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Angiotensin receptor (AT2R) agonist C21 prevents cognitive decline after permanent stroke in aged animals-A randomized double- blind pre-clinical study.
- Source :
-
Behavioural brain research [Behav Brain Res] 2019 Feb 01; Vol. 359, pp. 560-569. Date of Electronic Publication: 2018 Oct 05. - Publication Year :
- 2019
-
Abstract
- Post stroke cognitive impairment (PSCI) is an understudied, long-term complication of stroke, impacting nearly 30-40% of all stroke survivors. No cure is available once the cognitive deterioration manifests. To our knowledge, this is the first study to investigate the long-term effects of C21 treatment on the development of PSCI in aged animals. Treatments with C21 or vehicle were administered orally, 24 h post-stroke, and continued for 30 days. Outcome measures for sensorimotor and cognitive function were performed using a sequence of tests, all blindly conducted and assessed at baseline as well as at different time points post-stroke. Our findings demonstrate that the angiotensin receptor (AT2R) agonist C21 effectively prevents the development of PSCI in aged animals.<br /> (Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Administration, Oral
Aging physiology
Aging psychology
Animals
Body Weight drug effects
Cognitive Dysfunction etiology
Cognitive Dysfunction physiopathology
Disease Models, Animal
Double-Blind Method
Drug Evaluation, Preclinical
Male
Motor Activity drug effects
Random Allocation
Rats, Wistar
Recovery of Function drug effects
Stroke complications
Stroke physiopathology
Stroke psychology
Time Factors
Aging drug effects
Cognitive Dysfunction prevention & control
Nootropic Agents pharmacology
Receptor, Angiotensin, Type 2 agonists
Stroke drug therapy
Sulfonamides pharmacology
Thiophenes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-7549
- Volume :
- 359
- Database :
- MEDLINE
- Journal :
- Behavioural brain research
- Publication Type :
- Academic Journal
- Accession number :
- 30296528
- Full Text :
- https://doi.org/10.1016/j.bbr.2018.10.010