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首页> 外文期刊>Japanese Journal of Pharmacology >Dopamine Release and Presynaptic Dopaminergic Regulation in Guinea Pig Spinal Cord
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Dopamine Release and Presynaptic Dopaminergic Regulation in Guinea Pig Spinal Cord

机译:豚鼠脊髓中的多巴胺释放和突触前多巴胺能调节

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References(29) Cited-By(3) Using pharmacological approaches, we obtained evidence for the release of dopamine (DA) and its dopaminergic regulation in the guinea pig spinal cord. Electrical stimulation of the cord pieces increased the endogenous DA release and the efflux of [3H]dopamine ([3H] DA) from tissues preloaded with [3H] DA. The evoked release of [3H] DA was current- and frequency-dependent and was prevented by tetrodotoxin (10-6 M) or Ca2+-free medium containing EGTA (10-4 M), while benztropine allowed a recovery of a more extensive amount of [3H] DA in the superfusing medium by inhibiting the reuptake process. The stimulated [3H]-DA release was reduced by LY-171555, but not by SKF-38393 and 8-Br-cAMP. (-)Sulpiride enhanced the stimulated endogenous DA and [3H]DA release. (-)-Sulpiride reversed the inhibition of evoked [3H] DA release induced by LY-171555, while SKF-38393 and 8-Br-cAMP did not affect LY-171555-induced inhibition of evoked [3H] DA release. These findings provide additional evidence for the neurotransmitter role of DA in the spinal cord of the guinea pig, and they strongly suggest the presence of presynaptic regulation of DA release via the dopamine receptor which is the D2 type.
机译:参考文献(29)(3)使用药理学方法,我们获得了豚鼠脊髓中多巴胺(DA)释放及其多巴胺能调节的证据。脐带碎片的电刺激增加了内源性DA的释放以及预加载了[3H] DA的组织中[3H]多巴胺([3H] DA)的流出。 [3H] DA的诱发释放是电流和频率依赖性的,并被河豚毒素(10-6 M)或不含EGTA的不含Ca2 +的培养基(10-4 M)所阻止,而苄索平允许更广泛的恢复抑制再摄取过程,使超融合介质中的[3H] DA含量降低。 LY-171555降低了刺激的[3H] -DA释放,但SKF-38393和8-Br-cAMP并未降低。 (-)舒必利增强了刺激的内源性DA和[3H] DA的释放。 (-)-舒必利逆转了LY-171555诱导的[3H] DA释放的抑制作用,而SKF-38393和8-Br-cAMP并不影响LY-171555诱导的[3H] DA释放的抑制作用。这些发现为DA在豚鼠脊髓中的神经递质作用提供了额外的证据,并且它们强烈暗示突触前调节通过D2型多巴胺受体释放DA的存在。

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