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Kathryn A. Seely

Researcher at University of Arkansas for Medical Sciences

Publications -  19
Citations -  1750

Kathryn A. Seely is an academic researcher from University of Arkansas for Medical Sciences. The author has contributed to research in topics: Cannabinoid & Synthetic cannabinoids. The author has an hindex of 15, co-authored 19 publications receiving 1583 citations.

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Spice drugs are more than harmless herbal blends: a review of the pharmacology and toxicology of synthetic cannabinoids

TL;DR: A review of the legal status of common synthetic cannabinoids detected in Spice and analytical procedures used to test Spice products and human specimens collected under a variety of clinical circumstances is provided in this paper.
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The CB2 cannabinoid agonist AM-1241 prolongs survival in a transgenic mouse model of amyotrophic lateral sclerosis when initiated at symptom onset

TL;DR: It is demonstrated that mRNA, receptor binding and function of CB2, but not CB1, receptors are dramatically and selectively up‐regulated in spinal cords of G93A‐SOD1 mice in a temporal pattern paralleling disease progression, and CB2 agonists may slow motor neuron degeneration and preserve motor function.
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Cytochrome P450-mediated oxidative metabolism of abused synthetic cannabinoids found in K2/Spice: identification of novel cannabinoid receptor ligands.

TL;DR: Test the hypothesis that JWH-018 and its fluorinated counterpart AM2201 are subject to cytochrome P450 (P450)-mediated oxidation, forming potent hydroxylated metabolites that retain significant affinity and activity at the cannabinoid 1 (CB1) receptor.
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Resveratrol improves renal microcirculation, protects the tubular epithelium, and prolongs survival in a mouse model of sepsis-induced acute kidney injury

TL;DR: Resveratrol may have a dual mechanism of action to restore the renal microcirculation and scavenge reactive nitrogen species, thus protecting the tubular epithelium even when administered after the onset of sepsis.
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Development of oxidative stress in the peritubular capillary microenvironment mediates sepsis-induced renal microcirculatory failure and acute kidney injury.

TL;DR: The first time-dependent studies to document changes in renal hemodynamic changes occur early after sepsis demonstrate that targeting the later oxidant generation can break the cycle of injury and enable the microcirculation and renal function to recover.