Pharmacokinetics of vanillin and its effects on mechanical hypersensitivity in a rat model of neuropathic pain
Identifieur interne : 001D05 ( Main/Merge ); précédent : 001D04; suivant : 001D06Pharmacokinetics of vanillin and its effects on mechanical hypersensitivity in a rat model of neuropathic pain
Auteurs : Francis Beaudry [Canada] ; Andréanne Ross [Canada] ; Pablo Patricio Lema [Canada] ; Pascal Vachon [Canada]Source :
- Phytotherapy Research [ 0951-418X ] ; 2010-04.
English descriptors
- KwdEn :
Abstract
The analgesic effects of vanillin on neuropathic pain was evaluated using thermal sensitivity and mechanical allodynia using the sciatic nerve constriction model (n = 30 rats). To determine the pharmacokinetics of vanillin, rats (n = 6/administration route) received either 20 or 100 mg/kg of vanillin i.v. and p.o., respectively. For the pharmacodynamic study, baseline levels for hyperalgesia and allodynia were taken for 5 days prior to surgery. Following surgery each group (n = 6 rats/group) received either vanillin (50 mg/kg or 100 mg/kg), morphine (2 mg/kg or 6 mg/kg) or the vehicle only. Pharmacokinetic results following p.o. administrations are Cmax 290.24 ng/mL, Tmax 4 h, relative clearance 62.17 L/h/kg and T1/2 10.3 h. The bioavailability is 7.6%. Mechanical allodynia was decreased on treatment days 1, 2, 3, 5 (p < 0.003) and not on day 4 (p > 0.02) with 50 mg/kg vanillin, whereas at 100 mg/kg p.o. a decrease was noted only on days 7 and 8 (p < 0.003). No effect on hyperalgesia was seen following vanillin administration. In conclusion, vanillin is bioavailable and seems to have an alleviating effect on mechanical allodynia, and not on hyperalgesia, when evaluated with a chronic constriction nerve injury rat model of neuropathic pain. Copyright © 2009 John Wiley & Sons, Ltd.
Url:
DOI: 10.1002/ptr.2975
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001B81
- to stream Istex, to step Curation: 001B81
- to stream Istex, to step Checkpoint: 000578
Links to Exploration step
ISTEX:B49476264C36A83BAEC549863D45BECCEFAAED42Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Pharmacokinetics of vanillin and its effects on mechanical hypersensitivity in a rat model of neuropathic pain</title>
<author><name sortKey="Beaudry, Francis" sort="Beaudry, Francis" uniqKey="Beaudry F" first="Francis" last="Beaudry">Francis Beaudry</name>
</author>
<author><name sortKey="Ross, Andreanne" sort="Ross, Andreanne" uniqKey="Ross A" first="Andréanne" last="Ross">Andréanne Ross</name>
</author>
<author><name sortKey="Lema, Pablo Patricio" sort="Lema, Pablo Patricio" uniqKey="Lema P" first="Pablo Patricio" last="Lema">Pablo Patricio Lema</name>
</author>
<author><name sortKey="Vachon, Pascal" sort="Vachon, Pascal" uniqKey="Vachon P" first="Pascal" last="Vachon">Pascal Vachon</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:B49476264C36A83BAEC549863D45BECCEFAAED42</idno>
<date when="2010" year="2010">2010</date>
<idno type="doi">10.1002/ptr.2975</idno>
<idno type="url">https://api-v5.istex.fr/document/B49476264C36A83BAEC549863D45BECCEFAAED42/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001B81</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001B81</idno>
<idno type="wicri:Area/Istex/Curation">001B81</idno>
<idno type="wicri:Area/Istex/Checkpoint">000578</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000578</idno>
<idno type="wicri:doubleKey">0951-418X:2010:Beaudry F:pharmacokinetics:of:vanillin</idno>
<idno type="wicri:Area/Main/Merge">001D05</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Pharmacokinetics of vanillin and its effects on mechanical hypersensitivity in a rat model of neuropathic pain</title>
<author><name sortKey="Beaudry, Francis" sort="Beaudry, Francis" uniqKey="Beaudry F" first="Francis" last="Beaudry">Francis Beaudry</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>University of Montreal, Faculty of Veterinary Medicine, Department of Veterinary Biomedicine, Saint‐Hyacinthe, QC</wicri:regionArea>
<wicri:noRegion>QC</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Ross, Andreanne" sort="Ross, Andreanne" uniqKey="Ross A" first="Andréanne" last="Ross">Andréanne Ross</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>University of Montreal, Faculty of Veterinary Medicine, Department of Veterinary Biomedicine, Saint‐Hyacinthe, QC</wicri:regionArea>
<wicri:noRegion>QC</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Lema, Pablo Patricio" sort="Lema, Pablo Patricio" uniqKey="Lema P" first="Pablo Patricio" last="Lema">Pablo Patricio Lema</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>University of Montreal, Faculty of Veterinary Medicine, Department of Veterinary Biomedicine, Saint‐Hyacinthe, QC</wicri:regionArea>
<wicri:noRegion>QC</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Vachon, Pascal" sort="Vachon, Pascal" uniqKey="Vachon P" first="Pascal" last="Vachon">Pascal Vachon</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>University of Montreal, Faculty of Veterinary Medicine, Department of Veterinary Biomedicine, Saint‐Hyacinthe, QC</wicri:regionArea>
<wicri:noRegion>QC</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><country>Canada</country>
<wicri:regionArea>Department of Veterinary Biomedicine, Faculty of Veterinary Medicine, University of Montreal, 3200 Sicotte, Saint‐Hyacinthe, Québec</wicri:regionArea>
<wicri:noRegion>Québec</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Phytotherapy Research</title>
<title level="j" type="sub">An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives</title>
<title level="j" type="abbrev">Phytother. Res.</title>
<idno type="ISSN">0951-418X</idno>
<idno type="eISSN">1099-1573</idno>
<imprint><publisher>John Wiley & Sons, Ltd.</publisher>
<pubPlace>Chichester, UK</pubPlace>
<date type="published" when="2010-04">2010-04</date>
<biblScope unit="volume">24</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="525">525</biblScope>
<biblScope unit="page" to="530">530</biblScope>
</imprint>
<idno type="ISSN">0951-418X</idno>
</series>
<idno type="istex">B49476264C36A83BAEC549863D45BECCEFAAED42</idno>
<idno type="DOI">10.1002/ptr.2975</idno>
<idno type="ArticleID">PTR2975</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0951-418X</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>allodynia</term>
<term>neuropathic pain</term>
<term>pharmacokinetics</term>
<term>rats</term>
<term>vanillin</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The analgesic effects of vanillin on neuropathic pain was evaluated using thermal sensitivity and mechanical allodynia using the sciatic nerve constriction model (n = 30 rats). To determine the pharmacokinetics of vanillin, rats (n = 6/administration route) received either 20 or 100 mg/kg of vanillin i.v. and p.o., respectively. For the pharmacodynamic study, baseline levels for hyperalgesia and allodynia were taken for 5 days prior to surgery. Following surgery each group (n = 6 rats/group) received either vanillin (50 mg/kg or 100 mg/kg), morphine (2 mg/kg or 6 mg/kg) or the vehicle only. Pharmacokinetic results following p.o. administrations are Cmax 290.24 ng/mL, Tmax 4 h, relative clearance 62.17 L/h/kg and T1/2 10.3 h. The bioavailability is 7.6%. Mechanical allodynia was decreased on treatment days 1, 2, 3, 5 (p < 0.003) and not on day 4 (p > 0.02) with 50 mg/kg vanillin, whereas at 100 mg/kg p.o. a decrease was noted only on days 7 and 8 (p < 0.003). No effect on hyperalgesia was seen following vanillin administration. In conclusion, vanillin is bioavailable and seems to have an alleviating effect on mechanical allodynia, and not on hyperalgesia, when evaluated with a chronic constriction nerve injury rat model of neuropathic pain. Copyright © 2009 John Wiley & Sons, Ltd.</div>
</front>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Canada/explor/ParkinsonCanadaV1/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001D05 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 001D05 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Canada |area= ParkinsonCanadaV1 |flux= Main |étape= Merge |type= RBID |clé= ISTEX:B49476264C36A83BAEC549863D45BECCEFAAED42 |texte= Pharmacokinetics of vanillin and its effects on mechanical hypersensitivity in a rat model of neuropathic pain }}
![]() | This area was generated with Dilib version V0.6.29. | ![]() |