Various acetylcholinesterase inhibitors and passive avoidance behavior in the nucleus basalis lesioned rats (CROSBI ID 604193)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Simonić, Ante ; Župan, Gordana
engleski
Various acetylcholinesterase inhibitors and passive avoidance behavior in the nucleus basalis lesioned rats
The frontal neocortex, the hippocampus and the cholinergic afferents to these areas have an important role in memory processes. The major cholinergic innervation for neocortical regions originates from the nucleus basalis magnocellularis (NB). Lesions of the NB are associated with an impairment of cognitive functions. Therefore we have analyzed the influence of various acetylcholinesterase inhibitors on the passive avoidance in rats with bilateral electrolytic lesions of mentioned structure. Wistar albino rats weighing 200-250 g were used. Bilateral electrolytic NB lesions were made by using the coordinates 0.7 mm posterior ; 2.7 mm lateral to the bregma, 7 mm below the dura. 15 days after the surgery the lesioned rats started the passive avoidance test per the procedure of Ashford and Jones, 1976. The control animals received 0.9% NaCl solution. Other NB lesioned rats received physostigmine salicylate ( 0, 001 ; 0, 01 ; 0, 1 mg/kg) ; galanthamine hydrobromide (0, 01 ; 0, 1 ; 1 mg/kg) or tetrahydroaminoacridine (THA) hydrochloride (0, 01 ; 0, 1 ; 1, 0 mg/kg ). All tested drugs were given intraperitoneally, once per day in the course of four testing days. Physostigmine was injected 1/2 and the other substances 1 hr before the passive avoidance experiment started. The results of our experiments show that mentioned acetylcholinesterase inhibitors in some tested doses can improve the passive avoidance in the NB lesioned rats.
NB lesions; physostigmine; galanthamine; tetrahydroaminoacridine; passive avoidance; rat
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Podaci o prilogu
86-86.
1989.
objavljeno
Podaci o matičnoj publikaciji
Book of Abstracts
Berlin:
Podaci o skupu
Interdisciplinary Satellite Symposion to the IV. World Conference on Clinical Pharmacology and Therapeutics
poster
28.07.1989-30.07.1989
Berlin, Njemačka