10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Distinctive Evidence Involved in the Role of Endocannabinoid Signalling in Parkinson’s Disease: A Perspective on Associated Therapeutic Interventions

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Current pharmacotherapy of Parkinson’s disease (PD) is symptomatic and palliative, with levodopa/carbidopa therapy remaining the prime treatment, and nevertheless, being unable to modulate the progression of the neurodegeneration. No available treatment for PD can enhance the patient’s life-quality by regressing this diseased state. Various studies have encouraged the enrichment of treatment possibilities by discovering the association of the effects of the endocannabinoid system (ECS) in PD. These reviews delineate the reported evidence from the literature on the neuromodulatory role of the endocannabinoid system and expression of cannabinoid receptors in symptomatology, cause, and treatment of PD progression, wherein cannabinoid (CB) signalling experiences alterations of biphasic pattern during PD progression. Published papers to date were searched via MEDLINE, PubMed, etc., using specific key words in the topic of our manuscript. Endocannabinoids regulate the basal ganglia neuronal circuit pathways, synaptic plasticity, and motor functions via communication with dopaminergic, glutamatergic, and GABAergic signalling systems bidirectionally in PD. Further, gripping preclinical and clinical studies demonstrate the context regarding the cannabinoid compounds, which is supported by various evidence (neuroprotection, suppression of excitotoxicity, oxidative stress, glial activation, and additional benefits) provided by cannabinoid-like compounds (much research addresses the direct regulation of cannabinoids with dopamine transmission and other signalling pathways in PD). More data related to endocannabinoids efficacy, safety, and pharmacokinetic profiles need to be explored, providing better insights into their potential to ameliorate or even regress PD.

          Related collections

          Most cited references172

          • Record: found
          • Abstract: found
          • Article: not found

          The orphan receptor GPR55 is a novel cannabinoid receptor.

          The endocannabinoid system functions through two well characterized receptor systems, the CB1 and CB2 receptors. Work by a number of groups in recent years has provided evidence that the system is more complicated and additional receptor types should exist to explain ligand activity in a number of physiological processes. Cells transfected with the human cDNA for GPR55 were tested for their ability to bind and to mediate GTPgammaS binding by cannabinoid ligands. Using an antibody and peptide blocking approach, the nature of the G-protein coupling was determined and further demonstrated by measuring activity of downstream signalling pathways. We demonstrate that GPR55 binds to and is activated by the cannabinoid ligand CP55940. In addition endocannabinoids including anandamide and virodhamine activate GTPgammaS binding via GPR55 with nM potencies. Ligands such as cannabidiol and abnormal cannabidiol which exhibit no CB1 or CB2 activity and are believed to function at a novel cannabinoid receptor, also showed activity at GPR55. GPR55 couples to Galpha13 and can mediate activation of rhoA, cdc42 and rac1. These data suggest that GPR55 is a novel cannabinoid receptor, and its ligand profile with respect to CB1 and CB2 described here will permit delineation of its physiological function(s).
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            The molecular logic of endocannabinoid signalling.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              CB1 cannabinoid receptors and on-demand defense against excitotoxicity.

              Abnormally high spiking activity can damage neurons. Signaling systems to protect neurons from the consequences of abnormal discharge activity have been postulated. We generated conditional mutant mice that lack expression of the cannabinoid receptor type 1 in principal forebrain neurons but not in adjacent inhibitory interneurons. In mutant mice,the excitotoxin kainic acid (KA) induced excessive seizures in vivo. The threshold to KA-induced neuronal excitation in vitro was severely reduced in hippocampal pyramidal neurons of mutants. KA administration rapidly raised hippocampal levels of anandamide and induced protective mechanisms in wild-type principal hippocampal neurons. These protective mechanisms could not be triggered in mutant mice. The endogenous cannabinoid system thus provides on-demand protection against acute excitotoxicity in central nervous system neurons.
                Bookmark

                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                28 August 2020
                September 2020
                : 21
                : 17
                : 6235
                Affiliations
                [1 ]Department of Pharmacology, Chitkara College of Pharmacy, Chitkara University, Punjab 140401, India; kgagandeep060@ 123456gmail.com (G.K.); arundhiman431@ 123456gmail.com (A.K.)
                [2 ]Department of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, 410028 Oradea, Romania
                [3 ]National Agri Food Biotechnology Institute, Mohali, Punjab 140306, India; rj.kuk01@ 123456gmail.com
                [4 ]Department of Pharmacology, Government College of Pharmacy, Distt. Shimla, Himachal Pradesh, Rohru 171207, India; vineet.mehta20@ 123456gmail.com
                [5 ]Department of Biology, Faculty of Science, Selcuk University Campus, 42130 Konya, Turkey; biyologzengin@ 123456gmail.com
                [6 ]Department of Medical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, 410073 Oradea, Romania; roxana.gavrila@ 123456yahoo.com (R.B.); ovidiufr@ 123456yahoo.co.uk (O.F.)
                [7 ]Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China; Shams1327@ 123456yahoo.com
                [8 ]Department of Natural Product Chemistry, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China
                Author notes
                [* ]Correspondence: tapanbehl31@ 123456gmail.com (T.B.); sbungau@ 123456uoradea.ro (S.B.); Tel.: +91-85275-17931 (T.B.); Tel.: +40-726-776-588 (S.B.)
                Author information
                https://orcid.org/0000-0003-3236-1292
                https://orcid.org/0000-0001-5188-6540
                Article
                ijms-21-06235
                10.3390/ijms21176235
                7504186
                32872273
                f4d520bf-8da9-423d-9b0b-d8cdaef6926b
                © 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
                : 09 August 2020
                : 27 August 2020
                Categories
                Review

                Molecular biology
                endocannabinoid system,endocannabinoids,cannabinoid 1 receptor,cannabinoid 2 receptor,parkinson’s disease,neuroprotection

                Comments

                Comment on this article