Attenuation of scopolamine-induced spatial memory deficits in the rat by cholinomimetic and non-cholinomimetic drugs using a novel task in the 12-arm radial maze

1993 ◽  
Vol 111 (4) ◽  
pp. 435-441 ◽  
Author(s):  
Robert P. Dennes ◽  
Julie C. Barnes
2004 ◽  
Vol 151 (1-2) ◽  
pp. 287-293 ◽  
Author(s):  
Yu-Wen Huang ◽  
Wei-Wei Hu ◽  
Zhong Chen ◽  
Li-San Zhang ◽  
Hai-Qing Shen ◽  
...  

1989 ◽  
Vol 71 (1) ◽  
pp. 105-112 ◽  
Author(s):  
Matthew A. Howard ◽  
Alan Gross ◽  
M. Sean Grady ◽  
Robert S. Langer ◽  
Edith Mathiowitz ◽  
...  

✓ Pharmacological treatments directed at increasing cortical acetylcholine activity in patients with Alzheimer's disease have largely been disappointing, perhaps because denervated areas of brain may not be exposed to adequate amounts of drug. A new method has been developed to enable localized intracerebral delivery of neurotransmitter substances using a polymeric drug delivery system. Microspheres of a polyanhydride sebacic acid copolymer were impregnated with bethanechol, an acetylcholinesterase-resistant cholinomimetic. Twenty rats received bilateral fimbria-fornix lesions, producing cholinergic denervation of the hippocampus and marked impairment in spatial memory. The animals were trained for 2 weeks to run an eight-arm radial maze, after which they received bilateral intrahippocampal implants of saline (five rats), blank polymer (five rats), or bethanechol-impregnated polymer (10 rats). Following implantation, spatial memory was assessed by radial-maze performance testing for 40 days. Untreated lesioned rats showed persistently poor spatial memory, entering maze arms with near random frequency. Similarly, animals treated with saline and blank polymer did not improve after implantation. Rats treated with bethanechol-impregnated microspheres, however, displayed significant improvement within 10 days after implantation; this improvement persisted for the duration of the experiment (p < 0.05, Student's t-test). Histological analysis of regional acetylcholinesterase staining showed widespread loss of activity throughout the hippocampus bilaterally in all animals. The microsphere implants were visible within the hippocampus, with minimal reactive changes in surrounding brain. It is concluded that intracerebral polymeric drug delivery successfully reversed lesion-induced memory deficits, and has potential as a neurosurgical treatment method for Alzheimer's disease and other neurodegenerative disorders.


2012 ◽  
Vol 135 (1-3) ◽  
pp. 84-89 ◽  
Author(s):  
Elena A. Spieker ◽  
Robert S. Astur ◽  
Jeffrey T. West ◽  
Jacqueline A. Griego ◽  
Laura M. Rowland

1998 ◽  
Vol 86 (3_suppl) ◽  
pp. 1288-1290 ◽  
Author(s):  
L. L. Cook ◽  
M. A. Persinger

After training in an automated radial maze, 11 male rats were injected with either “subclinical” dosages of lithium and pilocarpine or saline and then tested 5 days or 4 months later. When employed as their own controls or when compared with a saline-injected reference group, the rats that had received the lithium and pilocarpine displayed memory deficits but not learning deficits after the longest of the two delays (effect size was 41%). These results suggest that subtle disruptions in memory but not learning to criterion could be associated with “subclinical electrical seizures” or the micromorphological changes associated with this activity.


2013 ◽  
Vol 34 (3) ◽  
pp. 716-730 ◽  
Author(s):  
Nour Yassine ◽  
Anelise Lazaris ◽  
Cornelia Dorner-Ciossek ◽  
Olivier Després ◽  
Laurence Meyer ◽  
...  

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