Page last updated: 2024-10-24

candesartan and Brain Infarction

candesartan has been researched along with Brain Infarction in 4 studies

candesartan: a nonpeptide angiotensin II receptor antagonist
candesartan : A benzimidazolecarboxylic acid that is 1H-benzimidazole-7-carboxylic acid substituted by an ethoxy group at position 2 and a ({2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl}methyl) group at position 1. It is a angiotensin receptor antagonist used for the treatment of hypertension.

Brain Infarction: Tissue NECROSIS in any area of the brain, including the CEREBRAL HEMISPHERES, the CEREBELLUM, and the BRAIN STEM. Brain infarction is the result of a cascade of events initiated by inadequate blood flow through the brain that is followed by HYPOXIA and HYPOGLYCEMIA in brain tissue. Damage may be temporary, permanent, selective or pan-necrosis.

Research Excerpts

ExcerptRelevanceReference
"To determine whether BP lowering with candesartan, initiated at reperfusion, can reduce neurovascular damage and improve outcome in a model of hypertension after experimental ischemic stroke."7.73Hypertension after experimental cerebral ischemia: candesartan provides neurovascular protection. ( Ergul, A; Fagan, SC; Hess, DC; Hill, WD; Johnson, MH; Kozak, A; Pollock, DM; Xu, L, 2006)
"To determine whether BP lowering with candesartan, initiated at reperfusion, can reduce neurovascular damage and improve outcome in a model of hypertension after experimental ischemic stroke."3.73Hypertension after experimental cerebral ischemia: candesartan provides neurovascular protection. ( Ergul, A; Fagan, SC; Hess, DC; Hill, WD; Johnson, MH; Kozak, A; Pollock, DM; Xu, L, 2006)
"Candesartan promotes angiogenesis and activates MMPs."1.42Sequential Therapy with Minocycline and Candesartan Improves Long-Term Recovery After Experimental Stroke. ( Fagan, SC; Fouda, AY; Ishrat, T; Patel, A; Pillai, B; Soliman, S, 2015)
"Focal cerebral ischemia, induced by middle cerebral artery occlusion/reperfusion (MCAO), was conducted at 4 wk after STZ injection."1.32Role of AT1 receptors and NAD(P)H oxidase in diabetes-aggravated ischemic brain injury. ( Granger, DN; Ishikawa, M; Kusaka, G; Kusaka, I; Nanda, A; Tang, J; Zhang, JH; Zhou, C, 2004)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Soliman, S1
Ishrat, T1
Fouda, AY1
Patel, A1
Pillai, B1
Fagan, SC3
Guan, W1
Kozak, A2
Kusaka, I1
Kusaka, G1
Zhou, C1
Ishikawa, M1
Nanda, A1
Granger, DN1
Zhang, JH1
Tang, J1
Hill, WD1
Pollock, DM1
Xu, L1
Johnson, MH1
Ergul, A1
Hess, DC1

Other Studies

4 other studies available for candesartan and Brain Infarction

ArticleYear
Sequential Therapy with Minocycline and Candesartan Improves Long-Term Recovery After Experimental Stroke.
    Translational stroke research, 2015, Volume: 6, Issue:4

    Topics: Angiotensin II Type 1 Receptor Blockers; Animals; Benzimidazoles; Biphenyl Compounds; Brain Infarcti

2015
Drug repurposing for vascular protection after acute ischemic stroke.
    Acta neurochirurgica. Supplement, 2011, Volume: 111

    Topics: Animals; Anticholesteremic Agents; Antihypertensive Agents; Atorvastatin; Benzimidazoles; Biphenyl C

2011
Role of AT1 receptors and NAD(P)H oxidase in diabetes-aggravated ischemic brain injury.
    American journal of physiology. Heart and circulatory physiology, 2004, Volume: 286, Issue:6

    Topics: Animals; Antihypertensive Agents; Benzimidazoles; Biphenyl Compounds; Blood Glucose; Blood Pressure;

2004
Hypertension after experimental cerebral ischemia: candesartan provides neurovascular protection.
    Journal of hypertension, 2006, Volume: 24, Issue:3

    Topics: Animals; Antihypertensive Agents; Behavior, Animal; Benzimidazoles; Biphenyl Compounds; Blood Pressu

2006