|
|
Relationship between the expression quantity of miR-21 and the degree of atherosclerosis and the influence of Vinpocetine on miR-21 |
WANG Shan YANG Huayu YAO Lan WANG Yunchao CHEN Haiping MA Qing▲ |
Medical Care Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China |
|
|
Abstract Objective To study the correlation between different degrees of atherosclerosis and the expression quantity of miR-21, and the influence of Vinpocetine application on the expression quantity of miR-21. Methods Forty patients with atherosclerosis hospitalized in Medical Care Center, Beijing Friendship Hospital, Capital Medical University from January 2014 to December 2016 were selected, and they were divided into mild (9 cases), moderate (6 cases) and severe (25 cases) according to the degree of atherosclerosis, and they were also divided into medication group (17 cases) and control group (23 cases) according to the treatment method. The serum RNA of patients was extracted and the levels of serum miR-21 in the patients with different degrees of atherosclerosis were analyzed by real-time quantitative PCR, the changes of miR-21 and haematocrit before and after treatment in the medication group and control group were compared. Results The expression of miR-21 in patients with severe atherosclerosis was higher than that in patients with mild atherosclerosis, the difference was statistically significant (P < 0.05). After treatment, the haematocrit and relative contents of miR-21 in the medication group were lower than those before treatment, the differences were statistically significant (P < 0.05), there was no statistically significant difference of the relative contents of miR-21 after treatment between medication group and control group (P > 0.05). Conclusion The levels of serum miR-21 in patients with atherosclerosis are increased with the increase of atherosclerosis, and the expression of miR-21 is significantly decreased after treatment with Vinpocetine, which indicates that miR-21 has correlation with atherosclerosis.
|
|
|
|
|
[1] 林聪,吴晓球,邓可.动脉粥样硬化的研究进展[J].医学综述,2013,19(6):975-977.
[2] Li S,Fan Q,He S,et al. MicroRNA-21 negatively regulates Treg cells through a TGF-β1/Smad-independent pathway in patients with coronary heart disease [J]. Cell Physiol Biochem,2015,37(3):866-878.
[3] Volny O,Ka?觢i■ková L,Coufalová D,et al. microRNAs in Cerebrovascular Disease[M]// microRNA:Medical Evidence. Springer International Publishing,2015:155-195.
[4] 任骞,张杰.长春西汀药理作用机制研究进展[J].中草药,2013,44(11):1517-1520.
[5] 周云建.急性脑梗死应用长春西汀治疗效果的临床观察[J].中国医院药学杂志,2013,33(19):1608-1610.
[6] 秦合伟,刘萍.中医药抗动脉粥样硬化作用机制的研究进展[J].中西医结合心脑血管病杂志,2013,19(9):1107-l108.
[7] Gray SP,Jandeleit-Dahm KA. The role of NADPH oxidase in vascular disease-hypertension,atherosclerosis & stroke [J]. Curr Pharm Des,2015,21(41):5933-5944.
[8] Weber M,Baker MB,Moore JP,et al. MiR-21 is induced in endothelial cells by shear stress and modulates apoptosis and eNOS activity [J]. Biochem Biophys Res Commun,2010,393(4):643-648.
[9] Xu X,Li H. Integrated microRNAgene analysis of coronary artery disease based on miRNA and gene expression profiles [J]. Mol Med Rep,2016,13(4):3063-3073.
[10] Ma X,Becker Buscaglia LE,Barker JR,et al. MicrRNAs in NF kappaB signaling [J]. J Mol Cell Biol,2011,3(3):159-166.
[11] 韩耀霞.miR-20a对apoE-/-小鼠ABCA1的表达及动脉粥样硬化病变的影响[D].太原:山西医科大学,2015.
[12] 张丽,谢建洪,陈明,等.miR-26a在动脉粥样硬化发生中的作用[J].中华全科医学,2015,13(4):532-534,666.
[13] 梁斌,蒋晓,边云飞,等.MicroRNA在胆固醇逆转运中的调节作用[J].中国动脉硬化杂志,2014,22(2):196-199.
[14] 吴春艳,吴婕翎,王馨,等.miR-31-5p通过靶向抑制胰岛素降解酶发挥促进动脉粥样硬化作用[J].中国动脉硬化杂志,2015,23(11):1100-1106.
[15] 仲威,严金川.miR-145在动脉粥样硬化发展中的作用[J].中国动脉硬化杂志,2015,23(5):522-526.
[16] 郝理,游盛中,马素华,等.miR-143、miR-145及血管紧张素Ⅱ在人冠状动脉粥样硬化斑块中的表达[J].热带医学杂志,2014,14(4):466-469.
[17] 杨长勇,吴剑锋,曾高峰.miR-758调控动脉粥样硬化研究进展[J].现代医药卫生,2016,32(4):530-532.
[18] 孟凡磊,王超,霍晓川,等.miR-146a促进动脉粥样硬化斑块形成调控机制研究[J].解放军医学院学报,2014, 35(8):847-849.
[19] 孟凡磊.miR-146a促进动脉粥样硬化斑块形成调控机制研究[J].辽宁医学院,2015,35(8):847-849.
[20] 王丽莉.MiR-146a对动脉粥样硬化免疫炎症的影响及普罗布考/瑞舒伐他汀的干预作用[D].天津:天津医科大学,2013. |
|
|
|