Establishment of recombinant cannabinoid receptor assays and characterization of several natural and synthetic ligands

Geiger, Sarah and Nickl, Kathrin and Schneider, Erich H. and Seifert, Roland and Heilmann, Joerg (2010) Establishment of recombinant cannabinoid receptor assays and characterization of several natural and synthetic ligands. NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 382 (2). pp. 177-191. ISSN 0028-1298, 1432-1912

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Abstract

Cannabinoid receptors (CBR) are important drug targets for the treatment of various inflammatory, metabolic and neurological diseases. Therefore, sensitive test systems for the assessment of ligands are needed. In this study, a steady-state GTPase assay for human CBR subtypes 1 and 2 was developed to characterize the pharmacological property of ligands at a very proximal point of the signal transduction cascade. Establishing these in vitro test sytems, we studied cell or tissue membranes heterogenously or endogenously expressing CBR, such as CBR-infected Human Embryonic Kidney (HEK) 293 cells, rat cerebellum and spleen cells. The lack of effects in the GTPase assay and in [S-35]GTP gamma S binding experiments in these expression system, directed us to use Spodoptera frugiperda (Sf9) cells. Co-expressing CBR, different G alpha-subunits, G beta gamma heterodimer, and RGS (Regulator of G-protein signaling)-proteins in Sf9 cell membranes greatly improved the sensitivity of the assay, with highest GTPase activation in the CBR + G alpha(i2) + G beta(1)gamma(2) + RGS4 system. We examined exogenous and endogenous standard ligands as well as secondary metabolites as Delta(9)-tetrahydrocannabinol (Delta(9)-THC), dodeca-2E,4E-dienoic acid isobutylamide, an alkylamide from Echinacea purpurea, and an E. purpurea hexane extract according their agonistic and antagonistic properties. The suitability of the assay for screening procedures was also proven by detecting the activity of Delta(9)-THC in a matrix of other less active compounds (Delta(9)-THC-free Cannabis sativa extract). In conclusion, we have developed highly sensitive test systems for the analysis of CBR ligands.

Item Type: Article
Uncontrolled Keywords: HIGH CONSTITUTIVE ACTIVITY; G-PROTEIN; ENDOCANNABINOID SYSTEM; SIGNAL-TRANSDUCTION; MOLECULAR ANALYSIS; FUSION PROTEINS; CB1; PHARMACOLOGY; AGONISTS; AFFINITY; Cannabinoid receptor; G-protein-coupled receptors; Steady-state gamma-GTPase assay; Anandamide Delta(9)-Tetrahydrocannabinol
Subjects: 600 Technology > 615 Pharmacy
Divisions: Chemistry and Pharmacy > Institute of Pharmacy > Pharmacology and Toxicology (Prof. Schlossmann, formerly Prof. Seifert)
Chemistry and Pharmacy > Institute of Pharmacy > Pharmaceutical Biology (Prof. Heilmann)
Depositing User: Dr. Gernot Deinzer
Date Deposited: 21 Jul 2020 12:21
Last Modified: 21 Jul 2020 12:21
URI: https://pred.uni-regensburg.de/id/eprint/24414

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