Satoru Yoshikawa

Izunokuni, 4102321, Japan

Last Updated: 09/26/2026

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Found 11 publications

LPA4 in the spinal dorsal horn is a potential therapeutic target for inflammatory pain and neuropathic mechanical hypersensitivity.

LPA4 in the spinal dorsal horn is a potential therapeutic target for inflammatory pain and neuropathic mechanical hypersensitivity.

Journal: iScience

Published: January 21, 2026

AK1780, a selective P2X7 receptor antagonist with high central nervous system penetration, exhibits analgesic effect in rat neuropathic pain model.

AK1780, a selective P2X7 receptor antagonist with high central nervous system penetration, exhibits analgesic effect in rat neuropathic pain model.

Journal: The journal of pain

Published: October 10, 2024

Cholesterol metabolism and neuroinflammatory changes in a non-human primate spinal nerve ligation model.

Cholesterol metabolism and neuroinflammatory changes in a non-human primate spinal nerve ligation model.

Journal: Scientific reports

Published: March 21, 2024

Peripheral tetrahydrobiopterin is involved in the pathogenesis of mechanical hypersensitivity in a rodent postsurgical pain model.

Peripheral tetrahydrobiopterin is involved in the pathogenesis of mechanical hypersensitivity in a rodent postsurgical pain model.

Journal: Pain

Published: June 17, 2020

Pain phenotypes classified by machine learning using electroencephalography features.

Pain phenotypes classified by machine learning using electroencephalography features.

Journal: NeuroImage

Published: July 30, 2019

An Electroencephalography Bioassay for Preclinical Testing of Analgesic Efficacy.

An Electroencephalography Bioassay for Preclinical Testing of Analgesic Efficacy.

Journal: Scientific reports

Published: April 11, 2018

Decreased Monoamine Oxidase A Expression and Activity in the Bladders of Rats With Partial Outlet Obstruction.

Decreased Monoamine Oxidase A Expression and Activity in the Bladders of Rats With Partial Outlet Obstruction.

Journal: Urology

Published: July 10, 2017

Mechanisms of inhibitory action of TRK-130 (Naltalimide), a μ-opioid receptor partial agonist, on the micturition reflex.

Mechanisms of inhibitory action of TRK-130 (Naltalimide), a μ-opioid receptor partial agonist, on the micturition reflex.

Journal: International urology and nephrology

Published: November 25, 2016

Characteristics of TRK-130 (Naltalimide), a novel opioid ligand, as a new therapeutic agent for overactive bladder.

Characteristics of TRK-130 (Naltalimide), a novel opioid ligand, as a new therapeutic agent for overactive bladder.

Journal: The Journal of pharmacology and experimental therapeutics

Published: June 15, 2014

TRK-380, a novel selective human β3-adrenoceptor agonist, ameliorates formalin-induced pollakiuria in rats and carbachol-induced bladder contraction in dogs.

TRK-380, a novel selective human β3-adrenoceptor agonist, ameliorates formalin-induced pollakiuria in rats and carbachol-induced bladder contraction in dogs.

Journal: Urology

Published: January 22, 2013

Discovery of potent transient receptor potential vanilloid 1 antagonists: design and synthesis of phenoxyacetamide derivatives.

Discovery of potent transient receptor potential vanilloid 1 antagonists: design and synthesis of phenoxyacetamide derivatives.

Journal: Bioorganic & medicinal chemistry letters

Published: December 25, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026