Cannabinoids inhibit ethanol‐induced activation of liver toxicity in rats through JNK/ERK/MAPK signaling pathways. Issue 2 (1st December 2022)

• Record Type: Journal Article
• Authors: Yan, Lei; Luo, Heng; Tang, Xiaolu; Wang, Haidong
• Is Part Of: Journal of biochemical and molecular toxicology. Volume 37:Issue 2(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-12-01
• Subjects: cannabinoids -- ethanol -- JNK/ERK signaling -- liver injury -- MAPK pathway; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Toxicology -- Periodicals; 574
• DOI: 10.1002/jbt.23260
• Languages: English
• ISSNs: 1095-6670

Abstract

Abstract: Cannabinoids (CBs) are psychoactive compounds, with reported anticancer, anti‐inflammatory, and anti‐neoplastic properties. The study was aimed at assessing the hepatoprotective effects of CB against ethanol (EtOH)‐induced liver toxicity in rats. The animals were divided into seven groups: control (Group I) and Group II were treated with 50% ethanol (EtOH 5 mg/kg). Groups III, IV, and VI were treated with (EtOH + CB 10 mg/kg), (EtOH + CB 20 mg/kg), and (EtOH + CB 30 mg/kg), respectively. Groups V and VII consisted of animals treated with 20 and 30 mg/kg, of CB, respectively. Biochemical analysis revealed that Group IV (EtOH + CB 20 mg/kg) had reduced levels of ALT—alanine transferase, AST—aspartate aminotransferase, ALP—alanine peroxidase, MDA—malondialdehyde and increased levels of GSH‐reduced glutathione. Histopathological analysis of liver and kidney tissues showed that EtOH + CB (20 and 30 mg/kg) treated animal groups exhibited normal tissue architecture similar to that of the control group. ELISA revealed that the inflammatory markers were reduced in the animal groups that were treated with EtOH + CB 20 mg/kg, in comparison to the animals treated only with EtOH. The mRNA expression levels of COX‐2, CD‐14, and MIP‐2 showed a remarkable decrease in EtOH + CB treated animal groups to control groups. Western blot analysis revealed that CB downregulated p38/JNK/ERK thereby exhibiting its hepatoprotective property by inhibiting mitogen‐activated protein kinase pathways. Thus, our findings suggest that CB is a potential candidate for the treatment of alcohol‐induced hepatotoxicity.