首页> 外文期刊>Life sciences >THE ENDOGENOUS CANNABINOID RECEPTOR LIGAND, ANANDAMIDE, INHIBITS THE MOTOR BEHAVIOR - ROLE OF NIGROSTRIATAL DOPAMINERGIC NEURONS
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THE ENDOGENOUS CANNABINOID RECEPTOR LIGAND, ANANDAMIDE, INHIBITS THE MOTOR BEHAVIOR - ROLE OF NIGROSTRIATAL DOPAMINERGIC NEURONS

机译:内源性大麻素配体金胺化物可抑制运动行为-黑人纹状体多巴胺能神经元的作用

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摘要

The present study has been designed to test whether the recently described endogenous ligand for the cannabinoid receptor, arachidonylethanolamide, termed anandamide, can mimic the effects produced by exogenous cannabinoids on motor behavior and to test possible neurochemical substrates for this potential effect. To this end, adult male rats were submitted to an acute i.p. injection of anandamide, Delta(9)-tetrahydrocannabinol (THC) or vehicle. Animals were behaviorally tested ten minutes after injection of the drug and, then, sacrificed and their brains used for dopaminergic analyses. Ambulation was not significantly affected by the treatment with either THC or anandamide, but a very pronounced increase was observed in the time spent in inactivity in rats treated with either THC or anandamide. This was accompanied by a marked decrease in the frequency of spontaneous non-ambulatory activities, such as grooming and rearing, although only the administration of THC decreased shaking behavior. The anandamide-induced decrease in grooming was dose-dependent, but the decrease in rearing was higher with the dose of 3 mg/kg than with the dose of 10 mg/kg. The administration of anandamide also caused a dose-dependent decrease in the activity of tyrosine hydroxylase and in the ratio between the number of D1 and D2 receptors in the striatum. Moreover, the administration of 3 mg/kg of anandamide significantly decreased the contents of dopamine and L-3,4-dihydroxyphenylacetic acid in the striatum although lesser and higher doses were less effective. THC only tended to decrease these parameters. No changes were seen in dopaminergic activity in the limbic forebrain after either cannabimimetics. In summary, anandamide, as well as THC, decreases motor behavior. This effect was paralleled by a reduction in the activity of nigrostriatal dopaminergic neurons. However, subtle differences in the behavioral and neurochemical effects between anandamide and THC could be observed. [References: 27]
机译:本研究旨在测试最近描述的大麻素受体的内源性配体花生四烯基乙醇酰胺(称为花生四烯酸酰胺)能否模拟外源性大麻素对运动行为产生的作用,并测试这种潜在作用的可能神经化学底物。为此,将成年雄性大鼠置于急性腹膜内。注射anandamide,Delta(9)-四氢大麻酚(THC)或赋形剂。注射药物十分钟后对动物进行行为测试,然后处死动物的大脑进行多巴胺能分析。用THC或anandamide处理不会显着影响运动,但在用THC或anandamide处理的大鼠中,无活动时间明显增加。尽管仅施用THC可以降低摇晃行为,但伴随的自发非走动活动(例如梳理和饲养)的频率显着下降。安南酰胺诱导的修饰减少是剂量依赖性的,但是3 mg / kg的剂量比10 mg / kg的剂量增加了饲养的减少。 Anandamide的使用还导致酪氨酸羟化酶活性以及纹状体中D1和D2受体数目之比的剂量依赖性降低。此外,给予3 mg / kg的anandamide会显着降低纹状体中多巴胺和L-3,4-二羟基苯基乙酸的含量,尽管剂量越来越小效果差。 THC仅倾向于减少这些参数。两种大麻素药后,在边缘前脑的多巴胺能活动均未见变化。总之,阿南酰胺和四氢大麻酚会降低运动行为。这种作用与黑质纹状体多巴胺能神经元活性的降低并行。但是,可以观察到anandamide和THC在行为和神经化学作用上的细微差异。 [参考:27]

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