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神经肽编码交感节前神经元;关注肾上腺投射群体。

Neuropeptide coding of sympathetic preganglionic neurons; focus on adrenally projecting populations.

机构信息

The Australian School of Advanced Medicine, Faculty of Human Sciences, Macquarie University, Sydney, NSW, 2109, Australia.

出版信息

Neuroscience. 2010 Oct 27;170(3):789-99. doi: 10.1016/j.neuroscience.2010.07.047. Epub 2010 Jul 29.

Abstract

Chemical coding of sympathetic preganglionic neurons (SPN) suggests that the chemical content of subpopulations of SPN can define their function. Since neuropeptides, once synthesized are transported to the axon terminal, most demonstrated chemical coding has been identified using immunoreactive terminals at the target organ. Here, we use a different approach to identify and quantify the subpopulations of SPN that contain the mRNA for pituitary adenylate cyclase activating polypeptide (PACAP) or enkephalin. Using double-labeled immunohistochemistry combined with in situ hybridization (ISH) we firstly identified the distribution of these mRNAs in the spinal cord and determined quantitatively, in Sprague-Dawley rats, that many SPN at the T4-T10 spinal level contain preproPACAP (PPP+, 80 ± 3%, n=3), whereas a very small percentage contain preproenkephalin (PPE+, 4 ± 2%, n=4). A similar neurochemical distribution was found at C8-T3 spinal level. These data suggest that PACAP potentially regulates a large number of functions dictated by SPN whereas enkephalins are involved in few functions. We extended the study to explore those SPN that control adrenal chromaffin cells. We found 97 ± 5% of adrenally projecting SPN (AP-SPN) to be PPP+ (n=4) with only 47 ± 3% that were PPE+ (n=5). These data indicate that adrenally projecting PACAPergic SPN regulate both adrenal adrenaline (Ad) and noradrenaline (NAd) release whereas the enkephalinergic SPN subpopulation must control a (sub) population of chromaffin cells - most likely those that release Ad. The sensory innervation of the adrenal gland was also determined. Of the few adrenally projecting dorsal root ganglia (AP-DRG) observed, 74 ± 12% were PPP+ (n=3), whereas 1 ± 1% were PPE+ (n=3). Therefore, if sensory neurons release peptides to the adrenal medulla, PACAP is most likely involved. Together, these data provide a neurochemical basis for differential control of sympathetic outflow particularly that to the adrenal medulla.

摘要

交感节前神经元(SPN)的化学编码表明,SPN 亚群的化学物质含量可以决定其功能。由于神经肽一旦合成就会被运送到轴突末梢,因此大多数已证明的化学编码都是通过在靶器官的免疫反应性末梢来确定的。在这里,我们采用一种不同的方法来识别和量化含有垂体腺苷酸环化酶激活肽(PACAP)或脑啡肽 mRNA 的 SPN 亚群。我们使用双标记免疫组织化学结合原位杂交(ISH)首先确定了这些 mRNA 在脊髓中的分布,并在 Sprague-Dawley 大鼠中定量确定,T4-T10 脊髓水平的许多 SPN 含有前垂体腺苷酸环化酶激活肽(PPP+,80±3%,n=3),而一小部分含有前脑啡肽(PPE+,4±2%,n=4)。在 C8-T3 脊髓水平也发现了类似的神经化学分布。这些数据表明,PACAP 可能调节由 SPN 决定的大量功能,而脑啡肽则参与很少的功能。我们扩展了这项研究,以探索那些控制肾上腺嗜铬细胞的 SPN。我们发现,97±5%的肾上腺投射 SPN(AP-SPN)为 PPP+(n=4),而只有 47±3%为 PPE+(n=5)。这些数据表明,肾上腺投射的 PACAP 能 SPN 调节肾上腺肾上腺素(Ad)和去甲肾上腺素(NAd)的释放,而脑啡肽能 SPN 亚群必须控制一个(亚)群的嗜铬细胞-很可能是那些释放 Ad 的细胞。肾上腺的感觉神经支配也被确定。在观察到的少数肾上腺投射背根神经节(AP-DRG)中,74±12%为 PPP+(n=3),而 1±1%为 PPE+(n=3)。因此,如果感觉神经元向肾上腺髓质释放肽,那么 PACAP 很可能参与其中。综上所述,这些数据为交感神经传出的差异控制提供了神经化学基础,特别是对肾上腺髓质的控制。

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