<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>42(6)</volume><submitter>Ling QS</submitter><pubmed_abstract>Stroke is a common cause of death and disability. Allisartan isoproxil (ALL) is a new angiotensin II receptor blocker and a new antihypertensive drug discovered and developed in China. In the present study we investigated the therapeutic effects of ALL in stroke-prone renovascular hypertensive rats (RHR-SP) and the underlying mechanisms. The model rats were generated via two-kidney two-clip (2K2C) surgery, which led to 100% of hypertension, 100% of cerebrovascular damage as well as 100% of mortality 1 year after the surgery. Administration of ALL (30 mg · kg&lt;sup>-1&lt;/sup> · d&lt;sup>-1&lt;/sup> in diet, for 55 weeks) significantly decreased stroke-related death and prolonged lifespan in RHR-SP, but the survival ALL-treated RHR-SP remained of hypertension and cardiovascular hypertrophy compared wi</pubmed_abstract><journal>Acta pharmacologica Sinica</journal><pagination>871-884</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8149727</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Allisartan isoproxil reduces mortality of stroke-prone rats and protects against cerebrovascular, cardiac, and aortic damage.</pubmed_title><pmcid>PMC8149727</pmcid><pubmed_authors>Fu FH</pubmed_authors><pubmed_authors>Tian JS</pubmed_authors><pubmed_authors>Zhang SL</pubmed_authors><pubmed_authors>Liu JG</pubmed_authors><pubmed_authors>Miao CY</pubmed_authors><pubmed_authors>Liu AJ</pubmed_authors><pubmed_authors>Ling QS</pubmed_authors><pubmed_authors>Cheng MH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Allisartan isoproxil reduces mortality of stroke-prone rats and protects against cerebrovascular, cardiac, and aortic damage.</name><description>Stroke is a common cause of death and disability. Allisartan isoproxil (ALL) is a new angiotensin II receptor blocker and a new antihypertensive drug discovered and developed in China. In the present study we investigated the therapeutic effects of ALL in stroke-prone renovascular hypertensive rats (RHR-SP) and the underlying mechanisms. The model rats were generated via two-kidney two-clip (2K2C) surgery, which led to 100% of hypertension, 100% of cerebrovascular damage as well as 100% of mortality 1 year after the surgery. Administration of ALL (30 mg · kg&lt;sup>-1&lt;/sup> · d&lt;sup>-1&lt;/sup> in diet, for 55 weeks) significantly decreased stroke-related death and prolonged lifespan in RHR-SP, but the survival ALL-treated RHR-SP remained of hypertension and cardiovascular hypertrophy compared wi</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2025-04-04T20:15:19.789Z</modification><creation>2025-04-04T20:15:19.789Z</creation></dates><accession>S-EPMC8149727</accession><cross_references><pubmed>34002042</pubmed><doi>10.1038/s41401-021-00684-7</doi></cross_references></HashMap>