دورية أكاديمية

Dietary Supplementation with D-Ribose-L-Cysteine Prevents Hepatic Stress and Pro-Inflammatory Responses in Male Wistar Rats Fed a High-Fructose High-Fat Diet

التفاصيل البيبلوغرافية
العنوان: Dietary Supplementation with D-Ribose-L-Cysteine Prevents Hepatic Stress and Pro-Inflammatory Responses in Male Wistar Rats Fed a High-Fructose High-Fat Diet
المؤلفون: Abodunrin Adebayo Ojetola, Jerome Ndudi Asiwe, Wale Johnson Adeyemi, Dare Joshua Ogundipe, Adesoji Adedipe Fasanmade
المصدر: Pathophysiology, Vol 29, Iss 4, Pp 631-639 (2022)
بيانات النشر: MDPI AG, 2022.
سنة النشر: 2022
المجموعة: LCC:Physiology
مصطلحات موضوعية: D-ribose-L-cysteine, oxidative stress, inflammation, liver, high-fat high-fructose, Physiology, QP1-981
الوصف: Diets rich in fats and fructose are associated with the pathogenesis of oxidative stress-induced non-alcoholic fatty liver disease. Therefore, we investigated the effect of D-ribose-L-cysteine (DRLC) in high-fructose high-fat (HFHF) diet-fed rats. Twenty rats (n = 5), divided into four groups, were simultaneously exposed to HFHF and/or DRLC (250 mg/kg) orally during the 8 weeks of the study. Results showed that HFHF precipitated pro-inflammation and selective disruption of the oxidative stress markers. There were significant decreases in the level of antioxidants such as superoxide dismutase (SOD), glutathione peroxidase (GPX), total antioxidant capacity (TAC), hepatic SOD and GPX. Significant increases in serum levels of uric acid (UA), tumour necrosis factor-alpha (TNF-α), C-reactive protein (CRP) and hepatic Xanthine oxidase (XO) were observed in the HFHF compared to the control. In the HFHF + DRLC group, oxidative stress was mitigated due to differences in serum levels of SOD, GPX, TAC, TNF-α, liver SOD, and XO relative to control. The administration of DRLC alone caused significant reductions in malondialdehyde, UA and CRP and a significant increase in SOD compared to the control. DRLC prevents hepatic and systemic oxidative stress and pro-inflammatory events in HFHF diet-fed rats.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1873-149X
Relation: https://www.mdpi.com/1873-149X/29/4/49; https://doaj.org/toc/1873-149X
DOI: 10.3390/pathophysiology29040049
URL الوصول: https://doaj.org/article/c80cca831ba048b1a5e63ad556232a0f
رقم الأكسشن: edsdoj.80cca831ba048b1a5e63ad556232a0f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1873149X
DOI:10.3390/pathophysiology29040049