Hepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats

Abstract Background The current study aimed to investigate the oxidative stress in rat liver with diabetes mellitus (DM) as well as the protective effects of N-acetylcysteine (NAC) on irisin expression. Methods Twenty-eight male Wistar rats were divided into four groups, 7 rats in each group, and 30...

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Main Authors: Mehmet Mustafa Erdogan, Mehmet Ali Erdogan, Suleyman Koc, Alper Yalcin, Ahmet Turk, Esra Akkus Yetkin
Format: Article
Language:English
Published: SpringerOpen 2023-07-01
Series:Egyptian Liver Journal
Subjects:
Online Access:https://doi.org/10.1186/s43066-023-00271-x
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author Mehmet Mustafa Erdogan
Mehmet Ali Erdogan
Suleyman Koc
Alper Yalcin
Ahmet Turk
Esra Akkus Yetkin
author_facet Mehmet Mustafa Erdogan
Mehmet Ali Erdogan
Suleyman Koc
Alper Yalcin
Ahmet Turk
Esra Akkus Yetkin
author_sort Mehmet Mustafa Erdogan
collection DOAJ
description Abstract Background The current study aimed to investigate the oxidative stress in rat liver with diabetes mellitus (DM) as well as the protective effects of N-acetylcysteine (NAC) on irisin expression. Methods Twenty-eight male Wistar rats were divided into four groups, 7 rats in each group, and 30-day regimens of experimental or control groups. NAC-treated group is as follows: 100 mg/kg once daily was administered intraperitoneally (i.p.). Diabetes-induced group is as follows: single-dose intraperitoneal injection of streptozotocin (STZ) (50 mg/kg) was used to induce DM in overnight fasting Wistar rats. By determining blood glucose concentration in STZ-induced rats 72 h after injection of STZ, DM was assessed. DM + NAC group is as follows: STZ-induced DM plus NAC is described previously. On the 30th day of the experiment, liver samples were collected after fasting and anesthesia. Biochemical analyses were performed to measure total antioxidant status (TAS), total oxidant status (TOS), and malondialdehyde (MDA) levels. Each liver sample was weighed and then prepared for histopathologic evaluation by light microscopy. Results There was a statistically significant decrease in TAS levels and an increase in TOS and MDA levels in the DM group compared to the control group. In contrast, TOS and MDA levels were found significantly decreased, and TAS levels increased in the serum and liver tissues of the DM + NAC group compared to the DM group. Liver samples were also used for histopathological examination using hematoxylin-eosin and immunohistochemical staining. STZ-induced liver damage was detected as oxidative stress, increased irisin immunoreactivity, sinusoidal dilatation, and hepatocyte degeneration. In the DM + NAC group, it was observed that NAC significantly reduced the aforementioned histopathological changes due to STZ. Conclusion In the early period of diabetes, due to the antioxidant properties of irisin related to the sudden response of liver tissue to oxidative stress, it is thought that the immunoreactivity in the tissue increases in the early period. As a result, NAC in diabetic rat liver tissue was found to suppress oxidative damage and irisin immunoreactivity.
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spelling doaj.art-9d97b061ce5d42618425919cf39bcc192023-07-16T11:10:06ZengSpringerOpenEgyptian Liver Journal2090-62262023-07-011311910.1186/s43066-023-00271-xHepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic ratsMehmet Mustafa Erdogan0Mehmet Ali Erdogan1Suleyman Koc2Alper Yalcin3Ahmet Turk4Esra Akkus Yetkin5Department of Histology and Embryology, Malatya Education and Research HospitalDepartment of Gastroenterology, Faculty of Medicine, Inonu UniversityDepartment of Surgery, Faculty of Medicine, Cumhuriyet UniversityDepartment of Histology and Embryology, Faculty of Medicine, Sutcu Imam UniversityDepartment of Histology and Embryology, Faculty of Medicine, Adiyaman UniversityDepartment of Anatomy, Faculty of Medicine, Adiyaman UniversityAbstract Background The current study aimed to investigate the oxidative stress in rat liver with diabetes mellitus (DM) as well as the protective effects of N-acetylcysteine (NAC) on irisin expression. Methods Twenty-eight male Wistar rats were divided into four groups, 7 rats in each group, and 30-day regimens of experimental or control groups. NAC-treated group is as follows: 100 mg/kg once daily was administered intraperitoneally (i.p.). Diabetes-induced group is as follows: single-dose intraperitoneal injection of streptozotocin (STZ) (50 mg/kg) was used to induce DM in overnight fasting Wistar rats. By determining blood glucose concentration in STZ-induced rats 72 h after injection of STZ, DM was assessed. DM + NAC group is as follows: STZ-induced DM plus NAC is described previously. On the 30th day of the experiment, liver samples were collected after fasting and anesthesia. Biochemical analyses were performed to measure total antioxidant status (TAS), total oxidant status (TOS), and malondialdehyde (MDA) levels. Each liver sample was weighed and then prepared for histopathologic evaluation by light microscopy. Results There was a statistically significant decrease in TAS levels and an increase in TOS and MDA levels in the DM group compared to the control group. In contrast, TOS and MDA levels were found significantly decreased, and TAS levels increased in the serum and liver tissues of the DM + NAC group compared to the DM group. Liver samples were also used for histopathological examination using hematoxylin-eosin and immunohistochemical staining. STZ-induced liver damage was detected as oxidative stress, increased irisin immunoreactivity, sinusoidal dilatation, and hepatocyte degeneration. In the DM + NAC group, it was observed that NAC significantly reduced the aforementioned histopathological changes due to STZ. Conclusion In the early period of diabetes, due to the antioxidant properties of irisin related to the sudden response of liver tissue to oxidative stress, it is thought that the immunoreactivity in the tissue increases in the early period. As a result, NAC in diabetic rat liver tissue was found to suppress oxidative damage and irisin immunoreactivity.https://doi.org/10.1186/s43066-023-00271-xIrisinLiver toxicityN-acetylcysteineOxidative stressDiabetes
spellingShingle Mehmet Mustafa Erdogan
Mehmet Ali Erdogan
Suleyman Koc
Alper Yalcin
Ahmet Turk
Esra Akkus Yetkin
Hepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats
Egyptian Liver Journal
Irisin
Liver toxicity
N-acetylcysteine
Oxidative stress
Diabetes
title Hepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats
title_full Hepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats
title_fullStr Hepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats
title_full_unstemmed Hepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats
title_short Hepatoprotective effects of N-acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats
title_sort hepatoprotective effects of n acetylcysteine on liver injury by irisin upregulation and oxidative stress reduction in diabetic rats
topic Irisin
Liver toxicity
N-acetylcysteine
Oxidative stress
Diabetes
url https://doi.org/10.1186/s43066-023-00271-x
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