Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese Mice

Obesity-associated hyperglycemia underlies insulin resistance, glucose intolerance, and related metabolic disorders including type 2 diabetes, renal damage, and nonalcoholic fatty liver disease. Turmeric root is commonly used in Asia, and curcumin, one of its pharmacological components, can play a r...

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Main Authors: Geng-Ruei Chang, Wen-Tsong Hsieh, Lan-Szu Chou, Chen-Si Lin, Ching-Fen Wu, Jen-Wei Lin, Wei-Li Lin, Tzu-Chun Lin, Huei-Jyuan Liao, Chen-Yung Kao, Chuen-Fu Lin
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Processes
Subjects:
Online Access:https://www.mdpi.com/2227-9717/9/7/1132
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spelling doaj-fe3952678454484d848f0eb79af806452021-07-23T14:03:04ZengMDPI AGProcesses2227-97172021-06-0191132113210.3390/pr9071132Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese MiceGeng-Ruei Chang0Wen-Tsong Hsieh1Lan-Szu Chou2Chen-Si Lin3Ching-Fen Wu4Jen-Wei Lin5Wei-Li Lin6Tzu-Chun Lin7Huei-Jyuan Liao8Chen-Yung Kao9Chuen-Fu Lin10Department of Veterinary Medicine, National Chiayi University, 580 Xinmin Road, Chiayi 60054, TaiwanDepartment of Pharmacology, China Medical University, 91 Hsueh-Shih Road, Taichung 404333, TaiwanDepartment of BioAgricultural Sciences, National Chiayi University, 300 Syuefu Road, Chiayi 60004, TaiwanSchool of Veterinary Medicine, National Taiwan University, 4 Section, 1 Roosevelt Road, Taipei 10617, TaiwanDepartment of Veterinary Medicine, National Chiayi University, 580 Xinmin Road, Chiayi 60054, TaiwanBachelor Degree Program in Animal Healthcare, Hungkuang University, 6 Section, 1018 Taiwan Boulevard, Shalu District, Taichung 433304, TaiwanBachelor Degree Program in Animal Healthcare, Hungkuang University, 6 Section, 1018 Taiwan Boulevard, Shalu District, Taichung 433304, TaiwanDepartment of Veterinary Medicine, National Chiayi University, 580 Xinmin Road, Chiayi 60054, TaiwanDepartment of Veterinary Medicine, National Chiayi University, 580 Xinmin Road, Chiayi 60054, TaiwanDepartment of Veterinary Medicine, National Chiayi University, 580 Xinmin Road, Chiayi 60054, TaiwanDepartment of Veterinary Medicine, College of Veterinary Medicine, National Pingtung University of Science and Technology, 1, Shuefu Road, Neipu, Pingtung 912301, TaiwanObesity-associated hyperglycemia underlies insulin resistance, glucose intolerance, and related metabolic disorders including type 2 diabetes, renal damage, and nonalcoholic fatty liver disease. Turmeric root is commonly used in Asia, and curcumin, one of its pharmacological components, can play a role in preventing and treating certain chronic physiological disorders. Accordingly, this study examined how high-fat diet (HFD)-induced hyperglycemia and hyperlipidemia are reduced by curcumin through changes in fatty liver scores, chromium distribution, and renal injury in mice. Relative to the control group, also fed an HFD, the curcumin group weighed less and had smaller adipocytes; it also had lower daily food efficiency, blood urea nitrogen and creatinine levels, serum alanine aminotransferase and aspartate aminotransferase levels, serum and hepatic triglyceride levels, and hepatic lipid regulation marker expression. The curcumin-treated obese group exhibited significantly lower fasting blood glucose, was less glucose intolerant, had higher Akt phosphorylation and glucose transporter 4 (GLUT4) expression, and had greater serum insulin levels. Moreover, the group showed renal damage with lower TNF-α expression along with more numerous renal antioxidative enzymes that included superoxide dismutase, glutathione peroxidase, and catalase. The liver histology of the curcumin-treated obese mice showed superior lipid infiltration and fewer FASN and PNPLA3 proteins in comparison with the control mice. Curcumin contributed to creating a positive chromium balance by decreasing the amount of chromium lost through urine, leading to the chromium mobilization needed to mitigate hyperglycemia. Thus, the results suggest that curcumin prevents HFD-induced glucose intolerance, kidney injury, and nonalcoholic fatty liver disease.https://www.mdpi.com/2227-9717/9/7/1132curcuminchromiumfatty liverglucose intolerancerenal injuryobesity
collection DOAJ
language English
format Article
sources DOAJ
author Geng-Ruei Chang
Wen-Tsong Hsieh
Lan-Szu Chou
Chen-Si Lin
Ching-Fen Wu
Jen-Wei Lin
Wei-Li Lin
Tzu-Chun Lin
Huei-Jyuan Liao
Chen-Yung Kao
Chuen-Fu Lin
spellingShingle Geng-Ruei Chang
Wen-Tsong Hsieh
Lan-Szu Chou
Chen-Si Lin
Ching-Fen Wu
Jen-Wei Lin
Wei-Li Lin
Tzu-Chun Lin
Huei-Jyuan Liao
Chen-Yung Kao
Chuen-Fu Lin
Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese Mice
Processes
curcumin
chromium
fatty liver
glucose intolerance
renal injury
obesity
author_facet Geng-Ruei Chang
Wen-Tsong Hsieh
Lan-Szu Chou
Chen-Si Lin
Ching-Fen Wu
Jen-Wei Lin
Wei-Li Lin
Tzu-Chun Lin
Huei-Jyuan Liao
Chen-Yung Kao
Chuen-Fu Lin
author_sort Geng-Ruei Chang
title Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese Mice
title_short Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese Mice
title_full Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese Mice
title_fullStr Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese Mice
title_full_unstemmed Curcumin Improved Glucose Intolerance, Renal Injury, and Nonalcoholic Fatty Liver Disease and Decreased Chromium Loss through Urine in Obese Mice
title_sort curcumin improved glucose intolerance, renal injury, and nonalcoholic fatty liver disease and decreased chromium loss through urine in obese mice
publisher MDPI AG
series Processes
issn 2227-9717
publishDate 2021-06-01
description Obesity-associated hyperglycemia underlies insulin resistance, glucose intolerance, and related metabolic disorders including type 2 diabetes, renal damage, and nonalcoholic fatty liver disease. Turmeric root is commonly used in Asia, and curcumin, one of its pharmacological components, can play a role in preventing and treating certain chronic physiological disorders. Accordingly, this study examined how high-fat diet (HFD)-induced hyperglycemia and hyperlipidemia are reduced by curcumin through changes in fatty liver scores, chromium distribution, and renal injury in mice. Relative to the control group, also fed an HFD, the curcumin group weighed less and had smaller adipocytes; it also had lower daily food efficiency, blood urea nitrogen and creatinine levels, serum alanine aminotransferase and aspartate aminotransferase levels, serum and hepatic triglyceride levels, and hepatic lipid regulation marker expression. The curcumin-treated obese group exhibited significantly lower fasting blood glucose, was less glucose intolerant, had higher Akt phosphorylation and glucose transporter 4 (GLUT4) expression, and had greater serum insulin levels. Moreover, the group showed renal damage with lower TNF-α expression along with more numerous renal antioxidative enzymes that included superoxide dismutase, glutathione peroxidase, and catalase. The liver histology of the curcumin-treated obese mice showed superior lipid infiltration and fewer FASN and PNPLA3 proteins in comparison with the control mice. Curcumin contributed to creating a positive chromium balance by decreasing the amount of chromium lost through urine, leading to the chromium mobilization needed to mitigate hyperglycemia. Thus, the results suggest that curcumin prevents HFD-induced glucose intolerance, kidney injury, and nonalcoholic fatty liver disease.
topic curcumin
chromium
fatty liver
glucose intolerance
renal injury
obesity
url https://www.mdpi.com/2227-9717/9/7/1132
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