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Michael J Caspers

4 papers in the library · 84 citations · publishing 2011-2016

Papers

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Time course of pharmacokinetic and hormonal effects of inhaled high-dose salvinorin A in humans.

Journal of psychopharmacology (Oxford, England) April 1, 2016 Matthew W Johnson, Katherine A Maclean, Michael J Caspers et al. 11 citations

Salvinorin A is a kappa opioid agonist and the principal psychoactive constituent of the Salvia divinorum plant, which has been used for hallucinogenic effects. Previous research on salvinorin A pharmacokinetics likely underestimated plasma levels typically resulting from the doses administered due to inefficient vaporization and not collecting samples during peak drug effects. Six healthy...

LC-MS/MS quantification of salvinorin A from biological fluids.

Analytical methods : advancing methods and applications December 21, 2013 Michael J Caspers, Todd D Williams, Kimberly M Lovell et al. 6 citations

A facile method for quantifying the concentration of the powerful and widely available hallucinogen salvinorin A (a selective kappa opioid agonist) from non-human primate cerebrospinal fluid (CSF) and human plasma has been developed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) in positive electrospray ionization (ESI) mode. With CSF solid phase extraction can be avoided...

Behavioral effects and central nervous system levels of the broadly available κ-agonist hallucinogen salvinorin A are affected by P-glycoprotein modulation in vivo.

The Journal of pharmacology and experimental therapeutics June 1, 2012 Eduardo R Butelman, Michael J Caspers, Kimberly M Lovell et al. 27 citations

Active blood-brain barrier mechanisms, such as the major efflux transporter P-glycoprotein (mdr1), modulate the in vivo/central nervous system (CNS) effects of many pharmacological agents, whether they are used for nonmedical reasons or in pharmacotherapy. The powerful, widely available hallucinogen salvinorin A (from the plant Salvia divinorum) is a high-efficacy, selective κ-opioid agonist...

Opioid receptor probes derived from cycloaddition of the hallucinogen natural product salvinorin A.

Journal of Natural Products April 25, 2011 Anthony Lozama, Christopher W Cunningham, Michael J Caspers et al. 40 citations

As part of our continuing efforts toward more fully understanding the structure-activity relationships of the neoclerodane diterpene salvinorin A, we report the synthesis and biological characterization of unique cycloadducts through [4+2] Diels-Alder cycloaddition. Microwave-assisted methods were developed and successfully employed, aiding in functionalizing the chemically sensitive salvinorin...