The release of catecholamines by an endogenous factor that inhibits neuronal Na+,K(+)-ATPase.

G Rodríguez de Lores Arnaiz, A Pellegrino de Iraldi
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Abstract

It is known that the inhibition of Na+,K(+)-ATPase induces neurotransmitter release in several experimental models. In this laboratory it was previously observed that a brain soluble fraction separated by Sephadex G-50 (peak II) is able to inhibit Na+,K(+)-ATPase but not other membrane-bound enzymes. The object of the present study was to test the effect of brain peak II fraction on neurotransmitter content of the pineal nerves synaptic vesicles. Uninjected rats and rats injected 30 min before with 5-hydroxydopamine (30 mg per kg,i.p.) were used. 5-hydroxydopamine produces a false neurotransmitter whose presence in the synaptic vesicles is visualized after fixation with glutaraldehyde-osmium as an electron dense material with the electron microscope which fills totally or partially the vesicles. In uninjected rats the osmiophilia and the chromaffin reaction of the electron dense core were studied. The pineal glands were incubated in Tyrode solution without calcium in the presence and absence of peak II at room temperature and processed for electron microscopy. When the glands from rats pretreated with 5-hydroxydopamine were incubated with peak II a significant decrease in the number of vesicles totally stained was observed. This indicates a reduction in false neurotransmitter content, specially in the matrix of the synaptic vesicles. In the presence of an aged peak II, which does not inhibit Na+,K(+)-ATPase, this effect on the synaptic vesicles was not observed. When the glands from uninjected rats were incubated with peak II no changes in the osmiophilia and the chromaffin reaction of the synaptic vesicles were found. The osmiophilia and the chromaffin reaction of the cores marks the monoamines storage site (catechol and indoleamines in the pineal nerves). These results are coherent with the idea of a relationship between the inhibition of Na+,K(+)-ATPase activity and the release of a pool of neurotransmitter stored in the nerve endings.

抑制神经元Na+,K(+)- atp酶的内源性因子释放儿茶酚胺。
在几种实验模型中,Na+,K(+)- atp酶的抑制可诱导神经递质释放。在本实验室中,先前观察到由Sephadex G-50(峰II)分离的脑可溶性部分能够抑制Na+,K(+)- atp酶,但不能抑制其他膜结合酶。研究脑ⅱ峰分数对松果体神经突触囊泡神经递质含量的影响。采用未注射大鼠和30 min前注射5-羟多巴胺(30 mg / kg,i.p)的大鼠。5-羟多巴胺产生一种假神经递质,其存在于突触囊泡中,经戊二醛锇固定后,在电子显微镜下可见其作为电子致密物质全部或部分填充囊泡。在未注射的大鼠中,研究了电子致密核的亲锇性和染色质反应。将松果体置于不含钙的Tyrode溶液中,在有和没有峰II的情况下室温孵育,并进行电镜处理。经5-羟多巴胺预处理的大鼠腺体经II峰孵育后,观察到完全染色的囊泡数量明显减少。这表明假神经递质含量减少,特别是在突触囊泡基质中。在不抑制Na+,K(+)- atp酶的老化峰II的存在下,未观察到这种对突触囊泡的影响。未注射的大鼠腺体在II峰孵育时,突触囊泡的亲锇性和嗜铬反应未见变化。核心区的亲渗透性和嗜铬反应标志着松果体神经中单胺类物质(儿茶酚类和吲哚胺类)的储存位置。这些结果与Na+,K(+)- atp酶活性的抑制与储存在神经末梢的神经递质的释放之间的关系的观点是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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