Decreased Brain Neurokinin-1 Receptor Availability in Chronic Tennis Elbow

Substance P is released in painful and inflammatory conditions, affecting both peripheral processes and the central nervous system neurokinin 1 (NK1) receptor. There is a paucity of data on human brain alterations in NK1 expression, how this system may be affected by treatment, and interactions betw...

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Veröffentlicht in:PloS one 2016-09, Vol.11 (9), p.e0161563-e0161563
Hauptverfasser: Linnman, Clas, Catana, Ciprian, Svärdsudd, Kurt, Appel, Lieuwe, Engler, Henry, Långström, Bengt, Sörensen, Jens, Furmark, Tomas, Fredrikson, Mats, Borsook, David, Peterson, Magnus
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container_issue 9
container_start_page e0161563
container_title PloS one
container_volume 11
creator Linnman, Clas
Catana, Ciprian
Svärdsudd, Kurt
Appel, Lieuwe
Engler, Henry
Långström, Bengt
Sörensen, Jens
Furmark, Tomas
Fredrikson, Mats
Borsook, David
Peterson, Magnus
description Substance P is released in painful and inflammatory conditions, affecting both peripheral processes and the central nervous system neurokinin 1 (NK1) receptor. There is a paucity of data on human brain alterations in NK1 expression, how this system may be affected by treatment, and interactions between central and peripheral tissue alterations. Ten subjects with chronic tennis elbow (lateral epicondylosis) were selected out of a larger (n = 120) randomized controlled trial evaluating graded exercise as a treatment for chronic tennis elbow (lateral epicondylosis). These ten subjects were examined by positron emission tomography (PET) with the NK1-specific radioligand 11C-GR205171 before, and eight patients were followed up after treatment with graded exercise. Brain binding in the ten patients before treatment, reflecting NK1-receptor availability (NK1-RA), was compared to that of 18 healthy subjects and, longitudinally, to the eight of the original ten patients that agreed to a second PET examination after treatment. Before treatment, patients had significantly lower NK1-RA in the insula, vmPFC, postcentral gyrus, anterior cingulate, caudate, putamen, amygdala and the midbrain but not the thalamus and cerebellum, with the largest difference in the insula contralateral to the injured elbow. No significant correlations between brain NK1-RA and pain, functional severity, or peripheral NK1-RA in the affected limb were observed. In the eight patients examined after treatment, pain ratings decreased in everyone, but there were no significant changes in NK1-RA. These findings indicate a role for the substance P (SP) / NK1 receptor system in musculoskeletal pain and tissue healing. As neither clinical parameters nor successful treatment response was reflected in brain NK1-RA after treatment, this may reflect the diverse function of the SP/NK1 system in CNS and peripheral tissue, or a change too small or slow to capture over the three-month treatment.
doi_str_mv 10.1371/journal.pone.0161563
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There is a paucity of data on human brain alterations in NK1 expression, how this system may be affected by treatment, and interactions between central and peripheral tissue alterations. Ten subjects with chronic tennis elbow (lateral epicondylosis) were selected out of a larger (n = 120) randomized controlled trial evaluating graded exercise as a treatment for chronic tennis elbow (lateral epicondylosis). These ten subjects were examined by positron emission tomography (PET) with the NK1-specific radioligand 11C-GR205171 before, and eight patients were followed up after treatment with graded exercise. Brain binding in the ten patients before treatment, reflecting NK1-receptor availability (NK1-RA), was compared to that of 18 healthy subjects and, longitudinally, to the eight of the original ten patients that agreed to a second PET examination after treatment. Before treatment, patients had significantly lower NK1-RA in the insula, vmPFC, postcentral gyrus, anterior cingulate, caudate, putamen, amygdala and the midbrain but not the thalamus and cerebellum, with the largest difference in the insula contralateral to the injured elbow. No significant correlations between brain NK1-RA and pain, functional severity, or peripheral NK1-RA in the affected limb were observed. In the eight patients examined after treatment, pain ratings decreased in everyone, but there were no significant changes in NK1-RA. These findings indicate a role for the substance P (SP) / NK1 receptor system in musculoskeletal pain and tissue healing. 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One</addtitle><date>2016-09-22</date><risdate>2016</risdate><volume>11</volume><issue>9</issue><spage>e0161563</spage><epage>e0161563</epage><pages>e0161563-e0161563</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Substance P is released in painful and inflammatory conditions, affecting both peripheral processes and the central nervous system neurokinin 1 (NK1) receptor. There is a paucity of data on human brain alterations in NK1 expression, how this system may be affected by treatment, and interactions between central and peripheral tissue alterations. Ten subjects with chronic tennis elbow (lateral epicondylosis) were selected out of a larger (n = 120) randomized controlled trial evaluating graded exercise as a treatment for chronic tennis elbow (lateral epicondylosis). These ten subjects were examined by positron emission tomography (PET) with the NK1-specific radioligand 11C-GR205171 before, and eight patients were followed up after treatment with graded exercise. Brain binding in the ten patients before treatment, reflecting NK1-receptor availability (NK1-RA), was compared to that of 18 healthy subjects and, longitudinally, to the eight of the original ten patients that agreed to a second PET examination after treatment. Before treatment, patients had significantly lower NK1-RA in the insula, vmPFC, postcentral gyrus, anterior cingulate, caudate, putamen, amygdala and the midbrain but not the thalamus and cerebellum, with the largest difference in the insula contralateral to the injured elbow. No significant correlations between brain NK1-RA and pain, functional severity, or peripheral NK1-RA in the affected limb were observed. In the eight patients examined after treatment, pain ratings decreased in everyone, but there were no significant changes in NK1-RA. These findings indicate a role for the substance P (SP) / NK1 receptor system in musculoskeletal pain and tissue healing. As neither clinical parameters nor successful treatment response was reflected in brain NK1-RA after treatment, this may reflect the diverse function of the SP/NK1 system in CNS and peripheral tissue, or a change too small or slow to capture over the three-month treatment.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27658244</pmid><doi>10.1371/journal.pone.0161563</doi><tpages>e0161563</tpages><oa>free_for_read</oa></addata></record>
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subjects Amygdala
Anesthesiology
Biology and Life Sciences
Brain
Brain-derived neurotrophic factor
Care and treatment
Central nervous system
Cerebellum
Clinical trials
Elbow
Elbow (anatomy)
Epidemiology
Gene expression
Hospitals
Hostages
Inflammation
Injuries
Medicine
Medicine and Health Sciences
Mesencephalon
Neurokinin NK1 receptors
Neurosciences
Oncology
Pain
Pain management
Patients
Positron emission
Positron emission tomography
Postcentral gyrus
Public health
Putamen
Research and Analysis Methods
Rodents
Social Sciences
Sports injuries
Substance P
Tennis
Tennis elbow
Thalamus
Tomography
title Decreased Brain Neurokinin-1 Receptor Availability in Chronic Tennis Elbow
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