Deficit of circulating stem – progenitor cells in opiate addiction: a pilot study

<p>Abstract</p> <p>A substantial literature describes the capacity of all addictive drugs to slow cell growth and potentiate apoptosis. Flow cytometry was used as a means to compare two lineages of circulating progenitor cells in addicted patients. Buprenorphine treated opiate addi...

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Main Authors: Davidson Peter, Reece Albert S
Format: Article
Language:English
Published: BMC 2007-07-01
Series:Substance Abuse Treatment, Prevention, and Policy
Online Access:http://www.substanceabusepolicy.com/content/2/1/19
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spelling doaj-fcf19735884c49f3b25667ac3ccdd5732020-11-24T21:53:01ZengBMCSubstance Abuse Treatment, Prevention, and Policy1747-597X2007-07-01211910.1186/1747-597X-2-19Deficit of circulating stem – progenitor cells in opiate addiction: a pilot studyDavidson PeterReece Albert S<p>Abstract</p> <p>A substantial literature describes the capacity of all addictive drugs to slow cell growth and potentiate apoptosis. Flow cytometry was used as a means to compare two lineages of circulating progenitor cells in addicted patients. Buprenorphine treated opiate addicts were compared with medical patients. Peripheral venous blood CD34<sup>+ </sup>CD45<sup>+ </sup>double positive cells were counted as haemopoietic stem cells (HSC's), and CD34<sup>+ </sup>KDR<sup>+ </sup>(VEGFR2<sup>+</sup>) cells were taken as endothelial progenitor cells (EPC's). 10 opiate dependent patients with substance use disorder (SUD) and 11 non-addicted (N-SUD) were studied. The ages were (mean + S.D.) 36.2 + 8.6 and 56.4 + 18.6 respectively (P <0.01). HSC's were not different in the SUD (2.38 + 1.09 Vs. 3.40 + 4.56 cells/mcl). EPC's were however significantly lower in the SUD (0.09 + 0.14 Vs. 0.26 + 0.20 cells/mcl; No. > 0.15, OR = 0.09, 95% C.I. 0.01–0.97), a finding of some interest given the substantially older age of the N-SUD group. These laboratory data are thus consistent with clinical data suggesting accelerated ageing in addicted humans and implicate the important stem cell pool in both addiction toxicology and ageing. They carry important policy implications for understanding the fundamental toxicology of addiction, and suggest that the toxicity both of addiction itself and of indefinite agonist maintenance therapies may have been seriously underestimated.</p> http://www.substanceabusepolicy.com/content/2/1/19
collection DOAJ
language English
format Article
sources DOAJ
author Davidson Peter
Reece Albert S
spellingShingle Davidson Peter
Reece Albert S
Deficit of circulating stem – progenitor cells in opiate addiction: a pilot study
Substance Abuse Treatment, Prevention, and Policy
author_facet Davidson Peter
Reece Albert S
author_sort Davidson Peter
title Deficit of circulating stem – progenitor cells in opiate addiction: a pilot study
title_short Deficit of circulating stem – progenitor cells in opiate addiction: a pilot study
title_full Deficit of circulating stem – progenitor cells in opiate addiction: a pilot study
title_fullStr Deficit of circulating stem – progenitor cells in opiate addiction: a pilot study
title_full_unstemmed Deficit of circulating stem – progenitor cells in opiate addiction: a pilot study
title_sort deficit of circulating stem – progenitor cells in opiate addiction: a pilot study
publisher BMC
series Substance Abuse Treatment, Prevention, and Policy
issn 1747-597X
publishDate 2007-07-01
description <p>Abstract</p> <p>A substantial literature describes the capacity of all addictive drugs to slow cell growth and potentiate apoptosis. Flow cytometry was used as a means to compare two lineages of circulating progenitor cells in addicted patients. Buprenorphine treated opiate addicts were compared with medical patients. Peripheral venous blood CD34<sup>+ </sup>CD45<sup>+ </sup>double positive cells were counted as haemopoietic stem cells (HSC's), and CD34<sup>+ </sup>KDR<sup>+ </sup>(VEGFR2<sup>+</sup>) cells were taken as endothelial progenitor cells (EPC's). 10 opiate dependent patients with substance use disorder (SUD) and 11 non-addicted (N-SUD) were studied. The ages were (mean + S.D.) 36.2 + 8.6 and 56.4 + 18.6 respectively (P <0.01). HSC's were not different in the SUD (2.38 + 1.09 Vs. 3.40 + 4.56 cells/mcl). EPC's were however significantly lower in the SUD (0.09 + 0.14 Vs. 0.26 + 0.20 cells/mcl; No. > 0.15, OR = 0.09, 95% C.I. 0.01–0.97), a finding of some interest given the substantially older age of the N-SUD group. These laboratory data are thus consistent with clinical data suggesting accelerated ageing in addicted humans and implicate the important stem cell pool in both addiction toxicology and ageing. They carry important policy implications for understanding the fundamental toxicology of addiction, and suggest that the toxicity both of addiction itself and of indefinite agonist maintenance therapies may have been seriously underestimated.</p>
url http://www.substanceabusepolicy.com/content/2/1/19
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