A study of the comparative distribution pattern of beta- and gamma-isomers of hexachlorocyclohexane (HCH) in albino rat tissues as a function of duration of treatment at two dose levels revealed different accumulation patterns for the two isomers in tissues. In general, the accumulation pattern was found to be in the order: fat greater than kidney greater than lungs greater than liver greater than muscle greater than heart greater than spleen greater than brain greater than blood for beta-HCH and fat greater than brain greater than kidney greater than muscle greater than lungs greater than heart greater than spleen greater than liver greater than blood for gamma-HCH. The tissue accumulation of beta-isomer was always greater than that of gamma-isomer in any tissue except in brain. Brain beta-HCH residue levels were relatively lower than in many other tissues except blood, whereas brain gamma-HCH concentration was only next to fat. A higher dose or a longer period of treatment generally produced a more marked elevation of tissue residue levels in beta-HCH fed rats, but not in gamma-HCH treated animals.
Dietary administration of beta- and gamma-hexachlorocyclohexane (HCH) to albino rats caused an abnormal excessive excretion of glucose in the urine, blood glucose level being nearly normal. Occurrence of glucosuria was also accompanied by increased excretions of the two low-threshold compounds - creatinine and urea, their levels in blood being normal. The interference of HCH isomers with renal function as evidenced by biochemical data was also indicated by histopathological lesions observed in the kidney sections, viz., hypertrophy and degeneration of the renal tubular epithelia.
The effect of the fungicide metalaxyl [methyl N-(2-methoxyacetyl)-N-(2,6-xylyl)-DL-alaniate] on cardiac activity was investigated in albino rats anesthetized with phentobarbitone. Metalaxyl caused dose-dependent bradycardia, and at higher doses (250 and 300 mg/kg body weight) the sustained bradycardia led to cardiac arrest. The acetylcholinesterase activities in brain and heart were not affected in metalaxyl-treated rats. However, the bradycardia induced by the fungicide was blocked by pretreatment of rats with the alpha-adrenoreceptor antagonist phentolamine (20 mg/kg, ip). The data suggest that the bradycardia-inducing effect of metalaxyl was not mediated by the cholinergic system but through alpha-adrenoreceptors.
In adult albino rats, maternal dietary beta- and gamma-hexachlorocyclohexane (HCH) intake during gestation upto 400 ppm level did not affect the number of litters produced. But about 50 and 100% pup mortality was found in 200 and 400 ppm beta-HCH group within 5 days of birth. Maternal mortality was observed in 800 ppm beta-HCH group during third week of gestation. The effect of maternal dietary intake of HCH isomers at 50 and 250 ppm level during gestation and/or lactation on perinatal development was also studied. The body weights and sizes of the newborn litters of mother rats exposed to dietary HCH isomers did not differ from controls. Similarly, the growth and development of the litters of HCH exposed mother rats that survived 28 day lactation period were found to be comparable to controls as evidenced by the body weight and weight of vital organs. However, liver weight increases were found in the 28 days weaned litters wherever the mothers had been exposed to HCH isomers during lactation. Lowered kidney weight was seen in litters of mother rats fed 250 ppm gamma-HCH during gestation and lactation. The brain and testis weights were not affected in the litters of any experimental groups.
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