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Anatomy of Primary Afferents and Projection Neurones in the Rat Spinal Dorsal Horn with Particular Emphasis on Substance P and the Neurokinin 1 Receptor
Author(s) -
Todd A. J.
Publication year - 2002
Publication title -
experimental physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.925
H-Index - 101
eISSN - 1469-445X
pISSN - 0958-0670
DOI - 10.1113/eph8702351
Subject(s) - neuroscience , substance p , medulla oblongata , nociception , spinal cord , biology , anatomy , nociceptor , medulla , tachykinin receptor 1 , population , neuropeptide , central nervous system , receptor , medicine , biochemistry , environmental health
The dorsal horn of the spinal cord plays an important role in transmitting information from nociceptive primary afferent neurones to the brain; however, our knowledge of its neuronal and synaptic organisation is still limited. Nociceptive afferents terminate mainly in laminae I and II and some of these contain substance P. Many projection neurones are located in lamina I and these send axons to various parts of the brain, including the caudal ventrolateral medulla (CVLM), parabrachial area, periaqueductal grey matter and thalamus. The neurokinin 1 (NK1) receptor on which substance P acts is expressed by certain neurones in the dorsal horn, including approximately 80% of lamina I projection neurones. There is also a population of large NK1 receptor‐immunoreactive neurones with cell bodies in laminae III and IV which project to the CVLM and parabrachial area. It has been shown that the lamina III/IV NK1 receptor‐immunoreactive projection neurones are densely and selectively innervated by substance P‐containing primary afferent neurones, and there is evidence that these afferents also target lamina I projection neurones with the receptor. Both types of neurone are innervated by descending serotoninergic axons from the medullary raphe nuclei. The lamina III/IV neurones also receive numerous synapses from axons of local inhibitory interneurones which contain GABA and neuropeptide Y, and again this input shows some specificity since post‐synaptic dorsal column neurones which also have cell bodies in laminae III and IV receive few contacts from neuropeptide Y‐containing axons. These observations indicate that there are specific patterns of synaptic connectivity within the spinal dorsal horn.

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