Expression of MicroRNAs (miR-15b, miR-16, miR-138, miR-221, and miR-222) as Biomarkers of Endothelial Corpus Cavernosum Dysfunction in a Diabetic Alcoholic Murine Model

被引:5
|
作者
Tiraboschi, Ricardo Brianezi [1 ,2 ]
Lizarte Neto, Fermino Sanches [3 ]
da Cunha Tirapelli, Daniela Pretti [3 ]
de Bessa Jr, Jose [1 ]
Miranda, Eduardo Paula [4 ]
de Assis Cirino, Mucio Luiz [3 ]
Tirapelli, Luis Fernando [3 ]
Tucci Jr, Silvio [2 ]
Fernandes Molina, Carlos Augusto [2 ]
机构
[1] Univ Estadual Feira de Santana, State Univ Feira de Santana, Med Sch, Dept Surg,Div Urol, Feira De Santana, BA, Brazil
[2] Univ Sao Paulo, Ribeirao Preto Med Sch, Div Urol, Surg & Anat, Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Ribeirao Preto Med Sch, Surg & Anat, Ribeirao Preto, SP, Brazil
[4] Univ Fed Ceara, Div Urol, Fortaleza, Ceara, Brazil
关键词
Alcoholism; Biomarkers; Diabetes mellitus; Endothelium; Erectile dysfunction; MicroRNAs; CARDIOVASCULAR RISK-FACTORS; CANNABINOID RECEPTOR CB2; NITRIC-OXIDE SYNTHASE; ERECTILE DYSFUNCTION; MARIJUANA USE; WESTERN DIET; OBESITY;
D O I
10.1016/j.esxm.2021.100326
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: MicroRNAs (miRNAs) are short noncoding RNA molecules that regulate gene expression and are related to endothelial dysfunction (EnD). Recently, miRNAs have also been explored as potential biomarkers and target molecular therapy of erectile dysfunction (ED). Could the miRNAs be the tip of the iceberg of chronic arterial disease foreshadowed by the ED? Aim: To investigate the expression of miR-15b, miR-16, miR-138, miR-221, and miR-222 in corpus cavernosum (CC) and peripheral blood in a rat model of endothelium dysfunction secondary to diabetes (DM) and alcohol consumption to assess potential endothelial lesion biomarkers. Methods: Twenty males Wistar rats were divided into 4 groups: control group (C), alcohol consumption group (A), diabetic group (D), diabetic-alcohol consumption group (D + A). DM was alloxan-induced and alcohol consumption was through progressive increase of ethanol concentration in drinkable water. After 7 weeks, miRNAs expressions from CC and blood sample were evaluated by real-time PCR. Functional assessment of CC was performed in an acetylcholine endothelium-dependent relaxation pharmacological study. Main Outcome Measure: miRNA expression in CC and blood were evaluated; pharmacological study in CC strips was conducted to validate EnD. Results: We found that 3 miRNAs (miR-16, miR-221, and miR-222) were downregulated in the CC in the D+A group, while all 5 miRNAs were downregulated in the blood of D and D + A groups. The endothelium-dependent relaxation induced by acetylcholine was significantly decreased in groups A, D, and D + A. Diagnostic accuracy estimated by AUC, to discriminating groups A, D, andD+ A fromcontrols, was superior to>0.9 in all plasmaticmiRNAs. Conclusion: miRNAs downregulation was identified in both CC and blood notably in DM associated with alcohol consumption animals (D + A), the greatest endothelial injury potential group. Serum miRNAs have also demonstrated high diagnostic accuracy properties in predicting CC relaxation dysfunction labeling EnD. Copyright (c) 2021 The Authors. Published by Elsevier Inc. on behalf of International Society for Sexual Medicine. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/bync-nd/4.0/).
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页数:10
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