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Alex Straiker

5 papers in the library · 2 citations · publishing 2007-2025

Papers

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Muscarinic cannabinoid suppression of excitation, a novel form of coincidence detection.

Pharmacological Research February 1, 2025 Michaela Dvorakova, Ken Mackie, Alex Straiker 2 citations

Δ9-tetrahydrocannabinol (THC), the chief psychoactive ingredient of cannabis, acts in the brain primarily via cannabinoid CB1 receptors. These receptors are implicated in several forms of synaptic plasticity - depolarization-induced suppression of excitation (DSE), metabotropic suppression of excitation (MSE), long term depression (LTD) and activation-dependent desensitization. Cultured...

DOI: 10.1016/j.phrs.2025.107606 (opens in new tab) Full text (opens in new tab) Synaptic plasticity Autaptic hippocampal neurons Cb1 receptor M3/m5 muscarinic receptors

Differential Enantiomer-Specific Signaling of Cannabidiol at CB1 Receptors.

Molecular Pharmacology December 2022 Taryn Bosquez-Berger, Sierra Wilson, Christos Iliopoulos-Tsoutsouvas et al.

The two main constituents of cannabis are Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD). While Δ9-THC pharmacology has been studied extensively, CBD-long considered inactive-is now the subject of vigorous research related to epilepsy, pain, and inflammation and is popularly embraced as a virtual cure-all. However, our understanding of CBD pharmacology remains limited, although CBD...

Mutation of putative GRK phosphorylation sites in the cannabinoid receptor 1 (CB1R) confers resistance to cannabinoid tolerance and hypersensitivity to cannabinoids in mice.

Journal of Neuroscience April 9, 2014 Daniel J Morgan, Brian J Davis, Chris S Kearn et al.

For many G-protein-coupled receptors (GPCRs), including cannabinoid receptor 1 (CB1R), desensitization has been proposed as a principal mechanism driving initial tolerance to agonists. GPCR desensitization typically requires phosphorylation by a G-protein-coupled receptor kinase (GRK) and interaction of the phosphorylated receptor with an arrestin. In simple model systems, CB1R is desensitized...

JWH018, a common constituent of 'Spice' herbal blends, is a potent and efficacious cannabinoid CB receptor agonist.

British Journal of Pharmacology June 2010 Brady K Atwood, John W Huffman, Alex Straiker et al.

'Spice' is an herbal blend primarily marketed in Europe as a mild hallucinogen with prominent cannabis-like effects and as a legal alternative to cannabis. However, a recent report identified a number of synthetic additives in samples of 'Spice'. One of these, the indole derivative JWH018, is a ligand for the cannabinoid receptor 1 (CB(1)) cannabinoid receptor and inhibits cAMP production in...

Cannabinoids and Their Receptors

Encyclopedia of Life Sciences December 21, 2007 Alex Straiker

Abstract: Exogenous cannabinoids are ∼60 molecules with a similar structural motif found in marijuana and hashish. Some of these are psychoactive – the chief being Δ 9 ‐tetrahydrocannabinol (Δ 9 ‐THC) – and have been found to exert their psychoactive effects via receptors in the body. The human body makes endogenous cannabinoids that are structurally distinct from exogenous cannabinoids. This...