Literature DB >> 32245321

The Association between Inflammatory Cytokines and miRNAs with Slow Coronary Flow Phenomenon.

Shahla Danaii1, Sadaf Shiri2, Sanam Dolati3, Majid Ahmadi4, Leila Ghahremani-Nasab5, Atefeh Amiri6, Amin Kamrani7, Hossein Samadi Kafil8, Forough Chakari-Khiavi9, Mohammad Hojjat-Farsangi10, Aida Malek Mahdavi11, Amir Mehdizadeh12, Mehdi Yousefi13.   

Abstract

Slow coronary flow (SCF) is a coronary artery disorder. Several inflammatory mediators have been reported to be associated with vascular homeostasis and endothelial dysfunction. The aim of this study was to investigate the association between cytokines and miRNAs in patients with SCF compared to the controls. In this regard, blood samples were acquired from 45 SCF patients and 45 age- and sex-matched healthy control subjects. Serum and peripheral blood mononuclear cells (PBMCs) were separated. Expression levels of miRNAs and cytokines in PBMCs were measured by real-time PCR. As a final point, serum levels of cytokines were quantified by ELISA. Expression levels of miR-1, miR-133, miR-208a, miR-206, miR-17, miR-29, miR-223, miR-326, and miR-155 as considerable indicators of inflammatory function significantly increased in SCF patients while the expression levels of miR-15a, miR-21, miR-25, miR-126, miR-17, miR-16 and miR-18a as considerable indicators of anti-inflammatory function significantly decreased in patients with SCF compared to the control group. Additionally, serum IL-1β, IL-8, and TNF-α concentrations were significantly higher in the SCF group than controls. However, no significant differences were observed in IL-10 production in SCF patients compared to the controls. This study provided the potential role of miRNAs as biomarkers for SCF diagnosis as well as suitable markers for monitoring coronary artery disease (CAD) development in these patients. More investigations are still necessary to unravel the detailed essential mechanisms of circulating miRNA levels in patients with heart failure and SCF.

Entities:  

Keywords:  Cytokines; Inflammation; Slow coronary flow; miRNA

Year:  2020        PMID: 32245321     DOI: 10.18502/ijaai.v19i1.2418

Source DB:  PubMed          Journal:  Iran J Allergy Asthma Immunol        ISSN: 1735-1502            Impact factor:   1.464


  4 in total

1.  Baicalin attenuates LPS-induced alveolar type II epithelial cell A549 injury by attenuation of the FSTL1 signaling pathway via increasing miR-200b-3p expression.

Authors:  Xin-Ya Duan; Yang Sun; Zhu-Feng Zhao; Yao-Qing Shi; Xun-Yan Ma; Li Tao; Ming-Wei Liu
Journal:  Innate Immun       Date:  2021-05-18       Impact factor: 2.680

Review 2.  Endothelial Dysfunction, Inflammation and Coronary Artery Disease: Potential Biomarkers and Promising Therapeutical Approaches.

Authors:  Diana Jhoseline Medina-Leyte; Oscar Zepeda-García; Mayra Domínguez-Pérez; Antonia González-Garrido; Teresa Villarreal-Molina; Leonor Jacobo-Albavera
Journal:  Int J Mol Sci       Date:  2021-04-08       Impact factor: 5.923

3.  Macrophage-derived exosomal miR-4532 promotes endothelial cells injury by targeting SP1 and NF-κB P65 signalling activation.

Authors:  Peng Liu; Shuya Wang; Guangxin Wang; Mingming Zhao; Fengli Du; Kaiyuan Li; Lei Wang; Huihui Wu; Jiamin Chen; Yang Yang; Guohai Su
Journal:  J Cell Mol Med       Date:  2022-09-07       Impact factor: 5.295

4.  LncRNA NEAT1 Promote Inflammatory Responses in Coronary Slow Flow Through Regulating miR-148b-3p/ICAM-1 Axis.

Authors:  Qing Zhu; Cuiting Zhao; Yonghuai Wang; Xinxin Li; Yixue Xue; Chunyan Ma
Journal:  J Inflamm Res       Date:  2021-06-09
  4 in total

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