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Anti-spastic effect induced by waggle needling correlates with KCC2-GABAA pathway in post-stroke spasticity rats.

Abstract
Although clinical efficacy of waggle needling has been confirmed, therapeutic mechanisms still remain poorly understood. Reduction of GABA was involved in the etiology of spasticity. Recently, accumulated evidences suggest that the inhibitory effect of GABA is determined by low intracellular chloride concentration, which is predominantly mediated by KCC2. This study was designed to investigate whether KCC2-GABAA pathway was involved in the mechanism underlying acupuncture intervention in rats with middle cerebral artery occlusion (MCAO). Three days after modeling, the rats received waggle needling, routine needling and placebo needling for 7 consecutive days. After treatment, the muscle spasticity, motor function and infarct volumes were tested. KCC2 and GABAAγ2 levels were detected via western blotting, RT-PCR and immunofluorescence. KCC2 antagonist and agonist were administered after the last intervention. We found that acupuncture, particularly waggle needling, could remarkably alleviate muscle spasticity, reverse motor deficits and reduce cerebral infraction in MCAO rats, possibly due to its effects on up-regulating expressions of KCC2 and GABAAγ2 in the cortical infarct regions. However, the effects were blocked by KCC2 antagonist. In summary, this study suggests that improvements in muscle spasticity and motor function induced by waggle needling correlates with the activation of KCC2-GABAA pathway.
AuthorsJun-Xiang Wang, Liang-Xiao Ma, Jie-Dan Mu, Tian-Yi Sun, Xu Qian, Wen-Yan Yu, Yuan Tian, Zhou Zhang
JournalNeuroscience letters (Neurosci Lett) Vol. 750 Pg. 135810 (04 17 2021) ISSN: 1872-7972 [Electronic] Ireland
PMID33705929 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2021. Published by Elsevier B.V.
Chemical References
  • Gabbr2 protein, rat
  • Receptors, GABA-B
  • Symporters
Topics
  • Acupuncture Points
  • Acupuncture Therapy (methods)
  • Animals
  • Infarction, Middle Cerebral Artery (rehabilitation, therapy)
  • Male
  • Muscle Spasticity (therapy)
  • Muscle, Skeletal (metabolism, physiopathology)
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA-B (genetics, metabolism)
  • Stroke Rehabilitation (methods)
  • Symporters (genetics, metabolism)
  • Up-Regulation
  • K Cl- Cotransporters

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