Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
1994-2-14
pubmed:abstractText
Morphine enhanced the noxious thermal stimulus-evoked responses in 4/13 (31%) selectively nocireceptive neurons in the superficial dorsal horn, inhibited the responses in 4/13 (31%) neurons and produced a biphasic effect in 2/13 (17%) neurons. Naloxone antagonized these effects in 7/7 neurons. In contrast, morphine produced a naloxone reversible reduction in the nociceptive responses of 4/4 (100%) multireceptive neurons in the deeper dorsal horn of the medulla. The data are interpreted to indicate that opiates may differentially modulate nociceptive input in the superficial versus the deeper dorsal horn.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0006-8993
pubmed:author
pubmed:issnType
Print
pubmed:day
29
pubmed:volume
626
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
318-21
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
Morphine differentially modulates nociceptive input in the superficial versus the deeper dorsal horn of the medulla (trigeminal nucleus caudalis) in the rat.
pubmed:affiliation
Department of Physiology, Meharry Medical College, Nashville, TN 37208.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.