Literature DB >> 26923013

Enalapril Alone or Co-Administered with Losartan Rescues Cerebrovascular Dysfunction, but not Mnemonic Deficits or Amyloidosis in a Mouse Model of Alzheimer's Disease.

Brice Ongali1, Nektaria Nicolakakis1, Xing-Kang Tong1, Tahar Aboulkassim1, Hans Imboden2, Edith Hamel1.   

Abstract

The co-administration of angiotensin converting enzyme inhibitors (ACEi) and angiotensin II (AngII) receptor blockers (ARB) that bind angiotensin type 1 receptors (AT1R) may protect from Alzheimer's disease (AD) better than each treatment taken alone. We tested the curative potential of the non brain-penetrant ACEi enalapril (3 mg/kg/day) administered for 3 months either alone or in combination with the brain penetrant ARB losartan (10 mg/kg/day) in aged (∼15 months) transgenic mice overexpressing a mutated form of the human amyloid-β protein precursor (AβPP, thereafter APP mice). We studied cerebrovascular function, protein levels of oxidative stress markers (superoxide dismutases SOD1, SOD2 and the NADPH oxidase subunit p67phox), amyloid-β (Aβ) pathology, astrogliosis, cholinergic innervation, AT1R and angiotensin IV receptor (AT4R) levels, together with cognitive performance. Both treatments normalized cerebrovascular reactivity and p67phox protein levels, but they did not reduce the cerebrovascular levels of SOD1. Combined treatment normalized cerebrovascular SOD2 levels, significantly attenuated astrogliosis, but did not reduce the increased levels of cerebrovascular AT1R. Yet, combined therapy enhanced thioflavin-S labeled Aβ plaque burden, a tendency not significant when Aβ1 - 42 plaque load was considered. None of the treatments rescued cognitive deficits, cortical AT4R or cholinergic innervation. We conclude that both treatments normalized cerebrovascular function by inhibiting the AngII-induced oxidative stress cascade, and that the positive effects of the combined therapy on astrogliosis were likely due to the ability of losartan to enter brain parenchyma. However, enalapril did not potentiate, and may even dampen, the reported cognitive benefits of losartan, raising caution when selecting the most appropriate antihypertensive therapy in AD patients.

Entities:  

Keywords:  APP mice; Alzheimer’s disease; angiotensin II; angiotensin converting enzyme inhibitors (ACEi); enalapril; losartan

Mesh:

Substances:

Year:  2016        PMID: 26923013     DOI: 10.3233/JAD-150868

Source DB:  PubMed          Journal:  J Alzheimers Dis        ISSN: 1387-2877            Impact factor:   4.472


  4 in total

1.  Multifunctional Nanostructure RAP-RL Rescues Alzheimer's Cognitive Deficits through Remodeling the Neurovascular Unit.

Authors:  Qian Zhang; Qingxiang Song; Xiao Gu; Mengna Zheng; Antian Wang; Gan Jiang; Meng Huang; Huan Chen; Yu Qiu; Bin Bo; Shanbao Tong; Rong Shao; Binyin Li; Gang Wang; Hao Wang; Yongbo Hu; Hongzhuan Chen; Xiaoling Gao
Journal:  Adv Sci (Weinh)       Date:  2020-12-10       Impact factor: 16.806

2.  Systemic Candesartan Treatment Modulates Behavior, Synaptic Protein Levels, and Neuroinflammation in Female Mice That Express Human APOE4.

Authors:  Sarah B Scheinman; Steve Zaldua; Adedoyin Dada; Kateryna Krochmaliuk; Katherine Dye; Felecia M Marottoli; Gregory R J Thatcher; Leon M Tai
Journal:  Front Neurosci       Date:  2021-02-10       Impact factor: 4.677

Review 3.  Vasculo-Neuronal Coupling and Neurovascular Coupling at the Neurovascular Unit: Impact of Hypertension.

Authors:  Jessica L Presa; Flavia Saravia; Zsolt Bagi; Jessica A Filosa
Journal:  Front Physiol       Date:  2020-09-25       Impact factor: 4.566

Review 4.  Effects of Antihypertensive Drugs on Cognitive Function in Elderly Patients with Hypertension: A Review.

Authors:  Wei Yang; Hongyu Luo; Yixin Ma; Sicong Si; Huan Zhao
Journal:  Aging Dis       Date:  2021-06-01       Impact factor: 6.745

  4 in total

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