Memory-related task performance by aged rhesus monkeys administered the muscarinic M1-preferring agonist, talsaclidine

被引:21
作者
Terry, AV
Buccafusco, JJ
Borsini, F
Leusch, A
机构
[1] Univ Georgia, Coll Pharm, Med Coll Georgia, Program Clin & Expt Therapeut, Augusta, GA 30912 USA
[2] Med Coll Georgia, Alzheimers Res Ctr, Augusta, GA 30912 USA
[3] Med Coll Georgia, Dept Pharmacol & Toxicol, Augusta, GA 30912 USA
[4] Dept Vet Affairs Med Ctr, Augusta, GA 30910 USA
[5] Boehringer Ingelheim Pharma, Dept CNS Res, D-88394 Biberach, Germany
[6] Boehringer Ingelheim Pharma, Dept Project Management Res & Dev, D-88397 Biberach, Germany
关键词
muscarinic; receptor; cholinergic; learning; memory; match to sample; monkey;
D O I
10.1007/s00213-002-1105-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: Muscarinic-acetylcholine receptor agonists are yet to be used clinically for the treatment of Alzheimer's disease (AD) even though laboratory evidence continues to support the potential for such an approach. Objectives: The purpose of this study was to evaluate the M-1-preferring agonist talsaclidine in aged monkeys for effects on working memory. Methods: Three doses (0.6, 1.2, and 2.4 mg/kg, PO) of talsaclidine and two time intervals (45 min and 8 h) after drug administration were evaluated in seven aged rhesus macaques trained to perform a computer-assisted delayed matching-to-sample (DMTS) task. The relative effectiveness of talsaclidine was also compared with another M-1-preferring agonist WAY-132983 that was previously studied in this laboratory. Results: Talsaclidine improved DMTS accuracy only during sessions initiated 8 h after administration of one of the doses (i.e. 0.6 mg/kg). The drug's enhanced effectiveness at the 8-h time point relative to the 45-min time point was surprising in view of the fact that plasma concentrations were highest 45 min after administration. A higher dose of talsaclidine (4.7 mg/kg) resulted in side effects (lethargy and excessive drooling) in some animals. Individualized optimal doses of talsaclidine were associated with 7.4% and 10.6% improvement in overall (all trials averaged) DMTS accuracy during the 45 min and 8 h post-administration sessions, respectively. Under similar experimental conditions WAY-132983 increased DMTS accuracy by up to 15.6% above control levels. Conclusion: Both talsaclidine and WAY 132983 provide at least modest improvements in DMTS accuracy in aged monkeys at some doses; however, challenges remain regarding the achievement of an adequate level of efficacy and reliability while minimizing side effects with these compounds. The positive findings do, however, support further study of the potential use of direct muscarinic agonists in the treatment age-related disorders of memory function.
引用
收藏
页码:292 / 300
页数:9
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