The initiation activity of norfloxacin does not result in the induction of hepatocellular tumors in rats

• Published in: Toxicology (Amsterdam) Vol. 231; no. 2; pp. 234 - 242
• Main Authors: Itoh, Tadashi, Moto, Mitsuyoshi, Kuroiwa, Yuichi, Sakai, Hiroki, Mitsumori, Kunitoshi
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier Ireland Ltd 07.03.2007; Amsterdam Elsevier Science
• Subjects: Administration, Oral; Animals; Anti-Infective Agents - toxicity; Biological and medical sciences; Carcinogenicity; Carcinogenicity Tests; Carcinogens - toxicity; Carcinoma, Hepatocellular - enzymology; Carcinoma, Hepatocellular - etiology; Carcinoma, Hepatocellular - pathology; Dose-Response Relationship, Drug; Emergency; Glutathione Transferase - metabolism; Hepatectomy; Initiation activity; Liver Neoplasms - enzymology; Liver Neoplasms - etiology; Liver Neoplasms - pathology; Male; Medical sciences; Norfloxacin; Norfloxacin - toxicity; Phenobarbital; Phenobarbital - pharmacology; Quinolone; Rats; Rats, Inbred F344; Toxicology; Quinolone; Phenobarbital; Norfloxacin; Initiation activity; Carcinogenicity; Rat; Digestive system; Psychotropic; Liver; Rodentia; Hypnotic; Anticonvulsant; Tumorigenicity; Biological activity; Fluoroquinolone derivatives; Vertebrata; Mammalia; Animal; Tumor; Sedative; Barbiturates; Antibacterial agent; Initiation; Quinolone derivatives
• ISSN: 0300-483X; 1879-3185
• DOI: 10.1016/j.tox.2006.12.003

Abstract In order to examine whether the in vivo initiation activity of a new quinolone antimicrobial agent – norfloxacin (NFLX) – results in the induction of hepatocellular tumors, F344 male rats were subjected to two-thirds partial hepatectomy and oral administration of 1500 or 750 mg/kg BW of NFLX or the vehicle once daily for 3 weeks. From 2 weeks after the completion of NFLX treatment, the rats were given 500 ppm phenobarbital (PB) in their drinking water for 51 weeks. After the promotion treatment with PB for 17, 34, or 51 weeks, the rats were euthanized under ether anesthesia, and the NFLX-induced hepatic tumors were examined macroscopically by thoroughly sectioning the liver at 5-mm intervals. The liver slices, one each from all liver lobes, were fixed in 10% neutral buffered formalin for immunohistochemical examination of glutathione S -transferase placental form (GST-P) positive foci. NFLX increased neither the incidence of macroscopic hepatic tumors nor the mean number or area of GST-P positive foci. These results suggest that under the present study conditions, the initiation activity of NFLX does not result in the induction of hepatocellular tumors in rats; thus, the initiation activity of NFLX is extremely weak.