The analgesic effect of electroacupuncture on acute thermal pain perception-a central neural correlate study with fMRI

被引:33
作者
Shukla, Shivshil [3 ]
Torossian, Artour [4 ]
Duann, Jeng-Ren [5 ]
Leung, Albert [1 ,2 ]
机构
[1] Univ Calif San Diego, Sch Med, Dept Anesthesiol, La Jolla, CA 92037 USA
[2] Vet Adm San Diego Healthcare Syst, La Jolla, CA 92037 USA
[3] Vet Adm San Diego Healthcare Syst, Anesthesia Serv, San Diego, CA 92161 USA
[4] Vanderbilt Univ, Sch Med, Nashville, TN 37232 USA
[5] Univ Calif San Diego, Inst Neural Computat, Swartz Ctr Computat Neurosci, La Jolla, CA 92093 USA
来源
MOLECULAR PAIN | 2011年 / 7卷
关键词
DORSOLATERAL PREFRONTAL CORTEX; PERIPHERAL-NERVE STIMULATION; SPINOTHALAMIC TRACT CELLS; AMYGDALA NEURONS; BRAIN ACTIVATION; ACUPUNCTURE; MODULATION; THRESHOLDS; MODEL; HYPERALGESIA;
D O I
10.1186/1744-8069-7-45
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Electrical acupuncture (EA) has been utilized in acute pain management. However, the neuronal mechanisms that lead to the analgesic effect are still not well defined. The current study assessed the intensity [optimal EA (OI-EA) vs. minimal EA (MI-EA)] effect of non-noxious EA on supraspinal regions related to noxious heat pain (HP) stimulation utilizing an EA treatment protocol for acute pain and functional magnetic resonance imaging (fMRI) with correlation in behavioral changes. Subjects underwent five fMRI scanning paradigms: one with heat pain (HP), two with OI-EA and MI-EA, and two with OI-EA and HP, and MI-EA and HP. Results: While HP resulted in activations (excitatory effect) in supraspinal areas known for pain processing and perception, EA paradigms primarily resulted in deactivations (suppressive effect) in most of these corresponding areas. In addition, OI-EA resulted in a more robust supraspinal sedative effect in comparison to MI-EA. As a result, OI-EA is more effective than MI-EA in suppressing the excitatory effect of HP in supraspinal areas related to both pain processing and perception. Conclusion: Intensities of EA plays an important role in modulating central pain perception.
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页数:11
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