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      Terpenoids, Cannabimimetic Ligands, beyond the Cannabis Plant

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          Abstract

          Medicinal use of Cannabis sativa L. has an extensive history and it was essential in the discovery of phytocannabinoids, including the Cannabis major psychoactive compound—Δ9-tetrahydrocannabinol (Δ9-THC)—as well as the G-protein-coupled cannabinoid receptors (CBR), named cannabinoid receptor type-1 (CB1R) and cannabinoid receptor type-2 (CB2R), both part of the now known endocannabinoid system (ECS). Cannabinoids is a vast term that defines several compounds that have been characterized in three categories: (i) endogenous, (ii) synthetic, and (iii) phytocannabinoids, and are able to modulate the CBR and ECS. Particularly, phytocannabinoids are natural terpenoids or phenolic compounds derived from Cannabis sativa. However, these terpenoids and phenolic compounds can also be derived from other plants (non-cannabinoids) and still induce cannabinoid-like properties. Cannabimimetic ligands, beyond the Cannabis plant, can act as CBR agonists or antagonists, or ECS enzyme inhibitors, besides being able of playing a role in immune-mediated inflammatory and infectious diseases, neuroinflammatory, neurological, and neurodegenerative diseases, as well as in cancer, and autoimmunity by itself. In this review, we summarize and critically highlight past, present, and future progress on the understanding of the role of cannabinoid-like molecules, mainly terpenes, as prospective therapeutics for different pathological conditions.

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          Structure of a cannabinoid receptor and functional expression of the cloned cDNA.

          Marijuana and many of its constituent cannabinoids influence the central nervous system (CNS) in a complex and dose-dependent manner. Although CNS depression and analgesia are well documented effects of the cannabinoids, the mechanisms responsible for these and other cannabinoid-induced effects are not so far known. The hydrophobic nature of these substances has suggested that cannabinoids resemble anaesthetic agents in their action, that is, they nonspecifically disrupt cellular membranes. Recent evidence, however, has supported a mechanism involving a G protein-coupled receptor found in brain and neural cell lines, and which inhibits adenylate cyclase activity in a dose-dependent, stereoselective and pertussis toxin-sensitive manner. Also, the receptor is more responsive to psychoactive cannabinoids than to non-psychoactive cannabinoids. Here we report the cloning and expression of a complementary DNA that encodes a G protein-coupled receptor with all of these properties. Its messenger RNA is found in cell lines and regions of the brain that have cannabinoid receptors. These findings suggest that this protein is involved in cannabinoid-induced CNS effects (including alterations in mood and cognition) experienced by users of marijuana.
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            Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome

            New England Journal of Medicine, 376(21), 2011-2020
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              Identification of an endogenous 2-monoglyceride, present in canine gut, that binds to cannabinoid receptors

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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                29 March 2020
                April 2020
                : 25
                : 7
                : 1567
                Affiliations
                [1 ]Laboratory of Autoimmunity and Immunopharmacology (LAIF), Department of Health Sciences, Campus Araranguá, Universidade Federal de Santa Catarina, Araranguá 88906-072, Brazil; elainecdalazen@ 123456gmail.com (E.C.D.G.); baldasso.gabriela@ 123456gmail.com (G.M.B.); rodrigosebbenp@ 123456gmail.com (R.S.P.)
                [2 ]Graduate Program of Neuroscience, Center of Biological Sciences, Campus Florianópolis, Universidade Federal de Santa Catarina, Florianópolis 88040-900, Brazil
                [3 ]Neurosurgery Department, Neurosurgery Pain Research institute, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA; bicca.ma@ 123456jhmi.edu
                [4 ]Department of Agricultural Sciences, University of Naples Federico II, 80,055 Portici, Italy
                Author notes
                [* ]Correspondence: rafcapas@ 123456unina.it (R.C.); rafaelcdutra@ 123456gmail.com or rafael.dutra@ 123456ufsc.br (R.C.D.); Tel.: +39-081-678664 (R.C.); +55-48-3721-21678 (R.C.D.); Fax: +55-48-3721-6448 (R.C. & R.C.D.)
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0003-0682-3019
                https://orcid.org/0000-0002-6254-2812
                https://orcid.org/0000-0002-3648-8824
                https://orcid.org/0000-0002-2330-4862
                https://orcid.org/0000-0002-3335-1822
                https://orcid.org/0000-0002-6938-2161
                Article
                molecules-25-01567
                10.3390/molecules25071567
                7181184
                32235333
                ca3d6c4c-72f2-4c66-815e-4191cb78b264
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 29 February 2020
                : 27 March 2020
                Categories
                Review

                phytocannabinoid,terpenoids,cannabinoid receptors,cannabis plant,endocannabinoids,inflammation.

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