World Bank assisted National Agricultural Research Project (NARP) - University of Port Harcourt
Abstract
The pharmacological effects of intraperitoneal administration of
different doses of vanadium pentoxide (V2O5) on the histological and
sperm parameters of male guinea pigs were investigated. Also
investigated were the effects of oral pretreatment with different doses
of vitamin E (a known protein kinase C inhibitor) on the V2O5 -induced
responses of the testis and liver of male guinea pigs. In n = 5
experiments, vanadium pentoxide in the dose range of 4.5-12.5mg/kg
caused destruction of the testicular and liver architecture. This was
characterized by a reduction in spermatogonia, destruction of
seminiferous tubules, necrosis of the testicular tissues, necrosis of
liver cells, fatty cells infiltration and vacoulation. Oral
administration/ pretreatment with vitamin E in the dose range of
500-2000I.U caused a reversal of the vanadium pentoxide \u2013induced
histological damages of the testis and the liver cells. Furthermore, in
n = 5 animals experiments, Vanadium pentoxide (4.5-12.5 mg/kg/) caused
a statistically significant increase in the percentage basal cell
death, from 5.0 to 75.0 \ub1 1.0%, reduction in sperm motility from
90.0 to 31.0 \ub1 3.9%, reduction in sperm count from 80.0
x106cells/ml to 25.0\ub1 4.0 x 106cells/ml and alteration in the
spermatic cell morphology ( i.e. causing a change in the cellular
structure of sperm cells and an increase in abnormal cells count) of
the male guinea pigs. These inhibitory effects were significant at P
< 0.05 (ANOVA). These effects were all dose- and time-dependent and
may have a role in oxidative pathology of vanadium pentoxide