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苯乙醇胺N-甲基转移酶在迷走神经感觉和运动核中的超微结构定位

Ultrastructural localization of phenylethanolamine N-methyltransferase in sensory and motor nuclei of the vagus nerve.

作者信息

Pickel V M, Chan J, Park D H, Joh T H, Milner T A

出版信息

J Neurosci Res. 1986;15(4):439-55. doi: 10.1002/jnr.490150402.

Abstract

The ultrastructural localization of phenylethanolamine N-methyltransferase (PNMT), the enzyme used in the final step in the synthesis of adrenaline, was examined in the medial nuclei of the solitary tracts (m-NTS) and in the dorsal motor nuclei of the vagus. Adult rats were anesthetized with Nembutal (50 mg/kg intraperitoneally), and the brains were fixed by vascular perfusion with a solution containing 3.75% acrolein and 2% paraformaldehyde in 0.1 M phosphate buffer. Coronal Vibratome sections were collected through the intermediate portions of the m-NTS at the level of the area postrema. These sections were immunocytochemically labeled employing a rabbit polyclonal antiserum against PNMT and the peroxidase-antiperoxidase method. Immunoreactivity was detected in perikarya, dendrites, and axon terminals in the intermediate portion of the m-NTS. The labeled perikarya were either small (10-15 microns diameter) and oval or large 20-30 microns) with two or more proximal processes. The PNMT-containing dendrites received synaptic input from unlabeled, small (0.5-1.0 microns) and large (2-3 microns) vagal-like afferents as well as from a few terminals, which also showed PNMT immunoreactivity. Axons and axon terminals containing immunoreactive PNMT were more frequently observed than the perikarya or dendrites in the m-NTS and were the only labeled profiles in the dorsal motor nuclei. In both regions the PNMT-labeled terminals formed principally symmetric synapses with unlabeled dendrites. However, a few asymmetric axodendritic and symmetric axosomatic synapses also were detected. These findings indicate that the adrenergic neurons may have multiple, but principally inhibitory, actions on other neurons within cardiovagal portions of baroreflex pathways.

摘要

苯乙醇胺N-甲基转移酶(PNMT)是肾上腺素合成最后一步所使用的酶,对其进行超微结构定位研究,观察对象为孤束内侧核(m-NTS)和迷走神经背运动核。成年大鼠用戊巴比妥(50mg/kg腹腔注射)麻醉,通过血管灌注含有3.75%丙烯醛和2%多聚甲醛的0.1M磷酸盐缓冲液来固定大脑。在最后区水平,通过m-NTS中间部分收集冠状振动切片。这些切片采用抗PNMT兔多克隆抗血清和过氧化物酶-抗过氧化物酶方法进行免疫细胞化学标记。在m-NTS中间部分的胞体、树突和轴突终末检测到免疫反应性。标记的胞体要么小(直径10-15微米)呈椭圆形,要么大(20-30微米)有两个或更多近端突起。含PNMT的树突接受来自未标记的小(0.5-1.0微米)和大(2-3微米)迷走样传入纤维以及一些也显示PNMT免疫反应性的终末的突触输入。在m-NTS中,含有免疫反应性PNMT的轴突和轴突终末比胞体或树突更常被观察到,并且是迷走神经背运动核中唯一被标记的结构。在这两个区域,PNMT标记的终末主要与未标记的树突形成对称突触。然而,也检测到一些不对称的轴-树突触和对称的轴-体突触。这些发现表明,肾上腺素能神经元可能对压力感受性反射通路的心血管迷走部分内的其他神经元有多种作用,但主要是抑制作用。

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