Acetyl-L-Carnitine and Liposomal Co-Enzyme Q10 Attenuate Hepatic Inflammation, Apoptosis, and Fibrosis Induced by Propionic Acid

被引:3
|
作者
Alhusaini, Ahlam M. [1 ]
Alsoghayer, Rahaf [2 ]
Alhushan, Lina [2 ]
Alanazi, Abeer M. [1 ]
Hasan, Iman H. [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, POB 22452, Riyadh 11459, Saudi Arabia
[2] King Saud Univ, Coll Pharm, Pharm Program D, POB 22452, Riyadh 11459, Saudi Arabia
关键词
propionic acid; acetyl-L-carnitine; liposomal-coenzyme Q(10); cytokeratin-18; transforming growth factor-& beta; 1; FATTY LIVER-DISEASE; OXIDATIVE STRESS; DAMAGE; EXPRESSION; ENZYMES;
D O I
10.3390/ijms241411519
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Propionic acid (PRA) is a metabolic end-product of enteric bacteria in the gut, and it is commonly used as a food preservative. Despite the necessity of PRA for immunity in the body, excessive exposure to this product may result in disruptive effects. The purpose of this study is to examine the hepatoprotective effects of acetyl-L-carnitine (A-CAR) and liposomal-coenzyme Q(10) (L-CoQ(10)) against PRA-induced injury. Liver injury in rats was induced by oral administration of PRA, and A-CAR and L-CoQ(10) were administered concurrently with PRA for 5 days. Oxidative stress, inflammatory, apoptotic, and fibrotic biomarkers were analyzed; the histology of liver tissue was assessed as well to further explore any pathological alterations. PRA caused significant increases in the levels of serum liver enzymes and hepatic oxidative stress, inflammatory, and apoptotic biomarker levels, along with histopathological alterations. Concurrent treatment with A-CAR and/or L-CoQ(10) with PRA prevented tissue injury and decreased the levels of oxidative stress, proinflammatory cytokines, and apoptotic markers. Additionally, A-CAR and/or L-CoQ(10) modulated the expression of high-mobility group box-1, cytokeratin-18, transforming growth factor-beta1, and SMAD3 in liver tissue. In conclusion, A-CAR and/or L-CoQ(10) showed hepatoprotective efficacy by reducing oxidative stress, the inflammatory response, apoptosis, and fibrosis in liver tissue.
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页数:12
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