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DOI 10.1007/s00210-019-01785-1

Медицинская библиотека · Naunyn-Schmiedeberg's archives of pharmacology · 2019

Adelmidrol protects against non-alcoholic steatohepatitis in mice.

Nageeb Mahitab Mohamed, Khatab Monira Ismaeil, Abdel-Sameea Ahmed Ahmed, Teleb Noha Abbas

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Аннотация

Non-alcoholic steatohepatitis (NASH) is a more serious condition of non-alcoholic fatty liver disease (NAFLD), a widely spread type of chronic liver disease. Oxidative stress and inflammation induced by lipotoxicity are involved in hepatic injury of NASH. This work aimed to investigate the possible protective effect of adelmidrol (PPAR α and γ agonist) against NASH in mice.Thirty-six mice were divided into six equal groups: sham-operated, NASH, vehicle, adelmidrol 5 mg/kg, adelmidrol 10 mg/kg, and adelmidrol 20 mg /kg. Adelmidrol was injected intraperitoneally once daily for 7 weeks along with high-fat diet (HFD). Mice were euthanized, and livers were removed for light microscopic examination and detection of reduced glutathione (GSH) content while blood samples were collected for assessment of transaminases (ALT& AST), tumor necrosis factor (TNF-α), matrix metalloproteinase-1 (MMP-1), adiponectin, cholesterol, high-density lipoprotein (HDL), and triglyceride. NASH mice had increments in MMP-1, TNF-α, AST, ALT, triglyceride, and cholesterol levels while HDL, adiponectin levels, and GSH content were decreased with vesicular steatosis, lobular inflammation, hepatocyte ballooning, and degeneration. Administration of adelmidrol decreased MMP-1, TNF-α, AST, ALT, triglyceride, and cholesterol levels while increased HDL, adiponectin levels, and GSH content as well as ameliorated the histopathological changes. Adelmidrol protected mice from NASH; an effect could be attributed to its anti-inflammatory and antioxidant actions.

Для цитирования: Nageeb Mahitab Mohamed, Khatab Monira Ismaeil, Abdel-Sameea Ahmed Ahmed, Teleb Noha Abbas. Adelmidrol protects against non-alcoholic steatohepatitis in mice.. Naunyn-Schmiedeberg's archives of pharmacology. 2019. DOI: 10.1007/s00210-019-01785-1.

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