Jiaji (EX-B2)-Based Electroacupuncture Preconditioning Attenuates Early Ischaemia Reperfusion Injury in the Rat Myocardium. (8th December 2020)

• Record Type: Journal Article
• Authors: Xiao, Ning; Li, Yang; Shao, Ming-lu; Cui, Hua-feng; Zhang, Chang-yun; Kong, Su-ping; Zhang, Xin; Yu, Hui-juan; Tan, Qi-wen
• Other Names: Zhao Jing Academic Editor.
• Is Part Of: Evidence-based complementary and alternative medicine. Volume 2020(2020)
• Publication Date: 2020-12-08
• Subjects: Alternative medicine -- Periodicals; 615.505
• DOI: 10.1155/2020/8854033
• Languages: English
• ISSNs: 1741-427X

Abstract

Abstract : Background . Acupuncture preconditioning was able to reduce the extent of ischaemia reperfusion ( I / R ) injury. Previous studies have shown that electroacupuncture (EA) pretreatment at T4-T5 Jiaji (EX-B2) acupoints had cardioprotective effects against myocardial I / R injury. However, the molecular mechanism remains inconclusive. Methods . Wistar rats were pretreated with electroacupuncture for 7 days at the Neiguan (PC6), T4-T5 Jiaji (EX-B2), Yanglingquan (GB34), and Quchi (LI11) acupoints, which belong to different meridians. Then, we investigated the genome-wide gene expression profiles of rats prestimulated at these acupoints after I / R injury. Results . Our study revealed previously unknown cardioprotective roles of T4-T5 Jiaji (EX-B2) acupoints in the I / R progression. The extent of myocardial injury was significantly decreased in the Jiaji group compared with the I / R group. In addition, our data are among the first to link the EA preconditioning at Neiguan (PC6) acupoints and circadian rhythm in the I / R model. Also, for the first time, we explored the meridian and acupoint specificity involved in EA pretreatment at the heart meridian, in which Yanglingquan and Quchi acupoints were selected as the control group for heart-divergent-meridian and nonheart-meridian acupoints. Conclusions . The present study suggested that EA pretreatment at Jiaji alters genome-wide gene expression and protects the rat myocardium against I / R injury, which are most likely through neurohumoral regulation.