Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic rats

Objective: To determine the effects of syringic acid on hepatic damage in diabetic rats. Methods: Diabetes was induced by streptozotocin. Diabetic rats were given syringic acid at doses of 25, 50 and 100 mg/kg by oral gavage for 6 weeks. Syringic acid effects on the liver were evaluated by examinati...

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Main Authors: Zahra Sabahi, Mohammad Javad Khoshnoud, Bahman Khalvati, Seyedeh-Sara Hashemi, Zahra Ghasempour Farsani, Hoda Mogholi Gerashi, Marzieh Rashedinia
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Asian Pacific Journal of Tropical Biomedicine
Subjects:
Online Access:http://www.apjtb.org/article.asp?issn=2221-1691;year=2020;volume=10;issue=3;spage=111;epage=119;aulast=Sabahi
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author Zahra Sabahi
Mohammad Javad Khoshnoud
Bahman Khalvati
Seyedeh-Sara Hashemi
Zahra Ghasempour Farsani
Hoda Mogholi Gerashi
Marzieh Rashedinia
author_facet Zahra Sabahi
Mohammad Javad Khoshnoud
Bahman Khalvati
Seyedeh-Sara Hashemi
Zahra Ghasempour Farsani
Hoda Mogholi Gerashi
Marzieh Rashedinia
author_sort Zahra Sabahi
collection DOAJ
description Objective: To determine the effects of syringic acid on hepatic damage in diabetic rats. Methods: Diabetes was induced by streptozotocin. Diabetic rats were given syringic acid at doses of 25, 50 and 100 mg/kg by oral gavage for 6 weeks. Syringic acid effects on the liver were evaluated by examination of plasma biochemical parameters, and pathological study. In addition, biomarkers of lipid peroxidation and antioxidant status of liver tissues were assessed. Real time-PCR was performed to investigate the mRNA expression levels of mitochondrial biogenesis indices in different groups. Results: Syringic acid significantly attenuated the increase in most of plasma biochemical parameters in diabetic rats. Moreover, syringic acid treatment increased the catalase activity while it reduced the superoxide dismutase activity and hepatic malondialdehyde level in diabetic rats. There was no difference between the glutathione content of the treated and untreated groups. These findings were supported by alleviation of histopathological damages in the syringic acid-treated groups compared to the untreated diabetic group. Syringic acid also significantly up-regulated the hepatic mRNA expression of PGC-1a, NRF-1, and NRF-2 and increased the mtDNA/nDNA ratio in diabetic rats. Conclusions: Syringic acid can be considered as a suitable candidate against hepatic complications since it can reduce oxidative damages in diabetic cases. Furthermore, it has the potential of targeting hepatic mitochondria in diabetes.
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spelling doaj.art-84c3d8c0aa8f4f70952c003a32116e182022-12-21T19:40:39ZengWolters Kluwer Medknow PublicationsAsian Pacific Journal of Tropical Biomedicine2588-92222020-01-0110311111910.4103/2221-1691.276317Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic ratsZahra SabahiMohammad Javad KhoshnoudBahman KhalvatiSeyedeh-Sara HashemiZahra Ghasempour FarsaniHoda Mogholi GerashiMarzieh RashediniaObjective: To determine the effects of syringic acid on hepatic damage in diabetic rats. Methods: Diabetes was induced by streptozotocin. Diabetic rats were given syringic acid at doses of 25, 50 and 100 mg/kg by oral gavage for 6 weeks. Syringic acid effects on the liver were evaluated by examination of plasma biochemical parameters, and pathological study. In addition, biomarkers of lipid peroxidation and antioxidant status of liver tissues were assessed. Real time-PCR was performed to investigate the mRNA expression levels of mitochondrial biogenesis indices in different groups. Results: Syringic acid significantly attenuated the increase in most of plasma biochemical parameters in diabetic rats. Moreover, syringic acid treatment increased the catalase activity while it reduced the superoxide dismutase activity and hepatic malondialdehyde level in diabetic rats. There was no difference between the glutathione content of the treated and untreated groups. These findings were supported by alleviation of histopathological damages in the syringic acid-treated groups compared to the untreated diabetic group. Syringic acid also significantly up-regulated the hepatic mRNA expression of PGC-1a, NRF-1, and NRF-2 and increased the mtDNA/nDNA ratio in diabetic rats. Conclusions: Syringic acid can be considered as a suitable candidate against hepatic complications since it can reduce oxidative damages in diabetic cases. Furthermore, it has the potential of targeting hepatic mitochondria in diabetes.http://www.apjtb.org/article.asp?issn=2221-1691;year=2020;volume=10;issue=3;spage=111;epage=119;aulast=Sabahisyringic acid; diabetic; liver; oxidative stress; mitochondrial biogenesis; rats
spellingShingle Zahra Sabahi
Mohammad Javad Khoshnoud
Bahman Khalvati
Seyedeh-Sara Hashemi
Zahra Ghasempour Farsani
Hoda Mogholi Gerashi
Marzieh Rashedinia
Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic rats
Asian Pacific Journal of Tropical Biomedicine
syringic acid; diabetic; liver; oxidative stress; mitochondrial biogenesis; rats
title Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic rats
title_full Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic rats
title_fullStr Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic rats
title_full_unstemmed Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic rats
title_short Syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin-induced diabetic rats
title_sort syringic acid improves oxidative stress and mitochondrial biogenesis in the liver of streptozotocin induced diabetic rats
topic syringic acid; diabetic; liver; oxidative stress; mitochondrial biogenesis; rats
url http://www.apjtb.org/article.asp?issn=2221-1691;year=2020;volume=10;issue=3;spage=111;epage=119;aulast=Sabahi
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