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豚鼠小肠中具有神经介素U样免疫反应性的神经元投射

Projections of neurons with neuromedin U-like immunoreactivity in the small intestine of the guinea-pig.

作者信息

Furness J B, Pompolo S, Murphy R, Giraud A

机构信息

Centre for Neuroscience, Medical School, Flinders University, Bedford Park, South Australia.

出版信息

Cell Tissue Res. 1989 Aug;257(2):415-22. doi: 10.1007/BF00261844.

DOI:10.1007/BF00261844
PMID:2476233
Abstract

Neuromedin U immunoreactivity was located histochemically in the guinea-pig small intestine. Projections of immunoreactive neurons were determined by analysing patterns of degeneration following nerve lesions. The co-localization of neuromedin U immunoreactivity with immunoreactivity for substance P, neuropeptide Y, vasoactive intestinal peptide and calbindin was also investigated. Neuromedin U immunoreactivity was found in nerve cells in the myenteric and submucous plexuses and in nerve fibres in these ganglionated plexuses, around submucous arterioles and in the mucosa. Reactive fibres did not supply the muscle layers. Most reactive nerve cells in the myenteric ganglia had Dogiel type-II morphology and in many there was co-localization of calbindin, although some Dogiel type-II neuromedin U neurons were calbindin negative. Lesion studies suggest that these myenteric neurons project circumferentially to local myenteric ganglia. Projections from myenteric neurons also run anally in the myenteric plexus, while other projections extend to submucous ganglia, and still further projections run from the intestine to provide terminals in the coeliac ganglia. In the submucous ganglia neuromedin U was co-localized in three populations of nerve cells: (i) those with vasoactive intestinal peptide immunoreactivity, (ii) neurons containing neuropeptide Y, and (iii) neurons containing substance P. Each of these populations sends nerve fibres to the mucosa. Neuromedin U immunoreactivity is thus located in a variety of neurons serving different functions in the intestine and therefore probably does not have a single role in intestinal physiology.

摘要

通过组织化学方法确定,神经介素U免疫反应性位于豚鼠小肠中。通过分析神经损伤后变性模式来确定免疫反应性神经元的投射。还研究了神经介素U免疫反应性与P物质、神经肽Y、血管活性肠肽和钙结合蛋白免疫反应性的共定位情况。在肌间神经丛和黏膜下神经丛的神经细胞中,以及在这些有神经节的神经丛中的神经纤维、黏膜下小动脉周围和黏膜中发现了神经介素U免疫反应性。反应性纤维不支配肌肉层。肌间神经节中的大多数反应性神经细胞具有多极II型形态,许多细胞中存在钙结合蛋白的共定位,尽管一些多极II型神经介素U神经元为钙结合蛋白阴性。损伤研究表明,这些肌间神经元向周围的局部肌间神经节投射。肌间神经元的投射也在肌间神经丛中向肛门方向延伸,而其他投射延伸至黏膜下神经节,还有一些投射从肠道延伸至腹腔神经节并提供终末。在黏膜下神经节中,神经介素U在三类神经细胞中共定位:(i)具有血管活性肠肽免疫反应性的细胞,(ii)含有神经肽Y的神经元,以及(iii)含有P物质的神经元。这些细胞群中的每一个都向黏膜发送神经纤维。因此,神经介素U免疫反应性位于肠道中具有不同功能的多种神经元中,因此可能在肠道生理学中不具有单一作用。

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本文引用的文献

1
The fine structure of the submucous plexus of the guinea-pig ileum. I. The ganglia, neurons, Schwann cells and neuropil.豚鼠回肠黏膜下神经丛的精细结构。I. 神经节、神经元、施万细胞和神经毡。
J Neurocytol. 1981 Oct;10(5):759-84. doi: 10.1007/BF01262652.
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Choline acetyltransferase- and peptide immunoreactivity of submucous neurons in the small intestine of the guinea-pig.豚鼠小肠黏膜下神经元的胆碱乙酰转移酶和肽免疫反应性
Cell Tissue Res. 1984;237(2):329-36. doi: 10.1007/BF00217152.
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Neurochemically similar myenteric and submucous neurons directly traced to the mucosa of the small intestine.
Mucosal Immunol. 2022 Jan;15(1):27-39. doi: 10.1038/s41385-021-00443-1. Epub 2021 Sep 1.
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Neuromedin U, a Key Molecule in Metabolic Disorders.神经调节素 U,代谢紊乱中的关键分子。
Int J Mol Sci. 2021 Apr 19;22(8):4238. doi: 10.3390/ijms22084238.
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Neuromedin U: potential roles in immunity and inflammation.神经钙黏素 U:在免疫和炎症中的潜在作用。
Immunology. 2021 Jan;162(1):17-29. doi: 10.1111/imm.13257. Epub 2020 Sep 16.
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Emerging pharmacology and physiology of neuromedin U and the structurally related peptide neuromedin S.神经调节素 U 和结构相关肽神经调节素 S 的新兴药理学和生理学。
Br J Pharmacol. 2009 Sep;158(1):87-103. doi: 10.1111/j.1476-5381.2009.00252.x. Epub 2009 Jun 10.
7
The antiobesity effects of centrally administered neuromedin U and neuromedin S are mediated predominantly by the neuromedin U receptor 2 (NMUR2).中枢给予神经介素U和神经介素S的抗肥胖作用主要由神经介素U受体2(NMUR2)介导。
Endocrinology. 2009 Jul;150(7):3101-9. doi: 10.1210/en.2008-1772. Epub 2009 Mar 26.
8
Neuromedin U can exert colon-specific, enteric nerve-mediated prokinetic activity, via a pathway involving NMU1 receptor activation.神经介素U可通过涉及NMU1受体激活的途径发挥结肠特异性、肠神经介导的促动力活性。
Br J Pharmacol. 2007 Feb;150(4):502-8. doi: 10.1038/sj.bjp.0707004. Epub 2007 Jan 8.
9
Species-dependent smooth muscle contraction to Neuromedin U and determination of the receptor subtypes mediating contraction using NMU1 receptor knockout mice.神经介素U对不同物种平滑肌的收缩作用以及利用NMU1受体敲除小鼠确定介导收缩的受体亚型
Br J Pharmacol. 2006 Apr;147(8):886-96. doi: 10.1038/sj.bjp.0706677.
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Cytoplasmic, but not nuclear, expression of the neuronal nuclei (NeuN) antibody is an exclusive feature of Dogiel type II neurons in the guinea-pig gastrointestinal tract.神经元细胞核(NeuN)抗体的细胞质而非细胞核表达是豚鼠胃肠道中Dogiel II型神经元的一个独特特征。
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神经化学性质相似的肌间神经丛和黏膜下神经元直接追溯至小肠黏膜。
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Neuromedin U-8 and U-25: novel uterus stimulating and hypertensive peptides identified in porcine spinal cord.神经介素U-8和U-25:在猪脊髓中发现的新型子宫刺激肽和升压肽。
Biochem Biophys Res Commun. 1985 Aug 15;130(3):1078-85. doi: 10.1016/0006-291x(85)91726-7.
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Occurrence and developmental pattern of neuromedin U-immunoreactive nerves in the gastrointestinal tract and brain of the rat.大鼠胃肠道和脑中神经介素U免疫反应性神经的发生及发育模式
Neuroscience. 1988 Jun;25(3):797-816. doi: 10.1016/0306-4522(88)90037-1.
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Electrophysiology of guinea-pig myenteric neurons correlated with immunoreactivity for calcium binding proteins.
J Auton Nerv Syst. 1988 Mar;22(2):141-50. doi: 10.1016/0165-1838(88)90087-2.
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Immunohistochemical evidence for the presence of calcium-binding proteins in enteric neurons.肠道神经元中存在钙结合蛋白的免疫组织化学证据。
Cell Tissue Res. 1988 Apr;252(1):79-87. doi: 10.1007/BF00213828.
8
Distribution and characterisation of neuromedin U-like immunoreactivity in rat brain and intestine and in guinea pig intestine.神经介素U样免疫反应性在大鼠脑和肠以及豚鼠肠中的分布与特性
Regul Pept. 1988 Apr;20(4):281-92. doi: 10.1016/0167-0115(88)90063-8.
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Topographic localization of neuromedin U-like structures in the rat brain: an immunohistochemical study.大鼠脑中神经介素U样结构的定位:一项免疫组织化学研究。
Neuroscience. 1987 Dec;23(3):1103-22. doi: 10.1016/0306-4522(87)90185-0.
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Neuromedin U octapeptide alters ion transport in porcine jejunum.神经介素U八肽改变猪空肠中的离子转运。
Eur J Pharmacol. 1988 Oct 11;155(1-2):159-62. doi: 10.1016/0014-2999(88)90415-3.