{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T13:45:41Z","timestamp":1791380741251,"version":"4.3.3"},"reference-count":46,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2004,10,9]],"date-time":"2004-10-09T00:00:00Z","timestamp":1097280000000},"content-version":"vor","delay-in-days":4219,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Comparative Neurology"],"published-print":{"date-parts":[[1993,3,22]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>The central arborizations in the dorsal horn of the spinal cord of 23 rapidly adapting (RA) A\u2010beta primary afferent neurons innervating different regions of the glabrous skin of the hindpaw were studied by the intra\u2010axonal injection of horseradish peroxidase in adult rats. A total of 284 arbors of the complex, simple, and blind\u2010ending variety were recovered. The arbors of RA afferents innervating the toes, paw pads, and non\u2010pad hindpaw differed from each other in branch pattern and dimensions. The simple and complex arbors, which are both bouton\u2010containing, were distributed mainly in laminae III\u2013V, although some complex arbors projected dorsally into lamina IIi.<\/jats:p>\n                  <jats:p>The hindpaw glabrous skin afferent terminals were located in the lumbar enlargement from caudal L3 to rostral L6. A crude somatotopic organization was observed such that toes 1\u20135 were represented successively in more caudal positions from mid\u2010L4 to caudal L5. The paw pads were organized in a rostrocaudal sequence moving from the paw pads proximal to toe 1 across the foot to the paw pads proximal to toe 5, from caudal L3 to mid\u2010L5. Non\u2010pad hindpaw afferents were located in caudal L5. Overlap between toe, paw pad and non\u2010pad afferent central fields was present, however, and the central terminals of afferents with non\u2010adjacent peripheral receptive fields were shown to occupy the same region of the dorsal horn. \u00a9 1993 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/cne.903290406","type":"journal-article","created":{"date-parts":[[2005,1,1]],"date-time":"2005-01-01T03:43:19Z","timestamp":1104550999000},"page":"491-511","source":"Crossref","is-referenced-by-count":47,"title":["Morphology and somatotopy of the central arborizations of rapidly adapting glabrous skin afferents in the rat lumbar spinal cord"],"prefix":"10.1002","volume":"329","author":[{"given":"Peter","family":"Shortland","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Clifford J.","family":"Woolf","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2004,10,9]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/978-1-4471-1305-8"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1113\/jphysiol.1981.sp013970"},{"key":"e_1_2_1_4_1","doi-asserted-by":"crossref","first-page":"770","DOI":"10.1113\/jphysiol.1977.sp012073","article-title":"Morphology of hair follicle afferent fibre collaterals in the cat spinal cord","volume":"272","author":"Brown A. 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University of London."},{"key":"e_1_2_1_35_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1460-9568.1991.tb00826.x"},{"key":"e_1_2_1_36_1","doi-asserted-by":"publisher","DOI":"10.1098\/rstb.1992.0120"},{"key":"e_1_2_1_37_1","doi-asserted-by":"publisher","DOI":"10.1002\/cne.902890307"},{"key":"e_1_2_1_38_1","first-page":"S29","article-title":"The somatotopic organization of single rapidly adapting afferent terminals in the dorsal horn of the rat lumbar spinal cord","volume":"36","author":"Shortland P.","year":"1989","journal-title":"Neurosci. Lett. 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