Source:http://linkedlifedata.com/resource/pubmed/id/18824159
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2008-11-17
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pubmed:abstractText |
Eugenol is an aromatic molecule found in several plants and widely used in dentistry for analgesic and antiseptic purposes. It inhibits pro-inflammatory mediators including nitric oxide synthase, cyclooxygenase and lipoxygenase. It also regulates ion channels involved in pain signaling, such as TRPV1 receptor, high-voltage-activated Ca(2+) channels, NMDA receptor and GABA(A) receptor. The expression and functional properties of voltage-gated Na(+) channels in primary sensory neurons are altered following inflammation or nerve injury. To elucidate an involvement of Na(+) channels in the eugenol-induced analgesia we investigated the effects of eugenol on tetrodotoxin-sensitive (TTX-S) and tetrodotoxin-resistant (TTX-R) Na(+) currents in acutely dissociated rat dorsal root ganglion neurons. Eugenol inhibited TTX-S and TTX-R Na(+) currents in a concentration-dependent manner. The K(d) values were 308 muM and 543 muM, respectively. Eugenol did not influence the activation voltage of either type of Na(+) current. However, eugenol moved the steady-state inactivation curves of both Na(+) currents to a hyperpolarizing direction and reduced the maximal Na(+) current. Thus eugenol appears to inhibit Na(+) currents through its interaction with both resting and inactivated Na(+) channels. The recovery from inactivation of both Na(+) currents was slowed by eugenol. The eugenol inhibition of Na(+) currents was not dependent on the stimulus frequency. The inhibition of Na(+) currents is considered as one of the mechanisms by which eugenol exerts analgesia.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Analgesics,
http://linkedlifedata.com/resource/pubmed/chemical/Eugenol,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrodotoxin
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1872-6240
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
3
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pubmed:volume |
1243
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
53-62
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pubmed:meshHeading |
pubmed-meshheading:18824159-Analgesics,
pubmed-meshheading:18824159-Animals,
pubmed-meshheading:18824159-Cells, Cultured,
pubmed-meshheading:18824159-Dose-Response Relationship, Drug,
pubmed-meshheading:18824159-Eugenol,
pubmed-meshheading:18824159-Ganglia, Spinal,
pubmed-meshheading:18824159-Ion Channel Gating,
pubmed-meshheading:18824159-Membrane Potentials,
pubmed-meshheading:18824159-Nociceptors,
pubmed-meshheading:18824159-Pain,
pubmed-meshheading:18824159-Patch-Clamp Techniques,
pubmed-meshheading:18824159-Rats,
pubmed-meshheading:18824159-Sensory Receptor Cells,
pubmed-meshheading:18824159-Sodium Channel Blockers,
pubmed-meshheading:18824159-Sodium Channels,
pubmed-meshheading:18824159-Tetrodotoxin
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pubmed:year |
2008
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pubmed:articleTitle |
Effects of eugenol on Na+ currents in rat dorsal root ganglion neurons.
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pubmed:affiliation |
Department of Pharmacology, College of Medicine, Chung-Ang University, 221 Heuksuk-Dong, Dongjak-Ku, Seoul 156-756, Republic of Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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