Ciprofloxacin prevents the inhibitory effects of acute ethanol exposure on hepatic regeneration in the rat
Autor: | Gu Qi Wang, Frank J. Burczynski, Xin K. Zhang, Gerald Y. Minuk, Tony Gauthier, Norman M. Pettigrew |
---|---|
Rok vydání: | 1995 |
Předmět: |
medicine.medical_specialty
Ethanol Hepatology DNA synthesis biology medicine.drug_class GABAA receptor medicine.medical_treatment Receptor antagonist Staining Proliferating cell nuclear antigen chemistry.chemical_compound Endocrinology chemistry Internal medicine medicine biology.protein Putrescine Saline |
Zdroj: | Hepatology. 22:1797-1800 |
ISSN: | 1527-3350 0270-9139 |
DOI: | 10.1002/hep.1840220628 |
Popis: | To determine whether the inhibitory effects of ethanol on hepatic regeneration could be prevented by ciprofloxacin, a fluroquinolone antibiotic with gammaaminobutyric acid (GABA A ), receptor antagonist properties, adult, male Sprague-Dawley rats (n = 6–8/group) received intraperitoneal injections of saline, putrescine (a hepatic growth promotor, 50 mg/kg), or ciprofloxacin (100 mg/kg), followed 1 hour later by gastric gavage with saline or ethanol (5 g/kg). One hour post-gavage, all rats underwent a 70% partial hepatectomy (PHx). Hepatic regenerative activity was documented 24 hours postPHx by 3 H-thymidine incorporation into hepatic DNA (DNA synthesis), proliferating cell nuclear antigen staining, and hepatic tissue putrescine levels. Compared with healthy controls, DNA synthesis rates were significantly lower in ethanol-gavaged/saline-treated rats (22.7 ± 4.4 × 10 3 vs. 12.3 ± 6.9 × 10 9 DPM/mg DNA, respectively, P 3 DPM/ mg DNA) and ciprofloxacin-treated (18.3 ± 2.6 × 10 3 DPM/mg DNA) rats. Hepatic proliferating cell nuclear antigen staining supported these findings. Hepatic putrescine levels also correlated with DNA synthesis data, being decreased in ethanol-gavaged/saline-treated rats (86 ± 14 pmoles/mg tissue) compared with healthy controls (120 ± 12 pmoles/mg, P P P A receptor-mediated changes in liver membrane potentials, intracellular membrane potentials were recorded before and 1 hour after PHx in healthy control, ethanol-gavaged/saline-treated and ethanol-gavaged/ciprofloxacin-treated rats. In these studies, ciprofloxacin prevented ethanol-induced depolarization of the liver (change in membrane potential of healthy controls, ethanol-gavaged/saline-treated, and ethanol-gavaged/ciprofloxacin-treated rats were −9 ± 1, −15 ± 2, and −3 ± 1 mV, respectively). In conclusion, the results of this study indicate that the inhibitory effects of acute ethanol exposure on hepatic regenerative activity in rats can be prevented by exogenous ciprofloxacin. |
Databáze: | OpenAIRE |
Externí odkaz: |