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机构地区:[1]阜外心血管病医院临床药理研究室 [2]北京医科大学临床药理研究所
出 处:《中国新药杂志》1998年第2期146-146,共1页Chinese Journal of New Drugs
摘 要:目的:从中枢递质的水平研究促智药阿尼西坦的作用机制。方法:采用反相HPLC电化学法测定了给药老龄大鼠脑内单胺类递质及其代谢产物的含量。结果:阿尼西坦500mg/(kg·d)连续ig5周后,在老龄给药鼠脑组织中(海马、下丘脑、纹状体)NA含量分别为699±183、696±123、364±68ng/g;DA含量分别为32±7、122±15、2986±416ng/g和77±27ng/g(大脑皮层),均显著高于老龄对照鼠(P<0.05)。在上述4个区域5HT含量与老龄对照鼠无显著性差异。结论:阿尼西坦促智作用机理可能与儿茶酚胺类递质的改变有关。OBJECTIVE:To investigate the possible mechanism of aniracetam(AM) in central transmitter level. METHODS:The monoamines and their metabolites in treated rat brain were determined by a reversed phase HPLCECD. RESULTS:After 5 weeks consecutive treatment with AM (500 mg/(kg·d),po), the NA level in Hippocampus(Hip), Hypothalamus(Hyp), and striatum(Str) were 699±183; 696±123; and 364±68ng/g rats brain tissue respectively. DA level in treated rats' brain were 77±27 (Cerebralcortex, Cer); 32±7(Hip); 122±15(Hyp); 2 986±416(Str)ng/g brain tissue. These data are significantly higher than those in control animals(P<0.05). The 5HT level in Hip, Hyp, Str and Cer showed no significant difference between active and control groups. CONCLUSION:Results obtained suggested that AM elicits nootropic action in rats may be possibly via monoamine mechanism.
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