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1.
Braz. j. med. biol. res ; 34(2): 233-240, Feb. 2001.
Article in English | LILACS | ID: lil-281601

ABSTRACT

Rats implanted bilaterally with cannulae in the CA1 region of the dorsal hippocampus or the entorhinal cortex were submitted to either a one-trial inhibitory avoidance task, or to 5 min of habituation to an open field. Immediately after training, they received intrahippocampal or intraentorhinal 0.5-æl infusions of saline, of a vehicle (2 percent dimethylsulfoxide in saline), of the glutamatergic N-methyl-D-aspartate (NMDA) receptor antagonist 2-amino-5-phosphono pentanoic acid (AP5), of the protein kinase A inhibitor Rp-cAMPs (0.5 æg/side), of the calcium-calmodulin protein kinase II inhibitor KN-62, of the dopaminergic D1 antagonist SCH23390, or of the mitogen-activated protein kinase kinase inhibitor PD098059. Animals were tested in each task 24 h after training. Intrahippocampal KN-62 was amnestic for habituation; none of the other treatments had any effect on the retention of this task. In contrast, all of them strongly affected memory of the avoidance task. Intrahippocampal Rp-cAMPs, KN-62 and AP5, and intraentorhinal Rp-cAMPs, KN-62, PD098059 and SCH23390 caused retrograde amnesia. In view of the known actions of the treatments used, the present findings point to important biochemical differences in memory consolidation processes of the two tasks


Subject(s)
Animals , Male , Rats , 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/pharmacology , Avoidance Learning/drug effects , Calcium-Calmodulin-Dependent Protein Kinases/pharmacology , Enzyme Inhibitors/pharmacology , Excitatory Amino Acid Agonists/pharmacology , Habituation, Psychophysiologic/drug effects , Memory/drug effects , Analysis of Variance , Dose-Response Relationship, Drug , Entorhinal Cortex/drug effects , Hippocampus/drug effects , Rats, Wistar , Task Performance and Analysis
2.
Braz. j. med. biol. res ; 33(11): 1329-35, Nov. 2000. ilus, tab
Article in English | LILACS | ID: lil-273225

ABSTRACT

Rats infected with the helminth Capillaria hepatica regularly develop septal hepatic fibrosis that may progress to cirrhosis in a relatively short time. Because of such characteristics, this experimental model was selected for testing drugs exhibiting antifibrosis potential, such as pentoxifylline, gadolinium chloride and vitamin A. Hepatic fibrosis was qualitatively and quantitatively evaluated in liver samples obtained by partial hepatectomy and at autopsy. The material was submitted to histological, biochemical and morphometric methods. A statistically significant reduction of fibrosis was obtained with pentoxifylline when administered intraperitoneally rather than intravenously. Gadolinium chloride showed moderate activity when administered prophylactically (before fibrosis had started), but showed a poor effect when fibrosis was well advanced. No modification of fibrosis was seen after vitamin A administration. Hydroxyproline content was correlated with morphometric measurements. The model appears to be adequate, since few animals die of the infection, fibrosis develops regularly in all animals, and the effects of different antifibrotic drugs and administration protocols can be easily detected


Subject(s)
Animals , Male , Female , Rats , Capillaria , Enoplida Infections/drug therapy , Gadolinium/therapeutic use , Liver Cirrhosis/parasitology , Pentoxifylline/therapeutic use , Vitamin A , Analysis of Variance , Case-Control Studies , Disease Models, Animal , Liver Cirrhosis/drug therapy , Rats, Wistar , Time Factors
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