The objective of this study was to examine the protective effects of S-methyl methionine sulfonium chloride (MMSC) against galactosamine (GalN)-induced brain and cerebellum injury in rats. A total of 22 female Sprague-Dawley rats were randomly divided into four groups as follows: Group I (n = 5), intact animals; Group II (n = 6), animals received 50 mg/kg/day of MMSC by gavage technique for 3 consecutive days; Group III (n = 5), animals injected with a single dose of 500 mg/kg of GalN intraperitoneally (ip); and Group IV (n = 6), animals injected with the same dose of GalN 1 h after MMSC treatment. After 6 h of the last GalN treatment (at the end of the experiments), all animals were killed under anesthesia, brain and cerebellum tissues were dissected out. Reduced glutathione, total antioxidant status levels, and antioxidant enzymes (catalase, superoxide dismutase, and glutathionerelated enzymes), aryl esterase, and carbonic anhydrase activities remarkably declined whereas advanced oxidized protein products, reactive oxygen species, total oxidant status, oxidative stress index levels, and myeloperoxidase, acetylcholinesterase, lactate dehydrogenase, and xanthine oxidase activities were significantly elevated in the GalN group compared with intact rats. In contrast, the administration of MMSC to GalN groups reversed these alterations. In conclusion, we may suggest that MMSC has protective effects against GalN-induced brain and cerebellar toxicity in rats.galactosamine, brain and cerebellum, antioxidant effect, oxidative stress, S-methyl methionine sulfonium chloride
| INTRODUCTIONGalactosamine (GalN) is an important amino derivative of D-galactose, it is extremely toxic when excessively formed or accumulated in an organism.In experimental animal models, it acts as a hepatotoxin and triggers hepatocellular damage and inflammation. [1][2][3] GalN interacts with uracilcontaining nucleotides in hepatocytes, thereby causing clinically similar effects like that of viral hepatitis and hepatic necrosis. [4] The resultant liver dysfunction may affect more than 500 metabolic processes, compromise detoxification processes, and thereafter result in the damage