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- Title
Manual Acupuncture at ST37 Modulates TRPV1 in Rats with Acute Visceral Hyperalgesia via Phosphatidylinositol 3-Kinase/Akt Pathway.
- Authors
Chen, Caiyi; Yu, Zhi; Lin, Dong; Wang, Xuan; Zhang, Xuejun; Ji, Feng; He, Lingling; Xu, Bin
- Abstract
Acupuncture can significantly ameliorate inflammatory pain in acute visceral hyperalgesia. Hyperalgesia is attenuated by inflammatory mediators that activate transient receptor potential vanilloid 1 (TRPV1), and TRPV1 is regulated by nerve growth factor (NGF)-induced phosphatidylinositol 3-kinase (PI3K)/Akt pathway. However, it is unknown whether NGF-induced PI3K/Akt pathway is associated with manual acupuncture (MA). In this study, the effect and mechanism of MA at Shangjuxu (ST37) and Quchi (LI11) were examined using an acetic acid-induced rat model with visceral hyperalgesia. We demonstrated that MA at ST37 significantly decreased abdominal withdrawal reflex (AWR) scores, proinflammatory cytokine expression (TNF-α, IL-1β, and IL-6), and TRPV1 protein and mRNA expression in rats with acute visceral hyperalgesia compared with the untreated controls, while MA at LI11 showed no effect. The effects of MA at ST37 were reversed after treatment with the PI3K agonist IGF-1 30 min before MA. In rats with visceral hyperalgesia, the upregulation of NGF, tropomyosin-receptor-kinase A (TrkA), PI3K, and phosphorylation-Akt (p-Akt) was decreased by MA at ST37, indicating that TRPV1 regulation via the NGF-induced PI3K/Akt pathway plays a vital role in the effects of MA-mediated amelioration of acute visceral hyperalgesia.
- Subjects
ABDOMINAL physiology; BIOLOGICAL models; CYTOKINES; NERVE growth factor; MUSCLE proteins; PHOSPHOTRANSFERASES; ANIMAL experimentation; HUMAN body; METABOLISM; REFLEXES; CELL receptors; RATS; GENE expression; ACETIC acid; ACUPUNCTURE points; MESSENGER RNA; PHOSPHOLIPIDS; INFLAMMATORY mediators; HYPERALGESIA; CARRIER proteins; PHOSPHORYLATION; CHEMICAL inhibitors
- Publication
Evidence-based Complementary & Alternative Medicine (eCAM), 2021, p1
- ISSN
1741-427X
- Publication type
Article
- DOI
10.1155/2021/5561999