AOAA和依托咪酯对儿茶酚胺末端影响的组织荧光研究。可能是GABA-NA在小脑皮层的相互作用。

Folia histochemica et cytochemica Pub Date : 1980-01-01
M Smiałowska
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引用次数: 0

摘要

采用Falck-Hillarp单胺组织荧光法研究了氨基乙酸(AOAA) (37,5 mg/kg)和依托咪酯(2 X 10 mg/kg)两种gaba能药物对大鼠脑去甲肾上腺素能(NA)和多巴胺能(DA)神经元的影响。两种药物均增强了小脑皮质NA末端的儿茶酚胺能荧光,提示NA含量增加。这种作用可通过微毒素(一种Gaba受体阻断化合物)预处理而被阻断。AOAA后尾壳核DA末端荧光增强(依托咪酯未见),5只大鼠中有3只被微毒素阻断。所得结果表明,除了先前描述的纹状体中GABA-DA的相互作用外,在小脑皮层中也存在GABA-NA的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histofluorescence studies of the effect of AOAA and etomidate on catecholamine terminals. Possible GABA-NA interaction in the cerebellar cortex.

The effect of two GABA-ergic drugs: aminooxyacetic acid (AOAA) (37,5 mg/kg) and etomidate (2 X 10 mg/kg) on noradrenergic (NA) and dopaminergic (DA) neurons in the rat brain was studied using the Falck-Hillarp histofluorescence method for monoamines. Both drugs enhanced the catecholaminergic fluorescence in NA terminals in the cerebellar cortex, which suggests an increase in NA content there. This effect was blocked by pretreatment with picrotoxin, a Gaba receptor blocking compound. The increase in fluorescence was also observed in DA terminals in nucleus caudatus-putamen after AOAA (but not after etomidate) and this effect was blocked by picrotoxin in 3 out of 5 rats. The obtained results indicate that apart from previously described GABA-DA interaction in the striatum, there exists also GABA-NA interaction seen in the cerebellar cortex.

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