Evidence map›Paper›PMID 23961275›Full record

ArticleJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences2013

Enalapril protects endothelial cells against induced apoptosis in Alzheimer's disease.

Rokhsareh Meamar, Leila Dehghani, Majid Ghasemi, Mohamad Saadatnia, Keivan Basiri, Nazanin Alaei Faradonbeh, Shaghayegh Haghjooy Javanmard

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Article in Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Rokhsareh MeamarIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran ; Department of Medical Science, Islamic Azad University, Najafabad Branch, Isfahan, Iran.
Leila Dehghani
Majid Ghasemi
Mohamad Saadatnia
Keivan Basiri
Nazanin Alaei Faradonbeh
Shaghayegh Haghjooy Javanmard

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is a progressive neurodegenerative disease in which endothelial cell (EC) can be affected. In brain, functional changes in ECs contribute to reductions in resting blood flow. Furthermore, angiotensin-converting enzyme inhibitors (ACE-I) have beneficial effects on endothelial dysfunction. This is the first study that presents direct experimental evidence associating endothelial apoptosis as a basis of AD pathogenesis and response to an ACE-I therapy. MATERIALS AND

methodsHuman umbilical vein ECs (HUVECs) were treated with sera from AD patients and sera from healthy volunteers (each group, n = 10). Apoptosis was determined by annexin V-propidium iodide staining and cell death detection kit. The effect of 50 μM enalapril on endothelial apoptosis was assessed. Nitrite (NO2 (-)) levels were determined in the culture supernatants.

resultsEnalapril suppressed the induction of apoptosis by the serum of patients only when used before treating HUVECs with the sera of AD. Mean ± SD of apoptosis induction in the control group was 6.7 ± 3.69; in the group treated with sera of AD for 24 h was 47.78 ± 0.65; in the group wherein sera from AD was added (pretreatment) after exposure of HUVECs by 50 μM enalapril for 24 h was 26.6 ± 2.63; and in the group wherein HUVECs were exposed in the sera of AD for 24 h and then 50 μM enalapril was added to these cells for another 24 h (post-treatment) was 56.87 ± 5.51. Also, the mean ± SD of NO2 (-) concentration showed significantly greater levels of dissolved NO2/NO3 metabolite in the culture media of untreated HUVECs by enalapril (1.03 ± 0.06) as compared with control (0.26 ± 0.13; P < 0.05), while the rate of nitric oxide (NO) significantly decreased when enalapril was presented in culture both in the pretreatment (0.07 ± 0.003) and in the post-treatment group (0.06 ± 0.005; P < 0.05).

conclusionIt could be concluded that EC treated with sera from AD patients activates apoptosis in HUVECs; this effect was reversed by enalapril pretreatment. This can be proposed as a therapeutic approach for Alzheimer's patients.

Indexed as

Apoptosisenalaprilendothelial cell

Identifiers

PMID23961275
PMCPMC3743309

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