The concomitant use of cannabis and cocaine coexists with increased LPS levels and systemic inflammation in male drug users

•Cannabis sativa and cocaine use promotes an inflammatory profile.•Cannabis sativa and cocaine use coexists with increased plasma levels of LPS.•Cocaine impaired the antioxidative defense system. Illicit drug use can cause a variety of effects including alterations in the immune system. The aim of t...

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Veröffentlicht in:Cytokine (Philadelphia, Pa.) Pa.), 2021-05, Vol.141, p.155472-155472, Article 155472
Hauptverfasser: Ribeiro, Camila Bastos, Castro, Fernanda de Oliveira Feitosa de, Dorneles, Gilson Pires, de Sousa Barros, Jéssica Barletto, Silva, Jacyelle Medeiros, Tavares, Camila, Carvalho, Hélio Rocha, Carlos da Cunha, Luiz, Nagib, Patrícia, Hoffmann, Christian, Peres, Alessandra, Torres Romão, Pedro Roosevelt, Pfrimer, Irmtraut Araci Hoffmann, Fonseca, Simone Gonçalves da
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container_title Cytokine (Philadelphia, Pa.)
container_volume 141
creator Ribeiro, Camila Bastos
Castro, Fernanda de Oliveira Feitosa de
Dorneles, Gilson Pires
de Sousa Barros, Jéssica Barletto
Silva, Jacyelle Medeiros
Tavares, Camila
Carvalho, Hélio Rocha
Carlos da Cunha, Luiz
Nagib, Patrícia
Hoffmann, Christian
Peres, Alessandra
Torres Romão, Pedro Roosevelt
Pfrimer, Irmtraut Araci Hoffmann
Fonseca, Simone Gonçalves da
description •Cannabis sativa and cocaine use promotes an inflammatory profile.•Cannabis sativa and cocaine use coexists with increased plasma levels of LPS.•Cocaine impaired the antioxidative defense system. Illicit drug use can cause a variety of effects including alterations in the immune system. The aim of this study was to investigate the effects of illicit drugs on circulating lipopolysaccharide (LPS), systemic inflammation and oxidative stress markers in drug users. We evaluated the levels of soluble CD14 (sCD14), LPS, inflammatory (TNF-α and IL-6) and regulatory (IL-10) cytokines, as well as C-reactive protein (CRP), lipid peroxidation (TBARS) and total thiols in the peripheral blood of 81 men included in groups of cannabis (n = 21), cocaine (n = 12), cannabis-plus-cocaine users (n = 27), and non-drug users (n = 21). The use of cannabis plus cocaine leads to higher systemic levels of LPS, CRP, IL-6 and higher IL-6/IL-10 ratio, characterizing a proinflammatory profile. In contrast, a regulatory profile as viewed by lower systemic TNF-α and IL-6 levels and lower TNF-α/IL-10 ratio were observed in cannabis users compared to the control group. Moreover, cocaine users presented a lower content of non-enzymatic antioxidant thiol compared to control group, cannabis group and cannabis plus cocaine group. In conclusion, our results indicate that the use of cannabis contributes to an anti-inflammatory/or regulatory profile while the concomitant cannabis plus cocaine consumption coexists with increased circulating amounts of LPS and proinflammatory status.
doi_str_mv 10.1016/j.cyto.2021.155472
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Illicit drug use can cause a variety of effects including alterations in the immune system. The aim of this study was to investigate the effects of illicit drugs on circulating lipopolysaccharide (LPS), systemic inflammation and oxidative stress markers in drug users. We evaluated the levels of soluble CD14 (sCD14), LPS, inflammatory (TNF-α and IL-6) and regulatory (IL-10) cytokines, as well as C-reactive protein (CRP), lipid peroxidation (TBARS) and total thiols in the peripheral blood of 81 men included in groups of cannabis (n = 21), cocaine (n = 12), cannabis-plus-cocaine users (n = 27), and non-drug users (n = 21). The use of cannabis plus cocaine leads to higher systemic levels of LPS, CRP, IL-6 and higher IL-6/IL-10 ratio, characterizing a proinflammatory profile. In contrast, a regulatory profile as viewed by lower systemic TNF-α and IL-6 levels and lower TNF-α/IL-10 ratio were observed in cannabis users compared to the control group. Moreover, cocaine users presented a lower content of non-enzymatic antioxidant thiol compared to control group, cannabis group and cannabis plus cocaine group. In conclusion, our results indicate that the use of cannabis contributes to an anti-inflammatory/or regulatory profile while the concomitant cannabis plus cocaine consumption coexists with increased circulating amounts of LPS and proinflammatory status.</description><identifier>ISSN: 1043-4666</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1016/j.cyto.2021.155472</identifier><identifier>PMID: 33618152</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; C-reactive protein ; C-Reactive Protein - metabolism ; Cannabis - adverse effects ; Cocaine - adverse effects ; Cocaine-Related Disorders - blood ; Cytokines - blood ; Drug Users ; Humans ; Illicit drugs ; Inflammation ; Inflammation - blood ; Lipopolysaccharides - blood ; LPS ; Male ; Marijuana Abuse - blood ; Oxidative stress</subject><ispartof>Cytokine (Philadelphia, Pa.), 2021-05, Vol.141, p.155472-155472, Article 155472</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. 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Illicit drug use can cause a variety of effects including alterations in the immune system. The aim of this study was to investigate the effects of illicit drugs on circulating lipopolysaccharide (LPS), systemic inflammation and oxidative stress markers in drug users. We evaluated the levels of soluble CD14 (sCD14), LPS, inflammatory (TNF-α and IL-6) and regulatory (IL-10) cytokines, as well as C-reactive protein (CRP), lipid peroxidation (TBARS) and total thiols in the peripheral blood of 81 men included in groups of cannabis (n = 21), cocaine (n = 12), cannabis-plus-cocaine users (n = 27), and non-drug users (n = 21). The use of cannabis plus cocaine leads to higher systemic levels of LPS, CRP, IL-6 and higher IL-6/IL-10 ratio, characterizing a proinflammatory profile. In contrast, a regulatory profile as viewed by lower systemic TNF-α and IL-6 levels and lower TNF-α/IL-10 ratio were observed in cannabis users compared to the control group. Moreover, cocaine users presented a lower content of non-enzymatic antioxidant thiol compared to control group, cannabis group and cannabis plus cocaine group. 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Illicit drug use can cause a variety of effects including alterations in the immune system. The aim of this study was to investigate the effects of illicit drugs on circulating lipopolysaccharide (LPS), systemic inflammation and oxidative stress markers in drug users. We evaluated the levels of soluble CD14 (sCD14), LPS, inflammatory (TNF-α and IL-6) and regulatory (IL-10) cytokines, as well as C-reactive protein (CRP), lipid peroxidation (TBARS) and total thiols in the peripheral blood of 81 men included in groups of cannabis (n = 21), cocaine (n = 12), cannabis-plus-cocaine users (n = 27), and non-drug users (n = 21). The use of cannabis plus cocaine leads to higher systemic levels of LPS, CRP, IL-6 and higher IL-6/IL-10 ratio, characterizing a proinflammatory profile. In contrast, a regulatory profile as viewed by lower systemic TNF-α and IL-6 levels and lower TNF-α/IL-10 ratio were observed in cannabis users compared to the control group. Moreover, cocaine users presented a lower content of non-enzymatic antioxidant thiol compared to control group, cannabis group and cannabis plus cocaine group. In conclusion, our results indicate that the use of cannabis contributes to an anti-inflammatory/or regulatory profile while the concomitant cannabis plus cocaine consumption coexists with increased circulating amounts of LPS and proinflammatory status.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>33618152</pmid><doi>10.1016/j.cyto.2021.155472</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-1331-0441</orcidid></addata></record>
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subjects Adult
C-reactive protein
C-Reactive Protein - metabolism
Cannabis - adverse effects
Cocaine - adverse effects
Cocaine-Related Disorders - blood
Cytokines - blood
Drug Users
Humans
Illicit drugs
Inflammation
Inflammation - blood
Lipopolysaccharides - blood
LPS
Male
Marijuana Abuse - blood
Oxidative stress
title The concomitant use of cannabis and cocaine coexists with increased LPS levels and systemic inflammation in male drug users
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