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NMDA receptor mediates chronic visceral pain induced by neonatal noxious somatic stimulation

机译:NMDA受体介导新生儿有害体细胞刺激引起的慢性内脏痛

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摘要

NMDA receptors (NMDAR) are important in the development and maintenance of central sensitization. Our objective was to investigate the role of spinal neurons and NMDAR in the maintenance of chronic visceral pain. Neonatal rats were injected with acidic saline adjusted to pH4.0 in the gastrocnemius muscle every other day for 12 days. In adult rats, NR1 and NR2B subunits were examined in the lumbo-sacral (LS) spinal cord. A baseline, visceromotor response (VMR) to graded colorectal distension (CRD) was recorded before and after administration of the NMDA antagonist, CGS-19755. Extracellular recordings were performed from CRD-sensitive LS spinal neurons and pelvic nerve afferents (PNA) before and after CGS-19755. Rats that received pH 4.0 saline injections demonstrated a significant increase in the expression NR2B subunits and VMR response to CRD >20mmHg. CGS-19755 (i.v. or i.t.) had no effect in naïve rats, but significantly decreased the response to CRD in pH4.0 saline injected rats. CGS-19755 had no effect on the spontaneous firing of SL-A, but decreased that of SL-S. Similarly, CGS-19755 attenuates the responses of SL-S neurons to CRD, but had no effect on SL-A neurons or on the response characteristics of PNA fibers. Neonatal noxious somatic stimulation results in chronic visceral hyperalgesia and sensitizes a specific subpopulation of CRD-sensitive spinal neurons. The sensitization of these SL-S spinal neurons is attenuated by the NMDAR antagonist. The results of this study suggest that spinal NMDARs play an important role in the development of hyperalgesia early in life.
机译:NMDA受体(NMDAR)在中枢敏化的发展和维持中很重要。我们的目的是研究脊髓神经元和NMDAR在维持慢性内脏痛中的作用。每隔一天在新生大鼠中注射腓肠肌的酸性盐水至pH4.0,持续12天。在成年大鼠中,在腰-(LS)脊髓中检查了NR1和NR2B亚基。在施用NMDA拮抗剂CGS-19755之前和之后,记录了对分级的大肠扩张(CRD)的基线内脏运动反应(VMR)。在CGS-19755之前和之后,从CRD敏感的LS脊髓神经元和骨盆神经传入(PNA)进行细胞外记录。接受pH 4.0生理盐水注射的大鼠表现出NR2B亚基的表达和VMR对CRD> 20mmHg的应答显着增加。 CGS-19755(静脉内或静脉内注射)对幼稚大鼠没有影响,但在注射pH4.0盐水的大鼠中对CRD的反应明显降低。 CGS-19755对SL-A的自发射击没有影响,但降低了SL-S的自发射击。同样,CGS-19755减弱了SL-S神经元对CRD的反应,但对SL-A神经元或PNA纤维的反应特性没有影响。新生儿有害的体细胞刺激导致慢性内脏痛觉过敏,并使CRD敏感的脊神经元的特定亚群敏感。这些SL-S脊髓神经元的敏化作用被NMDAR拮抗剂减弱。这项研究的结果表明,脊髓NMDAR在生命早期的痛觉过敏的发展中起着重要作用。

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