Abstract:
Endocrine disrupting chemicals (EDC) are the natural or synthetic
compounds which mimic or inhibit the actions of endogenous hormones or
modulate the synthesis of latter and are said to adversely affect the normal
functioning of the endocrine system. They can be broadly categorized as (anti)
androgenic, (anti)estrogenic or (anti) progestagenic chemicals depending on
their effects on the production or functions of those steroids (i.e. androgens,
estrogens, progesterone respectively). EDC may enter into the physiological
system of animals/humans through the diet or occupational exposure and have
been related with the occurrence of a number of hormone-sensitive
disease/disorders like reduced fecundity, abnormal fetal development, delayed
onset of puberty, cryptorchadism, abnormal lactation, testicular dysfunction
and even various types of cancers
The present work describes action of two major pesticides: Chlordane
and Monocrotophos. We investigated chlordane, monocrotophos for endocrine
disruptions and reproductive toxicity in animal model (in vivo). Our aim was
to evaluate the hazardous effects of chlordane and monocrotophos in order to
establish a relationship between the exposure to these insecticides (through
any modes) and occurrence of various human diseases.
Results showed that oral administration of chlordane and
monocrotophos caused a significant reduction in the overall body weight along
with weight of testis and accessory sex organs. However, the weight of the
liver was increased significantly. Negative fertility was observed at high dose
of chlordane and monocrotophos. Motility of sperms in cauda epididymides
was decreased markedly after oral administration of chlordane and
monocrotophos at all dose levels. Sperm density in the testis and cauda
epididymides was decreased significantly in rats treated with chlordane and
monocrotophos at all dose levels. A significant decrease was observed in
serum testosterone concentration in the chlordane and monocrotophos treated
rats at higher dose levels which was indicative of its anti-androgenic activities.
Total erythrocyte count (TEC), haemoglobin concentration and haematocrit
values were significantly decreased at various dose levels of chlordane and
monocrotophos treatment. Whereas the total leukocyte count (TLC) was
increased in chlordane and monocrotophos exposed rats at all the dose levels.
Blood urea and blood sugar, bilirubin concentration, serum protein were
significantly increased. Serum phospholipids, Serum cholesterol, HDL-Chol,
LDL-Chol and VLDL-Chol levels were increased at all the dose levels.
Degenerative changes in the histoarchitecture of testis and reduced amount of
secretion in seminal vesicle and prostate was also observed. The
histoarchitecture of testis was altered markedly. Inhibition of spermatogenesis,
shrunken and damaged seminiferous tubules with increased interstitial spaces,
degenerated and vacuolated Sertoli cells, presence of vacuoles in the
epithelium, disruption of Leydig cells were conspicuous. Epididymes showed
reduced number of spermatozoa in the lumen of caput and cauda regions after
the treatment with chlordane and monocrotophos. The epithelial lining was
regressed. Histopathologically size of the liver was found to be increased
(hypertrophy) and various histopathological alterations were observed in the
kidney which includes glomerulonephritis, glomeruloscleroses, odenema,
pycnotic nuclei and glomerulus deposits.
The results of the present study revealed that the administration of
chlordane and monocrotophos insecticides induces reproductive toxicity as
well as hepato-nephrotoxicity in male albino rats. In which mating test showed
100% negative fertility that is the state of sterility. Low concentration of
spermatozoa in testis and cauda epididymides and reduction in number of
spermatogenic elements in testis reflects antispermatogenic nature of
chlordane and monocrotophos insecticides. Increase in acid phosphatase,
aspartate, alanine transferase and bilirubin indicates the hepatotoxic action of
insecticides due to cellular damage. Increase blood urea and pathological
alterations further suggests the chlordane and monocrotophos induced
intoxication on the structure and function of kidney.