4.5 Article

Renin inhibitor aliskiren exerts neuroprotection against amyloid beta-peptide toxicity in rat cortical neurons

Journal

NEUROCHEMISTRY INTERNATIONAL
Volume 61, Issue 3, Pages 369-377

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2012.05.012

Keywords

Alzheimer's disease; Angiotensin; Angiotensin-converting enzyme; Anti-hypertensive; Renin-angiotensin system

Funding

  1. Chang Gung Memorial Hospital [CMRPG880801, CMRPG880802]
  2. National Science Council [NSC97-2314-B-010-008MY3, NSC98-2314-B-010-020MY3]

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Accumulation of amyloid beta-peptide (A beta) in senile plaques, a pathological hallmark of Alzheimer's disease (AD), has been implicated in neuronal degeneration. Renin-angiotensin system (RAS) blockers, including the renin inhibitor aliskiren, are a group of clinically relevant anti-hypertensive agents. The present study was initiated to investigate whether aliskiren may modulate A beta neurotoxicity as an additional function aside from its established property of lowering blood pressure. We found aliskiren conferred neuronal resistance to A beta toxicity in primary rat cortical cultures. Moreover, both A beta 25-35 and A beta 1-42 induced renin expression in cortical neurons; in parallel, a heightened expression of renin was detected in the cerebral cortices of 9-month-old AD transgenic mice. Notably, aliskiren blocked A beta-mediated neuronal induction of renin. We therefore concluded that aliskiren may carry neuroprotective action against A beta toxicity. Furthermore, the aliskiren effects may involve downregulation of renin expression induced by A beta. (C) 2012 Elsevier Ltd. All rights reserved.

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