Endogenous Cannabinoids in Crohn’s Disease
Source abstract
Abstract
Background: An increasing number of people around the world suffer from Crohn’s disease (CD), one of the inflammatory bowel diseases (IBDs). Recent evidence suggests that the endogenous cannabinoid system plays an important role in IBD. The main endocannabinoids, anandamide (AEA) and 2-arachidonoylglycerol (2-AG), are ligands of the CB1 and CB2 receptors that are expressed on immune cells. These receptors as well as endocannabinoids are believed to mediate inflammatory activity and participate in the pathophysiology of CD. Objective: Very little is known about the secretion of endogenous cannabinoids throughout the course of CD. Therefore, the aim of this study was to determine and analyze the 2-AG and AEA concentrations in children who suffered from CD. Methods: We studied 34 adolescents with CD, mean age 13.5 years ± 2.0. Blood samples were collected three times in the active phase of the disease (during admission to hospital, before treatment), 2–4 weeks later, during the treatment and clinical improvement of the patients, and 3–6 months later, in the period of remission. The control group included 33 healthy teenagers of the same age who were examined once. In all patients, fasting blood samples were collected in the morning. 2AG and AEA concentrations in serum were measured using EIA kits (Abclonal, Woburn, MA, USA and ELK Biotechnology Co., Ltd. Wuhan, China, respectively). Results: The median 2-AG concentration in the study group was stable: acute phase 907.4 [379.3; 1300.5] pg/mL, during treatment 715.1 [416.7; 1302.5] pg/mL; remission 991.1 [381.1; 1652.5] pg/mL, and similar to the values observed in the control group 761.8 [504.3; 1497.0] pg/mL. No significant differences were found between the results obtained at all time points in the study group and compared to the control group (in all cases p > 0.44). In the case of AEA, in the study group before treatment, the median concentration was 2.63 [2.24; 2.79] ng/mL and similar to values obtained during treatment 2.56 [2.33; 3.06] ng/mL, and in remission, with 2.61 [2.46; 2.85] ng/mL. All these concentrations were lower compared to the values measured in the control group of 3.18 [2.57; 3.88] ng/mL (p = 0.023, p = 0.035, p = 0.056, respectively). Conclusions: While 2-AG levels remained stable throughout the disease course and were comparable to controls, AEA concentrations were consistently lower in CD patients. Therefore, therapeutic interventions aimed at increasing AEA-related signaling, such as administration of its analogues or fatty acid amide hydrolase inhibitors, may improve symptoms associated with Crohn’s disease in children.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Cannabis and Cannabinoid Research · Dietary Effects on Health · Diet, Metabolism, and Disease
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Clinical Biochemistry, Students Scientific Society, Faculty of Medicine, Jagiellonian University Medical College, 30-663 Krakow, Poland
Department of Pediatrics, Gastroenterology and Nutrition, Faculty of Medicine, Jagiellonian University Medical College, 30-663 Krakow, Poland
Department of Clinical Biochemistry, Pediatric Institute, Faculty of Medicine, Jagiellonian University Medical College, 30-663 Krakow, Poland
Funding
Jagiellonian University
References (56)
Show source-provided references
1. Increasing Incidence and Prevalence of the Inflammatory Bowel Diseases With Time, Based on Systematic Review10.1053/j.gastro.2011.10.001 ↗
2. Worldwide Incidence and Prevalence of Inflammatory Bowel Disease in the 21st Century: A Systematic Review of Population-Based Studies10.1016/S0140-6736(17)32448-0 ↗
3. Crohn’s and Colitis in Children and Adolescents10.3748/wjg.v18.i41.5862 ↗
4. Crohn’s Disease10.1016/S0140-6736(16)31711-1 ↗
5. Frigstad, S.O., Høivik, M.L., Jahnsen, J., Cvancarova, M., Grimstad, T., Berset, I.P., Huppertz-Hauss, G., Hovde, Ø., Bernklev, T., and Moum, B. (2019). Pain Severity and Vitamin D Deficiency in IBD Patients. Nutrients, 12.10.3390/nu12010026 ↗
6. Mucosal Flora in Inflammatory Bowel Disease10.1053/gast.2002.30294 ↗
7. Gut Microbiota in the Pathogenesis of Inflammatory Bowel Disease10.1007/s12328-017-0813-5 ↗
8. Differences in the Intestinal Microbiome of Healthy Children and Patients with Newly Diagnosed Crohn’s Disease10.1038/s41598-019-55290-9 ↗
9. An Introduction to the Endogenous Cannabinoid System10.1016/j.biopsych.2015.07.028 ↗
10. The Diverse CB1 and CB2 Receptor Pharmacology of Three Plant Cannabinoids: Delta9-Tetrahydrocannabinol, Cannabidiol and Delta9-Tetrahydrocannabivarin10.1038/sj.bjp.0707442 ↗
11. CB1 and CB2 Receptor Pharmacology10.1016/bs.apha.2017.03.007 ↗
12. Cannabinoid Signalling in the Enteric Nervous System10.1111/j.1365-2982.2009.01372.x ↗
13. Localization of Cannabinoid and Cannabinoid Related Receptors in the Cat Gastrointestinal Tract10.1007/s00418-020-01854-0 ↗
14. Hryhorowicz, S., Kaczmarek-Ryś, M., Zielińska, A., Scott, R.J., Słomski, R., and Pławski, A. (2021). Endocannabinoid System as a Promising Therapeutic Target in Inflammatory Bowel Disease—A Systematic Review. Front. Immunol., 12.10.3389/fimmu.2021.790803 ↗
15. The Role of the Endocannabinoid System in the Brain-Gut Axis10.1053/j.gastro.2016.04.015 ↗
16. Cencioni, M.T., Chiurchiù, V., Catanzaro, G., Borsellino, G., Bernardi, G., Battistini, L., and Maccarrone, M. (2010). Anandamide Suppresses Proliferation and Cytokine Release from Primary Human T-Lymphocytes Mainly via CB2 Receptors. PLoS ONE, 5.10.1371/journal.pone.0008688 ↗
17. A Comprehensive Profile of Brain Enzymes That Hydrolyze the Endocannabinoid 2-Arachidonoylglycerol10.1016/j.chembiol.2007.11.006 ↗
18. Neurobiological Interactions Between Stress and the Endocannabinoid System10.1038/npp.2015.166 ↗
19. Lactobacillus Acidophilus Modulates Intestinal Pain and Induces Opioid and Cannabinoid Receptors10.1038/nm1521 ↗
20. Muccioli, G.G., Naslain, D., Bäckhed, F., Reigstad, C.S., Lambert, D.M., Delzenne, N.M., and Cani, P.D. (2010). The Endocannabinoid System Links Gut Microbiota to Adipogenesis. Mol. Syst. Biol., 6.10.1038/msb.2010.46 ↗
21. Dione, N., Lacroix, S., Taschler, U., Deschênes, T., Abolghasemi, A., Leblanc, N., Di Marzo, V., and Silvestri, C. (2020). Mgll Knockout Mouse Resistance to Diet-Induced Dysmetabolism Is Associated with Altered Gut Microbiota. Cells, 9.10.3390/cells9122705 ↗
22. Srivastava, R.K., Lutz, B., and Ruiz de Azua, I. (2022). The Microbiome and Gut Endocannabinoid System in the Regulation of Stress Responses and Metabolism. Front. Cell. Neurosci., 16.10.3389/fncel.2022.867267 ↗
23. Dysbiosis of the Faecal Microbiota in Patients with Crohn’s Disease and Their Unaffected Relatives10.1136/gut.2010.223263 ↗
24. Carding, S., Verbeke, K., Vipond, D.T., Corfe, B.M., and Owen, L.J. (2015). Dysbiosis of the Gut Microbiota in Disease. Microb. Ecol. Health Dis., 26.10.3402/mehd.v26.26191 ↗
25. Regulation of Nausea and Vomiting by Cannabinoids10.1111/j.1476-5381.2010.01176.x ↗
26. Martyniak, A., Wędrychowicz, A., and Tomasik, P.J. (2023). Endogenous Opioids in Crohn’s Disease. Biomedicines, 11.10.3390/biomedicines11072037 ↗
27. ESPGHAN Revised Porto Criteria for the Diagnosis of Inflammatory Bowel Disease in Children and Adolescents10.1097/MPG.0000000000000239 ↗
28. The Endogenous Cannabinoid System in the Gut of Patients with Inflammatory Bowel Disease10.1038/mi.2011.18 ↗
29. Members of the Endocannabinoid System Are Distinctly Regulated in Inflammatory Bowel Disease and Colorectal Cancer10.1038/s41598-019-38865-4 ↗
30. Tartakover Matalon, S., Azar, S., Meiri, D., Hadar, R., Nemirovski, A., Abu Jabal, N., Konikoff, F.M., Drucker, L., Tam, J., and Naftali, T. (2021). Endocannabinoid Levels in Ulcerative Colitis Patients Correlate With Clinical Parameters and Are Affected by Cannabis Consumption. Front. Endocrinol., 12.10.3389/fendo.2021.685289 ↗
31. The Endogenous Cannabinoid System Protects against Colonic Inflammation10.1172/JCI200419465 ↗
32. Role of Cannabis in Digestive Disorders10.1097/MEG.0000000000000779 ↗
33. Balestrieri, P., Ribolsi, M., Guarino, M.P.L., Emerenziani, S., Altomare, A., and Cicala, M. (2020). Nutritional Aspects in Inflammatory Bowel Diseases. Nutrients, 12.10.3390/nu12020372 ↗
34. Nutrition and IBD: Malnutrition and/or Sarcopenia? A Practical Guide
35. Weight Loss Is a Sufficient and Economical Single Outcome Measure of Murine Dextran Sulfate Sodium Colitis10.1096/fba.2019-00035 ↗
36. Analysis of Fat and Muscle Mass in Patients with Inflammatory Bowel Disease during Remission and Active Phase10.1017/S0007114508032224 ↗
37. Cannabis Use Provides Symptom Relief in Patients with Inflammatory Bowel Disease but Is Associated with Worse Disease Prognosis in Patients with Crohn’s Disease10.1097/01.MIB.0000440982.79036.d6 ↗
38. Cannabis Use in the United States and Its Impact on Gastrointestinal Health10.1002/ncp.11111 ↗
39. Full Fatty Acid Amide Hydrolase Inhibition Combined with Partial Monoacylglycerol Lipase Inhibition: Augmented and Sustained Antinociceptive Effects with Reduced Cannabimimetic Side Effects in Mice10.1124/jpet.115.222851 ↗
40. The Monoacylglycerol Lipase Inhibitor JZL184 Suppresses Inflammatory Pain in the Mouse Carrageenan Model10.1016/j.lfs.2012.06.020 ↗
41. Experimental Colitis in Mice Is Attenuated by Changes in the Levels of Endocannabinoid Metabolites Induced by Selective Inhibition of Fatty Acid Amide Hydrolase (FAAH)10.1016/j.crohns.2014.01.025 ↗
42. An Overview of Cannabis Based Treatment in Crohn’s Disease10.1080/17474124.2020.1740590 ↗
43. Cannabis for the Treatment of Crohn’s Disease
44. Cannabinoid-Induced Immune Suppression and Modulation of Antigen-Presenting Cells10.1007/s11481-005-9007-x ↗
45. The Multiple Functions of the Endocannabinoid System: A Focus on the Regulation of Food Intake10.1186/1758-5996-2-5 ↗
46. Carvalho, A.C.A.D., Souza, G.A.D., Marqui, S.V.D., Guiguer, É.L., Araújo, A.C., Rubira, C.J., Goulart, R.D.A., Flato, U.A.P., Bueno, P.C.D.S., and Buchaim, R.L. (2020). Cannabis and Canabidinoids on the Inflammatory Bowel Diseases: Going Beyond Misuse. Int. J. Mol. Sci., 21.10.3390/ijms21082940 ↗
47. Cannabis Induces a Clinical Response in Patients with Crohn’s Disease: A Prospective Placebo-Controlled Study10.1016/j.cgh.2013.04.034 ↗
48. Cannabis Use amongst Patients with Inflammatory Bowel Disease10.1097/MEG.0b013e328349bb4c ↗
49. The Gastrointestinal Tract—A Central Organ of Cannabinoid Signaling in Health and Disease10.1111/nmo.12931 ↗
50. Cannabinoid Exposure during Pregnancy and Its Impact on Immune Function10.1007/s00018-018-2955-0 ↗
51. Considering Cannabis: The Effects of Regular Cannabis Use on Neurocognition in Adolescents and Young Adults10.1007/s40429-014-0019-6 ↗
52. Cannabinoids for Medical Use: A Systematic Review and Meta-Analysis10.1001/jama.2015.6358 ↗
53. Chu, F., and Cascella, M. (2024). Cannabinoid Hyperemesis Syndrome. StatPearls, StatPearls Publishing.
54. Serotonin Syndrome versus Cannabis Toxicity in the Emergency Department10.5811/cpcem.2020.1.45410 ↗
55. Supply and Demand for Endocannabinoids10.1016/j.tins.2011.03.003 ↗
56. The Endogenous Cannabinoid Receptor Agonist Anandamide Impairs Memory in Rats10.1097/00008877-199605000-00008 ↗