Water-restraint stress enhances methamphetamine-induced cardiotoxicity

Methamphetamine (MAP) and stress both cause a variety of cardiovascular problems. Stress also increases stimulant drug-seeking or drug-taking behavior by both humans and animals. In addition to the physiological effects on circulation, metabolism, and excretion, stress affects subject's respons...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chemico-biological interactions 2011-03, Vol.190 (1), p.54-61
Hauptverfasser: Tomita, Masafumi, Katsuyama, Hironobu, Watanabe, Yoko, Hidaka, Kazuo, Yoshitome, Kei, Miyaishi, Satoru, Ishikawa, Takaki, Shinone, Kotaro, Nata, Masayuki
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 61
container_issue 1
container_start_page 54
container_title Chemico-biological interactions
container_volume 190
creator Tomita, Masafumi
Katsuyama, Hironobu
Watanabe, Yoko
Hidaka, Kazuo
Yoshitome, Kei
Miyaishi, Satoru
Ishikawa, Takaki
Shinone, Kotaro
Nata, Masayuki
description Methamphetamine (MAP) and stress both cause a variety of cardiovascular problems. Stress also increases stimulant drug-seeking or drug-taking behavior by both humans and animals. In addition to the physiological effects on circulation, metabolism, and excretion, stress affects subject's responses to stimulant drugs such as MAP. However, the mechanisms underlying the drug–stress interactions remain unknown. In the present study, we assessed the effects of stress on myocardial responses to MAP in mice. Mice were injected with MAP (30mg/kg) immediately before exposure to water-restraint stress (WRS), which has often been used as a stressor in animal experiments. The combination of MAP with WRS produced a significant increase (p
doi_str_mv 10.1016/j.cbi.2011.01.025
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1687664017</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0009279711000494</els_id><sourcerecordid>1687664017</sourcerecordid><originalsourceid>FETCH-LOGICAL-c409t-9e690eb2298c4526059ce08e16e754cb651a7c64cc8130ff91d47dac55f4397e3</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMoWqs_wIv26GXrJN0kGzxJ8QsEDyoeQzo7a1O6uzVJRf-9KVWPwsAw8Lwvw8PYCYcxB64uFmOc-bEAzseQR8gdNuCVFoXWldplAwAwhdBGH7DDGBf5BFHCPjsQXGiltRmwm1eXKBSBYgrOd2mUN8U4om7uOqQ4ainNXbuaU3Kt76jwXb1GqkfoQu371H969OnriO01bhnp-GcP2cvN9fP0rnh4vL2fXj0UWIJJhSFlgGZCmApLKRRIgwQVcUValjhTkjuNqkSs-ASaxvC61LVDKZtyYjRNhux827sK_fs6P21bH5GWS9dRv46Wq0orVQLXGeVbFEMfY6DGroJvXfiyHOxGn13YrM9u9FnII2TOnP7Ur2ct1X-JX18ZONsCjeutews-2pen3CCzWlVNhMrE5ZagrOHDU7ARPWWVtQ-Eyda9_-eBb1DEiZY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1687664017</pqid></control><display><type>article</type><title>Water-restraint stress enhances methamphetamine-induced cardiotoxicity</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Tomita, Masafumi ; Katsuyama, Hironobu ; Watanabe, Yoko ; Hidaka, Kazuo ; Yoshitome, Kei ; Miyaishi, Satoru ; Ishikawa, Takaki ; Shinone, Kotaro ; Nata, Masayuki</creator><creatorcontrib>Tomita, Masafumi ; Katsuyama, Hironobu ; Watanabe, Yoko ; Hidaka, Kazuo ; Yoshitome, Kei ; Miyaishi, Satoru ; Ishikawa, Takaki ; Shinone, Kotaro ; Nata, Masayuki</creatorcontrib><description>Methamphetamine (MAP) and stress both cause a variety of cardiovascular problems. Stress also increases stimulant drug-seeking or drug-taking behavior by both humans and animals. In addition to the physiological effects on circulation, metabolism, and excretion, stress affects subject's responses to stimulant drugs such as MAP. However, the mechanisms underlying the drug–stress interactions remain unknown. In the present study, we assessed the effects of stress on myocardial responses to MAP in mice. Mice were injected with MAP (30mg/kg) immediately before exposure to water-restraint stress (WRS), which has often been used as a stressor in animal experiments. The combination of MAP with WRS produced a significant increase (p&lt;0.01) in the leakage of proteins specific to myocardial damage and the levels of cytokines IL-6, TNF-α, and IL-10. The histological findings indicated the possibility that a combination of MAP with WRS induced cardiac myocytolysis. We also examined the expression of heat shock proteins (Hsps), which have cardioprotective effects. Administration of MAP alone significantly stimulated the RNA expressions of Hsp32, 60, 70, and 90 and the protein Hsp70 in cardiac muscles, whereas the expressions due to WRS or MAP plus WRS were not increased. These results reveal the fact that exposure to WRS depresses the induction of Hsps, in particular Hsp70, due to MAP injection, following to enhance MAP-induced myocardial damage. We believe that interactions between MAP and severe stress, including environmental temperature, affect the induction of Hsps, following to susceptibility of hosts to cardiotoxicity due to the stimulant drug.</description><identifier>ISSN: 0009-2797</identifier><identifier>EISSN: 1872-7786</identifier><identifier>DOI: 10.1016/j.cbi.2011.01.025</identifier><identifier>PMID: 21276779</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>ambient temperature ; animal experimentation ; Animals ; cardioprotective effect ; Cardiotoxicity ; Central Nervous System Stimulants - toxicity ; Chaperonin 60 - genetics ; Chaperonin 60 - metabolism ; drugs ; excretion ; Fatty Acid-Binding Proteins - metabolism ; Heart - drug effects ; Heat shock protein ; heat shock proteins ; hosts ; HSP70 Heat-Shock Proteins - genetics ; HSP70 Heat-Shock Proteins - metabolism ; HSP90 Heat-Shock Proteins - genetics ; HSP90 Heat-Shock Proteins - metabolism ; humans ; Immersion ; interleukin-10 ; Interleukin-10 - metabolism ; interleukin-6 ; Interleukin-6 - metabolism ; metabolism ; Methamphetamine ; Methamphetamine - toxicity ; Mice ; muscles ; Myocardia ; Myocardium - metabolism ; Myocardium - pathology ; RNA ; Stress, Physiological ; Temperature ; Tumor Necrosis Factor-alpha - metabolism ; Water-restraint stress</subject><ispartof>Chemico-biological interactions, 2011-03, Vol.190 (1), p.54-61</ispartof><rights>2011 Elsevier Ireland Ltd</rights><rights>2011 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-9e690eb2298c4526059ce08e16e754cb651a7c64cc8130ff91d47dac55f4397e3</citedby><cites>FETCH-LOGICAL-c409t-9e690eb2298c4526059ce08e16e754cb651a7c64cc8130ff91d47dac55f4397e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0009279711000494$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21276779$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tomita, Masafumi</creatorcontrib><creatorcontrib>Katsuyama, Hironobu</creatorcontrib><creatorcontrib>Watanabe, Yoko</creatorcontrib><creatorcontrib>Hidaka, Kazuo</creatorcontrib><creatorcontrib>Yoshitome, Kei</creatorcontrib><creatorcontrib>Miyaishi, Satoru</creatorcontrib><creatorcontrib>Ishikawa, Takaki</creatorcontrib><creatorcontrib>Shinone, Kotaro</creatorcontrib><creatorcontrib>Nata, Masayuki</creatorcontrib><title>Water-restraint stress enhances methamphetamine-induced cardiotoxicity</title><title>Chemico-biological interactions</title><addtitle>Chem Biol Interact</addtitle><description>Methamphetamine (MAP) and stress both cause a variety of cardiovascular problems. Stress also increases stimulant drug-seeking or drug-taking behavior by both humans and animals. In addition to the physiological effects on circulation, metabolism, and excretion, stress affects subject's responses to stimulant drugs such as MAP. However, the mechanisms underlying the drug–stress interactions remain unknown. In the present study, we assessed the effects of stress on myocardial responses to MAP in mice. Mice were injected with MAP (30mg/kg) immediately before exposure to water-restraint stress (WRS), which has often been used as a stressor in animal experiments. The combination of MAP with WRS produced a significant increase (p&lt;0.01) in the leakage of proteins specific to myocardial damage and the levels of cytokines IL-6, TNF-α, and IL-10. The histological findings indicated the possibility that a combination of MAP with WRS induced cardiac myocytolysis. We also examined the expression of heat shock proteins (Hsps), which have cardioprotective effects. Administration of MAP alone significantly stimulated the RNA expressions of Hsp32, 60, 70, and 90 and the protein Hsp70 in cardiac muscles, whereas the expressions due to WRS or MAP plus WRS were not increased. These results reveal the fact that exposure to WRS depresses the induction of Hsps, in particular Hsp70, due to MAP injection, following to enhance MAP-induced myocardial damage. We believe that interactions between MAP and severe stress, including environmental temperature, affect the induction of Hsps, following to susceptibility of hosts to cardiotoxicity due to the stimulant drug.</description><subject>ambient temperature</subject><subject>animal experimentation</subject><subject>Animals</subject><subject>cardioprotective effect</subject><subject>Cardiotoxicity</subject><subject>Central Nervous System Stimulants - toxicity</subject><subject>Chaperonin 60 - genetics</subject><subject>Chaperonin 60 - metabolism</subject><subject>drugs</subject><subject>excretion</subject><subject>Fatty Acid-Binding Proteins - metabolism</subject><subject>Heart - drug effects</subject><subject>Heat shock protein</subject><subject>heat shock proteins</subject><subject>hosts</subject><subject>HSP70 Heat-Shock Proteins - genetics</subject><subject>HSP70 Heat-Shock Proteins - metabolism</subject><subject>HSP90 Heat-Shock Proteins - genetics</subject><subject>HSP90 Heat-Shock Proteins - metabolism</subject><subject>humans</subject><subject>Immersion</subject><subject>interleukin-10</subject><subject>Interleukin-10 - metabolism</subject><subject>interleukin-6</subject><subject>Interleukin-6 - metabolism</subject><subject>metabolism</subject><subject>Methamphetamine</subject><subject>Methamphetamine - toxicity</subject><subject>Mice</subject><subject>muscles</subject><subject>Myocardia</subject><subject>Myocardium - metabolism</subject><subject>Myocardium - pathology</subject><subject>RNA</subject><subject>Stress, Physiological</subject><subject>Temperature</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Water-restraint stress</subject><issn>0009-2797</issn><issn>1872-7786</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMoWqs_wIv26GXrJN0kGzxJ8QsEDyoeQzo7a1O6uzVJRf-9KVWPwsAw8Lwvw8PYCYcxB64uFmOc-bEAzseQR8gdNuCVFoXWldplAwAwhdBGH7DDGBf5BFHCPjsQXGiltRmwm1eXKBSBYgrOd2mUN8U4om7uOqQ4ainNXbuaU3Kt76jwXb1GqkfoQu371H969OnriO01bhnp-GcP2cvN9fP0rnh4vL2fXj0UWIJJhSFlgGZCmApLKRRIgwQVcUValjhTkjuNqkSs-ASaxvC61LVDKZtyYjRNhux827sK_fs6P21bH5GWS9dRv46Wq0orVQLXGeVbFEMfY6DGroJvXfiyHOxGn13YrM9u9FnII2TOnP7Ur2ct1X-JX18ZONsCjeutews-2pen3CCzWlVNhMrE5ZagrOHDU7ARPWWVtQ-Eyda9_-eBb1DEiZY</recordid><startdate>20110315</startdate><enddate>20110315</enddate><creator>Tomita, Masafumi</creator><creator>Katsuyama, Hironobu</creator><creator>Watanabe, Yoko</creator><creator>Hidaka, Kazuo</creator><creator>Yoshitome, Kei</creator><creator>Miyaishi, Satoru</creator><creator>Ishikawa, Takaki</creator><creator>Shinone, Kotaro</creator><creator>Nata, Masayuki</creator><general>Elsevier Ireland Ltd</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20110315</creationdate><title>Water-restraint stress enhances methamphetamine-induced cardiotoxicity</title><author>Tomita, Masafumi ; Katsuyama, Hironobu ; Watanabe, Yoko ; Hidaka, Kazuo ; Yoshitome, Kei ; Miyaishi, Satoru ; Ishikawa, Takaki ; Shinone, Kotaro ; Nata, Masayuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-9e690eb2298c4526059ce08e16e754cb651a7c64cc8130ff91d47dac55f4397e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>ambient temperature</topic><topic>animal experimentation</topic><topic>Animals</topic><topic>cardioprotective effect</topic><topic>Cardiotoxicity</topic><topic>Central Nervous System Stimulants - toxicity</topic><topic>Chaperonin 60 - genetics</topic><topic>Chaperonin 60 - metabolism</topic><topic>drugs</topic><topic>excretion</topic><topic>Fatty Acid-Binding Proteins - metabolism</topic><topic>Heart - drug effects</topic><topic>Heat shock protein</topic><topic>heat shock proteins</topic><topic>hosts</topic><topic>HSP70 Heat-Shock Proteins - genetics</topic><topic>HSP70 Heat-Shock Proteins - metabolism</topic><topic>HSP90 Heat-Shock Proteins - genetics</topic><topic>HSP90 Heat-Shock Proteins - metabolism</topic><topic>humans</topic><topic>Immersion</topic><topic>interleukin-10</topic><topic>Interleukin-10 - metabolism</topic><topic>interleukin-6</topic><topic>Interleukin-6 - metabolism</topic><topic>metabolism</topic><topic>Methamphetamine</topic><topic>Methamphetamine - toxicity</topic><topic>Mice</topic><topic>muscles</topic><topic>Myocardia</topic><topic>Myocardium - metabolism</topic><topic>Myocardium - pathology</topic><topic>RNA</topic><topic>Stress, Physiological</topic><topic>Temperature</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Water-restraint stress</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tomita, Masafumi</creatorcontrib><creatorcontrib>Katsuyama, Hironobu</creatorcontrib><creatorcontrib>Watanabe, Yoko</creatorcontrib><creatorcontrib>Hidaka, Kazuo</creatorcontrib><creatorcontrib>Yoshitome, Kei</creatorcontrib><creatorcontrib>Miyaishi, Satoru</creatorcontrib><creatorcontrib>Ishikawa, Takaki</creatorcontrib><creatorcontrib>Shinone, Kotaro</creatorcontrib><creatorcontrib>Nata, Masayuki</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Chemico-biological interactions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tomita, Masafumi</au><au>Katsuyama, Hironobu</au><au>Watanabe, Yoko</au><au>Hidaka, Kazuo</au><au>Yoshitome, Kei</au><au>Miyaishi, Satoru</au><au>Ishikawa, Takaki</au><au>Shinone, Kotaro</au><au>Nata, Masayuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Water-restraint stress enhances methamphetamine-induced cardiotoxicity</atitle><jtitle>Chemico-biological interactions</jtitle><addtitle>Chem Biol Interact</addtitle><date>2011-03-15</date><risdate>2011</risdate><volume>190</volume><issue>1</issue><spage>54</spage><epage>61</epage><pages>54-61</pages><issn>0009-2797</issn><eissn>1872-7786</eissn><abstract>Methamphetamine (MAP) and stress both cause a variety of cardiovascular problems. Stress also increases stimulant drug-seeking or drug-taking behavior by both humans and animals. In addition to the physiological effects on circulation, metabolism, and excretion, stress affects subject's responses to stimulant drugs such as MAP. However, the mechanisms underlying the drug–stress interactions remain unknown. In the present study, we assessed the effects of stress on myocardial responses to MAP in mice. Mice were injected with MAP (30mg/kg) immediately before exposure to water-restraint stress (WRS), which has often been used as a stressor in animal experiments. The combination of MAP with WRS produced a significant increase (p&lt;0.01) in the leakage of proteins specific to myocardial damage and the levels of cytokines IL-6, TNF-α, and IL-10. The histological findings indicated the possibility that a combination of MAP with WRS induced cardiac myocytolysis. We also examined the expression of heat shock proteins (Hsps), which have cardioprotective effects. Administration of MAP alone significantly stimulated the RNA expressions of Hsp32, 60, 70, and 90 and the protein Hsp70 in cardiac muscles, whereas the expressions due to WRS or MAP plus WRS were not increased. These results reveal the fact that exposure to WRS depresses the induction of Hsps, in particular Hsp70, due to MAP injection, following to enhance MAP-induced myocardial damage. We believe that interactions between MAP and severe stress, including environmental temperature, affect the induction of Hsps, following to susceptibility of hosts to cardiotoxicity due to the stimulant drug.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>21276779</pmid><doi>10.1016/j.cbi.2011.01.025</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0009-2797
ispartof Chemico-biological interactions, 2011-03, Vol.190 (1), p.54-61
issn 0009-2797
1872-7786
language eng
recordid cdi_proquest_miscellaneous_1687664017
source MEDLINE; Elsevier ScienceDirect Journals
subjects ambient temperature
animal experimentation
Animals
cardioprotective effect
Cardiotoxicity
Central Nervous System Stimulants - toxicity
Chaperonin 60 - genetics
Chaperonin 60 - metabolism
drugs
excretion
Fatty Acid-Binding Proteins - metabolism
Heart - drug effects
Heat shock protein
heat shock proteins
hosts
HSP70 Heat-Shock Proteins - genetics
HSP70 Heat-Shock Proteins - metabolism
HSP90 Heat-Shock Proteins - genetics
HSP90 Heat-Shock Proteins - metabolism
humans
Immersion
interleukin-10
Interleukin-10 - metabolism
interleukin-6
Interleukin-6 - metabolism
metabolism
Methamphetamine
Methamphetamine - toxicity
Mice
muscles
Myocardia
Myocardium - metabolism
Myocardium - pathology
RNA
Stress, Physiological
Temperature
Tumor Necrosis Factor-alpha - metabolism
Water-restraint stress
title Water-restraint stress enhances methamphetamine-induced cardiotoxicity
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T00%3A38%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Water-restraint%20stress%20enhances%20methamphetamine-induced%20cardiotoxicity&rft.jtitle=Chemico-biological%20interactions&rft.au=Tomita,%20Masafumi&rft.date=2011-03-15&rft.volume=190&rft.issue=1&rft.spage=54&rft.epage=61&rft.pages=54-61&rft.issn=0009-2797&rft.eissn=1872-7786&rft_id=info:doi/10.1016/j.cbi.2011.01.025&rft_dat=%3Cproquest_cross%3E1687664017%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1687664017&rft_id=info:pmid/21276779&rft_els_id=S0009279711000494&rfr_iscdi=true