Effect of medial bulboreticular and raphe nuclear lesions on the excitation and modulation of supraspinal nocifensive behaviors in the cat
dc.contributor.author | Casey, Kenneth L. | en_US |
dc.contributor.author | Morrow, Thomas J. | en_US |
dc.date.accessioned | 2006-04-07T20:40:03Z | |
dc.date.available | 2006-04-07T20:40:03Z | |
dc.date.issued | 1989-10-30 | en_US |
dc.identifier.citation | Casey, Kenneth L., Morrow, Thomas J. (1989/10/30)."Effect of medial bulboreticular and raphe nuclear lesions on the excitation and modulation of supraspinal nocifensive behaviors in the cat." Brain Research 501(1): 150-161. <http://hdl.handle.net/2027.42/27712> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6SYR-484M7VY-10R/2/1626b8facdd438ca13c6b8b8d53a06d2 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/27712 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2804690&dopt=citation | en_US |
dc.description.abstract | Six cats were trained to eat while partially restrained and while thermal pulse stimuli (43-60 [deg]C, 5 s duration) were delivered to the upper hindlimbs. Food and stimulus delivery were under programmed electronic control. The probability and latency of 3 natural, unlearned nocifensive behaviors were electronically registered: interruption of eating of of exploring for food, hindlimb movement and vocalization. Preoperatively, all cats showed significant increases in the probability of two or more behaviors as stimulus temperature increased. Each cat also showed a significant food-induced suppression of one or more of these behaviors. Thermocoagulation lesions limited to the giganto- and magnocellular fields of the medial medullary reticular formation (4 cats) produced a decrease in nocifensive responsiveness. Larger lesions within the same area but with extension into the postpyramidal raphe nuclei, resulted in increased nocifensive responsiveness (2 cats). No lesion affected response latency or the food-induced modulation of nocifensive behavior. The results support the hypothesis that supraspinally organized nocifensive responses are: (1) tonically facilitated by neural activity originating in or passing through the medial bulboreticular formation; (2) tonically suppressed by midline raphe spinal neurons; and (3) phasically modulated by suprabulbar neural mechanisms that are related to changes in behavioral state. | en_US |
dc.format.extent | 970070 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.title | Effect of medial bulboreticular and raphe nuclear lesions on the excitation and modulation of supraspinal nocifensive behaviors in the cat | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Neurosciences | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Neurology, University of Michigan, VA Medical Center, Ann Arbor, MI 48105, U.S.A.; Department of Physiology, University of Michigan, VA Medical Center, Ann Arbor, MI 48105, U.S.A.; Department of Neurology Research Laboratories, University of Michigan, VA Medical Center, Ann Arbor, MI 48105, U.S.A. | en_US |
dc.contributor.affiliationum | Department of Neurology Research Laboratories, University of Michigan, VA Medical Center, Ann Arbor, MI 48105, U.S.A.; Department of Physiology, University of Michigan, VA Medical Center, Ann Arbor, MI 48105, U.S.A. | en_US |
dc.identifier.pmid | 2804690 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/27712/1/0000100.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0006-8993(89)91036-6 | en_US |
dc.identifier.source | Brain Research | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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