Decreased dopamine activity predicts relapse in methamphetamine abusers
Studies in methamphetamine (METH) abusers showed that the decreases in brain dopamine (DA) function might recover with protracted detoxification. However, the extent to which striatal DA function in METH predicts recovery has not been evaluated. Here we assessed whether striatal DA activity in METH...
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Veröffentlicht in: | Molecular psychiatry 2012-09, Vol.17 (9), p.918-925 |
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description | Studies in methamphetamine (METH) abusers showed that the decreases in brain dopamine (DA) function might recover with protracted detoxification. However, the extent to which striatal DA function in METH predicts recovery has not been evaluated. Here we assessed whether striatal DA activity in METH abusers is associated with clinical outcomes. Brain DA D2 receptor (D2R) availability was measured with positron emission tomography and [
11
C]raclopride in 16 METH abusers, both after placebo and after challenge with 60 mg oral methylphenidate (MPH) (to measure DA release) to assess whether it predicted clinical outcomes. For this purpose, METH abusers were tested within 6 months of last METH use and then followed up for 9 months of abstinence. In parallel, 15 healthy controls were tested. METH abusers had lower D2R availability in caudate than in controls. Both METH abusers and controls showed decreased striatal D2R availability after MPH and these decreases were smaller in METH than in controls in left putamen. The six METH abusers who relapsed during the follow-up period had lower D2R availability in dorsal striatum than in controls, and had no D2R changes after MPH challenge. The 10 METH abusers who completed detoxification did not differ from controls neither in striatal D2R availability nor in MPH-induced striatal DA changes. These results provide preliminary evidence that low striatal DA function in METH abusers is associated with a greater likelihood of relapse during treatment. Detection of the extent of DA dysfunction may be helpful in predicting therapeutic outcomes. |
doi_str_mv | 10.1038/mp.2011.86 |
format | Article |
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11
C]raclopride in 16 METH abusers, both after placebo and after challenge with 60 mg oral methylphenidate (MPH) (to measure DA release) to assess whether it predicted clinical outcomes. For this purpose, METH abusers were tested within 6 months of last METH use and then followed up for 9 months of abstinence. In parallel, 15 healthy controls were tested. METH abusers had lower D2R availability in caudate than in controls. Both METH abusers and controls showed decreased striatal D2R availability after MPH and these decreases were smaller in METH than in controls in left putamen. The six METH abusers who relapsed during the follow-up period had lower D2R availability in dorsal striatum than in controls, and had no D2R changes after MPH challenge. The 10 METH abusers who completed detoxification did not differ from controls neither in striatal D2R availability nor in MPH-induced striatal DA changes. These results provide preliminary evidence that low striatal DA function in METH abusers is associated with a greater likelihood of relapse during treatment. Detection of the extent of DA dysfunction may be helpful in predicting therapeutic outcomes.</description><identifier>ISSN: 1359-4184</identifier><identifier>EISSN: 1476-5578</identifier><identifier>DOI: 10.1038/mp.2011.86</identifier><identifier>PMID: 21747399</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/378/340 ; 631/92/436/1729 ; 692/53/2423 ; Abstinence ; Adult ; Amphetamine abuse ; Amphetamine-Related Disorders - diagnostic imaging ; Amphetamine-Related Disorders - metabolism ; Amphetamines ; Behavioral Sciences ; Biological and medical sciences ; Biological Psychology ; Brain ; Carbon Radioisotopes ; Case-Control Studies ; Caudate-putamen ; Clinical outcomes ; Corpus Striatum - diagnostic imaging ; Corpus Striatum - metabolism ; Detoxification ; Diagnosis ; Diseases ; Dopamine ; Dopamine - metabolism ; Dopamine D2 receptors ; Dopamine receptors ; Drugs ; Female ; Humans ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; Methamphetamine ; Methamphetamine - adverse effects ; Methylphenidate ; Methylphenidate - pharmacology ; Monkeys & apes ; Neostriatum ; Neuropharmacology ; Neurosciences ; original-article ; Pharmacology. Drug treatments ; Pharmacotherapy ; Physiological aspects ; Positron emission tomography ; Positron-Emission Tomography - methods ; Psychiatry ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychopharmacology ; Putamen ; Raclopride ; Receptors, Dopamine D2 - metabolism ; Recurrence ; Relapse ; Substance abuse treatment ; Time Factors ; Tomography</subject><ispartof>Molecular psychiatry, 2012-09, Vol.17 (9), p.918-925</ispartof><rights>Macmillan Publishers Limited 2012</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2012 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Sep 2012</rights><rights>Macmillan Publishers Limited 2012.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c666t-7707cb893c3bd36d4784f1d0cce9f75603770ce8dc7eef56c3a2a888e3c943893</citedby><cites>FETCH-LOGICAL-c666t-7707cb893c3bd36d4784f1d0cce9f75603770ce8dc7eef56c3a2a888e3c943893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/mp.2011.86$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/mp.2011.86$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26304499$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21747399$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, G J</creatorcontrib><creatorcontrib>Smith, L</creatorcontrib><creatorcontrib>Volkow, N D</creatorcontrib><creatorcontrib>Telang, F</creatorcontrib><creatorcontrib>Logan, J</creatorcontrib><creatorcontrib>Tomasi, D</creatorcontrib><creatorcontrib>Wong, C T</creatorcontrib><creatorcontrib>Hoffman, W</creatorcontrib><creatorcontrib>Jayne, M</creatorcontrib><creatorcontrib>Alia-Klein, N</creatorcontrib><creatorcontrib>Thanos, P</creatorcontrib><creatorcontrib>Fowler, J S</creatorcontrib><title>Decreased dopamine activity predicts relapse in methamphetamine abusers</title><title>Molecular psychiatry</title><addtitle>Mol Psychiatry</addtitle><addtitle>Mol Psychiatry</addtitle><description>Studies in methamphetamine (METH) abusers showed that the decreases in brain dopamine (DA) function might recover with protracted detoxification. However, the extent to which striatal DA function in METH predicts recovery has not been evaluated. Here we assessed whether striatal DA activity in METH abusers is associated with clinical outcomes. Brain DA D2 receptor (D2R) availability was measured with positron emission tomography and [
11
C]raclopride in 16 METH abusers, both after placebo and after challenge with 60 mg oral methylphenidate (MPH) (to measure DA release) to assess whether it predicted clinical outcomes. For this purpose, METH abusers were tested within 6 months of last METH use and then followed up for 9 months of abstinence. In parallel, 15 healthy controls were tested. METH abusers had lower D2R availability in caudate than in controls. Both METH abusers and controls showed decreased striatal D2R availability after MPH and these decreases were smaller in METH than in controls in left putamen. The six METH abusers who relapsed during the follow-up period had lower D2R availability in dorsal striatum than in controls, and had no D2R changes after MPH challenge. The 10 METH abusers who completed detoxification did not differ from controls neither in striatal D2R availability nor in MPH-induced striatal DA changes. These results provide preliminary evidence that low striatal DA function in METH abusers is associated with a greater likelihood of relapse during treatment. Detection of the extent of DA dysfunction may be helpful in predicting therapeutic outcomes.</description><subject>631/378/340</subject><subject>631/92/436/1729</subject><subject>692/53/2423</subject><subject>Abstinence</subject><subject>Adult</subject><subject>Amphetamine abuse</subject><subject>Amphetamine-Related Disorders - diagnostic imaging</subject><subject>Amphetamine-Related Disorders - metabolism</subject><subject>Amphetamines</subject><subject>Behavioral Sciences</subject><subject>Biological and medical sciences</subject><subject>Biological Psychology</subject><subject>Brain</subject><subject>Carbon Radioisotopes</subject><subject>Case-Control Studies</subject><subject>Caudate-putamen</subject><subject>Clinical outcomes</subject><subject>Corpus Striatum - diagnostic imaging</subject><subject>Corpus Striatum - metabolism</subject><subject>Detoxification</subject><subject>Diagnosis</subject><subject>Diseases</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Dopamine D2 receptors</subject><subject>Dopamine receptors</subject><subject>Drugs</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Methamphetamine</subject><subject>Methamphetamine - adverse effects</subject><subject>Methylphenidate</subject><subject>Methylphenidate - pharmacology</subject><subject>Monkeys & apes</subject><subject>Neostriatum</subject><subject>Neuropharmacology</subject><subject>Neurosciences</subject><subject>original-article</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacotherapy</subject><subject>Physiological aspects</subject><subject>Positron emission tomography</subject><subject>Positron-Emission Tomography - methods</subject><subject>Psychiatry</subject><subject>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer</subject><subject>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychopharmacology</subject><subject>Putamen</subject><subject>Raclopride</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>Recurrence</subject><subject>Relapse</subject><subject>Substance abuse treatment</subject><subject>Time Factors</subject><subject>Tomography</subject><issn>1359-4184</issn><issn>1476-5578</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp90t1rFDEQAPBFFFurL_4BsiCCKHfm--OlUNpahYIv-hxys7N3KbvZNdkt9L831zv7oSL7kCXzm0lmSFW9pmRJCTef-nHJCKVLo55Uh1RotZBSm6fln0u7ENSIg-pFzleEbIPyeXXAqBaaW3tYXZwhJPQZm7oZRt-HiLWHKVyH6aYeEzYBplwn7PyYsQ6x7nHa-H7c4LTHqzljyi-rZ63vMr7ar0fVj8_n30-_LC6_XXw9PblcgFJqWmhNNKyM5cBXDVeN0Ea0tCEAaFstFeFFAJoGNGIrFXDPvDEGOVjBS95RdbyrO86rHhvAOCXfuTGF3qcbN_jgHkdi2Lj1cO04U5QzVgq83xdIw88Z8-T6kAG7zkcc5uy2E5XWSi4LffsHvRrmFEt7jikhtbKU0f-pUksYYRnh92rtO3QhtkO5HWyPdiecMEq5MqKo5T9U-RrsAwwR21D2HyV82CVAGnJO2N5NgpLbVlw_uu3jcEYV_Obh7O7o79dQwLs98Bl81yYfIeR7pzgR4tZ93LlcQnGN6WHLfx37C276zik</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Wang, G J</creator><creator>Smith, L</creator><creator>Volkow, N D</creator><creator>Telang, F</creator><creator>Logan, J</creator><creator>Tomasi, D</creator><creator>Wong, C T</creator><creator>Hoffman, W</creator><creator>Jayne, M</creator><creator>Alia-Klein, N</creator><creator>Thanos, P</creator><creator>Fowler, J S</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20120901</creationdate><title>Decreased dopamine activity predicts relapse in methamphetamine abusers</title><author>Wang, G J ; Smith, L ; Volkow, N D ; Telang, F ; Logan, J ; Tomasi, D ; Wong, C T ; Hoffman, W ; Jayne, M ; Alia-Klein, N ; Thanos, P ; Fowler, J S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c666t-7707cb893c3bd36d4784f1d0cce9f75603770ce8dc7eef56c3a2a888e3c943893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>631/378/340</topic><topic>631/92/436/1729</topic><topic>692/53/2423</topic><topic>Abstinence</topic><topic>Adult</topic><topic>Amphetamine abuse</topic><topic>Amphetamine-Related Disorders - diagnostic imaging</topic><topic>Amphetamine-Related Disorders - metabolism</topic><topic>Amphetamines</topic><topic>Behavioral Sciences</topic><topic>Biological and medical sciences</topic><topic>Biological Psychology</topic><topic>Brain</topic><topic>Carbon Radioisotopes</topic><topic>Case-Control Studies</topic><topic>Caudate-putamen</topic><topic>Clinical outcomes</topic><topic>Corpus Striatum - diagnostic imaging</topic><topic>Corpus Striatum - metabolism</topic><topic>Detoxification</topic><topic>Diagnosis</topic><topic>Diseases</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Dopamine D2 receptors</topic><topic>Dopamine receptors</topic><topic>Drugs</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Methamphetamine</topic><topic>Methamphetamine - adverse effects</topic><topic>Methylphenidate</topic><topic>Methylphenidate - pharmacology</topic><topic>Monkeys & apes</topic><topic>Neostriatum</topic><topic>Neuropharmacology</topic><topic>Neurosciences</topic><topic>original-article</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacotherapy</topic><topic>Physiological aspects</topic><topic>Positron emission tomography</topic><topic>Positron-Emission Tomography - methods</topic><topic>Psychiatry</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Putamen</topic><topic>Raclopride</topic><topic>Receptors, Dopamine D2 - metabolism</topic><topic>Recurrence</topic><topic>Relapse</topic><topic>Substance abuse treatment</topic><topic>Time Factors</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, G J</creatorcontrib><creatorcontrib>Smith, L</creatorcontrib><creatorcontrib>Volkow, N D</creatorcontrib><creatorcontrib>Telang, F</creatorcontrib><creatorcontrib>Logan, J</creatorcontrib><creatorcontrib>Tomasi, D</creatorcontrib><creatorcontrib>Wong, C T</creatorcontrib><creatorcontrib>Hoffman, W</creatorcontrib><creatorcontrib>Jayne, M</creatorcontrib><creatorcontrib>Alia-Klein, N</creatorcontrib><creatorcontrib>Thanos, P</creatorcontrib><creatorcontrib>Fowler, J S</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, G J</au><au>Smith, L</au><au>Volkow, N D</au><au>Telang, F</au><au>Logan, J</au><au>Tomasi, D</au><au>Wong, C T</au><au>Hoffman, W</au><au>Jayne, M</au><au>Alia-Klein, N</au><au>Thanos, P</au><au>Fowler, J S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased dopamine activity predicts relapse in methamphetamine abusers</atitle><jtitle>Molecular psychiatry</jtitle><stitle>Mol Psychiatry</stitle><addtitle>Mol Psychiatry</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>17</volume><issue>9</issue><spage>918</spage><epage>925</epage><pages>918-925</pages><issn>1359-4184</issn><eissn>1476-5578</eissn><abstract>Studies in methamphetamine (METH) abusers showed that the decreases in brain dopamine (DA) function might recover with protracted detoxification. However, the extent to which striatal DA function in METH predicts recovery has not been evaluated. Here we assessed whether striatal DA activity in METH abusers is associated with clinical outcomes. Brain DA D2 receptor (D2R) availability was measured with positron emission tomography and [
11
C]raclopride in 16 METH abusers, both after placebo and after challenge with 60 mg oral methylphenidate (MPH) (to measure DA release) to assess whether it predicted clinical outcomes. For this purpose, METH abusers were tested within 6 months of last METH use and then followed up for 9 months of abstinence. In parallel, 15 healthy controls were tested. METH abusers had lower D2R availability in caudate than in controls. Both METH abusers and controls showed decreased striatal D2R availability after MPH and these decreases were smaller in METH than in controls in left putamen. The six METH abusers who relapsed during the follow-up period had lower D2R availability in dorsal striatum than in controls, and had no D2R changes after MPH challenge. The 10 METH abusers who completed detoxification did not differ from controls neither in striatal D2R availability nor in MPH-induced striatal DA changes. These results provide preliminary evidence that low striatal DA function in METH abusers is associated with a greater likelihood of relapse during treatment. Detection of the extent of DA dysfunction may be helpful in predicting therapeutic outcomes.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>21747399</pmid><doi>10.1038/mp.2011.86</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/378/340 631/92/436/1729 692/53/2423 Abstinence Adult Amphetamine abuse Amphetamine-Related Disorders - diagnostic imaging Amphetamine-Related Disorders - metabolism Amphetamines Behavioral Sciences Biological and medical sciences Biological Psychology Brain Carbon Radioisotopes Case-Control Studies Caudate-putamen Clinical outcomes Corpus Striatum - diagnostic imaging Corpus Striatum - metabolism Detoxification Diagnosis Diseases Dopamine Dopamine - metabolism Dopamine D2 receptors Dopamine receptors Drugs Female Humans Male Medical sciences Medicine Medicine & Public Health Methamphetamine Methamphetamine - adverse effects Methylphenidate Methylphenidate - pharmacology Monkeys & apes Neostriatum Neuropharmacology Neurosciences original-article Pharmacology. Drug treatments Pharmacotherapy Physiological aspects Positron emission tomography Positron-Emission Tomography - methods Psychiatry Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychopharmacology Putamen Raclopride Receptors, Dopamine D2 - metabolism Recurrence Relapse Substance abuse treatment Time Factors Tomography |
title | Decreased dopamine activity predicts relapse in methamphetamine abusers |
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