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大鼠黑质和纹状体中P物质与递质机制之间可能相互作用的研究。

Investigation of possible interactions between substance P and transmitter mechanisms in the substantia nigra and corpus striatum of the rat.

作者信息

Starr M S

出版信息

J Pharm Pharmacol. 1978 Jun;30(6):359-63. doi: 10.1111/j.2042-7158.1978.tb13256.x.

Abstract

The effect of substnace P (SP) on the uptake and release of radiolabelled dopamine (3H-DA), 5-hydroxytryptamine (3H-5-HT) and y-aminobutyric acid (3H-GABA) was studied in slices of rat substantia nigra and corpus triatum. SP, 10(-9) to 10(-5) m, failed to modify the uptakes of these compounds during incubations (10-90 min) with slices of either brain region. SP, 10(-6)M, had no apparent effect on the spontaneous output of any of these compounds in either substantia nigra or corpus striatum. In the corpus striatum, SP seemed to potentiate the potassium-stimulated outflow of 3H-DA and 3H-5-HT, but not 3H-GABA, while the realeases from substantia nigra were unaffected. Morphine (10(-3)M), but not met-enkephalin (5 X 10(-6)M), weakly antagonized K+- EVOKED RELEASE OF 3/-DA in the corpus striatum. These results are discussed with reference to the possible interaction of SP with transmitter mechanisms at presynaptic sites in the central nervous system.

摘要

研究了P物质(SP)对大鼠黑质和纹状体切片中放射性标记多巴胺(3H-DA)、5-羟色胺(3H-5-HT)及γ-氨基丁酸(3H-GABA)摄取和释放的影响。10^(-9)至10^(-5)m的SP在与任一脑区切片共同孵育(10 - 90分钟)期间未能改变这些化合物的摄取。10^(-6)M的SP对黑质或纹状体中任何一种此类化合物的自发释放均无明显影响。在纹状体中,SP似乎增强了钾离子刺激引起的3H-DA和3H-5-HT的外流,但对3H-GABA无此作用,而黑质中的释放未受影响。吗啡(10^(-3)M)而非甲硫氨酸脑啡肽(5×10^(-6)M)可轻度拮抗纹状体中钾离子诱发的3H-DA释放。结合SP与中枢神经系统突触前部位递质机制可能的相互作用对这些结果进行了讨论。

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