Thiamine supplementation modulates oxidative stress by inhibiting hepatic adenosine diphosphate (ADP)-ribosylation in obese diabetic rats
Author:
Affiliation:
1. Department of Pharmacotherapeutics, Osaka University of Pharmaceutical Sciences
Publisher
Japanese Society of Toxicology
Link
https://www.jstage.jst.go.jp/article/fts/6/1/6_1/_pdf
Reference51 articles.
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2. Adams, L.A. and Angulo, P. (2005): Recent concepts in non-alcoholic fatty liver disease. Diabet. Med., 22, 1129-1133.
3. Adams, L.A. (2007): Nonalcoholic fatty liver disease and diabetes mellitus. Endocr. Res., 32, 59-69.
4. Alkhalidy, H., Moore, W., Wang, A., Luo, J., McMillan, R.P., Wang, Y., Zhen, W., Hulver, M.W. and Liu, D. (2018): Kaempferol ameliorates hyperglycemia through suppressing hepatic gluconeogenesis and enhancing hepatic insulin sensitivity in diet-induced obese mice. J. Nutr. Biochem., 58, 90-101.
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2. Blood thiamine pyrophosphate concentration and its correlation with the stage of diabetic retinopathy;International Ophthalmology;2020-07-26
3. Obesity-related hypertension and enhanced plasma orexin-A level are attenuated by the consumption of thiamine water in diabetic rats under cerebral oxidative stress conditions;Fundamental Toxicological Sciences;2019
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