Cannabidiol attenuates alcohol-induced liver steatosis, metabolic dysregulation, inflammation and neutrophil-mediated injury
0000 0004 0481 4802grid.420085.bLaboratory of Cardiovascular Physiology and Tissue Injury, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD USA
grid.452244.1Department of Clinical Microbiology and Immunology, Affiliated Hospital of Guiyang Medical University, Guiyang, Guizhou Province China
0000 0004 0481 4802grid.420085.bLaboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD USA
0000 0000 8692 8176grid.469131.8Department of Surgery and Center for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, New Jersey USA
0000 0004 1937 0538grid.9619.7Institute for Drug Research, Medical Faculty, Hebrew University, Jerusalem, 91120 Israel
Abstract
Cannabidiol (CBD) is a non-psychoactive component of marijuana, which has anti-inflammatory effects. It has also been approved by FDA for various orphan diseases for exploratory trials. Herein, we investigated the effects of CBD on liver injury induced by chronic plus binge alcohol feeding in mice. CBD or vehicle was administered daily throughout the alcohol feeding study. At the conclusion of the feeding protocol, serums samples, livers or isolated neutrophils were utilized for molecular biology, biochemistry and pathology analysis. CBD significantly attenuated the alcohol feeding-induced serum transaminase elevations, hepatic inflammation (mRNA expressions of TNFα, MCP1, IL1β, MIP2 and E-Selectin, and neutrophil accumulation), oxidative/nitrative stress (lipid peroxidation, 3-nitrotyrosine formation, and expression of reactive oxygen species generating enzyme NOX2). CBD treatment also attenuated the respiratory burst of neutrophils isolated from chronic plus binge alcohol fed mice or from human blood, and decreased the alcohol-induced increased liver triglyceride and fat droplet accumulation. Furthermore, CBD improved alcohol-induced hepatic metabolic dysregulation and steatosis by restoring changes in hepatic mRNA or protein expression of ACC-1, FASN, PPARα, MCAD, ADIPOR-1, and mCPT-1. Thus, CBD may have therapeutic potential in the treatment of alcoholic liver diseases associated with inflammation, oxidative stress and steatosis, which deserves exploration in human trials.
Introduction
Chronic alcohol consumption is a leading cause of alcoholic liver disease in the USA and worldwide, which eventually may progress to cirrhosis or hepatocellular carcinoma in susceptible subjects1,2. Interestingly, while most heavy drinkers develop fatty liver, only about 20% of them will develop liver cirrhosis3. Although numerous advances have been made in the understanding the complex mechanisms of alcohol-induced steatohepatitis (involving inflammation and oxidative stress) in cellular systems and animal models, the translation of these findings to clinical practice is still limited.
Cannabidiol (CBD) is the most abundant non-psychoactive constituent of marijuana plant (Cannabis Sativa) with excellent safety profile in humans even after chronic use4–6. An extract containing 50% CBD (Sativex) is used for treatment of pain and spasticity associated multiple sclerosis in numerous European counties and Canada6. Recently, CBD received U.S. Food and Drug Administration (FDA) approval for the evaluation of its effect in refractory childhood epilepsy (Lennox-Gastaut Syndrome and Dravet Syndrome) and glioblastoma multiforme in phase 3 and 1 clinical trials, respectively. In multiple preclinical disease models, including cardiomyopathies7–9, nephrotoxicity10, neuroinflammation6,11, colitis12, diabetic complications13 and cancer14 CBD has been reported to exert potent anti-inflammatory and antioxidant effects6.
CBD improved brain and liver function in a fulminant hepatic failure-induced model of hepatic encephalopathy in mice15, decreased hepatic ischemia-reperfusion induced injury both in mice16 and rats17, attenuated alcohol-binge-induced injury in mice18 and hepatotoxicity of cadmium19 and cocaine20. Some of these studies have not explored the detailed mechanisms behind the protective effects of CBD against liver injury, but others proposed attenuation of the pro-inflammatory response and signaling (e.g. neutrophil infiltration, TNF-α, macrophage inflammatory protein-1α/2, cyclooxygenase 2, nuclear factor kappa B (NF-κB), oxidative/nitrative stress, stress signaling (p38MAPK and JNK) and cell death (apoptotic/necrotic), as well as promotion of autophagy16–18. CBD also attenuated bacterial endotoxin-triggered NF-κB activation and TNF-α production in isolated Kupffer cells16, and attenuated the intracellular adhesion molecule 1 expression in TNF-α stimulated primary human liver sinusoidal endothelial cells, and attachment of human neutrophils to the activated endothelium16. Silvestri et al. investigated the effects of CBD on lipid levels using in vitro and in vivo models of hepatosteatosis21. Using nuclear magnetic resonance-based metabolomics they demonstrated that CBD directly reduced lipid accumulation in vitro in hepatocytes and adipocytes and induced post-translational changes in CREB, PRAS40, AMPKa2 and several STATs indicating increased lipid metabolism21. They also demonstrated that CBD increased lipid mobilization and inhibited development of hepatosteatosis in zebrafish and obese mouse models21.
Since hepatic steatosis and neutrophil infiltration1,22,23 are critical pathological features of alcohol-induced liver injury, and the previously discussed studies suggested that CBD had beneficial effect on these processes, we investigated the effects of CBD on alcohol-induced liver steatosis, metabolic changes, inflammation and neutrophil-mediated oxidative injury, using a well-established model of chronic ethanol feeding plus binge alcohol gavage (NIAAA model)24,25, which closely relates to human drinking behavior26. Our results may have important implication for treatment of liver steatosis in alcoholic liver disease.
Method
Mice, alcohol feeding and treatments
Mice (C57BL/6 J) were purchased from The Jackson Laboratory (Bar Harbor, ME). All animal experiments were approved by the National Institute on Alcohol Abuse and Alcoholism Animal Care and Use Committee. The study was carried out in line with the National Institutes of Health (NIH) Guidelines for the Care and Use of Laboratory Animals. Ten to twelve-week-old female mice with weight over 25 g were subjected to the following feeding protocol. Initially mice were fed the control Lieber- DeCarli diet (Bio-Serv, Frenchtown, NJ) ad libitum for 5 days to acclimatize them to a liquid diet. Then mice were pair-fed with an isocaloric control diet (control-fed groups) or Lieber-DeCarli diet (alcohol-fed groups) containing 5% ethanol for 10 days. On day 11, ethanol and pair-fed mice were gavaged early morning with a single dose of ethanol (5 g/kg b.w.) or isocaloric dextrin-maltose, respectively, and sacrificed 9 hours later24.
CBD was isolated as described27. It was dissolved in vehicle solution (one drop of Tween 80 in 3 ml 2.5% dimethyl sulfoxide (DMSO) in saline) and injected i.p. (5 or 10 mg/kg/day) for 11 days during the ethanol exposure. Vehicle solution was used in control experiments.
Biochemical assays
Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels were determined using a clinical chemistry analyzer Idexx VetTest 8008 (Idexx Laboratories, Westbrook, ME, USA) as described28. Liver triglycerides were extracted with a 2:1 chloroform:methanol mixture and measured using the EnzyChrom Triglyceride Assay Kit (BioAssays Systems, Hayward, CA)29.
Hepatic protein 3-nitrotyrosine (NT) content
Hepatic NT levels were determined using ELISA kit from Hycult biotechnology, Cell sciences, Canton, MA, USA, as described earlier29.
Hepatic 4-hydroxynonenal (HNE) content
Levels of hepatic HNE were measured by using the kit from Cell Biolabs, San Diego, CA, USA. In brief, BS A or hepatic tissue homogenates (10 μg/ml) were absorbed on to the 96- well plates for 12 h at 4 °C. The HNE adducts contained in the samples were captured with anti-HNE antibody, followed by a HRP-conjugated secondary antibody. The HNE protein adducts in liver samples was determined based on standard curve generated with BSA-HNE according to the protocol supplied by the manufacturer29.
Liver histology and immunohistochemistry
Liver specimens were fixed in 10% buffered formalin, embedded in paraffin, and cut into 5 µm sections. Paraffin embedded tissues were deparaffinized by changes of xylene and rehydrated in decreasing concentrations of ethanol. The sections were then subjected to hematoxylin and eosin (H&E) staining. For myeloperoxidase (MPO) staining slides were deparaffinized and hydrated in descending gradations of ethanol, followed by antigen retrieval procedure. Next, sections were incubated in 0.3% H2O2 in PBS to block endogenous peroxidase activity. The sections were then incubated with anti-MPO (Biocare Medical, Concord, CA, USA) or anti-malondialdehyde or anti-HNE (Genox, Baltimore, MD, USA) or anti –NT(cayman chemical, Ca) antibodies overnight at 4 °C in a moist chamber. Biotinylated secondary antibodies and ABC reagent were added according to the kit’s instructions (Vector Laboratories, Burlingame, CA, USA). Color development was induced by incubation with a DAB kit (Vector Laboratories) for 2–6 min, and the sections were counterstained16,30. Finally, the sections were dehydrated in ethanol and cleared in xylene and mounted. The specific staining was visualized and images were acquired using an IX-81 microscope (Olympus, Center Valley, PA). The morphometric examination was performed in a blinded manner by two independent investigators. The quantification of MPO positive cells was performed as described earlier29.
Oil-O-Red staining and liver triglyceride content measurement
Liver samples embedded in optimal cutting temperature compound were cut at 10 μM sections and stained with Oil Red O to evaluate the hepatic lipid content. Briefly, cryosections were air-dried and fixed in 10% formalin and then stained with 0.5% Oil Red O in propylene glycol for 10 mins at 60 °C and subsequently washed with 85% propylene glycol. Sections were counterstained with hematoxylin, washed in water and mounted with aqueous solution.
Triglyceride content was measured from liver tissue by Triglyceride Quantification Colorimetric Kit (Biovision) according to manufacturer’s instruction.
Isolation of hepatic leukocytes and flow cytometry analysis
Liver tissues were passed through a 70 µm cell strainer in phosphate-buffered saline (PBS), and the cell suspension was centrifuged at 30 g for 5 minutes to pellet the hepatocytes. The supernatant, which was enriched in nonparenchymal cells, was centrifuged at 300 g for 10 minutes. The pellet was resuspended in 15 ml of 35% Percoll (GE Healthcare, Pittsburgh, PA) and centrifuged at 500 g for 15 minutes. The resulting leukocyte pellet was resuspended in 2 ml of ACK lysing buffer (BioWhittaker, Walkersville, MD). After incubation for 5 minutes on ice, the cells were washed in PBS containing 2% fetal bovine serum. The cells were pre-incubated with Mouse BD Fc Block™ (purified rat anti-mouse CD16/CD32, clone 2.4G2, BD Biosciences, San Diego, CA) for 10 minutes at 4 °C and then stained with the designated antibodies for 30 minutes at 4 °C. The following antibodies were used: anti-F4/80 (clone BM8, eBioscience, San Diego, CA), anti-Gr-1 (clone RB6–8C5, eBioscience), anti-CD11b (clone M1/70, BD Biosciences), and anti-CD62L (clone MEL-14, BD Biosciences). Flow cytometry analysis was performed using a FACSCalibur (BD Biosciences).
Oxidative burst assay from isolated liver leukocytes and human neutrophils
For detection of superoxide production we used Dihydrorhodamine 123 (30 mM stock in DMSO; Sigma Chemicals, St Louis, MO) at a final concentration of 100 μM with a modified method of Rothe et al.31. Isolated leukocytes from mouse liver were stained with Gr1-PE-Cy7.7 and CD11b-APC. Human granulocytes were isolated from human blood obtained from NIH clinical center by Polymorphprep according to manufacturer’s instruction (Axis-Shield, Norway). Human neutrophils were stained with CD11b-PE-Cy7.7 and CD66b-APC. The IRB was approved (99-CC-0168) by Department of Transfusion Medicine (NIH clinical center) for Collection and Distribution of Blood Components from Healthy Donors for In Vitro Research Use.
Cells were incubated with DHR and catalase (1000 U/ml, Sigma Chemicals, St Louis, MO) in the dark at 37 °C for 20 minutes. Cells loaded with DHR were treated with phorbol ester (PMA) at indicated concentration for 30 mins. For human cells, CBD and cannabinoid 2 receptor antagonist SR144528 were added as described in the text for 1 hour at 37 °C followed by phorbol ester (PMA) at 100 µg/ml for 30 mins. Finally, DHR intensities were measured by flow cytometry (FACS Calibur, BD Bioscience) in FL1 channel. Polymorphonuclear neutrophils were gated on the basis of their surface staining.
Real-time quantitative polymerase chain reaction (real-time PCR)
Total RNA was extracted from liver tissue using the TRIzol reagent (Invitrogen, Carlsbad, CA) and treated with Turbo DNA-free (Ambion, Austin, TX) according to the manufacturer’s protocols. cDNA was synthesized using HT Fisrt stand CDNA synthesis kit (Qiagen, MD). Real-time PCR was performed in duplicate for each sample using the ABI PRISM 7500 Real-Time PCR System and SYBR Green Master Mix (Applied Biosystems) according to the manufacturer’s instructions. The specificity of transcript amplification was confirmed by melting curve profiles generated at the end of the PCR program. The expression levels of target genes were normalized to the expression of beta-actin and calculated based on the comparative cycle threshold Ct method (2−ΔΔCt). Primer sequences used were previously described29,32. The data shown represents the means ± SEM.
Western Blot
Western blot was performed as described earlier29. The primary antibodies used are gp91phox (Biolegend, San Diego, CA), FASN, ACC1, PPAR-αl, and beta-actin (Abcam, Cambridge, MA).
Quantitative ELISA
E–selectin and TNF-α were quantified using Simple Step Mouse E-Selectin ELISA Kit (Abcam) and Mouse TNF-alpha Quantikine ELISA Kit (R&D system) according to manufacturer’s instruction.
Statistical Analysis
All the values are represented as mean ± SEM. Student’s t-test was used to determine difference between two groups. One-way analysis of variance (ANOVA) test was used to determine difference among more than two groups. Tukey’s post hoc tests were then performed to find significant differences between groups. The analysis was conducted using GraphPad-Prism 4 software. P < 0.05 was considered statistically significant.
Results
CBD treatment attenuates chronic-plus-binge ethanol-induced liver injury and steatosis
Chronic-plus-binge ethanol feeding induced significant liver injury as shown by H&E staining (Fig. 1A) and by elevated serum transaminases ALT and AST (Fig. 1B). Marked alcohol-induced hepatic lipid/triglyceride accumulation was also observed, indicated by Oil Red O staining (Fig. 2A) and elevated liver triglyceride content (Fig. 2B). All these pathological changes were markedly attenuated by CBD treatment (Figs 1 and 2). CBD treated did not cause any changes in pair-fed groups.
Cannabidiol modulates genes and proteins involved in metabolism and liver steatosis
Because dysregulated metabolism plays an important role in alcohol-induced liver steatosis we examined a series of metabolic genes involved in fatty acid biosynthetic, oxidation and mitochondrial pathways (Fig. 3A–D). We found that alcohol enhanced hepatic expression of several genes involved in fatty acid biosynthesis (Fatty Acid Synthase (FASN), malonyl-CoA decarboxylase (Mlycd), and acetyl-Coenzyme A carboxylase alpha (ACC1)), while decreasing gene expressions involved in fatty acid oxidation (adiponectin receptor 1 (Adipor1) and medium-chain acyl-CoA dehydrogenase (MCAD); (Fig. 3AB). All these effects were attenuated by CBD treatment (Fig. 3AB). Alcohol feeding decreased hepatic carnitine palmitoyltransferase 1α (mCPT1α) and transcription factor peroxisome proliferator-activated receptor α (PPARα) mRNA expression levels (Fig. 3C,D). Alcohol also increased the protein expressions of FASN and ACC1 and decreased PPARα (Fig. 3E,F). These alcohol-induced effects were ameliorated by CBD treatment (Fig. 3C–F). CBD treatment had no effect on the above mentioned variables in pair-fed mice (Fig. 3A–D).
Cannabidiol attenuates alcohol-induced neutrophil accumulation in the liver
Chronic-plus-binge ethanol feeding induced significant hepatic neutrophil accumulation indicated by increased myeloperosidase (MPO) positive cells in histological sections, which was attenuated by CBD treatment (Fig. 4A,B).
Cannabidiol attenuates oxidative burst in mouse and human neutrophils independent from cannabinoid 2 receptors
CBD treatment of mice markedly attenuated the oxidative burst induced by PMA in neutrophil isolated from livers of ethanol-fed mice (Fig. 5A).
We also investigated the effects of CBD on PMA-induced oxidative burst in human neutrophils. CBD attenuated the PMA-induced neutrophil oxidative burst in concentration-dependent fashion (Fig. 5D) in human neutrophils. These beneficial effects of CBD could not be prevented by cannabinoid 2 receptor (CB2) antagonist SR144528 (Fig. 5C–E), indicating that this effect is independent from CB2.
Cannabidiol attenuates liver oxidative/nitrative stress
Because the alcohol-induced liver injury is known to be associated with increased oxidative and nitrative stress we also examined the effect of CBD treatment on alcohol induced oxidative/nitrative stress markers. We found that alcohol feeding markedly enhanced the hepatic mRNA expression of reactive oxygen species (ROS) generating NADPH oxidase 2 (NOX2) isoforms gp91phox and p67phox (Fig. 6A,B), increased protein expression of gp91phox (Fig. 6C), malondialdehyde (MDA, marker of lipid peroxidation) and 3-nitrotyrosine (NT, marker of nitrative stress) immunostaining (Fig. 7AB) and 4-hydroxynonenal (HNE, marker of lipid peroxidation) and NT content (measured by ELISA; Fig. 7CD). CBD treatment significantly attenuated the alcohol diet-induced oxidative and nitrative stress in the liver (Figs 6 and 7). CBD treatment did not affect ROS in pair-fed groups.
Cannabidiol attenuates chronic-binge ethanol-induced liver inflammation
To understand the mechanism of the beneficial effects of CBD on alcohol-induced neutrophil accumulation in the liver, we studied the effect of CBD on alcohol induced pro-inflammatory chemokines, cytokines and adhesion molecules. Chronic CBD treatment markedly decreased alcohol diet-induced increased hepatic mRNA expressions of pro-inflammatory chemokines (macrophage inflammatory protein 2-alpha (MIP-2)/chemokine (C-X-C motif) ligand 2 (CXCL2), monocyte chemotactic protein 1 (MCP-1/CCL2)), cytokines (tumor necrosis factor alpha (TNF-α) and interleukin 1 beta (IL1-β)), and adhesion molecule selectin E (SELE)(Fig. 8A–E). It also attenuated the hepatic TNFα and SELE levels measured by ELISA. CBD had no significant effect on these variables in pair-fed mice.
Discussion
Chronic alcohol consumption is a major cause of alcoholic liver disease characterized by metabolic dysregulation, enhanced oxidative stress, inflammation and steatosis in the liver, which may eventually culminate in cirrhosis or hepatocellular carcinoma in susceptible subjects1,2. Despite significant advances in our understanding of the pathology of alcoholic liver disease the therapeutical options are still very limited.
The recently FDA approved for exploratory trials non-psychoactive constituent of Cannabis sativa, cannabidiol (CBD), has been reported to exert antioxidant, cytoprotective and anti-inflammatory effects independently of cannabinoid 1 and 2 receptors in preclinical disease models.
In the present study, we describe that CBD treatment improves chronic-plus-binge-alcohol-induced hepatocellular liver injury in mice by attenuating oxidative and nitrative stress, expression of adhesion molecule E-selectin, neutrophil infiltration and neutrophil-mediated oxidative injury and inflammation. We also show that CBD attenuates alcohol-induced liver steatosis and dysregulation of numerous key genes of fatty acid biosynthetic and oxidation pathways, mitochondrial pathways, and transcription factor PPARα, implicated in development of alcohol-induced steatohepatitis. Furthermore, we demonstrate that CBD attenuates the oxidative burst in human neutrophils independently from anti-inflammatory cannabinoid 2 receptor.
Chronic-plus-binge alcohol leads to hepatocyte necrosis in the liver, causing proinflammatory response. It is known that neutrophils are linked to alcoholic hepatitis22,33. We also found increased neutrophil recruitment in livers and enhanced expressions of ROS generating NAD(P)H enzyme NOX2 isoforms, coupled with enhanced oxidative and nitrative stress in our model, which were all attenuated by CBD treatment. CBD treatment also attenuated the response of neutrophils isolated from alcoholic livers to generate ROS upon stimulation. Consistent with its previously described antioxidant effect7,11, CBD treatment also decreased the neutrophil burst in human neutrophils in vitro independent from anti-inflammatory CB2 receptor.
Numerous recent studies described potent anti-inflammatory effects of CBD reaching far beyond its initially reported antioxidant properties in models of colitis, ischemic-reperfusion injury, diabetic complications, autoimmune arthritis, hepatitis, myocarditis and neuroinflammation6,9,11,12,16,34. One of the most characteristic effects of CBD in these preclinical models of inflammation is the attenuation of the inflammatory cell infiltration and pro-inflammatory response6. In agreement with these reports in our chronic plus binge alcohol induced liver injury model, CBD suppressed the alcohol induced pro-inflammatory cytokines/chemokines (TNFα, IL-1β, MIP2 and MCP-1) expressions/levels in the liver.
Kupffer cell polarization (M1-M2 phenotype) has been importantly implicated in the initiation of alcoholic liver diseases35. In the current study CBD treatment significantly reduced expression of M1-related genes (TNFα and MCP-1) suggesting that M1 polarization could contribute to the anti-inflammatory effects of CBD, which should be explored in the future studies.
E-selectin/CD62/or endothelial-leukocyte adhesion molecule 1 is a key adhesion factor expressed in activated endothelium, which is involved in recruitment of leukocytes, particularly neutrophils during tissue injury36. An important role of E selectin in chronic plus binge alcohol-induced liver injury has recently been suggested25. Interestingly, CBD treatment attenuated the alcohol-induced hepatic E-selectin expression, consistently with its anti-inflammatory effects in activated endothelium37.
Most intriguingly CBD also attenuated the alcohol-induced metabolic dysregulation and steatosis in the liver. These results suggests that CBD may exert direct beneficial effects on lipid metabolism independent from its antioxidant and anti-inflammatory effects, which is consistent with a recent report demonstrating attenuation of lipid accumulation in hepatocytes and adipocytes by CBD in vitro, as well as in obese mice in vivo 21.
In conclusion, we demonstrate that CBD treatment significantly attenuates liver injury induced by chronic plus binge alcohol in a mouse model and oxidative burst in human neutrophils. CBD ameliorates alcohol-induced liver injury by attenuating inflammatory response involving E-selectin expression and neutrophil recruitment, and consequent oxidative/nitrative stress, in addition to attenuation of the alcohol-induced hepatic metabolic dysregulation and steatosis. These beneficial effects, coupled with the proven safety of CBD in human clinical trials and its current orphan drug approval by FDA for various indications suggest that it may have therapeutic potential in liver disease associated with inflammation, oxidative stress, metabolic dysregulation and steatosis.
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Acknowledgements
This work was supported by the Intramural Research Program of NIAAA/NIH (to P.P and B.G.), the National Natural Science Foundation of China grant 81460125(YP.W.) and China Scholarship Council (YP.W.). Dr. Yuping Wang is the recipient of fellowship from Affiliated Hospital of Guiyang Medical University, Guiyang, Guizhou Province, China during this work at NIH.
Notes
Competing Interests
The authors declare that they have no competing interests.