首页> 美国卫生研究院文献>The Journal of Physiology >Concomitant changes in formaldehyde-induced fluorescence of dopamine interneurones and in slow inhibitory post-synaptic potentials of the rabbit superior cervical ganglion induced by stimulation of the preganglionic nerve or by a muscarinic agent
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Concomitant changes in formaldehyde-induced fluorescence of dopamine interneurones and in slow inhibitory post-synaptic potentials of the rabbit superior cervical ganglion induced by stimulation of the preganglionic nerve or by a muscarinic agent

机译:刺激神经节前神经或毒蕈碱剂诱导的甲醛诱导的多巴胺中间神经元荧光变化和兔上颈神经节的缓慢抑制突触后电位变化

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摘要

1. Dopamine was identified by formaldehyde histochemistry and cytospectrofluorometry in the rabbit's superior cervical ganglion. Dopamine was localized to the intraganglionic `small intensely fluorescent' cells, and also to the characteristically beaded fibres forming a network in close contact with virtually all ganglion cell bodies. The extensive beaded fibres are therefore presumed to be processes of the small intensely fluorescent cells.2. Changes in the dopamine content of these interneurones were studied by recording alterations in their relative fluorescence intensity in conjunction with changes in the slow inhibitory post-synaptic potential (s.-i.p.s.p.) response of the ganglion to orthodromic nerve input.3. Dopamine content was lower after several hours in vitro even without special stimulation; this was in accord with a regularly observed spontaneous reduction of the s.-i.p.s.p. response.4. After a period of conditioning stimulation of the preganglionic nerve, in the presence of an anticholinesterase agent (eserine) and an inhibitor of catecholamine synthesis (α-methyl-p-tyrosine), the s.-i.p.s.p. was selectively and markedly reduced. The dopamine fluorescence in the small intensely fluorescent cell interneurones was also significantly reduced, to a mean value of about 55 or 60% of the fluorescence in the dopamine interneurones of the paired but unstimulated control ganglion. A significant reduction in dopamine fluorescence was always accompanied by a marked loss of s.-i.p.s.p. response; the reverse was not always true.5. Treatment with the muscarinic agent bethanechol for 30 min, with no α-methyl-p-tyrosine or eserine present, similarly resulted in reductions in the s.-i.p.s.p. response of the ganglia and in the formaldehyde-induced fluorescence of the dopamine interneurones.6. A functional uptake of extrinsic dopamine by the dopamine interneurones was also demonstrated: temporary exposure to dopamine restored a large fraction of both the s.-i.p.s.p. response and the dopamine fluorescence of the small intensely fluorescent cells, in ganglia already subjected either to the conditioning stimulation of the preganglionic nerve or to the action of bethanechol.7. It is concluded that (a) preganglionic impulses, by a cholinergic muscarinic synaptic action, can induce a release of dopamine from dopamine interneurones (small intensely fluorescent cells) in the superior cervical ganglion, (b) the ability of the ganglion to respond with a s.-i.p.s.p. to orthodromic input may be viewed as being dependent on the supply of functionally releasable dopamine in these interneurones, (c) the functionally releasable transmitter in vitro appears to comprise roughly 50% of the total dopamine content of the interneurones, and (d) the results fulfil some of the requirements of the hypothesis that a dopamine interneurone is activated muscarinically by preganglionic nerve impulses and mediates the production of s.-i.p.s.p. in sympathetic ganglion cells.
机译:1.通过甲醛组织化学和细胞荧光光谱法鉴定了兔上颈神经节中的多巴胺。多巴胺定位于神经节内的“小强荧光”细胞,并定位于形成与几乎所有神经节细胞体紧密接触的网络的特征性串珠纤维。因此,粗大的串珠纤维被认为是小的强荧光细胞的过程。2。研究了这些中间神经元的多巴胺含量的变化,方法是记录它们的相对荧光强度的变化,以及神经节对正畸神经输入的缓慢抑制性突触后电位(s.-i.p.s.p.)的变化; 3。即使在没有特殊刺激的情况下,体外几个小时后多巴胺的含量也会降低;这与定期观察到的s.-i.p.s.p的自发减少是一致的。回应4。在一段节律性刺激神经节前神经后,在抗胆碱酯酶药(丝氨酸)和儿茶酚胺合成抑制剂(α-甲基-对-酪氨酸)存在下,s.-i.p.s.p。被选择性地显着降低。较小的强荧光细胞间神经元中的多巴胺荧光也显着降低,为配对但未刺激的对照神经节中多巴胺间质中荧光的平均值的约55或60%。多巴胺荧光的显着降低总是伴随着s.-i.p.s.p的明显损失。响应;相反并非总是如此5。用毒蕈碱剂苯甲酚处理30分钟,不存在α-甲基-对-酪氨酸或色氨酸,同样导致s.-i.p.s.p.降低。神经节的响应和在多巴胺中间神经元的甲醛诱导的荧光中6。多巴胺中间神经元对外源性多巴胺的功能吸收也得到了证实:暂时暴露于多巴胺可恢复大部分的s.-i.p.s.p.神经节中已经受到神经节前神经的条件性刺激或苯甲酰胆碱作用的神经节中的强荧光小细胞的多巴胺反应和多巴胺荧光。7。结论是:(a)神经节前冲动通过胆碱能毒蕈碱突触作用,可诱导上颈神经节中多巴胺中间神经元(小的强荧光细胞)释放多巴胺,(b)神经节对神经节蛋白的反应能力。 ips输入到正畸输入可能被视为取决于这些中间神经元中功能可释放的多巴胺的供应,(c)体外功能可释放的递质似乎占中间神经元总多巴胺含量的大约50%,并且(d)结果满足以下假设的某些要求:多巴胺中间神经元通过节前神经冲动经毒蕈碱激活并介导s.ipsp的产生在交感神经节细胞中。

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