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fasudil and Hypertension, Renal

fasudil has been researched along with Hypertension, Renal in 4 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.

Hypertension, Renal: Persistent high BLOOD PRESSURE due to KIDNEY DISEASES, such as those involving the renal parenchyma, the renal vasculature, or tumors that secrete RENIN.

Research Excerpts

ExcerptRelevanceReference
" In the present study, the effect of a subdose of fasudil, a selective ROCK inhibitor, on systemic hypertension and myocardium fibrosis induced by aldosterone was investigated in uninephrectomized Sprague-Dawley rats (SD)."7.77Subdose of fasudil suppresses myocardial fibrosis in aldosterone-salt-treated uninephrectomized rats. ( Guo, P; Masaki, T; Mori, H; Nishiyama, A; Wu, C, 2011)
"Late fasudil treatment significantly improved kidney function, morphological changes, and alterations of mRNA expression in the renal cortex, although late untreated controls did not show any improvement."5.35Fasudil, a Rho-kinase inhibitor, reverses L-NAME exacerbated severe nephrosclerosis in spontaneously hypertensive rats. ( Akimoto, K; Inaba, C; Koshikawa, S; Matsuoka, H; Nishikimi, T, 2008)
" In the present study, the effect of a subdose of fasudil, a selective ROCK inhibitor, on systemic hypertension and myocardium fibrosis induced by aldosterone was investigated in uninephrectomized Sprague-Dawley rats (SD)."3.77Subdose of fasudil suppresses myocardial fibrosis in aldosterone-salt-treated uninephrectomized rats. ( Guo, P; Masaki, T; Mori, H; Nishiyama, A; Wu, C, 2011)
"Late fasudil treatment significantly improved kidney function, morphological changes, and alterations of mRNA expression in the renal cortex, although late untreated controls did not show any improvement."1.35Fasudil, a Rho-kinase inhibitor, reverses L-NAME exacerbated severe nephrosclerosis in spontaneously hypertensive rats. ( Akimoto, K; Inaba, C; Koshikawa, S; Matsuoka, H; Nishikimi, T, 2008)
"Fasudil treatment reduced both MAP and RVR responses to Ang II in each group."1.33Androgens potentiate renal vascular responses to angiotensin II via amplification of the Rho kinase signaling pathway. ( Kost, CK; Martin, DS; Song, J, 2006)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Koshikawa, S1
Nishikimi, T2
Inaba, C1
Akimoto, K2
Matsuoka, H2
Guo, P1
Wu, C1
Masaki, T1
Mori, H1
Nishiyama, A1
Wang, X1
Mori, Y1
Tadokoro, K1
Ishikawa, Y1
Shimokawa, H1
Ono, H1
Song, J1
Kost, CK1
Martin, DS1

Other Studies

4 other studies available for fasudil and Hypertension, Renal

ArticleYear
Fasudil, a Rho-kinase inhibitor, reverses L-NAME exacerbated severe nephrosclerosis in spontaneously hypertensive rats.
    Journal of hypertension, 2008, Volume: 26, Issue:9

    Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Animals; Collagen Type I; Collagen Type III; Drug Int

2008
Subdose of fasudil suppresses myocardial fibrosis in aldosterone-salt-treated uninephrectomized rats.
    Die Pharmazie, 2011, Volume: 66, Issue:9

    Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Aldosterone; Animals; Antihypertensive Agents; Biomar

2011
Fasudil, a Rho-kinase inhibitor, attenuates glomerulosclerosis in Dahl salt-sensitive rats.
    Journal of hypertension, 2004, Volume: 22, Issue:9

    Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Animals; Arterioles; Blood Pressure; Blotting, Wester

2004
Androgens potentiate renal vascular responses to angiotensin II via amplification of the Rho kinase signaling pathway.
    Cardiovascular research, 2006, Dec-01, Volume: 72, Issue:3

    Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Angiotensin II; Angiotensin II Type 1 Receptor Blocke

2006