Disodium Guanylate Alleviates Acute Hepatic Injury Induced by Carbon Tetrachloride Via Antioxidative Stress and Antiapoptosis In Vivo and In Vitro

• Published in: Journal of food science Vol. 84; no. 9; pp. 2658 - 2665
• Main Authors: Jin, Shao‐Ju, Liu, Chen, Wang, Rong, Guo, Kun‐Peng, Huang, Ya‐Nan, Li, Pan‐Xin, Ma, Yong‐Chao, Xu, Song‐Tao, Ding, Chang‐He, Zhou, Jun‐Jun, Chen, Fu‐Sheng
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.09.2019
• Subjects: Alanine; Alanine transaminase; Animal models; Animal tissues; Animals; Antioxidants; Antioxidants - pharmacology; apoptosis; Apoptosis - drug effects; Aspartate aminotransferase; Bax protein; Carbon; Carbon tetrachloride; Carbon Tetrachloride - toxicity; Caspase; Chemical and Drug Induced Liver Injury - metabolism; Digestive system; Digestive system diseases; disodium guanylate; Glutathione; Glutathione peroxidase; Guanosine; Guanosine Monophosphate - pharmacology; hepatic injury; Injuries; Liver; Liver - drug effects; Liver - metabolism; Malondialdehyde; Mice; mRNA; Nucleotides; oxidative stress; Oxidative Stress - drug effects; Peroxidase; Sodium; Sodium salts; Superoxide dismutase; Transaminase; apoptosis; disodium guanylate; hepatic injury; oxidative stress
• ISSN: 0022-1147; 1750-3841
• DOI: 10.1111/1750-3841.14677

Hepatic injury is one of the most common digestive system diseases worldwide in clinic. Guanylic acid or guanosine monophosphate (GMP) was an important component of nucleotides, which is mainly in the form of sodium salt (disodium guanylate, GMP‐Na2). However, its effect on hepatic injury has not yet been investigated. This study is to investigate the protective effects of GMP‐Na2 on acute hepatic injury induced by carbon tetrachloride (CCl4), and to explore its mechanism. The hepatic injury models of mice and HL‐7702 cells were induced by CCl4. The alanine transaminase (ALT), aspartate aminotransferase (AST), superoxide dismutase (SOD), glutathione peroxidase (GSH‐Px), malondialdehyde (MDA), total antioxidant capacity (T‐AOC) were determined by biochemical method. Hematoxylin–eosin staining were used to determine the morphological changes on liver tissue in mice. The mRNA and protein expressions of caspase‐3, Bax, and Bcl‐2 were detected by RT‐PCR and Western blot analysis. Our results show that GMP‐Na2 treatment significantly decreased the activities of ALT and AST, and the levels of MDA as well as increased the levels of SOD, GSH‐Px, and T‐AOC. Importantly, GMP‐Na2 effectively enhanced the antiapoptosis function by upregulating Bcl‐2 expression and downregulating caspase‐3 and Bax expressions in vivo and in vitro. Moreover, the histopathological changes of liver tissue were obviously improved after GMP‐Na2 treatment. These findings suggest that GMP‐Na2 has protective effects on hepatic injury, and its mechanisms may be associated with antioxidative stress and antiapoptosis.