Abstract

Abstract:This study investigated the effect of nitric oxide on lipid peroxide formation during endotoxaemia. Nitric oxide synthase inhibitors NG‐monomethyl‐L‐arginine acetate (L‐NMMA, 20 mg/kg, intravenously), NG‐nitro‐L‐arginine‐methyl ester (L‐NAME, 10 mg/kg, intravenously), and NG‐nitro‐L‐arginine (L‐NA, 10 mg/kg, intravenously), and a relatively selective inducible nitric oxide synthase inhibitor aminoguanidine (10 mg/kg, intravenously), did not protect against endotoxin‐induced death of mice. Superoxide dismutase activity in liver 18 hr after administration of endotoxin (6 mg/kg, intraperitoneally) to L‐arginine analogues (L‐NMMA, L‐NAME, L‐NA)‐treated mice was lower than in mice treated with endotoxin alone, whereas the administration of L‐arginine analogues increased xanthine oxidase activity in the livers of endotoxin‐injected mice compared with mice treated with endotoxin alone. In mice treated with L‐arginine analogues and aminoguanidine, the levels of non‐protein sulfhydryl and lipid peroxide in liver 18 hr after endotoxin injection did not show significant differences from mice treated with endotoxin alone. L‐Arginine analogues and aminoguanidine had little effect on lipid peroxide formation in liver caused by endotoxin. Treatment with aminoguanidine (300 μM) significantly inhibited endotoxin‐induced intracellular peroxide in J774A.1 cells, however, aminoguanidine did not affect endotoxin‐induced cytotoxicity in J774A.1 cells. Our results clearly demonstrate that treatment with catalase (10 μg/ml), D‐mannitol (10 mM), or superoxide dismutase (100 U/ml), has little or no effect on nitric oxide production by endotoxin (1 μg/ml)‐activated J774A.1 cells. These findings suggest that nitric oxide is not crucial for lipid peroxide formation during endotoxaemia. Therefore, it is unlikely that nitric oxide plays a significant role in liver injury caused by free radical generation in endotoxaemia.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.