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  <identifier identifierType="DOI">10.7910/DVN/CYOOXJ</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Dong-ho Youn</creatorName>
      <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="https://orcid.org">https://orcid.org/0000-0003-2460-4610</nameIdentifier>
      <affiliation>Department of Oral Physiology, School of Dentistry, Kyungpook National University, Daegu, Korea</affiliation>
    </creator>
    <creator>
      <creatorName nameType="Personal">Jiyeon Jun</creatorName>
      <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="https://orcid.org">https://orcid.org/0000-0002-4238-2751</nameIdentifier>
      <affiliation>Department of Oral Physiology, School of Dentistry, Kyungpook National University, Daegu, Korea</affiliation>
    </creator>
    <creator>
      <creatorName nameType="Personal">Tae Wan Kim</creatorName>
      <givenName>Tae Wan</givenName>
      <familyName>Kim</familyName>
      <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="https://orcid.org">https://orcid.org/0000-0002-7943-4682</nameIdentifier>
      <affiliation>Department of Physiology, College of Veterinary Medicine, Kyungpook National University, Daegu, Korea</affiliation>
    </creator>
    <creator>
      <creatorName nameType="Personal">Kibeom Park</creatorName>
      <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="https://orcid.org">https://orcid.org/0000-0002-1432-8301</nameIdentifier>
      <affiliation>Department of Anesthesiology and Pain Medicine, Keimyung University Dongsan Hospital, Keimyung University School of Medicine, Daegu, Korea</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Spinal orexin A attenuates opioid-induced mechanical hypersensitivity in the rat</title>
  </titles>
  <publisher>Harvard Dataverse</publisher>
  <publicationYear>2022</publicationYear>
  <subjects>
    <subject>Medicine, Health and Life Sciences</subject>
    <subject>Analgesics, Opioid</subject>
    <subject>Dynorphins</subject>
    <subject>Enkephalin, Ala(2)-MePhe(4)-Gly(5)-</subject>
    <subject>Hyperalgesia</subject>
    <subject>Orexins</subject>
    <subject>Orexin Receptors</subject>
    <subject>Pain</subject>
    <subject>Spinal Cord Dorsal Horn</subject>
  </subjects>
  <contributors>
    <contributor contributorType="ContactPerson">
      <contributorName nameType="Personal">Kibeom Park</contributorName>
      <affiliation>Department of Anesthesiology and Pain Medicine, Keimyung University Dongsan Hospital, Keimyung University School of Medicine, Daegu, Korea</affiliation>
    </contributor>
  </contributors>
  <dates>
    <date dateType="Submitted">2022-09-20</date>
    <date dateType="Available">2022-09-20</date>
  </dates>
  <resourceType resourceTypeGeneral="Dataset"/>
  <sizes>
    <size>14382</size>
    <size>13844</size>
    <size>571973</size>
    <size>20309</size>
  </sizes>
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  <version>1.0</version>
  <rightsList>
    <rights rightsURI="info:eu-repo/semantics/openAccess"/>
    <rights rightsURI="http://creativecommons.org/publicdomain/zero/1.0" rightsIdentifier="CC0-1.0" rightsIdentifierScheme="SPDX" schemeURI="https://spdx.org/licenses/" xml:lang="en">Creative Commons CC0 1.0 Universal Public Domain Dedication.</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Repeated administration of opioid analgesics for pain treatment can
produce paradoxical hyperalgesia via peripheral and/or central mechanisms. Thus,
this study investigated whether spinally (centrally) administered orexin A attenuates
opioid-induced hyperalgesia (OIH).
[D-Ala2, N-Me-Phe4, Gly5-ol]-enkephalin (DAMGO), a selective μ-opioid
receptor agonist, was used to induce mechanical hypersensitivity and was administered
intradermally (4 times, 1-hour intervals) on the rat hind paw dorsum. To determine
whether post- or pretreatments with spinal orexin A, dynorphin A, and antidynorphin
A were effective in OIH, the drugs were injected through an intrathecal
catheter whose tip was positioned dorsally at the L3 segment of the spinal cord (5
μg for all). Mechanical hypersensitivity was assessed using von Frey monofilaments.</description>
    <description descriptionType="Other">KJP-22-174</description>
  </descriptions>
</resource>
