Robert Laprairie
Assistant Professor
Pharmacy
University of Saskatchewan
Canada
Biography
Dr. Laprairie is a member of the Drug Discovery and Development Research Group and the Cannabinoid Research Initiative of Saskatchewan (CRIS). He is a member of the Canadian Society for Pharmacology and Therapeutics (CSPT), the Canadian Consortium for the Investigators of Cannabinoids (CCIC), the American Society for Pharmacology and Experimental Therapeutics (ASPET), and the International Cannabinoids Research Society (ICRS).
Research Interest
Dr. Laprairie’s research focuses on the endocannabinoid system and specifically the type 1 cannabinoid receptor (CB1R). CB1R is activated by the body’s own cannabinoids, synthetic cannabinoids, and cannabinoids from marijuana (e.g. THC and cannabidiol). CB1R is a potential target for the regulation of appetite and the treatment of pain, spasticity in multiple sclerosis, Huntington’s disease, epilepsy, and anxiety, among others. Despite its potential as a therapeutic target, we are still learning how CB1R is regulated by cannabinoids to alter physiology. His laboratory is working to (1) understand how the many different cannabinoids from marijuana affect CB1R function; and (2) develop new compounds known as allosteric modulators that increase or decrease CB1R activity. Dr. Laprairie’s research utilizes molecular biology, cell culture and animal models to study the endocannabinoid system in an attempt to further our understanding of marijuana as a medicine, and possibly lead to the development of new drug compounds.
Publications
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Hua T, Vemuri K, Pu M, Qu L, Han GW, Wu Y, Zhao S, Shui W, Li S, Korde A, Laprairie RB. Crystal structure of the human cannabinoid receptor CB 1. Cell. 2016 Oct 20;167(3):750-62.
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Laprairie RB, Bagher AM, Denovan-Wright EM. Cannabinoid receptor ligand bias: implications in the central nervous system. Current opinion in pharmacology. 2017 Feb 28;32:32-43.
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Bagher AM, Laprairie RB, Toguri JT, Kelly ME, Denovan-Wright EM. bidirectional allosteric interactions between cannabinoid receptor 1 (cb1) and dopamine receptor 2 long (d2l) heterotetramers. European Journal of Pharmacology. 2017 Oct 15;813:66-83.