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.
引用
收藏
页数:12
相关论文
共 16 条
  • [1] Acetyl-L-carnitine and/or liposomal co-enzyme Q10 prevent propionic acid-induced neurotoxicity by modulating oxidative tissue injury, inflammation, and ALDH1A1-RA-RAR? signaling in rats
    Alhusaini, Ahlam
    Sarawi, Wedad
    Mattar, Dareen
    Abo-Hamad, Amjad
    Almogren, Renad
    Alhumaidan, Sara
    Alsultan, Ebtesam
    Alsaif, Shaikha
    Hasan, Iman
    Hassanein, Emad
    Mahmoud, Ayman
    BIOMEDICINE & PHARMACOTHERAPY, 2022, 153
  • [2] Co-enzyme Q10 and acetyl salicylic acid enhance Hsp70 expression in primary chicken myocardial cells to protect the cells during heat stress
    Xu, Jiao
    Tang, Shu
    Yin, Bin
    Sun, Jiarui
    Song, Erbao
    Bao, Endong
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2017, 435 (1-2) : 73 - 86
  • [3] Acetyl-L-carnitine attenuates arsenic-induced liver injury by abrogation of mitochondrial dysfunction, inflammation, and apoptosis in rats
    Bodaghi-Namileh, Vida
    Sepand, Mohammad Reza
    Omidi, Ameneh
    Aghsami, Mehdi
    Seyednejad, Seyed Afshin
    Kasirzadeh, Sara
    Sabzevari, Omid
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2018, 58 : 11 - 20
  • [4] Hsp70 expression induced by Co-Enzyme Q10 protected chicken myocardial cells from damage and apoptosis under in vitro heat stress
    Xu, J.
    Tang, S.
    Song, E.
    Yin, B.
    Wu, D.
    Bao, E.
    POULTRY SCIENCE, 2017, 96 (05) : 1426 - 1437
  • [5] Liposomal coenzyme Q10 abates inflammation, apoptosis and DNA damage induced by an overdose of paracetamol in rat's liver
    Alhusaini, Ahlam
    Fadda, Laila
    Albogami, Leena
    Alnaim, Noura
    Sarawi, Wedad
    Mattar, Dareen
    Hasan, Iman
    JOURNAL OF KING SAUD UNIVERSITY SCIENCE, 2022, 34 (06)
  • [6] The Effect of acetyl-L-carnitine, Alpha-lipoic Acid, and Coenzyme Q10 Combination in Preventing Anti-tuberculosis Drug-induced Hepatotoxicity: A Randomized, Double-blind, Placebo-controlled Clinical Trial
    Hakimizad, Reza
    Soltani, Rasool
    Khorvash, Farzin
    Marjani, Majid
    Dastan, Farzaneh
    IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH, 2021, 20 (03): : 431 - 440
  • [7] Modulatory role of Co-enzyme Q10 on methionine and choline deficient diet-induced non-alcoholic steatohepatitis (NASH) in albino rats
    Saleh, Dalia O.
    Ahmed, Rania F.
    Amin, Mohamed M.
    APPLIED PHYSIOLOGY NUTRITION AND METABOLISM, 2017, 42 (03) : 243 - 249
  • [8] Protective Effects of Co-Enzyme Q10 on Thioacetamide-Induced Acute Liver Damage and Its Correlation With Behavioral, Biochemical, and Pathological Factors
    Ashkani-Esfahani, Soheil
    Bagheri, Fereshteh
    Emami, Yasaman
    Esmaeilzadeh, Elmira
    Azarpira, Negar
    Hassanabadi, Nazila
    Keshtkar, Marzieh
    Farjam, Mojtaba
    Koohi-Hosseinabadi, Omid
    Noorafshan, Ali
    IRANIAN RED CRESCENT MEDICAL JOURNAL, 2016, 18 (08)
  • [9] Influence of titanium dioxide nanoparticles and/or cadmium chloride oral exposure on testicular morphology, oxidative stress, and apoptosis in rats: Ameliorative role of co-enzyme Q10
    Behairy, Amany
    Hashem, Mohamed M. M.
    Abo-EL-Sooud, Khaled
    Soliman, Ahmed M.
    Mouneir, Samar M.
    El-Metwally, Abeer E.
    Ismail, Sameh H.
    Hassan, Bayan A.
    Abd-Elhakim, Yasmina M.
    HELIYON, 2024, 10 (01)
  • [10] Chemo- and Mechano-Induced Reactions of Vascular Smooth Muscles in Rats with Chronic Insufficiency of Cerebral Dopamine: Effect of Co-Enzyme Q10
    Talanov, S. A.
    Tkachenko, M. N.
    Bazilyuk, O. V.
    Stepanenko, L. G.
    Sagach, V. F.
    NEUROPHYSIOLOGY, 2009, 41 (03) : 171 - 175