Cannabinoid receptors in regulating the GI tract: Experimental evidence and therapeutic relevance
Handbook of Experimental Pharmacology, ISSN: 1865-0325, Vol: 239, Page: 343-362
2017
- 14Citations
- 52Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations14
- Citation Indexes13
- 13
- CrossRef12
- Policy Citations1
- Policy Citation1
- Captures52
- Readers52
- 52
Book Chapter Description
Cannabinoid receptors are fundamentally involved in all aspects of intestinal physiology, such as motility, secretion, and epithelial barrier function. They are part of a broader entity, the so-called endocannabinoid system which also includes their endocannabinoid ligands and the ligands’ synthesizing/degrading enzymes. The system has a strong impact on the pathophysiology of the gastrointestinal tract and is believed to maintain homeostasis in the gut by controlling hypercontractility and by promoting regeneration after injury. For instance, genetic knockout of cannabinoid receptor 1 leads to inflammation and cancer of the intestines. Derivatives of Δ-tetrahydrocannabinol, such as nabilone and dronabinol, activate cannabinoid receptors and have been introduced into the clinic to treat chemotherapy-induced emesis and loss of appetite; however, they may cause many psychotropic side effects. New drugs that interfere with endocannabinoid degradation to raise endocannabinoid levels circumvent this obstacle and could be used in the future to treat emesis, intestinal inflammation, and functional disorders associated with visceral hyperalgesia.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85018513503&origin=inward; http://dx.doi.org/10.1007/164_2016_105; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85017915161&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/28161834; http://link.springer.com/10.1007/164_2016_105; https://doi.org/10.1007%2F164_2016_105; https://dx.doi.org/10.1007/164_2016_105; https://link.springer.com/chapter/10.1007/164_2016_105
Springer Science and Business Media LLC
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