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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Dopamine D1 receptors and adenosine A1 receptors in the rat nucleus accumbens regulate motor activity but not prepulse inhibition.
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Dopamine D1 receptors and adenosine A1 receptors in the rat nucleus accumbens regulate motor activity but not prepulse inhibition.

机译:大鼠伏隔核中的多巴胺D1受体和腺苷A1受体调节运动活动,但不调节脉冲前抑制。

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摘要

Locomotor activity and sensorimotor gating (measured as prepulse inhibition of startle) are regulated by mesoaccumbal dopamine. Recent evidence indicated antagonistic interactions between adenosine A(1) receptors and dopamine D(1) receptors, as well as between adenosine A(2) receptors and dopamine D(2) receptors in the nucleus accumbens. Therefore, it is conceivable that accumbal dopamine and adenosine are both involved in the regulation of prepulse inhibition and locomotion. We tested whether accumbal adenosine A(1) and dopamine D(1) receptors control locomotor activity and prepulse inhibition using the following four treatments. (1) Injections of the selective adenosine A(1) receptor agonist N(6)-cyclopentanyladenosine (CPA 1.5 and 3 microg/microl per side) into the nucleus accumbens. (2) Stimulation of the ventral tegmental area by local infusion of the GABA(A) receptor antagonist picrotoxin (25-100 ng/0.5 microl bilaterally). (3) Picrotoxin injections into the ventral tegmental area (100 ng/0.5 microl) and simultaneous bilateral injections of CPA (3 microg/microl per side) into the nucleus accumbens. (4) Injections of the selective dopamine D(1) receptor antagonist SCH 23390 (3 microg/0.5 microl per side) into the nucleus accumbens and ventral tegmental area stimulation by picrotoxin. Intra-accumbal CPA infusion reduced locomotor activity but had no effect on prepulse inhibition. Picrotoxin stimulation of the ventral tegmental area increased locomotor activity which was antagonized by co-administration of CPA or SCH 23390 into the nucleus accumbens. An enhancement of prepulse inhibition was observed after stimulation of the ventral tegmental area and co-administration of SCH 23390 into the nucleus accumbens. These findings demonstrate that adenosine A(1) and dopamine D(1) receptors are involved in the regulation of locomotor activity mediated by the mesoaccumbal dopamine system. The finding that locomotor effects induced by stimulation of the mesoaccumbal dopamine system were not accompanied by a prepulse inhibition-deficit suggests a dissociation of the neuronal substrates involved in the control of locomotion and the regulation of sensorimotor gating.
机译:运动能力和感觉运动门控(测量为惊吓的脉冲前抑制)由中累积的多巴胺调节。最新证据表明伏隔核中腺苷A(1)受体与多巴胺D(1)受体之间以及腺苷A(2)受体与多巴胺D(2)受体之间存在拮抗作用。因此,可以想象,多巴胺多巴胺和腺苷都参与了前脉冲抑制和运动的调节。我们使用以下四种方法测试了伏隔腺苷A(1)和多巴胺D(1)受体是否控制运动活性和前脉冲抑制。 (1)向伏隔核注射选择性腺苷A(1)受体激动剂N(6)-环戊腺腺苷(每侧CPA 1.5和3 microg / microl)。 (2)通过局部输注GABA(A)受体拮抗剂微毒素(双侧25-100 ng / 0.5 microl)刺激腹侧被盖区。 (3)向腹侧被盖区注射微毒素(100 ng / 0.5 microl),同时向伏隔核同时注射CPA(每侧3 microg / microl)。 (4)将选择性多巴胺D(1)受体拮抗剂SCH 23390(每侧3微克/0.5微升)注射到伏隔核中,并通过微毒素刺激腹侧被盖区。腔内CPA输注可降低运动能力,但对脉冲前抑制没有影响。腹侧被盖区的微毒素刺激增加了运动活性,这通过在伏隔核中共同施用CPA或SCH 23390来对抗。在刺激腹侧被盖区和将SCH 23390共同伏入伏隔核后,观察到前脉冲抑制作用增强。这些发现表明,腺苷A(1)和多巴胺D(1)受体参与了由中累积多巴胺系统介导的运动活动的调节。通过刺激中肩部多巴胺系统诱导的运动功能没有伴随脉冲前抑制缺陷的发现表明神经元底物的解离与运动控制和感觉运动门控的调节有关。

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