Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1998-7-20
pubmed:abstractText
Ginseng root, a traditional oriental medicine, contains more than a dozen biologically active saponins called ginsenosides, including one present in only trace amounts called ginsenoside-Rf (Rf). Previously, we showed that Rf inhibits Ca2+ channels in mammalian sensory neurons through a mechanism requiring G-proteins, whereas a variety of other ginsenosides were relatively ineffective. Since inhibition of Ca2+ channels in sensory neurons contributes to antinociception by opioids, we tested for analgesic actions of Rf. We find dose-dependent antinociception by systemic administration of Rf in mice using two separate assays of tonic pain: in the acetic acid abdominal constriction test, the ED50 was 56+/-9 mg/kg, a concentration similar to those reported for aspirin and acetaminophen in the same assay; in the tonic phase of the biphasic formalin test, the ED50 was 129+/-32 mg/kg. Rf failed to affect nociception measured in three assays of acute pain: the acute phase of the formalin test, and the thermal (49 degrees C) tail-flick and increasing-temperature (3 degrees C/min) hot-plate tests. The simplest explanation is that Rf inhibits tonic pain without affecting acute pain, but other possibilities exist. Seeking a cellular explanation for the effect, we tested whether Rf suppresses Ca2+ channels on identified nociceptors. Inhibition was seen on large, but not small, nociceptors. This is inconsistent with a selective effect on tonic pain, so it seems unlikely that Ca2+ channel inhibition on primary sensory neurons can fully explain the behavioral antinociception we have demonstrated for Rf.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0006-8993
pubmed:author
pubmed:copyrightInfo
Copyright 1998 Elsevier Science B.V.
pubmed:issnType
Print
pubmed:day
11
pubmed:volume
792
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
218-28
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:9593902-Abdominal Muscles, pubmed-meshheading:9593902-Analgesics, pubmed-meshheading:9593902-Animals, pubmed-meshheading:9593902-Behavior, Animal, pubmed-meshheading:9593902-Body Temperature, pubmed-meshheading:9593902-Calcium Channel Blockers, pubmed-meshheading:9593902-Calcium Channels, pubmed-meshheading:9593902-Dose-Response Relationship, Drug, pubmed-meshheading:9593902-Formaldehyde, pubmed-meshheading:9593902-Ginsenosides, pubmed-meshheading:9593902-Hot Temperature, pubmed-meshheading:9593902-Locomotion, pubmed-meshheading:9593902-Mice, pubmed-meshheading:9593902-Neurons, Afferent, pubmed-meshheading:9593902-Nociceptors, pubmed-meshheading:9593902-Pain, pubmed-meshheading:9593902-Panax, pubmed-meshheading:9593902-Patch-Clamp Techniques, pubmed-meshheading:9593902-Plants, Medicinal, pubmed-meshheading:9593902-Saponins, pubmed-meshheading:9593902-Tail
pubmed:year
1998
pubmed:articleTitle
Ginsenoside Rf, a trace component of ginseng root, produces antinociception in mice.
pubmed:affiliation
Dept. of Psychology, University of Illinois at Urbana-Champaign, Champaign, IL 61820, USA. jmogil@s.psych.uiuc.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't