S. Chattopadhyay et al., Protection of sodium arsenite-induced ovarian toxicity by coadministrationof L-ascorbate (vitamin C) in mature Wistar strain rat, ARCH ENV C, 41(1), 2001, pp. 83-89
Citations number
62
Categorie Soggetti
Environment/Ecology,"Pharmacology & Toxicology
Journal title
ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY
Arsenic, a major water pollutant in India, produces toxic effects on female
reproductive system in rodent models at the dose available in drinking wat
er in arsenic-intoxicated zones. This study examines the coadministration o
f L-ascorbate (vitamin C) on ovarian steroidogenesis, plasma levels of gona
dotrophins, brain monoamines, and ovarian as well as uterine peroxidase act
ivities in sodium arsenite-treated rats. After sodium arsenite treatment, r
elative ovarian and uterine weights, ovarian Delta (5)-3 beta -HSD and 17 b
eta -HSD activities, plasma levels of gonadotrophins, norepinephrine levels
in midbrain and diencephalon, and the activities of peroxidase in ovary an
d uterus were decreased significantly. On the other hand, serotonin levels
in midbrain and diencephalon were increased significantly 28 days after sod
ium arsenite treatment at the dose of 0.4 ppm/100 g body weight/rat/day. Al
l these parameters were protected significantly and in most cases were unch
anged from control level when L-ascorbate at 25 mg/100 g body weight/rat/da
y was coadministered orally with sodium arsenite. This cotreatment of L-asc
orbate with sodium arsenite also restored the estrous cycle in a regular ma
nner. We concluded that L-ascorbate plays a pivotal role in maintaining nor
mal ovarian activities and brain monoamines in arsenic-treated rats.