine plus HFD-induced hepatic steatosis were mediated by suppression of oxidative stress and activation of adenosine 5'-monophosphate-activated protein kinase (AMPK) together with inhibition of its downstream target sterol regulatory element binding protein 1c (SREBP1c), fatty acid synthase (FAS), and acetyl-coenzyme A-carboxylase (ACC). We conclude that the α7nAChR agonist PNU protects against nicotine plus HFD-induced hepatic steatosis in obese mice. PNU appears to work at various steps of signaling pathways involving suppression of oxidative stress, activation of AMPK, and inhibition of SREBP1c, FAS, and ACC. α7nAChR agonists may be an effective therapeutic strategy for ameliorating fatty liver disease, especially in obese smokers.
وصف الملف: application/pdf
اللغة: English
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_______325::bc479d12bc01c03a0b19a20ee4f8dfba
http://www.escholarship.org/uc/item/9qc962kh
حقوق: OPEN
رقم الأكسشن: edsair.od.......325..bc479d12bc01c03a0b19a20ee4f8dfba
قاعدة البيانات: OpenAIRE