Literature DB >> 11881119

Pre-treatment with candesartan protects from cerebral ischaemia.

T Ito1, Y Nishimura, J Saavedra.   

Abstract

Angiotensin II (Ang II) regulates cerebral blood flow by stimulating cerebral vasoconstriction via AT1-receptors. In adult spontaneously hypertensive rats (SHR), the cerebrovascular autoregulatory curve is shifted to the right, in the direction of higher blood pressures, an indication of excessive cerebrovascular vasoconstriction. A restricted capacity to dilate cerebral blood vessels may be responsible for the enhanced vulnerability to cerebrovascular ischaemia during hypertension. We found that chronic treatment with the AT1-receptor antagonist, candesartan, (0.5 mg/kg/day for 14 days, via osmotic minipumps implanted in the subcutaneous tissue) blocked Ang II binding to AT1-receptors in cerebral blood vessels and in brain areas involved in the regulation of cerebrovascular flow, and increased the ratio of lumen-wall area in the middle cerebral artery. Candesartan treatment normalised the lower part of the autoregulatory curve in SHR, and markedly decreased cerebral ischaemia as a consequence of middle cerebral artery occlusion with reperfusion. Protection from ischaemia is related to arterial remodelling, enhanced compensatory vasodilatation in the peripheral area of ischaemia, decreased reduction in cerebral blood flow following the occlusion of a major cerebral blood vessel, and protection from injury in the periphery of the lesion. Our results indicate that pre-treatment with AT1-antagonists such as candesartan could be of benefit in the prevention and treatment of brain ischaemia.

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Year:  2001        PMID: 11881119     DOI: 10.3317/jraas.2001.024

Source DB:  PubMed          Journal:  J Renin Angiotensin Aldosterone Syst        ISSN: 1470-3203            Impact factor:   1.636


  6 in total

1.  Candesartan, an angiotensin II AT₁-receptor blocker and PPAR-γ agonist, reduces lesion volume and improves motor and memory function after traumatic brain injury in mice.

Authors:  Sonia Villapol; Alexandra K Yaszemski; Trevor T Logan; Enrique Sánchez-Lemus; Juan M Saavedra; Aviva J Symes
Journal:  Neuropsychopharmacology       Date:  2012-08-15       Impact factor: 7.853

2.  Transgenic Mice Overexpressing Human Angiotensin I Receptor Gene Are Susceptible to Stroke Injury.

Authors:  Sudhir Jain; Jatin Tulsulkar; Anita Rana; Ashok Kumar; Zahoor A Shah
Journal:  Mol Neurobiol       Date:  2015-02-05       Impact factor: 5.590

Review 3.  Brain angiotensin II: new developments, unanswered questions and therapeutic opportunities.

Authors:  Juan M Saavedra
Journal:  Cell Mol Neurobiol       Date:  2005-06       Impact factor: 5.046

4.  ACE (Angiotensin-Converting Enzyme) Inhibition Reverses Vasoconstriction and Impaired Dilation of Pial Collaterals in Chronic Hypertension.

Authors:  Zhaojin Li; Devon P Lindner; Nicole M Bishop; Marilyn J Cipolla
Journal:  Hypertension       Date:  2020-05-18       Impact factor: 10.190

5.  Effects of different classes of antihypertensive agents on the outcome of acute ischemic stroke.

Authors:  Konstantinos Tziomalos; Vasilios Giampatzis; Stella D Bouziana; Marianna Spanou; Maria Papadopoulou; Pavlina Kazantzidou; Stavroula Kostaki; Antonios Kouparanis; Christos Savopoulos; Apostolos I Hatzitolios
Journal:  J Clin Hypertens (Greenwich)       Date:  2015-03-13       Impact factor: 3.738

6.  Effects of angiotensin II type 1 receptor blocker and adiponectin on adipocyte dysfunction in stroke-prone spontaneously hypertensive rats.

Authors:  Kumiko Takemori; Takao Inoue; Hiroyuki Ito
Journal:  Lipids Health Dis       Date:  2013-07-22       Impact factor: 3.876

  6 in total

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