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Systemic Administration of Monosodium Glutamate Elevates Intramuscular Glutamate Levels and Sensitizes Rat Masseter Muscle Afferent Fibers

机译:味精的全身给药可提高肌内谷氨酸水平并使大鼠咬肌肌肉传入纤维敏感。

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摘要

There is evidence that elevated tissue concentrations of glutamate may contribute to pain and sensitivity in certain musculoskeletal pain conditions. In the present study the food additive monosodium glutamate (MSG) was injected intravenously into rats to determine whether it could significantly elevate interstitial concentrations of glutamate in the masseter muscle and whether MSG administration could excite and/or sensitize slowly conducting masseter afferent fibers through N-methyl-D-aspartate (NMDA) receptor activation. The interstitial concentration of glutamate after systemic injection of isotonic phosphate-buffered saline (control) or MSG (10 and 50 mg/kg) was measured with a glutamate selective biosensor. The pre-injection baseline interstitial concentration of glutamate in the rat masseter muscle was 24±11 μM. Peak interstitial concentration after injection of 50 mg/kg MSG was 63±18 μM and remained elevated above baseline for ~18 minutes In vivo single unit recording experiments were undertaken to assess the effect of MSG (50 mg/kg) on masseter afferent fibers. Injection of MSG evoked a brief discharge in one afferent fiber, and significantly decreased (~25%) the average afferent mechanical threshold (n=10) during the first 5 min after injection of MSG. Intravenous injection of ketamine (1 mg/kg), 5 minutes prior to MSG, prevented the MSG-induced decreases in the mechanical threshold of masseter afferent fibers. The present results indicate that a 2–3 fold elevation in interstitial glutamate levels in the masseter muscle is sufficient to excite and induce afferent mechanical sensitization through NMDA receptor activation. These findings suggest that modest elevations of interstitial glutamate concentration could alter musculoskeletal pain sensitivity in humans.
机译:有证据表明,在某些肌肉骨骼疼痛情况下,谷氨酸的组织浓度升高可能会导致疼痛和敏感性。在本研究中,将食品添加剂谷氨酸一钠(MSG)静脉内注射到大鼠中,以确定它是否可以显着提高咬肌中谷氨酸的间质浓度,以及施用MSG是否可以通过N-兴奋和/或敏化缓慢传导的咬肌传入纤维D-天冬氨酸甲酯(NMDA)受体激活。用谷氨酸选择性生物传感器测量系统注射等渗磷酸盐缓冲盐水(对照)或MSG(10和50 mg / kg)后谷氨酸的间质浓度。大鼠咬肌中谷氨酸盐的注射前基线间质浓度为24±11μM。注射50 mg / kg味精后的最高组织间质浓度为63±18μM,并在高于基线水平的情况下持续升高约18分钟。进行体内单单位记录实验以评估味精(50 mg / kg)对咬肌传入纤维的作用。注射味精会在一根传入纤维中引起短暂放电,并且在味精注射后的前5分钟内会显着降低(〜25%)平均传入机械阈值(n = 10)。 MSG前5分钟静脉注射氯胺酮(1 mg / kg),可防止MSG引起的咬肌传入纤维机械阈值降低。目前的结果表明,咬肌中间质谷氨酸水平升高2-3倍足以激发并通过NMDA受体激活诱导传入的机械敏化。这些发现表明,间质谷氨酸浓度的适度升高可能会改变人的肌肉骨骼疼痛敏感性。

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