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在佐剂或福尔马林诱导的伤害感受过程中,大鼠脊髓背角中NK-1和NK-3型速激肽受体mRNA表达增加。

NK-1 and NK-3 type tachykinin receptor mRNA expression in the rat spinal cord dorsal horn is increased during adjuvant or formalin-induced nociception.

作者信息

McCarson K E, Krause J E

机构信息

Department of Anatomy and Neurobiology, Washington University School of Medicine, Saint Louis, Missouri 63110.

出版信息

J Neurosci. 1994 Feb;14(2):712-20. doi: 10.1523/JNEUROSCI.14-02-00712.1994.

Abstract

Substance P (SP) and other related tachykinins such as neurokinin B (NKB) have been studied widely as mediators of sensory information. The release of SP into the dorsal horn of the spinal cord is increased during nociception, and SP activates nociception-specific dorsal horn neurons. The tachykinin NKB has antinociceptive effects in the spinal cord and is contained in intrinsic spinal neurons; thus, NKB may also contribute to the processing of sensory information. Both neurokinin-1 (NK-1) and neurokinin-3 (NK-3) receptors have been localized in the superficial laminae of the dorsal horn. This study investigated changes in NK-1 and NK-3 receptor mRNA expression during nociception. Following injection of either formalin or complete Freund's adjuvant (CFA) into one hindpaw, the levels of expression of NK-1 and NK-3 mRNAs in the spinal cord dorsal horn and preprotachykinin (PPT) mRNA expression in the lumbar dorsal root ganglia (DRG) were quantitated using solution hybridization-nuclease protection assays. Peptide and receptor mRNA expression levels were normalized to beta-actin mRNA levels, which did not change during the treatments. Formalin (2 or 6 hr) or CFA (4 d) injection produced approximately a twofold increase in SP-encoding PPT mRNA expression in the ipsilateral lumbar DRG. Increased activity in primary afferent neurons containing SP may stimulate the production of SP precursors, providing substrate for increased SP production, release, and turnover in the dorsal horn and periphery.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

P物质(SP)和其他相关速激肽,如神经激肽B(NKB),作为感觉信息的介质已被广泛研究。在伤害感受过程中,SP释放到脊髓背角增加,且SP激活伤害感受特异性背角神经元。速激肽NKB在脊髓中具有抗伤害感受作用,且存在于脊髓固有神经元中;因此,NKB也可能参与感觉信息的处理。神经激肽-1(NK-1)和神经激肽-3(NK-3)受体均已定位在背角的浅层。本研究调查了伤害感受过程中NK-1和NK-3受体mRNA表达的变化。在一侧后爪注射福尔马林或完全弗氏佐剂(CFA)后,使用溶液杂交-核酸酶保护试验定量脊髓背角中NK-1和NK-3 mRNA的表达水平以及腰段背根神经节(DRG)中前速激肽原(PPT)mRNA的表达水平。将肽和受体mRNA表达水平标准化为β-肌动蛋白mRNA水平,其在处理过程中未发生变化。注射福尔马林(2或6小时)或CFA(4天)使同侧腰段DRG中编码SP的PPT mRNA表达增加约两倍。含有SP的初级传入神经元活性增加可能刺激SP前体的产生,为背角和外周中SP产生、释放及周转增加提供底物。(摘要截短于250字)

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