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The angiotensin AT4 receptor subtype as a target for the treatment of memory dysfunction associated with Alzheimer's disease
Author(s) -
John W. Wright,
Joseph W. Harding
Publication year - 2008
Publication title -
journal of the renin-angiotensin-aldosterone system
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 46
eISSN - 1752-8976
pISSN - 1470-3203
DOI - 10.1177/1470320308099084
Subject(s) - disease , dementia , cognition , angiotensin receptor , mechanism (biology) , angiotensin ii , angiotensin receptor blockers , memory impairment , alzheimer's disease , medicine , vascular dementia , angiotensin converting enzyme , neuroscience , cognitive impairment , receptor , pharmacology , psychology , blood pressure , philosophy , epistemology
Over recent years antihypertensive drugs, particularly angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs), have been reported to have beneficial effects upon cognitive impairment. Such findings suggest that pharmacological manipulation of angiotensin ligands may be of clinical importance in slowing or halting the cognitive deterioration seen in vascular dementia and Alzheimer's disease.The mechanism(s) underlying these improvements in cognitive function remains unclear; however, important leads are emerging. The angiotensin AT 4 receptor subtype, discovered by our laboratory in 1992, influences several important behaviours and physiologies, including learning and memory, and may play a role in this cognitive improvement.This review initially describes the therapeutic drugs approved by the Federal Drug Administration and new approaches presently being developed to treat Alzheimer's disease-induced cognitive impairment. Next, the biologically-active angiotensin ligands and their respective receptor subtypes are discussed, followed by the roles of angiotensin II, angiotensin IV, ACE inhibitors and ARBs in cognitive function.We conclude with a working hypothesis concerning the importance of the AT 4 receptor subtype as a new potential drug target for the treatment of Alzheimer's disease-associated memory loss.

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