Protective Effect of Compound Tongluo Decoction on Brain Vascular Endothelial Cells after Ischemia‐Reperfusion by Inhibition of Ferroptosis Through Regulating Nrf2/ARE/SLC7A11 Signaling Pathway

Author:

Li Peiyi12,Wang Zhongda3,Zhao Tong1,Cheng Xiaolan1,Zhang Zhennian4,Wang Jingqing4,Wang Sulei4,Huang Ruiou5,Hui Zhen4ORCID

Affiliation:

1. School of Chinese Medicine School of Integrated Chinese and Western Medicine Nanjing University of Chinese Medicine Nanjing 210023 P. R. China

2. The First School of Clinical Medicine Nanjing University of Chinese Medicine Nanjing 210023 P. R. China

3. Affiliated Hospital of Integrated Traditional Chinese and Western Medicine Nanjing University of Chinese Medicine Nanjing 210028 P. R. China

4. Department of Neurology Nanjing Hospital of Chinese Medicine affiliated to Nanjing University of Chinese Medicine Nanjing Jiangsu 210001 P. R. China

5. Department of Infectious Diseases Children's Hospital of Nanjing Medical University Nanjing Jiangsu 210017 P. R. China

Abstract

AbstractCerebral infarction is one of the most common diseases for aged people. Compound Tongluo Decoction (CTLD), a classic traditional Chinese Medicine prescription, has been widely used in the treatment of ischemic cerebral infarction. Transient middle cerebral artery occlusion (tMCAO) rat model is established for the animal experiment and oxygen‐glucose deprivation and reperfusion (OGD/R) human umbilical vein endothelial cells (HUVECs) model are established for the cell experiment. This also use Nrf2‐/‐ rats to detect the role of nuclear factor erythroid 2‐related factor 2 (Nrf2). Longa score, Evans blue staining, brain water content measurement, and histological observation are done. The levels of reactive oxygen species (ROS), malondialdehyde (MDA), superoxide dismutase (SOD), and other ferroptosis‐related components are detected respectively. In the vivo experiment, CTLD relieved ischemia‐reperfusion (IR) injury symptoms and attenuated IR injury in brain tissues of tMCAO rats by relieving peroxidation injury in brain tissues and inhibiting ferroptosis in tMCAO rats. Moreover, CTLD reversed OGD/R‐induced oxidative damage of endothelial cells via suppressing ferroptosis. After knocking out the Nrf2 gene, the protective effect of CTLD is sharply reduced. This study put forward that CTLD can inhibit ferroptosis in I/R‐injured vascular endothelium by regulating Nrf2/ARE/SLC7A11 signaling to improve the relative symptoms of rats after cerebral I/R injury, thus providing a viable treatment option for cerebrovascular disease.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

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