电针对慢性内脏痛觉过敏大鼠脊髓背角c-fos蛋白表达的影响。

De-bo Qi, Wei-min Li
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引用次数: 17

摘要

目的:针刺对肠易激综合征(IBS)患者慢性内脏痛的抑制作用在临床上得到广泛应用;然而,其治疗作用的确切神经生物学机制还有待进一步探索。本研究的目的是探讨脊髓神经元可能参与电针(EA)缓解肠易激综合征大鼠模型慢性内脏痛觉过敏的作用。方法:对雄性新生大鼠进行结肠机械刺激,建立肠易激综合征模型。通过对大鼠结肠膨胀刺激下腹部退缩反射(AWR)反应的行为测试,判断大鼠结肠的敏感程度。足三里穴(ST36)和上巨虚穴(ST37)双侧EA共4次,每隔一天一次,相似穴的假EA采用无电刺激的插针方式。采用免疫组织化学方法显示原癌基因蛋白c-fos在脊髓背角的表达。结果:发现IBS模型大鼠AWR评分明显升高(p)。结论:脊髓背角神经兴奋性异常高可能是IBS模型大鼠内脏痛觉过敏的重要原因。EA治疗可通过抑制脊髓背角异常神经元兴奋性来缓解IBS大鼠慢性内脏痛觉过敏。
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Effects of electroacupuncture on expression of c-fos protein in the spinal dorsal horn of rats with chronic visceral hyperalgesia.

Objective: Acupuncture is widely used in clinics to suppress chronic visceral pain in patients with irritable bowel syndrome (IBS); however, the exact neurobiological mechanisms for its therapeutic effects need further exploration. The aim of this study was to investigate the possible involvement of spinal neurons in the effects of electroacupuncture (EA) in relieving chronic visceral hyperalgesia in a rat model of IBS.

Methods: Colon mechanical irritation was applied to male neonatal Sprague-Dawley rats to establish the IBS model. Behavioral test of the abdominal withdraw reflex (AWR) response to colorectal distention stimuli was conducted to judge the degree of colorectal sensitivity. EA at acupoints Zusanli (ST36) and Shangjuxu (ST37) was applied bilaterally in a total of four times every other day, while sham-EA at similar acupoints was done by inserting needles without electrical stimulation. Immunohistochemical methods were used to display the expression of proto-oncogene protein c-fos in the spinal dorsal horn.

Results: It was found that AWR scores were significantly increased in the IBS model rats (P<0.01), accompanied with significant increase in the expression of c-fos protein in the superficial laminae (SDH, laminae I and II) and nucleus proprius (NP, laminae III and IV), the neck of the dorsal horn (NECK, laminae V and VI) at lumbosacral (L6-S2) spinal level, and in NECK at thoracolumbar (T13-L2) spinal level, when compared with normal rats (P<0.05). After EA treatment, AWR scores and the expression of c-fos protein in SDH, NP and NECK at similar spinal levels were significantly decreased in the IBS model rats (P<0.05). No such effects on either AWR scores or the expression of c-fos protein were observed in IBS model rats after sham-EA treatment.

Conclusion: The abnormally high neuronal excitability in the spinal dorsal horn may be an important reason underlying the visceral hyperalgesia in IBS model rats. EA treatment can relieve the chronic visceral hyperalgesia in IBS rats by suppressing the abnormal neuronal excitability in the spinal dorsal horn.

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