PMID- 24250582 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20131119 LR - 20211021 IS - 1735-0328 (Print) IS - 1726-6890 (Electronic) IS - 1726-6882 (Linking) VI - 12 IP - 1 DP - 2013 Winter TI - Protective Effects of Vitamin C and NAC on the Toxicity of Rifampin on Hepg2 Cells. PG - 141-6 AB - Rifampin, an antibiotic widely used for the treatment of mycobacterial infections, produces hepatic, renal and bone marrow toxicity in human and animals. In this study, the protective effects of vitamin C and n-acetylcysteine (NAC) on the toxicity of rifampin on HepG2 cells were investigated. Human hepatoma cells (HepG2) were cultured in 96-well M of rifampin in the presence of microplate and exposed to 10, 20, 50 and 100 vitamin C (0.1 mg/mL) and NAC (0.2 mg/mL). Protective effect of the two drugs against rifampin toxicity was assessed by MTT assay. Results show that both vitamin C and NAC significantly inhibited HepG2 cellular damage due to rifampin, and vitamin C was relatively more potent than NAC. Rifampin is metabolized by the liver and its toxic metabolites are responsible for the drug›s hepatic toxicity. Based on our results, it seems that reactive metabolites are the main agents responsible for rifampin hepatotoxicity. The importance of this finding is that if vitamin C or NAC do not affect the antibacterial activity of rifampin, they could be used as preventive agents in rifampin users. FAU - Vahdati-Mashhadian, Nasser AU - Vahdati-Mashhadian N AD - Department of Pharmacodynamy and Toxicology, Faculty of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran. FAU - Jafari, Mahmoud Reza AU - Jafari MR FAU - Sharghi, Nasim AU - Sharghi N FAU - Sanati, Toktam AU - Sanati T LA - eng PT - Journal Article PL - Netherlands TA - Iran J Pharm Res JT - Iranian journal of pharmaceutical research : IJPR JID - 101208407 PMC - PMC3813199 OTO - NOTNLM OT - Cell toxicity OT - HepG2 OT - MTT assay OT - NAC OT - Vitamin C EDAT- 2013/11/20 06:00 MHDA- 2013/11/20 06:01 PMCR- 2013/01/01 CRDT- 2013/11/20 06:00 PHST- 2013/11/20 06:00 [entrez] PHST- 2013/11/20 06:00 [pubmed] PHST- 2013/11/20 06:01 [medline] PHST- 2013/01/01 00:00 [pmc-release] AID - ijpr-12-141 [pii] PST - ppublish SO - Iran J Pharm Res. 2013 Winter;12(1):141-6.