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Endocannabinoids

Drugs and Chemicals · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 4 min read

Fatty acid derivatives that have specificity for cannabinoid receptors.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (731 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

Fatty acid derivatives that have specificity for cannabinoid receptors. They are structurally distinct from cannabinoids and were originally discovered as a group of endogenous cannabinoid receptor agonists.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Endocannabinoid.

Where it fits in the MeSH classification

Broader topics
Fatty Acids

Related concepts

  • Cannabinoid Receptors
  • Cannabinoids
  • Cannabinoid Receptor Agonists

Research landscape

PubMed indexes 7,996 records tagged with the MeSH heading “Endocannabinoids” (counts retrieved 2026-10-31). 2,249 of them (28.1%) were published from 2020 onward, and the busiest period so far is 2010-2019 with 3,262 records.

Reviews account for 2,036 records (25.5%) and meta-analyses for 14. Randomized controlled trials number 104 (1.3%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 260 records; 2000-2009: 2,225 records; 2010-2019: 3,262 records; 2020 onward: 2,249 records260through 19992,2252000-20093,2622010-20192,2492020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 1999260
2000-20092,225
2010-20193,262
2020 onward2,249
Share of records by publication typeReviews: 25.5 percent; Meta-analyses: 0.2 percent; Randomized controlled trials: 1.3 percentReviews25.5% (2,036)Meta-analyses0.2% (14)Randomized controlled trials1.3% (104)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 7,996 PubMed records
TypeRecordsShare
Reviews2,03625.5%
Meta-analyses140.2%
Randomized controlled trials1041.3%

Method: PubMed query "Endocannabinoids"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in drugs and chemicals

Studies of a chemical or drug can answer very different questions: what it is and how it behaves in cells and animals, how the body handles it, and whether it changes outcomes in people. Laboratory and animal findings often do not carry over to patients, and observational studies of exposures are confounded by who uses a substance and why. Nothing on this page is a recommendation to use, avoid, start or stop any substance or medicine; talk to a qualified clinician or pharmacist about your own situation. Check the dose, the species, the comparison group and whether a patient-relevant outcome was measured.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
The Endocannabinoid System: A Potential Target for the Treatment of Various Diseases
Lowe H, Toyang N, Steele B, Bryant J, Ngwa W
2021Review article
Design not recorded in structured metadata
205cc by
PMID 34502379 · DOI · PMC8430969
ω-3 and ω-6 Polyunsaturated Fatty Acids, Obesity and Cancer
D'Angelo S, Motti ML, Meccariello R
2020Review article
Design not recorded in structured metadata
183cc by
PMID 32927614 · DOI · PMC7551151
The Endocannabinoid System and Physical Exercise
Matei D, Trofin D, Iordan DA, Onu I, Condurache I, Ionite C, et al.
2023Review article
Design not recorded in structured metadata
73cc by
PMID 36768332 · DOI · PMC9916354
CYP4X1/sEH-Dependent Endocannabinoid Metabolism Drives Fibroblast-Mediated Immunosuppression to Limit Immunotherapy in Colon Cancer
Mo M, Chen X, Liu Y, Wang C, Chen X, Zhang N, et al.
2026Research article
Design not recorded in structured metadata
2cc by
PMID 41276938 · DOI · PMC12849875

The Endocannabinoid System: A Potential Target for the Treatment of Various Diseases [1]

Review article Lowe H, Toyang N, Steele B, Bryant J, Ngwa W · · 2021 · cited 205 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
The Endocannabinoid System (ECS) is primarily responsible for maintaining homeostasis, a balance in internal environment (temperature, mood, and immune system) and energy input and output in living, biological systems.
Closing excerpt
or "medical cannabis"), may also have potential as lead compounds in the development of cannabinoid-based pharmaceuticals for a variety of diseases.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (246 words)

The Endocannabinoid System (ECS) is primarily responsible for maintaining homeostasis, a balance in internal environment (temperature, mood, and immune system) and energy input and output in living, biological systems. In addition to regulating physiological processes, the ECS directly influences anxiety, feeding behaviour/appetite, emotional behaviour, depression, nervous functions, neurogenesis, neuroprotection, reward, cognition, learning, memory, pain sensation, fertility, pregnancy, and pre-and post-natal development. The ECS is also involved in several pathophysiological diseases such as cancer, cardiovascular diseases, and neurodegenerative diseases. In recent years, genetic and pharmacological manipulation of the ECS has gained significant interest in medicine, research, and drug discovery and development. The distribution of the components of the ECS system throughout the body, and the physiological/pathophysiological role of the ECS-signalling pathways in many diseases, all offer promising opportunities for the development of novel cannabinergic, cannabimimetic, and cannabinoid-based therapeutic drugs that genetically or pharmacologically modulate the ECS via inhibition of metabolic pathways and/or agonism or antagonism of the receptors of the ECS. This modulation results in the differential expression/activity of the components of the ECS that may be beneficial in the treatment of a number of diseases. This manuscript in-depth review will investigate the potential of the ECS in the treatment of various diseases, and to put forth the suggestion that many of these secondary metabolites of Cannabis sativa L. (hereafter referred to as "C. sativa L." or "medical cannabis"), may also have potential as lead compounds in the development of cannabinoid-based pharmaceuticals for a variety of diseases.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 34502379 · DOI · PMC8430969

ω-3 and ω-6 Polyunsaturated Fatty Acids, Obesity and Cancer [2]

Review article D'Angelo S, Motti ML, Meccariello R · · 2020 · cited 183 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Recently, nutraceutical bioactive compounds in foods have been discovered for their potential health benefits regarding the prevention of chronic disorders, such as cancer, and inflammatory, cardiovascular, and metabolic diseases.
Closing excerpt
In this review, we present ω-3 and ω-6PUFAs and their derivatives, endocannabinoids; discuss the anti-obesity effects of ω-3PUFAs; their roles in inflammation and colorectal cancer development; and how their action can be co-preventative and co-therapeutic.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (151 words)

Recently, nutraceutical bioactive compounds in foods have been discovered for their potential health benefits regarding the prevention of chronic disorders, such as cancer, and inflammatory, cardiovascular, and metabolic diseases. Dietary omega-3 polyunsaturated fatty acids (ω-3PUFAs), including alpha-linolenic acid, docosapentaenoic acid, and eicosapentaenoic acid, are mostly attractive. They are available for the customers worldwide from commonly used foods and/or as components of commercial food supplements. The anti-inflammatory and hypotriglyceridemic effects of these fatty acids are well known, whereas pro-inflammatory properties have been recognized in their dietary counterparts, the ω-6PUFAs. Both ω-3 and ω-6PUFAs contribute to the production of lipid mediators such as endocannabinoids that are notably involved in control of food intake, energy sensing, and food-related disorders. In this review, we present ω-3 and ω-6PUFAs and their derivatives, endocannabinoids; discuss the anti-obesity effects of ω-3PUFAs; their roles in inflammation and colorectal cancer development; and how their action can be co-preventative and co-therapeutic.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 32927614 · DOI · PMC7551151

The Endocannabinoid System and Physical Exercise [3]

Review article Matei D, Trofin D, Iordan DA, Onu I, Condurache I, Ionite C, et al. · · 2023 · cited 73 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
The endocannabinoid system (ECS) is involved in various processes, including brain plasticity, learning and memory, neuronal development, nociception, inflammation, appetite regulation, digestion, metabolism, energy balance, motility, and regulation of stress and emotions.
Closing excerpt
This review provides information about the current state of knowledge about endocannabinoids and physical effort and also an overview of the studies published in the specialized literature about this subject.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (190 words)

The endocannabinoid system (ECS) is involved in various processes, including brain plasticity, learning and memory, neuronal development, nociception, inflammation, appetite regulation, digestion, metabolism, energy balance, motility, and regulation of stress and emotions. Physical exercise (PE) is considered a valuable non-pharmacological therapy that is an immediately available and cost-effective method with a lot of health benefits, one of them being the activation of the endogenous cannabinoids. Endocannabinoids (eCBs) are generated as a response to high-intensity activities and can act as short-term circuit breakers, generating antinociceptive responses for a short and variable period of time. A runner's high is an ephemeral feeling some sport practitioners experience during endurance activities, such as running. The release of eCBs during sustained physical exercise appears to be involved in triggering this phenomenon. The last decades have been characterized by an increased interest in this emotional state induced by exercise, as it is believed to alleviate pain, induce mild sedation, increase euphoric levels, and have anxiolytic effects. This review provides information about the current state of knowledge about endocannabinoids and physical effort and also an overview of the studies published in the specialized literature about this subject.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 36768332 · DOI · PMC9916354

CYP4X1/sEH-Dependent Endocannabinoid Metabolism Drives Fibroblast-Mediated Immunosuppression to Limit Immunotherapy in Colon Cancer [4]

Research article Mo M, Chen X, Liu Y, Wang C, Chen X, Zhang N, et al. · · 2026 · cited 2 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Cytochrome P450 (CYP) 4X1 and soluble epoxide hydrolase (sEH), the key enzymes responsible for endocannabinoid oxidative metabolism, have been implicated in inflammation and cancer.
Closing excerpt
Together, this study highlights that CYP4X1/sEH-dependent endocannabinoid metabolism controls CAF-mediated immune evasion, and targeting the CYP4X1/sEH-14,15-EET-EA-GPR119 axis represents a promising therapeutic strategy for improving anti-PD-1 therapy in colon cancer.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (144 words)

Cytochrome P450 (CYP) 4X1 and soluble epoxide hydrolase (sEH), the key enzymes responsible for endocannabinoid oxidative metabolism, have been implicated in inflammation and cancer. However, the precise role of CYP4X1 and sEH in tumor immune evasion is poorly understood. Here, it is elucidated that CYP4X1/sEH-dependent endocannabinoid metabolism governs immune evasion in colon cancer by promoting the infiltration of regulatory T cells (Tregs) and impairing CD8+ T cell effector function. Mechanistically, CYP4X1/sEH-derived 14,15-EET-EA upregulates PD-L1, CXCL12, and TGF-β in cancer-associated fibroblasts (CAFs) via the GPR119-Gs/β-arrestin 2 signaling axis. Importantly, targeted regulation of the CYP4X1/sEH-GPR119 axis enhances the efficacy of anti-PD-1 therapy. Moreover, CYP4X1 and sEH levels jointly predict prognosis and immune infiltration in human colon cancer. Together, this study highlights that CYP4X1/sEH-dependent endocannabinoid metabolism controls CAF-mediated immune evasion, and targeting the CYP4X1/sEH-14,15-EET-EA-GPR119 axis represents a promising therapeutic strategy for improving anti-PD-1 therapy in colon cancer.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41276938 · DOI · PMC12849875

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Cannabinoid Receptors and the Endocannabinoid System: Signaling and Function in the Central Nervous System [5]
    Zou S, Kumar U · Int J Mol Sci · 2018 · cited 951 times (Europe PMC)
  • Research article An Introduction to the Endogenous Cannabinoid System [6]
    Lu HC, Mackie K · Biol Psychiatry · 2016 · cited 859 times (Europe PMC)
  • Research article Cannabinoids and the expanded endocannabinoid system in neurological disorders [7]
    Cristino L, Bisogno T, Di Marzo V · Nat Rev Neurol · 2020 · cited 711 times (Europe PMC)
  • Research article Review of the Endocannabinoid System [8]
    Lu HC, Mackie K · Biol Psychiatry Cogn Neurosci Neuroimaging · 2021 · cited 384 times (Europe PMC)
  • Research article Circulating Endocannabinoids: From Whence Do They Come and Where are They Going? [9]
    Hillard CJ · Neuropsychopharmacology · 2018 · cited 343 times (Europe PMC)
  • Research article CB1 Receptor Signaling in the Brain: Extracting Specificity from Ubiquity [10]
    Busquets-Garcia A, Bains J, Marsicano G · Neuropsychopharmacology · 2018 · cited 274 times (Europe PMC)

References

  1. Lowe H, Toyang N, Steele B, Bryant J, Ngwa W. The Endocannabinoid System: A Potential Target for the Treatment of Various Diseases. . 2021. PMID 34502379 · DOI · PMC8430969
  2. D'Angelo S, Motti ML, Meccariello R. ω-3 and ω-6 Polyunsaturated Fatty Acids, Obesity and Cancer. . 2020. PMID 32927614 · DOI · PMC7551151
  3. Matei D, Trofin D, Iordan DA, Onu I, Condurache I, Ionite C, et al.. The Endocannabinoid System and Physical Exercise. . 2023. PMID 36768332 · DOI · PMC9916354
  4. Mo M, Chen X, Liu Y, Wang C, Chen X, Zhang N, et al.. CYP4X1/sEH-Dependent Endocannabinoid Metabolism Drives Fibroblast-Mediated Immunosuppression to Limit Immunotherapy in Colon Cancer. . 2026. PMID 41276938 · DOI · PMC12849875
  5. Zou S, Kumar U. Cannabinoid Receptors and the Endocannabinoid System: Signaling and Function in the Central Nervous System. Int J Mol Sci. 2018. PMID 29533978 · DOI · PMC5877694
  6. Lu HC, Mackie K. An Introduction to the Endogenous Cannabinoid System. Biol Psychiatry. 2016. PMID 26698193 · DOI · PMC4789136
  7. Cristino L, Bisogno T, Di Marzo V. Cannabinoids and the expanded endocannabinoid system in neurological disorders. Nat Rev Neurol. 2020. PMID 31831863 · DOI
  8. Lu HC, Mackie K. Review of the Endocannabinoid System. Biol Psychiatry Cogn Neurosci Neuroimaging. 2021. PMID 32980261 · DOI · PMC7855189
  9. Hillard CJ. Circulating Endocannabinoids: From Whence Do They Come and Where are They Going?. Neuropsychopharmacology. 2018. PMID 28653665 · DOI · PMC5719092
  10. Busquets-Garcia A, Bains J, Marsicano G. CB1 Receptor Signaling in the Brain: Extracting Specificity from Ubiquity. Neuropsychopharmacology. 2018. PMID 28862250 · DOI · PMC5719111

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

7,996
PubMed records on this heading
28%
published since 2020
2,036
review articles
104
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

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