Elevated Levels of Endocannabinoids in Chronic Hepatitis C May Modulate Cellular Immune Response and Hepatic Stellate Cell Activation

The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explor...

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Published inInternational journal of molecular sciences Vol. 16; no. 4; pp. 7057 - 7076
Main Authors Patsenker, Eleonora, Sachse, Philip, Chicca, Andrea, Gachet, María, Schneider, Vreni, Mattsson, Johan, Lanz, Christian, Worni, Mathias, De Gottardi, Andrea, Semmo, Mariam, Hampe, Jochen, Schafmayer, Clemens, Brenneisen, Rudolf, Gertsch, Jürg, Stickel, Felix, Semmo, Nasser
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Published Switzerland MDPI AG 27.03.2015
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Abstract The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explored. To study this question, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) were quantified in samples of HCV patients and healthy controls by gas and liquid chromatography mass spectrometry. Fatty acid amide hydrolase (FAAH) and monoaclyglycerol lipase (MAGL) activity was assessed by [3H]AEA and [3H]2-AG hydrolysis, respectively. Gene expression and cytokine release were assayed by TaqMan PCR and ELISpot, respectively. AEA and 2-AG levels were increased in plasma of HCV patients, but not in liver tissues. Hepatic FAAH and MAGL activity was not changed. In peripheral blood mononuclear cells (PBMC), ECs inhibited IFN-γ, TNF-α, and IL-2 secretion. Inhibition of IL-2 by endogenous AEA was stronger in PBMC from HCV patients. In hepatocytes, 2-AG induced the expression of IL-6, -17A, -32 and COX-2, and enhanced activation of hepatic stellate cells (HSC) co-cultivated with PBMC from subjects with CHC. In conclusion, ECs are increased in plasma of patients with CHC and might reveal immunosuppressive and profibrogenic effects.
AbstractList The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explored. To study this question, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) were quantified in samples of HCV patients and healthy controls by gas and liquid chromatography mass spectrometry. Fatty acid amide hydrolase (FAAH) and monoaclyglycerol lipase (MAGL) activity was assessed by [3H]AEA and [3H]2-AG hydrolysis, respectively. Gene expression and cytokine release were assayed by TaqMan PCR and ELISpot, respectively. AEA and 2-AG levels were increased in plasma of HCV patients, but not in liver tissues. Hepatic FAAH and MAGL activity was not changed. In peripheral blood mononuclear cells (PBMC), ECs inhibited IFN-γ, TNF-α, and IL-2 secretion. Inhibition of IL-2 by endogenous AEA was stronger in PBMC from HCV patients. In hepatocytes, 2-AG induced the expression of IL-6, -17A, -32 and COX-2, and enhanced activation of hepatic stellate cells (HSC) co-cultivated with PBMC from subjects with CHC. In conclusion, ECs are increased in plasma of patients with CHC and might reveal immunosuppressive and profibrogenic effects.The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explored. To study this question, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) were quantified in samples of HCV patients and healthy controls by gas and liquid chromatography mass spectrometry. Fatty acid amide hydrolase (FAAH) and monoaclyglycerol lipase (MAGL) activity was assessed by [3H]AEA and [3H]2-AG hydrolysis, respectively. Gene expression and cytokine release were assayed by TaqMan PCR and ELISpot, respectively. AEA and 2-AG levels were increased in plasma of HCV patients, but not in liver tissues. Hepatic FAAH and MAGL activity was not changed. In peripheral blood mononuclear cells (PBMC), ECs inhibited IFN-γ, TNF-α, and IL-2 secretion. Inhibition of IL-2 by endogenous AEA was stronger in PBMC from HCV patients. In hepatocytes, 2-AG induced the expression of IL-6, -17A, -32 and COX-2, and enhanced activation of hepatic stellate cells (HSC) co-cultivated with PBMC from subjects with CHC. In conclusion, ECs are increased in plasma of patients with CHC and might reveal immunosuppressive and profibrogenic effects.
The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explored. To study this question, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) were quantified in samples of HCV patients and healthy controls by gas and liquid chromatography mass spectrometry. Fatty acid amide hydrolase (FAAH) and monoaclyglycerol lipase (MAGL) activity was assessed by [3H]AEA and [3H]2-AG hydrolysis, respectively. Gene expression and cytokine release were assayed by TaqMan PCR and ELISpot, respectively. AEA and 2-AG levels were increased in plasma of HCV patients, but not in liver tissues. Hepatic FAAH and MAGL activity was not changed. In peripheral blood mononuclear cells (PBMC), ECs inhibited IFN-γ, TNF-α, and IL-2 secretion. Inhibition of IL-2 by endogenous AEA was stronger in PBMC from HCV patients. In hepatocytes, 2-AG induced the expression of IL-6, -17A, -32 and COX-2, and enhanced activation of hepatic stellate cells (HSC) co-cultivated with PBMC from subjects with CHC. In conclusion, ECs are increased in plasma of patients with CHC and might reveal immunosuppressive and profibrogenic effects.
The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explored. To study this question, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) were quantified in samples of HCV patients and healthy controls by gas and liquid chromatography mass spectrometry. Fatty acid amide hydrolase (FAAH) and monoaclyglycerol lipase (MAGL) activity was assessed by [ super(3)H]AEA and [ super(3)H]2-AG hydrolysis, respectively. Gene expression and cytokine release were assayed by TaqMan PCR and ELISpot, respectively. AEA and 2-AG levels were increased in plasma of HCV patients, but not in liver tissues. Hepatic FAAH and MAGL activity was not changed. In peripheral blood mononuclear cells (PBMC), ECs inhibited IFN-[gamma], TNF-[alpha], and IL-2 secretion. Inhibition of IL-2 by endogenous AEA was stronger in PBMC from HCV patients. In hepatocytes, 2-AG induced the expression of IL-6, -17A, -32 and COX-2, and enhanced activation of hepatic stellate cells (HSC) co-cultivated with PBMC from subjects with CHC. In conclusion, ECs are increased in plasma of patients with CHC and might reveal immunosuppressive and profibrogenic effects.
The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explored. To study this question, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) were quantified in samples of HCV patients and healthy controls by gas and liquid chromatography mass spectrometry. Fatty acid amide hydrolase (FAAH) and monoaclyglycerol lipase (MAGL) activity was assessed by [ 3 H]AEA and [ 3 H]2-AG hydrolysis, respectively. Gene expression and cytokine release were assayed by TaqMan PCR and ELISpot, respectively. AEA and 2-AG levels were increased in plasma of HCV patients, but not in liver tissues. Hepatic FAAH and MAGL activity was not changed. In peripheral blood mononuclear cells (PBMC), ECs inhibited IFN-γ, TNF-α, and IL-2 secretion. Inhibition of IL-2 by endogenous AEA was stronger in PBMC from HCV patients. In hepatocytes, 2-AG induced the expression of IL-6, -17A, -32 and COX-2, and enhanced activation of hepatic stellate cells (HSC) co-cultivated with PBMC from subjects with CHC. In conclusion, ECs are increased in plasma of patients with CHC and might reveal immunosuppressive and profibrogenic effects.
Author Chicca, Andrea
Lanz, Christian
De Gottardi, Andrea
Semmo, Mariam
Hampe, Jochen
Patsenker, Eleonora
Mattsson, Johan
Brenneisen, Rudolf
Sachse, Philip
Stickel, Felix
Gertsch, Jürg
Semmo, Nasser
Schneider, Vreni
Worni, Mathias
Gachet, María
Schafmayer, Clemens
AuthorAffiliation 3 Department of Clinical Research, Laboratory of Phytopharmacology, Bioanalytics and Pharmacokinetics, University of Bern, Bern 3010, Switzerland; E-Mails: Johan.Mattsson@insel.ch (J.M.); christian.lanz@dkf.unibe.ch (C.L.); rudolf.brenneisen@dkf.unibe.ch (R.B.)
4 Department of Visceral Surgery and Medicine, Inselspital, University of Bern, Bern 3010, Switzerland; E-Mails: christian.lanz@dkf.unibe.ch (M.W.); andrea.degottardi@ikp.unibe.ch (A.G.)
5 Department of Nephrology, Inselspital, University of Bern, Bern 3010, Switzerland; E-Mail: Mariam.Semmo@insel.ch
7 Department of Visceral Surgery, University of Schleswig-Holstein, Campus Kiel, Kiel 24105, Germany; E-Mail: clemens.schafmayer@uksh-kiel.de
2 Institute of Biochemistry and Molecular Medicine, University of Bern, Bern 3012, Switzerland; E-Mails: andrea.chicca@ibmm.unibe.ch (A.C.); maria.gachet@ibmm.unibe.ch (M.S.G.); juerg.gertsch@ibmm.unibe.ch (J.G.)
6 Department of Medicine II, Division of Gastroenterology, University of Dresden, Dres
AuthorAffiliation_xml – name: 2 Institute of Biochemistry and Molecular Medicine, University of Bern, Bern 3012, Switzerland; E-Mails: andrea.chicca@ibmm.unibe.ch (A.C.); maria.gachet@ibmm.unibe.ch (M.S.G.); juerg.gertsch@ibmm.unibe.ch (J.G.)
– name: 7 Department of Visceral Surgery, University of Schleswig-Holstein, Campus Kiel, Kiel 24105, Germany; E-Mail: clemens.schafmayer@uksh-kiel.de
– name: 3 Department of Clinical Research, Laboratory of Phytopharmacology, Bioanalytics and Pharmacokinetics, University of Bern, Bern 3010, Switzerland; E-Mails: Johan.Mattsson@insel.ch (J.M.); christian.lanz@dkf.unibe.ch (C.L.); rudolf.brenneisen@dkf.unibe.ch (R.B.)
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– name: 4 Department of Visceral Surgery and Medicine, Inselspital, University of Bern, Bern 3010, Switzerland; E-Mails: christian.lanz@dkf.unibe.ch (M.W.); andrea.degottardi@ikp.unibe.ch (A.G.)
– name: 5 Department of Nephrology, Inselspital, University of Bern, Bern 3010, Switzerland; E-Mail: Mariam.Semmo@insel.ch
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Cites_doi 10.1021/pr300683a
10.1016/j.jhep.2013.03.032
10.1016/j.ijid.2013.12.017
10.1002/hep.20669
10.1016/S0083-6729(09)81019-4
10.1074/jbc.M112.373241
10.1097/MOL.0b013e32803dbdec
10.1038/nrd2553
10.1053/j.gastro.2012.12.028
10.1194/jlr.M017368
10.1053/j.gastro.2007.11.039
10.1371/journal.pone.0062741
10.1152/ajpgi.00523.2007
10.1099/vir.0.067231-0
10.1002/hep.20895
10.3748/wjg.14.6109
10.1111/j.1478-3231.2009.02137.x
10.2119/molmed.2011.00149
10.1053/j.gastro.2004.12.050
10.1111/liv.12263
10.1111/j.1365-2893.2007.00842.x
10.1016/S0140-6736(05)17787-3
10.1172/JCI200523057
10.1189/jlb.0303101
10.1002/hep.24524
10.1016/j.jneuroim.2003.10.019
10.1002/hep.20733
10.1053/j.gastro.2008.04.009
10.1124/mol.108.047035
10.1016/j.jhep.2009.12.038
10.1152/ajpgi.00456.2007
10.1016/j.jhep.2013.04.029
10.1124/mol.105.019117
10.1074/jbc.M509706200
10.4155/fmc.09.93
10.1016/j.intimp.2012.03.022
10.1053/jhep.2003.50459
10.1371/journal.pone.0012841
10.1038/nm1421
10.1111/j.1476-5381.2011.01397.x
10.1002/hep.26598
10.1371/journal.pone.0008688
10.1016/j.cgh.2007.10.021
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References Semmo (ref_43) 2005; 365
Hegde (ref_14) 2008; 74
Mueller (ref_34) 2010; 52
Klein (ref_16) 2003; 74
Rockwell (ref_17) 2006; 70
Cao (ref_38) 2013; 144
Siegmund (ref_10) 2006; 281
Baldassarre (ref_11) 2013; 33
Klein (ref_15) 2004; 147
Semmo (ref_40) 2007; 14
Patsenker (ref_42) 2008; 135
Pacher (ref_3) 2008; 294
Semmo (ref_44) 2005; 41
Shahidi (ref_32) 2014; 95
Clugston (ref_27) 2011; 52
Ishida (ref_21) 2008; 6
Petrosino (ref_29) 2007; 18
Caraceni (ref_7) 2009; 30
Patsenker (ref_33) 2011; 17
Mallat (ref_20) 2013; 59
Patsenker (ref_39) 2014; 35
Parfieniuk (ref_25) 2008; 14
Glassner (ref_35) 2013; 59
Shahidi (ref_24) 2010; 5
Hezode (ref_22) 2005; 42
Julien (ref_2) 2005; 128
Hauer (ref_30) 2013; 8
Chicca (ref_41) 2012; 287
(ref_37) 2008; 7
Biswas (ref_8) 2003; 38
Cencioni (ref_12) 2010; 5
Zhou (ref_19) 2012; 11
Siegmund (ref_26) 2008; 294
Pandey (ref_13) 2009; 81
Balvers (ref_28) 2012; 13
Mallat (ref_6) 2011; 163
Sun (ref_31) 2014; 23
Guillot (ref_4) 2014; 59
Nagarkatti (ref_1) 2009; 1
Louvet (ref_18) 2011; 54
Julien (ref_5) 2006; 12
DePetrillo (ref_9) 2005; 115
Hezode (ref_23) 2008; 134
Schwabe (ref_36) 2005; 42
20098669 - PLoS One. 2010;5(1):e8688
18239059 - Am J Physiol Gastrointest Liver Physiol. 2008 Apr;294(4):G850-4
25053565 - J Gen Virol. 2014 Nov;95(Pt 11):2468-79
21856784 - J Lipid Res. 2011 Nov;52(11):2021-31
22879589 - J Biol Chem. 2012 Oct 5;287(41):34660-82
15864349 - J Clin Invest. 2005 May;115(5):1298-305
23890208 - Liver Int. 2013 Oct;33(9):1298-308
18006606 - Am J Physiol Gastrointest Liver Physiol. 2008 Feb;294(2):G357-62
23665286 - J Hepatol. 2013 Sep;59(3):427-33
21735467 - Hepatology. 2011 Oct;54(4):1217-26
23567085 - J Hepatol. 2013 Oct;59(4):891-6
23295443 - Gastroenterology. 2013 Apr;144(4):808-817.e15
14578855 - Hepatology. 2003 Nov;38(5):1167-77
21863215 - Mol Med. 2011;17(11-12):1285-94
18446159 - Nat Rev Drug Discov. 2008 May;7(5):438-55
12960289 - J Leukoc Biol. 2003 Oct;74(4):486-96
19840245 - Liver Int. 2010 Jul;30(6):816-25
18538673 - Gastroenterology. 2008 Aug;135(2):660-70
16175591 - Hepatology. 2005 Oct;42(4):975-6; author reply 976-7
20416967 - J Hepatol. 2010 Jun;52(6):800-11
23813495 - Hepatology. 2014 Jan;59(1):296-306
18985799 - World J Gastroenterol. 2008 Oct 28;14(40):6109-14
22498761 - Int Immunopharmacol. 2012 Jun;13(2):204-14
15765409 - Gastroenterology. 2005 Mar;128(3):742-55
18166478 - Clin Gastroenterol Hepatol. 2008 Jan;6(1):69-75
18242211 - Gastroenterology. 2008 Feb;134(2):432-9
15841456 - Hepatology. 2005 May;41(5):1019-28
16418162 - J Biol Chem. 2006 Apr 14;281(15):10431-8
24484068 - Liver Int. 2015 Jan;35(1):207-14
17576391 - J Viral Hepat. 2007 Jul;14(7):492-502
16611855 - Mol Pharmacol. 2006 Jul;70(1):101-11
21457226 - Br J Pharmacol. 2011 Aug;163(7):1432-40
20862263 - PLoS One. 2010;5(9). pii: e12841. doi: 10.1371/journal.pone.0012841
14741435 - J Neuroimmunol. 2004 Feb;147(1-2):91-4
17353660 - Curr Opin Lipidol. 2007 Apr;18(2):129-40
18388242 - Mol Pharmacol. 2008 Jul;74(1):20-33
20191092 - Future Med Chem. 2009 Oct;1(7):1333-49
22946841 - J Proteome Res. 2012 Nov 2;11(11):5433-42
24704332 - Int J Infect Dis. 2014 Jun;23:75-81
19647124 - Vitam Horm. 2009;81:487-504
23667516 - PLoS One. 2013;8(5):e62741
15664228 - Lancet. 2005 Jan 22-28;365(9456):327-9
15892090 - Hepatology. 2005 Jul;42(1):63-71
16715087 - Nat Med. 2006 Jun;12(6):671-6
References_xml – volume: 11
  start-page: 5433
  year: 2012
  ident: ref_19
  article-title: Serum metabolic profiling study of hepatocellular carcinoma infected with hepatitis B or hepatitis C virus by using liquid chromatography-mass spectrometry
  publication-title: J. Proteome Res.
  doi: 10.1021/pr300683a
– volume: 59
  start-page: 891
  year: 2013
  ident: ref_20
  article-title: Cannabinoid signaling and liver therapeutics
  publication-title: J. Hepatol.
  doi: 10.1016/j.jhep.2013.03.032
– volume: 23
  start-page: 75
  year: 2014
  ident: ref_31
  article-title: Endocannabinoid system activation contributes to glucose metabolism disorders of hepatocytes and promotes hepatitis C virus replication
  publication-title: Int. J. Infect. Dis.
  doi: 10.1016/j.ijid.2013.12.017
– volume: 41
  start-page: 1019
  year: 2005
  ident: ref_44
  article-title: Preferential loss of IL-2-secreting CD4+ T helper cells in chronic HCV infection
  publication-title: Hepatology
  doi: 10.1002/hep.20669
– volume: 81
  start-page: 487
  year: 2009
  ident: ref_13
  article-title: Use of cannabinoids as a novel therapeutic modality against autoimmune hepatitis
  publication-title: Vitam. Horm.
  doi: 10.1016/S0083-6729(09)81019-4
– volume: 287
  start-page: 34660
  year: 2012
  ident: ref_41
  article-title: Evidence for bidirectional endocannabinoid transport across cell membranes
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M112.373241
– volume: 18
  start-page: 129
  year: 2007
  ident: ref_29
  article-title: Endocannabinoids and the regulation of their levels in health and disease
  publication-title: Curr. Opin. Lipidol.
  doi: 10.1097/MOL.0b013e32803dbdec
– volume: 7
  start-page: 438
  year: 2008
  ident: ref_37
  article-title: Targeting the endocannabinoid system: To enhance or reduce?
  publication-title: Nat. Rev. Drug Discov.
  doi: 10.1038/nrd2553
– volume: 144
  start-page: 808
  year: 2013
  ident: ref_38
  article-title: Monoacylglycerol lipase controls endocannabinoid and eicosanoid signaling and hepatic injury in mice
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2012.12.028
– volume: 52
  start-page: 2021
  year: 2011
  ident: ref_27
  article-title: Altered hepatic lipid metabolism in c57bl/6 mice fed alcohol: A targeted lipidomic and gene expression study
  publication-title: J. Lipid Res.
  doi: 10.1194/jlr.M017368
– volume: 134
  start-page: 432
  year: 2008
  ident: ref_23
  article-title: Daily cannabis use: A novel risk factor of steatosis severity in patients with chronic hepatitis c
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2007.11.039
– volume: 8
  start-page: e62741
  year: 2013
  ident: ref_30
  article-title: Plasma concentrations of endocannabinoids and related primary fatty acid amides in patients with post-traumatic stress disorder
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0062741
– volume: 294
  start-page: G850
  year: 2008
  ident: ref_3
  article-title: Endocannabinoids and liver disease. III. Endocannabinoid effects on immune cells: Implications for inflammatory liver diseases
  publication-title: Am. J. Physiol. Gastrointest. Liver Physiol.
  doi: 10.1152/ajpgi.00523.2007
– volume: 95
  start-page: 2468
  year: 2014
  ident: ref_32
  article-title: Endocannabinoid CB1 antagonists inhibit hepatitis C virus production, providing a novel class of antiviral host targeting agents
  publication-title: J. Gen. Virol.
  doi: 10.1099/vir.0.067231-0
– volume: 42
  start-page: 975
  year: 2005
  ident: ref_36
  article-title: Potential role of CB2 receptors in cannabis smokers with chronic hepatitis C
  publication-title: Hepatology
  doi: 10.1002/hep.20895
– volume: 14
  start-page: 6109
  year: 2008
  ident: ref_25
  article-title: Role of cannabinoids in chronic liver diseases
  publication-title: World J. Gastroenterol.
  doi: 10.3748/wjg.14.6109
– volume: 30
  start-page: 816
  year: 2009
  ident: ref_7
  article-title: Circulating and hepatic endocannabinoids and endocannabinoid-related molecules in patients with cirrhosis
  publication-title: Liver Int.
  doi: 10.1111/j.1478-3231.2009.02137.x
– volume: 17
  start-page: 1285
  year: 2011
  ident: ref_33
  article-title: Cannabinoid receptor type I modulates alcohol-induced liver fibrosis
  publication-title: Mol. Med.
  doi: 10.2119/molmed.2011.00149
– volume: 128
  start-page: 742
  year: 2005
  ident: ref_2
  article-title: Antifibrogenic role of the cannabinoid receptor CB2 in the liver
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2004.12.050
– volume: 33
  start-page: 1298
  year: 2013
  ident: ref_11
  article-title: The endocannabinoid system in advanced liver cirrhosis: Pathophysiological implication and future perspectives
  publication-title: Liver Int.
  doi: 10.1111/liv.12263
– volume: 14
  start-page: 492
  year: 2007
  ident: ref_40
  article-title: Analysis of the relationship between cytokine secretion and proliferative capacity in hepatitis C virus infection
  publication-title: J. Viral Hepat.
  doi: 10.1111/j.1365-2893.2007.00842.x
– volume: 365
  start-page: 327
  year: 2005
  ident: ref_43
  article-title: T-cell responses and previous exposure to hepatitis c virus in indeterminate blood donors
  publication-title: Lancet
  doi: 10.1016/S0140-6736(05)17787-3
– volume: 115
  start-page: 1298
  year: 2005
  ident: ref_9
  article-title: Endocannabinoid activation at hepatic cb1 receptors stimulates fatty acid synthesis and contributes to diet-induced obesity
  publication-title: J. Clin. Investig.
  doi: 10.1172/JCI200523057
– volume: 74
  start-page: 486
  year: 2003
  ident: ref_16
  article-title: The cannabinoid system and immune modulation
  publication-title: J. Leukoc. Biol.
  doi: 10.1189/jlb.0303101
– volume: 54
  start-page: 1217
  year: 2011
  ident: ref_18
  article-title: Cannabinoid CB2 receptors protect against alcoholic liver disease by regulating kupffer cell polarization in mice
  publication-title: Hepatology
  doi: 10.1002/hep.24524
– volume: 147
  start-page: 91
  year: 2004
  ident: ref_15
  article-title: Cannabinoid receptors and T helper cells
  publication-title: J. Neuroimmunol.
  doi: 10.1016/j.jneuroim.2003.10.019
– volume: 42
  start-page: 63
  year: 2005
  ident: ref_22
  article-title: Daily cannabis smoking as a risk factor for progression of fibrosis in chronic hepatitis c
  publication-title: Hepatology
  doi: 10.1002/hep.20733
– volume: 135
  start-page: 660
  year: 2008
  ident: ref_42
  article-title: Inhibition of integrin αvβ6 on cholangiocytes blocks transforming growth factor-β activation and retards biliary fibrosis progression
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2008.04.009
– volume: 74
  start-page: 20
  year: 2008
  ident: ref_14
  article-title: Attenuation of experimental autoimmune hepatitis by exogenous and endogenous cannabinoids: Involvement of regulatory t cells
  publication-title: Mol. Pharmacol.
  doi: 10.1124/mol.108.047035
– volume: 52
  start-page: 800
  year: 2010
  ident: ref_34
  article-title: Virus-specific cd4+ T cell responses in chronic hcv infection in blood and liver identified by antigen-specific upregulation of cd154
  publication-title: J. Hepatol.
  doi: 10.1016/j.jhep.2009.12.038
– volume: 294
  start-page: G357
  year: 2008
  ident: ref_26
  article-title: Endocannabinoids and liver disease. II. Endocannabinoids in the pathogenesis and treatment of liver fibrosis
  publication-title: Am. J. Physiol. Gastrointest. Liver Physiol.
  doi: 10.1152/ajpgi.00456.2007
– volume: 59
  start-page: 427
  year: 2013
  ident: ref_35
  article-title: Impaired CD4+ T cell stimulation of nk cell anti-fibrotic activity may contribute to accelerated liver fibrosis progression in HIV/HCV patients
  publication-title: J. Hepatol.
  doi: 10.1016/j.jhep.2013.04.029
– volume: 35
  start-page: 207
  year: 2014
  ident: ref_39
  article-title: Metabolomic tissue signature in human non-alcoholic fatty liver disease identifies protective candidate metabolites
  publication-title: Liver Int.
– volume: 70
  start-page: 101
  year: 2006
  ident: ref_17
  article-title: Interleukin-2 suppression by 2-arachidonyl glycerol is mediated through peroxisome proliferator-activated receptor γ independently of cannabinoid receptors 1 and 2
  publication-title: Mol. Pharmacol.
  doi: 10.1124/mol.105.019117
– volume: 281
  start-page: 10431
  year: 2006
  ident: ref_10
  article-title: Fatty acid amide hydrolase determines anandamide-induced cell death in the liver
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M509706200
– volume: 1
  start-page: 1333
  year: 2009
  ident: ref_1
  article-title: Cannabinoids as novel anti-inflammatory drugs
  publication-title: Future Med. Chem.
  doi: 10.4155/fmc.09.93
– volume: 13
  start-page: 204
  year: 2012
  ident: ref_28
  article-title: Time-dependent effect of in vivo inflammation on eicosanoid and endocannabinoid levels in plasma, liver, ileum and adipose tissue in c57bl/6 mice fed a fish-oil diet
  publication-title: Int. Immunopharmacol.
  doi: 10.1016/j.intimp.2012.03.022
– volume: 38
  start-page: 1167
  year: 2003
  ident: ref_8
  article-title: Membrane cholesterol but not putative receptors mediates anandamide-induced hepatocyte apoptosis
  publication-title: Hepatology
  doi: 10.1053/jhep.2003.50459
– volume: 5
  start-page: e12841
  year: 2010
  ident: ref_24
  article-title: Hepatitis C virus induces the cannabinoid receptor 1
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0012841
– volume: 12
  start-page: 671
  year: 2006
  ident: ref_5
  article-title: CB1 cannabinoid receptor antagonism: A new strategy for the treatment of liver fibrosis
  publication-title: Nat. Med.
  doi: 10.1038/nm1421
– volume: 163
  start-page: 1432
  year: 2011
  ident: ref_6
  article-title: The endocannabinoid system as a key mediator during liver diseases: New insights and therapeutic openings
  publication-title: Br. J. Pharmacol.
  doi: 10.1111/j.1476-5381.2011.01397.x
– volume: 59
  start-page: 296
  year: 2014
  ident: ref_4
  article-title: Cannabinoid receptor 2 counteracts interleukin-17-induced immune and fibrogenic responses in mouse liver
  publication-title: Hepatology
  doi: 10.1002/hep.26598
– volume: 5
  start-page: e8688
  year: 2010
  ident: ref_12
  article-title: Anandamide suppresses proliferation and cytokine release from primary human t-lymphocytes mainly via CB2 receptors
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0008688
– volume: 6
  start-page: 69
  year: 2008
  ident: ref_21
  article-title: Influence of cannabis use on severity of hepatitis c disease
  publication-title: Clin. Gastroenterol. Hepatol.
  doi: 10.1016/j.cgh.2007.10.021
– reference: 18388242 - Mol Pharmacol. 2008 Jul;74(1):20-33
– reference: 18242211 - Gastroenterology. 2008 Feb;134(2):432-9
– reference: 20416967 - J Hepatol. 2010 Jun;52(6):800-11
– reference: 21457226 - Br J Pharmacol. 2011 Aug;163(7):1432-40
– reference: 16715087 - Nat Med. 2006 Jun;12(6):671-6
– reference: 15864349 - J Clin Invest. 2005 May;115(5):1298-305
– reference: 14741435 - J Neuroimmunol. 2004 Feb;147(1-2):91-4
– reference: 15892090 - Hepatology. 2005 Jul;42(1):63-71
– reference: 22498761 - Int Immunopharmacol. 2012 Jun;13(2):204-14
– reference: 24704332 - Int J Infect Dis. 2014 Jun;23:75-81
– reference: 23890208 - Liver Int. 2013 Oct;33(9):1298-308
– reference: 16175591 - Hepatology. 2005 Oct;42(4):975-6; author reply 976-7
– reference: 21863215 - Mol Med. 2011;17(11-12):1285-94
– reference: 15765409 - Gastroenterology. 2005 Mar;128(3):742-55
– reference: 20862263 - PLoS One. 2010;5(9). pii: e12841. doi: 10.1371/journal.pone.0012841
– reference: 18538673 - Gastroenterology. 2008 Aug;135(2):660-70
– reference: 18446159 - Nat Rev Drug Discov. 2008 May;7(5):438-55
– reference: 20098669 - PLoS One. 2010;5(1):e8688
– reference: 21856784 - J Lipid Res. 2011 Nov;52(11):2021-31
– reference: 23667516 - PLoS One. 2013;8(5):e62741
– reference: 24484068 - Liver Int. 2015 Jan;35(1):207-14
– reference: 23295443 - Gastroenterology. 2013 Apr;144(4):808-817.e15
– reference: 15664228 - Lancet. 2005 Jan 22-28;365(9456):327-9
– reference: 22879589 - J Biol Chem. 2012 Oct 5;287(41):34660-82
– reference: 23567085 - J Hepatol. 2013 Oct;59(4):891-6
– reference: 16418162 - J Biol Chem. 2006 Apr 14;281(15):10431-8
– reference: 17353660 - Curr Opin Lipidol. 2007 Apr;18(2):129-40
– reference: 12960289 - J Leukoc Biol. 2003 Oct;74(4):486-96
– reference: 20191092 - Future Med Chem. 2009 Oct;1(7):1333-49
– reference: 18166478 - Clin Gastroenterol Hepatol. 2008 Jan;6(1):69-75
– reference: 16611855 - Mol Pharmacol. 2006 Jul;70(1):101-11
– reference: 22946841 - J Proteome Res. 2012 Nov 2;11(11):5433-42
– reference: 19647124 - Vitam Horm. 2009;81:487-504
– reference: 19840245 - Liver Int. 2010 Jul;30(6):816-25
– reference: 15841456 - Hepatology. 2005 May;41(5):1019-28
– reference: 23813495 - Hepatology. 2014 Jan;59(1):296-306
– reference: 23665286 - J Hepatol. 2013 Sep;59(3):427-33
– reference: 17576391 - J Viral Hepat. 2007 Jul;14(7):492-502
– reference: 21735467 - Hepatology. 2011 Oct;54(4):1217-26
– reference: 18239059 - Am J Physiol Gastrointest Liver Physiol. 2008 Apr;294(4):G850-4
– reference: 14578855 - Hepatology. 2003 Nov;38(5):1167-77
– reference: 18006606 - Am J Physiol Gastrointest Liver Physiol. 2008 Feb;294(2):G357-62
– reference: 25053565 - J Gen Virol. 2014 Nov;95(Pt 11):2468-79
– reference: 18985799 - World J Gastroenterol. 2008 Oct 28;14(40):6109-14
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Snippet The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated...
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SubjectTerms Adult
Amidohydrolases - metabolism
Arachidonic Acids - blood
Arachidonic Acids - metabolism
Cells, Cultured
Cellular biology
Cytokines - metabolism
Endocannabinoids - blood
Endocannabinoids - metabolism
Female
Glycerides - blood
Glycerides - metabolism
Hepatic Stellate Cells - metabolism
Hepatic Stellate Cells - pathology
Hepatitis
Hepatitis C virus
Hepatitis C, Chronic - enzymology
Hepatitis C, Chronic - immunology
Hepatitis C, Chronic - pathology
Humans
Immune system
Immunity, Cellular
Liver
Male
Marijuana
Middle Aged
Monoacylglycerol Lipases - metabolism
Polyunsaturated Alkamides - blood
Polyunsaturated Alkamides - metabolism
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Title Elevated Levels of Endocannabinoids in Chronic Hepatitis C May Modulate Cellular Immune Response and Hepatic Stellate Cell Activation
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Volume 16
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