前列腺素E2和透明质酸钠对缓激肽所致大鼠膝关节疼痛的影响。

Nihon Seikeigeka Gakkai zasshi Pub Date : 1995-09-01
I Yamashita, Y Atsuta, S Shimazaki, M Miyatsu
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引用次数: 0

摘要

研究前列腺素E2和透明质酸钠对大鼠膝关节关节内注射缓激肽诱导的反应性肌肉活动的影响。我们建立了一个动物模型来评估膝关节疼痛。在未麻醉和脊髓化的大鼠膝关节注射缓激肽(BK),评估膝关节屈肌反应活动的持续时间。反应持续时间随注射BK剂量(0.025 ~ 2.5 μ g)的增加而延长。前列腺素E2 (PG E2)注射BK后,反应持续时间明显延长(p < 0.01)。相比之下,提前3 ~ 24小时注射透明质酸钠(Na-HA:平均MW 900 kD)可显著抑制BK诱导的反应(p < 0.05 ~ 0.01)。组织学研究显示荧光素标记的Na-HA弥漫性浸润到软组织表面。从这些结果来看,本研究中使用的动物模型对定量评估膝关节疼痛有价值。客观证明了PG E2对关节疼痛的增敏作用和Na-HA对关节疼痛的抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of prostaglandin E2 and sodium hyaluronate on bradykinin induced knee joint pain in rat].

We studied effects of prostaglandin E2 and sodium hyaluronate on the reactive muscle activity induced by intra-articular injection of bradykinin into the knee joint of rat. An animal model was developed to evaluate knee joint pain. In unanesthetized and spinalized rat, bradykinin (BK) was injected into the knee joint and the duration of the reactive activity of the knee flexor was evaluated. The duration of the reaction was elongated dependent on the injected BK dosage (0.025-2.5 micrograms). When prostaglandin E2 (PG E2) was injected with BK, the duration of the reaction increased significantly (p < 0.01). In contrast, sodium hyaluronate (Na-HA: average MW 900 kD) injected into the joint 3-24 hours in advance significantly inhibited the BK induced reaction (p < 0.05-0.01). A histological study demonstrated the fluorescein-labeled Na-HA diffusely infiltrating into the surface of the soft tissue. From these results, the animal model used in the present study was valuable to evaluate quantitatively knee joint pain. Furthermore, the sensitizing effect of PG E2 and the inhibitory effect of Na-HA on joint pain was objectively demonstrated.

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