TESTICULAR CREATINE AND URINARY CREATINE-CREATININE PROFILES IN MICE AFTER THE ADMINISTRATION OF THE REPRODUCTIVE TOXICANT METHOXYACETIC ACID

Citation
Me. Traina et al., TESTICULAR CREATINE AND URINARY CREATINE-CREATININE PROFILES IN MICE AFTER THE ADMINISTRATION OF THE REPRODUCTIVE TOXICANT METHOXYACETIC ACID, Biomarkers, 2(2), 1997, pp. 103-110
Citations number
32
Categorie Soggetti
Toxicology
Journal title
ISSN journal
1354750X
Volume
2
Issue
2
Year of publication
1997
Pages
103 - 110
Database
ISI
SICI code
1354-750X(1997)2:2<103:TCAUCP>2.0.ZU;2-M
Abstract
It was previously observed that the acute or subchronic administration of some testicular toxicants, caused a significant raise in urinary c reatine in rats. The aim of this study was to verify whether creatinur ia could be detected in mice (a species with a different excretion pro file of creatine) and whether it could be correlated to the levels of creatine in testis and to other parameters of testicular toxicity. The well known testicular toxicant methoxyacetic acid (MAA) was orally ad ministered as a single dose (400 or 600 mg kg(-1)) to male adult mice B6C3F1, Twenty-four hours after dosing, urinary creatine and creatinin e showed a significant reduction with respect to the pre-treatment val ues. At the following times post-dosing (48 and 72 h) the creatine exc eeded the control and pre-treatment values, while creatinine had not y et recovered, The ratio creatine/creatinine was significantly higher t han control and pre-treatment values, at 24 and 48 h after the treatme nts, In testis a significant, dose-dependent, decrease of creatine was observed 24 h after dosing, with a pattern related to the histopathol ogic alterations observed at different times after the treatments, Cre atine determination was the earlier quantitative parameter of testicul ar toxicity, since at this time testis weights, sperm head number and enzyme activities (LDH-C4, SDH) were less affected, their maximum decr ease being reached at 14 days after the treatments, These data suggest that in mice, 2-MAA could interfere with the metabolism of creatine, both in testis and other biosynthetically active tissues.