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1.
Bulletin of Faculty of Pharmacy-Cairo University. 1999; 37 (3): 155-166
in English | IMEMR | ID: emr-50492

ABSTRACT

Effect of insulin [0.5, 1 and 2 IUkg-1] on monoamines and gamma aminobutyric acid [GABA] contents in different brain regions of normal and diabetic mice with a relationship to their behavioral activity was investigated after seven daily SC doses. Non-treated alloxan-diabetic animals showed a significant decrease in norepinephrine [NE] content in the medulla, pons and cerebellum. The dopamine [DA] content was also reduced in all tested brain regions. On the other h and, serotonin [5-HT] was significantly increased in cerebral cortex and thalamus-hypothalamus. No change in mice brain gamma GABA content was observed after alloxan-induced diabetes


Subject(s)
Animals, Laboratory , Biogenic Monoamines , gamma-Aminobutyric Acid/drug effects , Brain/drug effects , Diabetes Mellitus, Experimental/physiopathology , Behavior, Animal/drug effects , Norepinephrine , Serotonin , Dopamine
2.
Bulletin of Faculty of Pharmacy-Cairo University. 1998; 36 (1): 21-8
in English | IMEMR | ID: emr-47769

ABSTRACT

The effect of glibenclamide, glipizide and gliclazide on brain norepinephrine, dopamine and serotonin contents in different brain regions of diabetic mice with correlation to behavioral activities were investigated. Alloxan-induced diabetes produced a significant decrease in norepinephrine contents in medulla, pons and cerebellum, with a decrease in dopamine contents in all tested brain regions, while serotonin contents was increased in cerebral cortex and thalamus hypothalamus. These effects were accompanied by reduction in behavioral activities of mice [sniffing, rearing, grooming, chewing, stillness, time of immobility, and pain threshold]. Sulphonylureas significantly increased brain norepinephrine and dopamine contents in different brain regions and antagonized the behavioral activities of diabetic mice. On the other h and, these drugs produced a significant decrease in serotonin contents, an action accompanied by an increase in time of immobility and pain threshold


Subject(s)
Animals, Laboratory , Glyburide/pharmacology , Glipizide/pharmacology , Gliclazide/pharmacology , Norepinephrine , Dopamine , Serotonin , Behavior , Mice/drug effects , Diabetes Mellitus, Experimental
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