实用医学杂志 ›› 2022, Vol. 38 ›› Issue (15): 1901-1907.doi: 10.3969/j.issn.1006⁃5725.2022.15.010

• 基础研究 • 上一篇    下一篇

血管软化丸抑制血管炎症反应防治动脉粥样硬化的分子机制 

秦合伟 牛雨晴 宋雪梅 王梦楠 孙孟艳    

  1. 河南中医药大学第二附属医院康复科(郑州 450002)

  • 出版日期:2022-08-10 发布日期:2022-08-10
  • 通讯作者: 牛雨晴 E⁃mail:niuyy126@126.com
  • 基金资助:
    国家自然科学基金(编号:81704030);河南省中医药科学研究专项重点课题(编号:20⁃21ZY1023);中原英才计划中原青年拔尖人才项目(编号:豫组通[2021]44 号);河南省科技攻关计划项目(编号:212102310359);河南省中医药拔尖人才培养项目资助(编号:豫卫中医函[2021]15 号)

Molecular mechanism of Xueguan Ruanhua Pill in preventing atherosclerosis through inhibiting vascular inflammation

QIN Hewei,NIU Yuqing,SONG Xuemei,WANG Mengnan,SUN Mengyan.   

  1. The Second Affiliated Hospital of He′nan University of Chinese Medicine,Zhengzhou 450002,China

  • Online:2022-08-10 Published:2022-08-10

摘要:

目的 观察中药复方血管软化丸防治动脉粥样硬化(atherosclerosis,AS)是否通过靶向调 控长链非编码 RNA⁃TGFB2⁃OT1、miR4459 及其下游信号抑制炎症反应产生效果。方法 建立 AS 模型, 采用血管软化丸干预、以 TGFB2⁃OT1 inhibitor 作为阳性对照;干预 8 周后进行生化检测,HE 染色观察主 动脉病理改变,Real⁃time PCR 法和 Western blot 法检测主动脉 TGFB2⁃OT1、miRNA4459、LARP1、SQSTM1 CASP1、IL1B 水平。结果 与模型组相比,血管软化丸组 TC、TG LDL⁃C 水平降低(均 P < 0.05),主动脉 LA 较大、IMT 较薄、PA 较小、LCA 较小(P < 0.05),主动脉 TGFB2⁃OT1 光密度值和荧光强度较低(均 P < 0.05),血清 ICAM⁃1、VCAM⁃1、IL⁃8 MCP⁃1 水平较低(均 P < 0.05),主动脉 TGFB2⁃OT1、miRNA4459 LARP1、SQSTM1 水平较低(均P < 0.05),主动脉TGFB2⁃OT1、CASP1、IL1B蛋白表达水平较低(均P < 0.05)。 结论 血管软化丸防治AS 的分子机制与靶向调控长链非编码RNA⁃TGFB2⁃OT1、miR4459及其下游信号抑 制炎症反应有关。

关键词:

动脉粥样硬化, 长链非编码RNA?TGFB2?OT1, 血管软化丸, 炎症反应

Abstract:

Objective To observe whether the Chinese medicine Xueguan Ruanhua Pill can prevent and treat atherosclerosis(AS)by targeting the regulation of long⁃chain non⁃coding RNA⁃TGFB2⁃OT1,miR4459 and their downstream signals to inhibit inflammatory response. Methods AS model was established;Xueguan Ruanhua Pill was used for intervention,and TGFB2⁃OT1 inhibitor was used as a positive control. After 8 weeks of interven⁃ tion,biochemical detection was performed,HE staining was used to observe the pathological changes of the aorta and real ⁃time PCR and western ⁃blot were used to detect aortic TGFB2⁃ OT1,miRNA4459,LARP1,SQSTM1 CASP1,and IL1B level. Results Compared with the model group,the level of TC,TG and LDL ⁃C in Fufang Xueguan Ruanhua Pill group decreased(all P < 0.05);larger aortic LA,thinner IMT,and smaller PA and LCA were found(all P < 0.05). The optical density and fluorescence intensity of aortic TGFB2⁃OT1 were lower(all P < 0.05),and the level of serum ICAM⁃1,VCAM⁃1,IL⁃8 and MCP⁃1 was lower(all P < 0.05). The level of OT1 miRNA4459,LARP1,and SQSTM1 was reduced(all P < 0.05),and the protein expression level of TGFB2⁃OT1 CASP1,and IL1B in the aorta was lower(all P < 0.05). Conclusion The molecular mechanism of Xueguan Ruanhua Pill in the prevention and treatment of AS is related to the targeted regulation of long ⁃chain non ⁃coding RNA⁃TGFB2⁃OT1,miR4459 and their downstream signals to inhibit the inflammatory response.

Key words:

atherosclerosis, long non?coding RNA?TGFB2?OT1, angiomalacia pills, inflammatory response