Healthy Volunteers Can Be Phenotyped Using Cutaneous Sensitization Pain Models

Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeate...

Full description

Saved in:
Bibliographic Details
Published inPloS one Vol. 8; no. 5; p. e62733
Main Authors Werner, Mads U., Petersen, Karin L., Rowbotham, Michael C., Dahl, Jørgen B.
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 09.05.2013
Public Library of Science (PLoS)
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models. We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models. Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1(st) quartile [<25%]) and 'large area' (4(th) quartile [>75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models. Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
AbstractList Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models. We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models. Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1.sup.st quartile [75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models. Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
Background Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models. Methods We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models. Results Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into ‘small area’ (1st quartile [<25%]) and ‘large area’ (4th quartile [>75%]) responders: 56–76% of subjects consistently fell into same ‘small-area’ or ‘large-area’ category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models. Conclusion Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
Background Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models. Methods We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models. Results Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1.sup.st quartile [75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models. Conclusion Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models.BACKGROUNDHuman experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models.We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models.METHODSWe performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models.Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1(st) quartile [<25%]) and 'large area' (4(th) quartile [>75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models.RESULTSWithin-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1(st) quartile [<25%]) and 'large area' (4(th) quartile [>75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models.Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.CONCLUSIONSecondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
BACKGROUND: Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models. METHODS: We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models. RESULTS: Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1(st) quartile [<25%]) and 'large area' (4(th) quartile [>75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models. CONCLUSION: Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models. We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models. Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into 'small area' (1(st) quartile [<25%]) and 'large area' (4(th) quartile [>75%]) responders: 56-76% of subjects consistently fell into same 'small-area' or 'large-area' category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models. Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
Background Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability to develop an area of secondary hyperalgesia varies substantially between subjects, but little is known about the agreement following repeated measurements. The aim of this study was to determine if the areas of secondary hyperalgesia were consistently robust to be useful for phenotyping subjects, based on their pattern of sensitization by the heat pain models. Methods We performed post-hoc analyses of 10 completed healthy volunteer studies (n = 342 [409 repeated measurements]). Three different models were used to induce secondary hyperalgesia to monofilament stimulation: the heat/capsaicin sensitization (H/C), the brief thermal sensitization (BTS), and the burn injury (BI) models. Three studies included both the H/C and BTS models. Results Within-subject compared to between-subject variability was low, and there was substantial strength of agreement between repeated induction-sessions in most studies. The intraclass correlation coefficient (ICC) improved little with repeated testing beyond two sessions. There was good agreement in categorizing subjects into ‘small area’ (1st quartile [<25%]) and ‘large area’ (4th quartile [>75%]) responders: 56–76% of subjects consistently fell into same ‘small-area’ or ‘large-area’ category on two consecutive study days. There was moderate to substantial agreement between the areas of secondary hyperalgesia induced on the same day using the H/C (forearm) and BTS (thigh) models. Conclusion Secondary hyperalgesia induced by experimental heat pain models seem a consistent measure of sensitization in pharmacodynamic and physiological research. The analysis indicates that healthy volunteers can be phenotyped based on their pattern of sensitization by the heat [and heat plus capsaicin] pain models.
Audience Academic
Author Werner, Mads U.
Rowbotham, Michael C.
Dahl, Jørgen B.
Petersen, Karin L.
AuthorAffiliation 1 Multidisciplinary Pain Center, Neuroscience Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
University of Arizona, United States of America
3 Department of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
2 California Pacific Medical Center Research Institute, San Francisco, California, United States of America
AuthorAffiliation_xml – name: 3 Department of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
– name: 2 California Pacific Medical Center Research Institute, San Francisco, California, United States of America
– name: 1 Multidisciplinary Pain Center, Neuroscience Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
– name: University of Arizona, United States of America
Author_xml – sequence: 1
  givenname: Mads U.
  surname: Werner
  fullname: Werner, Mads U.
– sequence: 2
  givenname: Karin L.
  surname: Petersen
  fullname: Petersen, Karin L.
– sequence: 3
  givenname: Michael C.
  surname: Rowbotham
  fullname: Rowbotham, Michael C.
– sequence: 4
  givenname: Jørgen B.
  surname: Dahl
  fullname: Dahl, Jørgen B.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23671631$$D View this record in MEDLINE/PubMed
BookMark eNqNk19v0zAUxSM0xP7AN0AQCQnBQ0tsJ07CA9KogFUabGJsr5Zj36SuXLvEDqJ8epw2m5ppQigPia5_99g-Ofc4OjDWQBQ9R8kUkRy9W9quNVxP16E8TRKKc0IeRUeoJHhCcUIO9r4Po2PnlkmSkYLSJ9EhJjRHlKCj6NsZcO0Xm_jG6s54gNbFM27ijxBfLsBYv1mDjK-dMk086zw3YDsXX4Fxyqs_3Ctr4kuuTPzVStDuafS45trBs-F9El1__vRjdjY5v_gyn52eTwQtsZ9UMs_LShBSp6LMCilInRMoaMFlBhLhrCp4mVIqZZoKnpaCCCKhqmuEc4rTgpxEL3e6a20dG6xwDJEsIbRM8iQQ8x0hLV-ydatWvN0wyxXbFmzbMN56JTSwjPKqly0xqlOei7LkhNYVqcJJBBYQtD4Mu3XVCqQA41uuR6LjFaMWrLG_GKFZMB0FgTeDQGt_duA8WyknQOudn_25EUUJxjSgr-6hD99uoBoeLqBMbcO-ohdlp2lekPCjszxQ0weo8EhYKRFyU6tQHzW8HTUExsNv3_DOOTa_-v7_7MXNmH29xy62kXMhcH183Bh8se_0ncW3gQ1AugNEa51rob5DUML6ubi1i_VzwYa5CG3v77UJ5bfpDY4o_e_mv_Q2ExI
CitedBy_id crossref_primary_10_1186_s12871_016_0193_2
crossref_primary_10_1097_MD_0000000000005336
crossref_primary_10_1371_journal_pone_0242169
crossref_primary_10_1371_journal_pone_0114840
crossref_primary_10_1016_j_joen_2015_12_010
crossref_primary_10_1097_j_pain_0000000000002803
crossref_primary_10_1111_anae_12717
crossref_primary_10_2196_resprot_5680
crossref_primary_10_1097_j_pain_0000000000000460
crossref_primary_10_1371_journal_pone_0254790
crossref_primary_10_1371_journal_pone_0201642
crossref_primary_10_1515_sjpain_2020_0091
crossref_primary_10_1097_PSY_0000000000000638
crossref_primary_10_1371_journal_pone_0134441
crossref_primary_10_1186_s13063_015_1021_6
crossref_primary_10_1002_ejp_1613
crossref_primary_10_1097_PR9_0000000000000790
crossref_primary_10_1093_pm_pnaa082
crossref_primary_10_1097_PR9_0000000000000697
crossref_primary_10_1371_journal_pone_0155284
crossref_primary_10_1097_ALN_0000000000001000
crossref_primary_10_1016_j_jneumeth_2015_08_018
crossref_primary_10_1111_aas_12492
crossref_primary_10_1371_journal_pone_0099507
crossref_primary_10_1016_j_jpain_2020_01_005
crossref_primary_10_1097_SPC_0000000000000045
Cites_doi 10.1097/00000542-200101000-00008
10.1097/00115550-200107000-00008
10.1016/j.pain.2012.02.022
10.1016/S0304-3959(97)00160-7
10.1016/j.pain.2007.09.019
10.1093/brain/awm233
10.2307/2529310
10.1191/096228099673819272
10.1097/00000542-200401000-00020
10.1037/0033-2909.86.2.420
10.2147/JPR.S33925
10.1097/00000539-200010000-00037
10.1093/bja/86.6.871
10.1016/j.pain.2012.04.004
10.1016/j.pain.2011.02.037
10.1002/9780470773666.ch19
10.1097/00000542-200207000-00015
10.1054/jpai.2003.10
10.1016/j.pain.2010.09.030
10.1016/j.pain.2010.11.013
10.1097/00115550-200109000-00005
10.1016/j.jpain.2006.05.010
ContentType Journal Article
Copyright COPYRIGHT 2013 Public Library of Science
2013 Werner et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2013 Werner et al 2013 Werner et al
Copyright_xml – notice: COPYRIGHT 2013 Public Library of Science
– notice: 2013 Werner et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2013 Werner et al 2013 Werner et al
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
IOV
ISR
3V.
7QG
7QL
7QO
7RV
7SN
7SS
7T5
7TG
7TM
7U9
7X2
7X7
7XB
88E
8AO
8C1
8FD
8FE
8FG
8FH
8FI
8FJ
8FK
ABJCF
ABUWG
AEUYN
AFKRA
ARAPS
ATCPS
AZQEC
BBNVY
BENPR
BGLVJ
BHPHI
C1K
CCPQU
D1I
DWQXO
FR3
FYUFA
GHDGH
GNUQQ
H94
HCIFZ
K9.
KB.
KB0
KL.
L6V
LK8
M0K
M0S
M1P
M7N
M7P
M7S
NAPCQ
P5Z
P62
P64
PATMY
PDBOC
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
PTHSS
PYCSY
RC3
7X8
5PM
DOA
DOI 10.1371/journal.pone.0062733
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Gale In Context: Opposing Viewpoints
Gale In Context: Science
ProQuest Central (Corporate)
Animal Behavior Abstracts
Bacteriology Abstracts (Microbiology B)
Biotechnology Research Abstracts
Nursing & Allied Health Database
Ecology Abstracts
Entomology Abstracts (Full archive)
Immunology Abstracts
Meteorological & Geoastrophysical Abstracts
Nucleic Acids Abstracts
Virology and AIDS Abstracts
Agricultural Science Collection
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
ProQuest Pharma Collection
ProQuest Public Health Database
Technology Research Database
ProQuest SciTech Collection
ProQuest Technology Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
Materials Science & Engineering Collection
ProQuest Central (Alumni)
ProQuest One Sustainability (subscription)
ProQuest Central UK/Ireland
Advanced Technologies & Aerospace Collection
Agricultural & Environmental Science Collection
ProQuest Central Essentials
Biological Science Collection
ProQuest Central (NC Live)
Technology Collection
Natural Science Collection
Environmental Sciences and Pollution Management
ProQuest One Community College
ProQuest Materials Science Collection
ProQuest Central Korea
Engineering Research Database
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
AIDS and Cancer Research Abstracts
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
Materials Science Database
Nursing & Allied Health Database (Alumni Edition)
Meteorological & Geoastrophysical Abstracts - Academic
ProQuest Engineering Collection
ProQuest Biological Science Collection
Agricultural Science Database
ProQuest Health & Medical Collection
Medical Database
Algology Mycology and Protozoology Abstracts (Microbiology C)
Biological Science Database
Engineering Database
Nursing & Allied Health Premium
Advanced Technologies & Aerospace Database
ProQuest Advanced Technologies & Aerospace Collection
Biotechnology and BioEngineering Abstracts
Environmental Science Database
Materials Science Collection
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
Engineering Collection
Environmental Science Collection
Genetics Abstracts
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Agricultural Science Database
Publicly Available Content Database
ProQuest Central Student
ProQuest Advanced Technologies & Aerospace Collection
ProQuest Central Essentials
Nucleic Acids Abstracts
SciTech Premium Collection
ProQuest Central China
Environmental Sciences and Pollution Management
ProQuest One Applied & Life Sciences
ProQuest One Sustainability
Health Research Premium Collection
Meteorological & Geoastrophysical Abstracts
Natural Science Collection
Health & Medical Research Collection
Biological Science Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
Engineering Collection
Advanced Technologies & Aerospace Collection
Engineering Database
Virology and AIDS Abstracts
ProQuest Biological Science Collection
ProQuest One Academic Eastern Edition
Agricultural Science Collection
ProQuest Hospital Collection
ProQuest Technology Collection
Health Research Premium Collection (Alumni)
Biological Science Database
Ecology Abstracts
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
Environmental Science Collection
Entomology Abstracts
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
Environmental Science Database
ProQuest Nursing & Allied Health Source (Alumni)
Engineering Research Database
ProQuest One Academic
Meteorological & Geoastrophysical Abstracts - Academic
ProQuest One Academic (New)
Technology Collection
Technology Research Database
ProQuest One Academic Middle East (New)
Materials Science Collection
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Central
ProQuest Health & Medical Research Collection
Genetics Abstracts
ProQuest Engineering Collection
Biotechnology Research Abstracts
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Bacteriology Abstracts (Microbiology B)
Algology Mycology and Protozoology Abstracts (Microbiology C)
Agricultural & Environmental Science Collection
AIDS and Cancer Research Abstracts
Materials Science Database
ProQuest Materials Science Collection
ProQuest Public Health
ProQuest Nursing & Allied Health Source
ProQuest SciTech Collection
Advanced Technologies & Aerospace Database
ProQuest Medical Library
Animal Behavior Abstracts
Materials Science & Engineering Collection
Immunology Abstracts
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList


MEDLINE - Academic



MEDLINE

Agricultural Science Database
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: 8FG
  name: ProQuest Technology Collection
  url: https://search.proquest.com/technologycollection1
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Sciences (General)
Medicine
DocumentTitleAlternate Phenotyping by Cutaneous Sensitization Pain Models
EISSN 1932-6203
ExternalDocumentID 1350369070
oai_doaj_org_article_56ab7624921f4a7c99a36fb3bd12c2ce
PMC3650051
2969014581
A478353857
23671631
10_1371_journal_pone_0062733
Genre Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations United States--US
San Francisco California
California
GeographicLocations_xml – name: San Francisco California
– name: United States--US
– name: California
GroupedDBID ---
123
29O
2WC
53G
5VS
7RV
7X2
7X7
7XC
88E
8AO
8C1
8CJ
8FE
8FG
8FH
8FI
8FJ
A8Z
AAFWJ
AAUCC
AAWOE
AAYXX
ABDBF
ABIVO
ABJCF
ABUWG
ACGFO
ACIHN
ACIWK
ACPRK
ACUHS
ADBBV
ADRAZ
AEAQA
AENEX
AEUYN
AFKRA
AFPKN
AFRAH
AHMBA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
APEBS
ARAPS
ATCPS
BAWUL
BBNVY
BCNDV
BENPR
BGLVJ
BHPHI
BKEYQ
BPHCQ
BVXVI
BWKFM
CCPQU
CITATION
CS3
D1I
D1J
D1K
DIK
DU5
E3Z
EAP
EAS
EBD
EMOBN
ESX
EX3
F5P
FPL
FYUFA
GROUPED_DOAJ
GX1
HCIFZ
HH5
HMCUK
HYE
IAO
IEA
IGS
IHR
IHW
INH
INR
IOV
IPNFZ
IPY
ISE
ISR
ITC
K6-
KB.
KQ8
L6V
LK5
LK8
M0K
M1P
M48
M7P
M7R
M7S
M~E
NAPCQ
O5R
O5S
OK1
OVT
P2P
P62
PATMY
PDBOC
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
PTHSS
PYCSY
RIG
RNS
RPM
SV3
TR2
UKHRP
WOQ
WOW
~02
~KM
BBORY
CGR
CUY
CVF
ECM
EIF
NPM
PV9
RZL
PMFND
3V.
7QG
7QL
7QO
7SN
7SS
7T5
7TG
7TM
7U9
7XB
8FD
8FK
AZQEC
C1K
DWQXO
FR3
GNUQQ
H94
K9.
KL.
M7N
P64
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQUKI
PRINS
RC3
7X8
5PM
PUEGO
-
02
AAPBV
ABPTK
ADACO
BBAFP
KM
ID FETCH-LOGICAL-c692t-bd779bc33f4c958dc3f73e868ad5ed125b8a9466dd44ca49c3c3debff12762483
IEDL.DBID M48
ISSN 1932-6203
IngestDate Fri Nov 26 17:12:30 EST 2021
Wed Aug 27 01:00:41 EDT 2025
Thu Aug 21 18:02:22 EDT 2025
Thu Aug 07 14:46:43 EDT 2025
Fri Jul 25 10:31:21 EDT 2025
Tue Jun 17 21:17:48 EDT 2025
Tue Jun 10 20:24:01 EDT 2025
Fri Jun 27 04:58:29 EDT 2025
Fri Jun 27 04:40:55 EDT 2025
Thu May 22 21:19:31 EDT 2025
Thu Apr 03 07:06:22 EDT 2025
Tue Jul 01 03:27:41 EDT 2025
Thu Apr 24 23:10:37 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Language English
License This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
Creative Commons Attribution License
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c692t-bd779bc33f4c958dc3f73e868ad5ed125b8a9466dd44ca49c3c3debff12762483
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
Conceived and designed the experiments: JBD MUW KLP MCR. Performed the experiments: JBD MUW KLP MCR. Analyzed the data: MUW KLP. Contributed reagents/materials/analysis tools: N/A. Wrote the paper: MUW KLP JBD MCR.
Competing Interests: The authors have declared that no competing interests exist.
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1371/journal.pone.0062733
PMID 23671631
PQID 1350369070
PQPubID 1436336
PageCount e62733
ParticipantIDs plos_journals_1350369070
doaj_primary_oai_doaj_org_article_56ab7624921f4a7c99a36fb3bd12c2ce
pubmedcentral_primary_oai_pubmedcentral_nih_gov_3650051
proquest_miscellaneous_1351610226
proquest_journals_1350369070
gale_infotracmisc_A478353857
gale_infotracacademiconefile_A478353857
gale_incontextgauss_ISR_A478353857
gale_incontextgauss_IOV_A478353857
gale_healthsolutions_A478353857
pubmed_primary_23671631
crossref_primary_10_1371_journal_pone_0062733
crossref_citationtrail_10_1371_journal_pone_0062733
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2013-05-09
PublicationDateYYYYMMDD 2013-05-09
PublicationDate_xml – month: 05
  year: 2013
  text: 2013-05-09
  day: 09
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: San Francisco
– name: San Francisco, USA
PublicationTitle PloS one
PublicationTitleAlternate PLoS One
PublicationYear 2013
Publisher Public Library of Science
Public Library of Science (PLoS)
Publisher_xml – name: Public Library of Science
– name: Public Library of Science (PLoS)
References KL Petersen (ref11) 2008; 137
AR Frymoyer (ref8) 2007; 8
MU Werner (ref20) 2004; 100
(ref3); 26
C Geber (ref22) 2011; 152
CJ Woolf (ref1) 2011; 152
JL Pedersen (ref18) 1998; 74
DB Pfau (ref19) 2011; 152
P Ravn (ref12) 2012; 5
ref17
JM Bland (ref16) 1999; 8
TA Norbury (ref9) 2007; 130
PE Shrout (ref14) 1979; 86
V Martinez (ref21) 2012; 153
S Mikkelsen (ref6) 2001; 86
J Dirks (ref13) 2003; 4
J Dirks (ref7) 2002; 97
JR Landis (ref15) 1977; 33
MS Angst (ref10) 2012; 153
J Dirks (ref5) 2001; 26
KL Petersen (ref4) 2001; 94
J Dirks (ref2) 2000; 91
12131110 - Anesthesiology. 2002 Jul;97(1):102-7
11561260 - Reg Anesth Pain Med. 2001 Sep-Oct;26(5):414-9
18839484 - Psychol Bull. 1979 Mar;86(2):420-8
17932101 - Brain. 2007 Nov;130(Pt 11):3041-9
21440369 - Pain. 2011 Jul;152(7):1532-9
11573598 - Br J Anaesth. 2001 Jun;86(6):871-3
14622709 - J Pain. 2003 Apr;4(3):122-8
23055774 - J Pain Res. 2012;5:313-26
10501650 - Stat Methods Med Res. 1999 Jun;8(2):135-60
11464350 - Reg Anesth Pain Med. 2001 Jul-Aug;26(4):322-8
22560289 - Pain. 2012 Jul;153(7):1478-83
11135717 - Anesthesiology. 2001 Jan;94(1):15-20
9520228 - Pain. 1998 Feb;74(2-3):139-51
17113353 - J Pain. 2007 Jan;8(1):19-25
20961685 - Pain. 2011 Mar;152(3 Suppl):S2-15
14695732 - Anesthesiology. 2004 Jan;100(1):115-9; discussion 5A
21237569 - Pain. 2011 Mar;152(3):548-56
11004058 - Anesth Analg. 2000 Oct;91(4):967-72
843571 - Biometrics. 1977 Mar;33(1):159-74
22444188 - Pain. 2012 Jul;153(7):1397-409
17977662 - Pain. 2008 Jul 15;137(2):395-404
References_xml – volume: 94
  start-page: 15
  year: 2001
  ident: ref4
  article-title: Effect of remifentanil on pain and secondary hyperalgesia associated with the heat–capsaicin sensitization model in healthy volunteers
  publication-title: Anesthesiology
  doi: 10.1097/00000542-200101000-00008
– volume: 26
  start-page: 322
  ident: ref3
  article-title: Werner MU, Perkins FM, Holte K, Pedersen JL, Kehlet H (20011) Effects of gabapentin in acute inflammatory pain in humans
  publication-title: Reg Anesth Pain Med
  doi: 10.1097/00115550-200107000-00008
– volume: 153
  start-page: 1397
  year: 2012
  ident: ref10
  article-title: Pain sensitivity and opioid analgesia: a pharmacogenomic twin study
  publication-title: Pain
  doi: 10.1016/j.pain.2012.02.022
– volume: 74
  start-page: 139
  year: 1998
  ident: ref18
  article-title: Hyperalgesia in a human model of acute inflammatory pain: a methodological study
  publication-title: Pain
  doi: 10.1016/S0304-3959(97)00160-7
– volume: 137
  start-page: 395
  year: 2008
  ident: ref11
  article-title: Changes in morphine analgesia and side effects during daily subcutaneous administration in healthy volunteers
  publication-title: Pain
  doi: 10.1016/j.pain.2007.09.019
– volume: 130
  start-page: 3041
  year: 2007
  ident: ref9
  article-title: Heritability of responses to painful stimuli in women: a classical twin study
  publication-title: Brain
  doi: 10.1093/brain/awm233
– volume: 33
  start-page: 159
  year: 1977
  ident: ref15
  article-title: The measurement of observer agreement for categorical data
  publication-title: Biometrics
  doi: 10.2307/2529310
– volume: 8
  start-page: 135
  year: 1999
  ident: ref16
  article-title: Measuring agreement in method comparison studies
  publication-title: Stat Methods Med Res
  doi: 10.1191/096228099673819272
– volume: 100
  start-page: 115
  year: 2004
  ident: ref20
  article-title: Prediction of postoperative pain by preoperative nociceptive responses to heat stimulation
  publication-title: Anesthesiology
  doi: 10.1097/00000542-200401000-00020
– volume: 86
  start-page: 420
  year: 1979
  ident: ref14
  article-title: Intraclass correlations: uses in assessing rater reliability
  publication-title: Psychol Bull
  doi: 10.1037/0033-2909.86.2.420
– volume: 5
  start-page: 313
  year: 2012
  ident: ref12
  article-title: Prediction of pain sensitivity in healthy volunteers
  publication-title: J Pain Res
  doi: 10.2147/JPR.S33925
– volume: 91
  start-page: 967
  year: 2000
  ident: ref2
  article-title: The effect of systemic lidocaine on pain and secondary hyperalgesia associated with the heat/capsaicin sensitization model in healthy volunteers
  publication-title: Anesth Analg
  doi: 10.1097/00000539-200010000-00037
– volume: 86
  start-page: 871
  year: 2001
  ident: ref6
  article-title: Effect of intravenous magnesium on pain and secondary hyperalgesia associated with the heat/capsaicin sensitization model in healthy volunteers
  publication-title: Br J Anaesth
  doi: 10.1093/bja/86.6.871
– volume: 153
  start-page: 1478
  year: 2012
  ident: ref21
  article-title: Risk factors predictive of chronic postsurgical neuropathic pain: The value of the iliac crest bone harvest model
  publication-title: Pain
  doi: 10.1016/j.pain.2012.04.004
– volume: 152
  start-page: 1532
  year: 2011
  ident: ref19
  article-title: Analysis of hyperalgesia time courses in humans after painful electrical high-frequency stimulation identifies a possible transition from early to late LTP-like pain plasticity
  publication-title: Pain
  doi: 10.1016/j.pain.2011.02.037
– ident: ref17
  doi: 10.1002/9780470773666.ch19
– volume: 97
  start-page: 102
  year: 2002
  ident: ref7
  article-title: Gabapentin suppresses cutaneous hyperalgesia following heat-capsaicin sensitization
  publication-title: Anesthesiology
  doi: 10.1097/00000542-200207000-00015
– volume: 4
  start-page: 122
  year: 2003
  ident: ref13
  article-title: The heat/capsaicin sensitization model: a methodologic study
  publication-title: J Pain
  doi: 10.1054/jpai.2003.10
– volume: 152
  start-page: S2
  year: 2011
  ident: ref1
  article-title: Central sensitization: implications for the diagnosis and treatment of pain
  publication-title: Pain
  doi: 10.1016/j.pain.2010.09.030
– volume: 152
  start-page: 548
  year: 2011
  ident: ref22
  article-title: Test-retest and interobserver reliability of quantitative sensory testing according to the protocol of the German Research Network on Neuropathic Pain (DFNS): a multi-centre study
  publication-title: Pain
  doi: 10.1016/j.pain.2010.11.013
– volume: 26
  start-page: 414
  year: 2001
  ident: ref5
  article-title: Effect of systemic adenosine on pain and secondary hyperalgesia associated with the heat/capsaicin sensitization model in healthy volunteers
  publication-title: Reg Anesth Pain Med
  doi: 10.1097/00115550-200109000-00005
– volume: 8
  start-page: 19
  year: 2007
  ident: ref8
  article-title: Placebo-controlled comparison of a morphine/dextromethorphan combination with morphine on experimental pain and hyperalgesia in healthy volunteers
  publication-title: J Pain
  doi: 10.1016/j.jpain.2006.05.010
– reference: 11004058 - Anesth Analg. 2000 Oct;91(4):967-72
– reference: 17932101 - Brain. 2007 Nov;130(Pt 11):3041-9
– reference: 843571 - Biometrics. 1977 Mar;33(1):159-74
– reference: 17113353 - J Pain. 2007 Jan;8(1):19-25
– reference: 14695732 - Anesthesiology. 2004 Jan;100(1):115-9; discussion 5A
– reference: 21237569 - Pain. 2011 Mar;152(3):548-56
– reference: 11464350 - Reg Anesth Pain Med. 2001 Jul-Aug;26(4):322-8
– reference: 9520228 - Pain. 1998 Feb;74(2-3):139-51
– reference: 22444188 - Pain. 2012 Jul;153(7):1397-409
– reference: 21440369 - Pain. 2011 Jul;152(7):1532-9
– reference: 18839484 - Psychol Bull. 1979 Mar;86(2):420-8
– reference: 20961685 - Pain. 2011 Mar;152(3 Suppl):S2-15
– reference: 11561260 - Reg Anesth Pain Med. 2001 Sep-Oct;26(5):414-9
– reference: 12131110 - Anesthesiology. 2002 Jul;97(1):102-7
– reference: 11573598 - Br J Anaesth. 2001 Jun;86(6):871-3
– reference: 17977662 - Pain. 2008 Jul 15;137(2):395-404
– reference: 22560289 - Pain. 2012 Jul;153(7):1478-83
– reference: 14622709 - J Pain. 2003 Apr;4(3):122-8
– reference: 10501650 - Stat Methods Med Res. 1999 Jun;8(2):135-60
– reference: 11135717 - Anesthesiology. 2001 Jan;94(1):15-20
– reference: 23055774 - J Pain Res. 2012;5:313-26
SSID ssj0053866
Score 2.265155
Snippet Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics. The ability...
Background Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics....
BACKGROUND: Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics....
Background Human experimental pain models leading to development of secondary hyperalgesia are used to estimate efficacy of analgesics and antihyperalgesics....
SourceID plos
doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage e62733
SubjectTerms Analgesics
Analysis
Anesthesiology
Antipruritics - adverse effects
Burns
Burns - complications
Capsaicin
Capsaicin - administration & dosage
Correlation analysis
Correlation coefficient
Correlation coefficients
Forearm
Healthy Volunteers - classification
Heat
Hot Temperature - adverse effects
Humans
Hyperalgesia
Hyperalgesia - classification
Hyperalgesia - etiology
Hyperalgesia - physiopathology
Medicine
Models, Biological
Narcotics
Pain
Pain - classification
Pain - etiology
Pain - physiopathology
Pain Measurement - methods
Pain Measurement - statistics & numerical data
Pain perception
Pharmacodynamics
Pharmacology
Phenotyping
Reproducibility of Results
Skin - drug effects
Skin - physiopathology
Statistical methods
Studies
Thigh
Volunteers
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELbQnrggyquBFgxCAg6mm_gVHwuiKhyKBBT1FtmOXSpVyYrsHvrvmXG8UYMqlQPX9WS1-83rSzIPQl5HWepl7RVTvhUMUwCzyyowAbmZG45LttO0zxN1fCq-nMmza6u-sCZsHA88AncglXXgsMJUZRRWe2MsV9Fx15aVr3zA6As5b3szNcZg8GKlcqMc1-VB1sv7Vd8FrOSCnM1niSjN65-i8mJ12Q83Uc6_KyevpaKj--Re5pD0cPztO-RO6B6QneylA32bR0m_e0hOxi6jK4pBCCAErkcBS-oCxdquHh_AthRr38-p3wBPDP1moAMWta9zgyZd2YuOpoU5wyNyevTpx8djljcoMK9MtWau1do4z3kU3si69TxqHmpV21YGAFC62uKA-bYVwlthPPe8DS7GskLMa_6YLDrAbJfQ4GvI9C4CHQlAOrDxUgfJK2mtKoOMBeFbOBufx4vjlovLJr0z03CbMaLToBKarISCsOmq1The4xb5D6ipSRaHY6cPwGSabDLNbSZTkBeo52bsNJ1cvDkU-BiM11IX5FWSwAEZHVbgnNvNMDSfv_78B6Hv32ZCb7JQ7AEOb3PXA_wnHLw1k9ybSYKb-9nxLlrlFpUBMJLAPgyEbLhya6k3H7-cjvFLsaoumRPKAOEHFqcK8mQ07AlZnOwHXL0siJ6Z_Az6-Ul38SvNJ-fA-iHWP_0funpG7lZpAYlkS7NHFuvfm7APNHDtnieP_wP_qVuk
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: ProQuest Technology Collection
  dbid: 8FG
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Jb9QwFLZguHBBlK2BAgYhAYfQSbwlJ9SOGAqHUlFa9WY5jt1WGiVDM3Pg3_Oe4wkEVcA1ftne-sV5CyGvvMjUtLAylbbmKYaA1Exzl3KIzaxkOGQ7dPs8lAcn_POZOIsbbl1Mq9z4xOCo69biHvluxgQ4W_iUm75ffk9xahT-XY0jNG6SWxncBlO6ivnHjScGW5Yylssxle1G6bxbto3DfC6I3GwUjkLX_sE3T5aLtrsOeP6ZP_lbQJrfJXcikqR7vei3yA3X3CNb0VY7-iY2lH57nxz2tUY_6CnoGTASEB-dmYbuO3p04ZoWt2FrGpIH6GwNaNG1644eY2r7KpZp0iNz2VAcnLboHpCT-Ydvs4M0zlFIrSzzVVrVSpWVZcxzW4qitswr5gpZmFq4GhBOVRhsM1_XnFvDS8ssq13lfZaDq-QFe0gmDfBsm1BnC4j3lQdQ4gB6YPmlcoLlwhiZOeETwjbs1DY2GcdZFwsd_pwp-NjouaNRCDoKISHpcNayb7LxD_p9lNRAiy2yw4H26lxHi9NCmgofv8wzz42yZWmY9BWr4I1tbl1CnqOcdV9vOhi63uO4GcYKoRLyMlBgm4wG83DOzbrr9Kcvp_9BdPx1RPQ6EvkW2GFNrH2Ad8L2WyPKnRElGLsdLW-jVm640ulfZgFnbjT1-uUXwzJeFHPrgjohDcB-wHIyIY96xR44i_39ALFnCVEjlR-xfrzSXF6ELuUMsD94_Md_f6wn5HYeBoyIdFrukMnqau2eAsxbVc-CLf8Eo-RRgg
  priority: 102
  providerName: ProQuest
Title Healthy Volunteers Can Be Phenotyped Using Cutaneous Sensitization Pain Models
URI https://www.ncbi.nlm.nih.gov/pubmed/23671631
https://www.proquest.com/docview/1350369070
https://www.proquest.com/docview/1351610226
https://pubmed.ncbi.nlm.nih.gov/PMC3650051
https://doaj.org/article/56ab7624921f4a7c99a36fb3bd12c2ce
http://dx.doi.org/10.1371/journal.pone.0062733
Volume 8
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELe2TkK8IDY-FhjFICTgIVMTJ3bygNBarQyklWqjU98ix3G2SVVSmlZi_z13jhMRVATiJQ_xuWrO57vf2fdByJs89MQgUtzlKgtcNAGuHPjaDcA2s5hhk21T7XPCz2bBl3k43yFNz1bLwGqra4f9pGarxfGP73cfYcN_MF0bhNdMOl6WhcY4LbDIbJfsgW0S2NPgPGjvFWB3c24T6P40E8sDMw5uBPM6tsqU9G8Vd2-5KKttqPT34MpfrNX4IXlgYSY9qeVin-zo4oDcO7cX6Qdk3-7pir6zhaffPyKTOifpjl6BPALDARnSkSzoUNPpjS5KPK7NqAkyoKMNoEpdbip6iSHwa5vOSafytqDYYG1RPSaz8em30Zlr-y24isf-2k0zIeJUMZYHKg6jTLFcMB3xSGahzgAJpZHEcvRZFgRKBrFiimU6zXPPB5UaROwJ6RXAyUNCtYoAF6Q5gBcNEAXTNIUOmR9KyT0d5g5hDWcTZYuRY0-MRWJu2AQ4JTWjElyaxC6NQ9x21rIuxvEX-iEuWkuLpbTNi3J1ndidmYRcpvj3Y9_LAylUHEvG85Sl8MXKV9ohL3HJkzovtVUIyUmAh2YsCoVDXhsKLKdRYLzOtdxUVfL569U_EF1edIjeWqK8BHYoaXMk4JuwTFeH8qhDCUpBdYYPUUAbrlTAoxCwSgwKHmY2Qrt9-FU7jD-KMXhGnJAG3APAfNwhT2sZbznb7BiHiI70d1jfHSlub0w1cwY-AliGZ_898zm575seJaE7iI9Ib73a6BeAFNdpn-yKuYBnNPLwOf7UJ3vD08n0om_OXvpGOfwELqhtBw
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELbKcoALank1UKhBIOCQdhPHTnJAqF1YdmlZKvpQb8ZxnLbSKtk2u0L9U_xGZhInEFQBl17jSZTMjOfhzHxDyIuMe2E_0sIVOg1cdAGu6vvGDcA3s5jhkO0K7XMiRofBp2N-vER-NL0wWFbZ2MTKUKeFxjPyTY9xMLaQyvXfzc5dnBqFf1ebERq1WuyYy--QspVvx-9Bvi99f_jhYDBy7VQBV4vYn7tJGoZxohnLAh3zKNUsC5mJRKRSblLw90mkEHQ9TYNAqyDWTLPUJFnm-WA4gojBc2-Qm_gpmOxFw4-N5QfbIYRtz2Oht2m1YWNW5AbrxyBSYB33V00JaH1BbzYtyqsC3T_rNX9zgMNlcsdGrnSrVrUVsmTyu2TF2oaSvrYA1m_ukUnd23RJj0CvQXAQYdKByum2oXunJi_w2DelVbECHSwgOjXFoqT7WEo_t22hdE-d5RQHtU3L--TwWjj8gPRy4NkqoUZHEF8kGQRBBkIdbPcMDWc-V0p4hmcOYQ07pbag5jhbYyqrP3UhJDc1dyQKQVohOMRt75rVoB7_oN9GSbW0CMldXSguTqTd4ZILleDrx76XBSrUcayYyBKWwBdrXxuHrKOcZd3f2hoWuRXg4RuLeOiQ5xUFwnLkWPdzohZlKcdfjv6DaP9rh-iVJcoKYIdWttcCvgnhvjqUax1KMC66s7yKWtlwpZS_tiHc2Wjq1cvP2mV8KNbyVeqENJBmQOwoHPKwVuyWs4gnCBmC55Cwo_Id1ndX8rPTChWdQa4BHubR319rndwaHXzelbvjyc5jctuvhptwtx-vkd78YmGeQIg5T55W-5qSb9dtSH4CvGyPkA
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwELdGkRAviPG1wGAGgYCH0CaO4-QBoa2jWhkqFWPT3ozj2NukKilLK7R_jb-Ou8QNBE3Ay17jS5Tcne_DufsdIc8tD8Qg0bEf6zzy0QX4ahAaPwLfzFKGQ7ZrtM9JvHcYfTjmx2vkx6oXBssqVzaxNtR5qfGMvB8wDsYWUrlB37qyiOnu6N38m48TpPBP62qcRqMi--biO6Rv1dvxLsj6RRiO3n8Z7vluwoCv4zRc-FkuRJppxmykU57kmlnBTBInKucmB9-fJQoB2PM8irSKUs00y01mbRCCEYkSBs-9Rq4LJhLcY8mwLS8BOxLHrlWPiaDvNOPNvCwM1pJB1MA6rrCeGND6hd58VlaXBb1_1m7-5gxHt8ktF8XS7Ubt1smaKe6QdWcnKvrKgVm_vksmTZ_TBT0CHQchQrRJh6qgO4ZOT01R4hFwTuvCBTpcQqRqymVFD7CsfuFaROlUnRUUh7bNqnvk8Eo4fJ_0CuDZBqFGJxBrZBYCIgNhD7Z-CsNZyJWKA8OtR9iKnVI7gHOcszGT9V87AYlOwx2JQpBOCB7x27vmDcDHP-h3UFItLcJz1xfK8xPpdrvkscrw9dMwsJESOk0Vi23GMvhiHWrjkS2Us2x6XVsjI7cjPIhjCRceeVZTIERHgcp-opZVJcefjv6D6OBzh-ilI7IlsEMr13cB34TQXx3KzQ4lGBrdWd5ArVxxpZK_tiTcudLUy5eftsv4UKzrq9UJaSDlgDgy9siDRrFbziK2IGQLgUdER-U7rO-uFGenNUI6g7wDvM3Dv7_WFrkBJkR-HE_2H5GbYT3nhPuDdJP0FudL8xiizUX2pN7WlHy9ajvyE-STk5E
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Healthy+Volunteers+Can+Be+Phenotyped+Using+Cutaneous+Sensitization+Pain+Models&rft.jtitle=PloS+one&rft.au=Werner%2C+Mads+U.&rft.au=Petersen%2C+Karin+L.&rft.au=Rowbotham%2C+Michael+C.&rft.au=Dahl%2C+J%C3%B8rgen+B.&rft.date=2013-05-09&rft.pub=Public+Library+of+Science&rft.eissn=1932-6203&rft.volume=8&rft.issue=5&rft_id=info:doi/10.1371%2Fjournal.pone.0062733&rft_id=info%3Apmid%2F23671631&rft.externalDocID=PMC3650051
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1932-6203&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1932-6203&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1932-6203&client=summon