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1.
Assiut Medical Journal. 2006; 30 (3): 9-40
in English | IMEMR | ID: emr-182184

ABSTRACT

The objective of this study was to document teratogenicity observed in chick embryos following administration of insecticide malathion in a dose of 2mg in 0.1 ml corn oil, and to suggest reasonable explanations for these anomalies. A total number of 300 eggs of Gallus domesticus species were used. After 48 hours of incubation eggs were divided into 5 groups, of 60 eggs each. The individual groups were subdivided into control [20], and treated [40] eggs. The control eggs were injected with 0.1 ml of corn oil, while the treated eggs were injected with 0.1 ml of corn oil in which 2 mg of malathion were dissolved. Eggs of both control and treated groups were examined at the 5[th], 7[th], 10[th], 14[th] and 18[th] days of incubation, for weight, mortality and morbidity, external malformations and body measurements. Embryos were prepared for skeletal examination with Alizarin red stain and Victoria blue stain. It's observed from the present study that lethality; external malformations and growth retardation, are characteristic features for malathion toxicity in chick embryo. It is observed that, malathion mortality is more frequent in higher age groups [14[th] and 18[th] days of incubation] while teratogenicity is more frequent in younger age groups [5[th] and 7[th] day of incubation]. Significant loss of weight in the treated groups is also observed. The characteristic external malformations were in the form of short lower peak, parrot beak, short neck, wry neck, micromelia of both fore limbs and hind limbs. In addition, tibiotarsal angulations and claw toes were also observed. Abnormal feather distribution, persistence of mesencephalic bulge, eye anomalies and visceral herniation could also be detected. It is concluded from this study that malathion injection is teratogenc in chick embryo when given in the 2[nd] day of incubation. The lethality detected in older age groups could be explained to be secondary to marked teratogenicity in vital organs such as heart [congestive heart failure] or neural tube defects. The toxicity of malathion on developing chick embryo could be explained by its anticholinesterase action or its suppressive effect on nicotinamid dinucleotide [NAD] levels. Also, its genotoxicity or mutagenicity could not be excluded


Subject(s)
Animals, Laboratory , Chick Embryo , Skeleton , Mutagenicity Tests/methods
2.
Assiut Medical Journal. 1995; 19 (3): 68-87
in English | IMEMR | ID: emr-36480

ABSTRACT

The emergence of laminar organization and the developmental changes in cellular and fibrous components of the layers of the superior colliculus of the newborn five, ten, twenty and sixty-day-old-albino rats [Wester Strain] were studied by using three staining techniques; the gallocyanine- chrom alum method for Nissl bodies, nuclei and nucleoli, the Golgi-Cox method for cell bodies and their processes and Holm's method for axons. The superior colliculus of the newborn rat appeared as a large collection of densely packed cells without any evidence of lamination. At the age of five days, a definite pattern of stratification started to appear transforming it into a six-layered structure. At ten days age, there were certain structural changes in the superficial layers of the colliculus, while the intermediate and deep layers showed no additional structural changes except the increase in the layers' thickness. At twenty days age onwards, there were no additional structural changes except the increase in cellular size and laminar thickness in all layers. It was concluded that the intermediate and deep layers of the superior colliculus reached their maturity earlier than the superficial layers. This could be explained as the intermediate and deep layers were involved in connections controlling the adaptive behaviors essential for the still closed-eyes animal, while the superficial layers responsible for controlling visual reflexes and eye movements were delayed in maturation till the animal's eyes start to open


Subject(s)
Rats , Brain/physiology , Brain/growth & development
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