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. 2014 Sep;232(9):2721-9.
doi: 10.1007/s00221-014-3965-2. Epub 2014 Apr 26.

Depressing effect of electroacupuncture on the spinal non-painful sensory input of the rat

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Depressing effect of electroacupuncture on the spinal non-painful sensory input of the rat

Salvador Quiroz-González et al. Exp Brain Res. 2014 Sep.

Abstract

The aim of this study was to explore the effect of electroacupuncture (EA) applied in the Zusanli (ST36) and Sanyinjiao (SP6) points on the N1 component of the cord dorsum potential (CDP) evoked by electrical stimulation of the sural nerve (SU) in the rat. The experiments were performed in 44 Wistar rats (250-300 g) anesthetized with ketamine (100 mg/kg) and xylazine (2 mg/kg). A bilateral laminectomy was performed to expose the L3 to S2 segments of the spinal cord. The SU nerve was exposed and placed on pairs of hook electrodes for electrical stimulation. The N1-CDPs were recorded with three silver-ball electrodes located on the dorsal surface of the L5 to S1 segments. Ipsilateral high and low EA stimulation (100, 2 Hz, 6 mA, 30 min) induced a considerable reduction in the amplitude (45 ± 5.6, 41 ± 6.2%) of the N1-CDP recorded at the L6 segmental level. Recovery of the N1-CDP amplitude occurred approximately 1-3 s after EA. Sectioning of the saphenous and superficial peroneal nerves reduced the depressing effect provoked by the EA stimulation (18.7 ± 1.3, 27 ± 3.8%). Similarly, sectioning of the posterior and anterior tibial, deep peroneal and gastrocnemius nerves partially reduced the effect provoked by EA (11 ± 1.5, 9.8 ± 1.1, 12.6 ± 1.9%). Intravenous picrotoxin (1 mg/kg) also reduced the action of low and high EA (23 ± 4.8, 27 ± 5.2%). It is suggested that EA stimulation depresses non-painful sensory pathways through the activation of specific inhibitory pathways that receive modulatory actions from other sensory and muscle afferent inputs in the rat spinal cord.

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References

    1. Neuroscience. 2008 Aug 13;155(2):463-8 - PubMed
    1. Brain Res Bull. 2011 Apr 25;85(1-2):68-74 - PubMed
    1. J Neurophysiol. 1998 May;79(5):2581-92 - PubMed
    1. Brain Res. 1992 Jan 8;569(1):123-35 - PubMed
    1. Curr Opin Neurol. 1994 Oct;7(5):407-14 - PubMed

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