Page last updated: 2024-10-28

fasudil and Pain

fasudil has been researched along with Pain in 1 studies

fasudil: intracellular calcium antagonist; structure in first source
fasudil : An isoquinoline substituted by a (1,4-diazepan-1-yl)sulfonyl group at position 5. It is a Rho-kinase inhibitor and its hydrochloride hydrate form is approved for the treatment of cerebral vasospasm and cerebral ischemia.

Pain: An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS.

Research Excerpts

ExcerptRelevanceReference
"In this article, the potential analgesic effects of Fasudil in a range of preclinical pain models were assessed."7.76Characterization of Fasudil in preclinical models of pain. ( Boyce-Rustay, JM; Chu, KL; Honore, P; McGaraughty, S; Simler, GH; Vasudevan, A; Wensink, EJ, 2010)
"In this article, the potential analgesic effects of Fasudil in a range of preclinical pain models were assessed."3.76Characterization of Fasudil in preclinical models of pain. ( Boyce-Rustay, JM; Chu, KL; Honore, P; McGaraughty, S; Simler, GH; Vasudevan, A; Wensink, EJ, 2010)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boyce-Rustay, JM1
Simler, GH1
McGaraughty, S1
Chu, KL1
Wensink, EJ1
Vasudevan, A1
Honore, P1

Other Studies

1 other study available for fasudil and Pain

ArticleYear
Characterization of Fasudil in preclinical models of pain.
    The journal of pain, 2010, Volume: 11, Issue:10

    Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Analgesics; Animals; Disease Models, Animal; Male; Pa

2010