Effects of sodium arsenite in the modulation of testosterone synthesis by the hypothalamo-pituitary testicular axis and its effect on memory and learning in the rat
Sodium arsenite is a toxic metalloid that exists ubiquitously in the environment. Human exposure to arsenic compounds is a significant public health concern. In most populations, the main source of arsenic exposure is the drinking water. Chronic exposure to arsenic is associated with increased ri...
Saved in:
| Main Author: | |
|---|---|
| Format: | Thesis |
| Language: | English |
| Published: |
2018
|
| Subjects: | |
| Online Access: | http://eprints.usm.my/47866/1/Dr.%20Saima%20Ashraf-24%20pages.pdf |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Sodium arsenite is a toxic metalloid that exists ubiquitously in the
environment. Human exposure to arsenic compounds is a significant public health
concern. In most populations, the main source of arsenic exposure is the drinking
water. Chronic exposure to arsenic is associated with increased risks of various
diseases. Recent emerging evidences suggest that arsenic exposure affects the
reproductive and developmental toxicity that leads to the decrease of cognition by
affecting on nervous system. The aim of this current research was to investigate the
morphological changes in structure of testis, hormonal imbalance and effect on
cognition in rats treated with different doses of sodium arsenite. Mature male
Sprague Dawley rats at the age of 90 days were divided into 4 groups of 8 animals
each. Group I received saline water whereas the other three groups received sodium
arsenite at doses of 3, 5 and 8mg/kg of body weight of rats respectively, for 60 days
by intraperitoneal injection. The blood samples were collected for follicle stimulating
hormone (FSH), Luteinizing hormone (LH), testosterone and Brain-derived
neurotrophic factor (BDNF) measurements at day 60. The Morris water maze
(MWM) test was performed for spatial memory at day 60. Following this, the
animals were then dissected and their testes were collected for histological studies. It
was found that the effect of chronic exposure was dose dependent. A significant
decrease (p≤0.05) was observed in plasma levels of testosterone, LH, FSH andBDNF in the higher dose groups (5mg/kg and 8mg/kg of body weight) in
comparison to the control group. To characterize behavioural alterations induced by
arsenic exposure, Morris water maze test was used. The Morris Water Maze test was
performed for spatial memory at day 60. Following this, the animals were then
dissected and their hippocampus was collected for histological studies. A significant
decrease (p < 0.05) was observed in cognitive behaviour, during Morris water maze
test, in the higher dose groups 5mg/kg and 8mg/kg) in comparison to the control
group. Histological evaluation revealed dose-dependent, gradual damage in
histoarchitecture of hippocampus. Moreover no significant change was observed in
any experimental parameter in the low dose group (3mg/kg) in comparison to the
control group. The results revealed that sub chronic exposure to sodium arsenite
caused degenerative changes in hippocampus; decrease the level of BDNF and
effects spatial memory in a dose dependent manner. Sodium arsenite exposure
caused complete arrest of spermatogenesis with disrupted seminiferous tubules in the
testes in high dose groups (5 and 8mg/kg). Moreover, no significant change was
observed in any experimental parameter in the low dose group (3mg/kg of body
weight) in comparison to the control group. Testosterone level was decreased by the
exposure of sodium arsenite. Low levels of endogenous testosterone can be
associated with poor performance on cognitive tests. For men with both cognitive
impairment and low testosterone, testosterone substitution may be considered. Large,
long- term studies evaluating the effects of testosterone substitution on cognitive
function in older men and testosterone substitution on cognitive function in affected
men exposed by sodium arsenite are warranted. |
|---|