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首页> 外文期刊>Experimental Brain Research >Glutamate and capsaicin-induced pain, hyperalgesia and modulatory interactions in human tendon tissue.
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Glutamate and capsaicin-induced pain, hyperalgesia and modulatory interactions in human tendon tissue.

机译:谷氨酸和辣椒素引起的人肌腱组织中的疼痛,痛觉过敏和调节性相互作用。

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摘要

Experimental glutamate and capsaicin-induced pain has not been described in tendon tissue despite the implications of addressing these receptors in pain management strategies. This study investigated pain induction and modulatory interactions by injecting glutamate (0.5 ml, 1 M) and capsaicin (0.5 ml, 5 microg, 33 microM) to human tendon tissue. Following the initial glutamate or capsaicin injection, a second injection of either glutamate (following capsaicin), capsaicin (following glutamate) or hypertonic saline (after both glutamate and capsaicin) was given. Twelve male volunteers participated. Subjects had four sequences of injections to tibialis anterior tendon over two sessions 1 week apart. Pain intensity responses were scored on a visual analogue scale (VAS). Pressure pain thresholds (PPTs) were assessed before, during and after pain induction. Capsaicin caused significantly higher peak pain scores compared to glutamate (P < 0.003) whilst glutamate pain was of significantly longer duration (P < 0.0003). Capsaicin following glutamate resulted in significantly higher average VAS scores 180-450 s after injection compared to capsaicin as primary injection (P < 0.05). PPTs were significantly reduced during capsaicin pain (72 +/- 5 and 80 +/- 6% of pre-pain values at the injection site and 2 cm proximal, P < 0.002). Following capsaicin, hypertonic saline and glutamate showed significant reductions in PPT at the same sites and to a similar degree compared to baseline (P < 0.002). The results indicate in tendon tissue a facilitation of response to capsaicin injection following glutamate injection. PPTs were only reliably reduced by capsaicin injection. These results emphasize the possible importance of peripheral glutamate receptor antagonists in pain management in musculoskeletal conditions.
机译:尽管在疼痛管理策略中涉及解决这些受体的意义,但尚未在肌腱组织中描述实验性谷氨酸和辣椒素诱导的疼痛。这项研究通过向人的肌腱组织注射谷氨酸(0.5 ml,1 M)和辣椒素(0.5 ml,5 microg,33 microM)来研究疼痛诱导和调节性相互作用。初次注射谷氨酸盐或辣椒素后,再次注射谷氨酸盐(在辣椒素之后),辣椒素(谷氨酸之后)或高渗盐水(在谷氨酸盐和辣椒素之后)。十二名男性志愿者参加了。受试者在相隔1周的两个疗程中进行了四次胫骨前肌腱注射序列。用视觉模拟量表(VAS)对疼痛强度反应进行评分。在疼痛诱发之前,期间和之后评估压力痛阈值(PPT)。与谷氨酸相比,辣椒素引起的峰值疼痛评分明显更高(P <0.003),而谷氨酸疼痛的持续时间明显更长(P <0.0003)。与初次注射辣椒素相比,谷氨酸注射后的辣椒素导致180-450 s的平均VAS评分明显更高(P <0.05)。辣椒素疼痛期间PPT显着降低(注射部位和近端2 cm处疼痛前值的72 +/- 5和80 +/- 6%,P <0.002)。辣椒素后,与基线相比,高渗盐水和谷氨酸在相同部位以相似程度显着降低了PPT(P <0.002)。结果表明在肌腱组织中谷氨酸盐注射后对辣椒素注射的反应的促进。只有通过辣椒素注射才能可靠地降低PPT。这些结果强调了外周谷氨酸受体拮抗剂在肌肉骨骼疾病的疼痛管理中的重要性。

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