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Effects of ferulic acid on diabetic nephropathy in a rat model of type 2 diabetes

Authors
Choi, RanKim, Bo HwanNaowaboot, JarinyapornLee, Mi YoungHyun, Mi RiCho, Eun JuLee, Eun SooLee, Eun YoungYang, Young ChulChung, Choon Hee
Issue Date
31-Dec-2011
Publisher
생화학분자생물학회
Keywords
diabetes mellitus; experimental; diabetic nephropathies; ferulic acid; inflammation; oxidative stress
Citation
Experimental & Molecular Medicine, v.43, no.12, pp 676 - 683
Pages
8
Journal Title
Experimental & Molecular Medicine
Volume
43
Number
12
Start Page
676
End Page
683
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/16001
DOI
10.3858/emm.2011.43.12.078
ISSN
1226-3613
2092-6413
Abstract
Diabetic nephropathy is the most serious complication in diabetes mellitus. It is known that oxidative stress and inflammation play a central role in the development of diabetic nephropathy. In this study, we investigated that ferulic acid (FA) known as anti-oxidative agent could effect on diabetic nephropathy by anti-oxidative and anti-inflammatory mechanism. We examined the effects of FA in obese diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) rats and non-diabetic control Long-Evans Tokushima Otsuka (LETO) rats. We treated FA to experimental rats from 26 to 45 weeks of age. We evaluated ACR, MDA and MCP-1 in 24 h urine and examined renal histopathology and morphologic change in extracted kidneys from rats. Also, we evaluated the ROS production and MCP-1 levels in cultured podocyte after FA treatment. In the FA-treated OLETF rats, blood glucose was significantly decreased and serum adiponectin levels were increased. Urinary ACR was significantly reduced in FA-treated OLETF rats compared with diabetic OLETF rats. In renal histopathology, FA-treated OLETF rats showed decreased glomerular basement membrane thickness, glomerular volume, and mesangial matrix expansion. FA treatment decreased oxidative stress markers and MCP-1 levels in 24 h urine of rats and supernatants of cultured podocyte. In conclusion, it was suggested that FA have protective and therapeutic effects on diabetic nephropathy by reducing oxidative stress and inflammation.
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