Suppr超能文献

延长神经阻滞对大鼠炎性痛觉过敏的影响:预防迟发性痛觉过敏。

Effect of prolonged nerve block on inflammatory hyperalgesia in rats: prevention of late hyperalgesia.

作者信息

Kissin I, Lee S S, Bradley E L

机构信息

Department of Anesthesia, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Anesthesiology. 1998 Jan;88(1):224-32. doi: 10.1097/00000542-199801000-00031.

Abstract

BACKGROUND

Recent evidence suggests that the duration of the nociceptive block may be an important factor in determining the effect of the block on injury-induced hyperalgesia after block resolution. The authors examined whether a tonicaine nerve block lasting for 12 to 16 h could prevent late inflammatory hyperalgesia.

METHODS

Inflammatory hyperalgesia was induced by injection of carrageenan into the rat paw. A threshold of motor response to increasing pressure was determined for the injected paw, contralateral paw, and tail The development of edema of the paw and an increase in paw temperature also were determined. The block was achieved by simultaneous percutaneous injections of tonicaine (a new long-acting anesthetic agent) or lidocaine at the sciatic nerve (greater trochanter level) and the saphenous nerve (midthigh level).

RESULTS

Carrageenan without nerve block caused a profound primary (injected paw) and secondary (contralateral paw and tail) hyperalgesia that lasted for 3-5 days. Tonicaine nerve block administered before carrageenan completely prevented primary and secondary hyperalgesia. Tonicaine block administered 5 h after carrageenan injection reversed secondary hyperalgesia and prevented the development of late (> or = 24 h) primary and secondary hyperalgesia. Edema and temperature of the paw were not significantly affected by the nerve block administered before or after carrageenan.

CONCLUSIONS

A prolonged nerve block (12-16 h) can prevent the development of long-lasting (3-5 days) inflammatory hyperalgesia. Prevention of late hyperalgesia can be provided not only by the preinjury block but also by the postinjury block administered when hyperalgesia is already well established.

摘要

背景

近期证据表明,伤害性阻滞的持续时间可能是决定阻滞后伤害性阻滞对损伤诱导的痛觉过敏影响的重要因素。作者研究了持续12至16小时的丁卡因神经阻滞是否能预防晚期炎症性痛觉过敏。

方法

通过向大鼠爪内注射角叉菜胶诱导炎症性痛觉过敏。测定注射爪、对侧爪和尾巴对逐渐增加压力的运动反应阈值。还测定爪部水肿的发展和爪部温度的升高。通过在坐骨神经(大转子水平)和隐神经(大腿中部水平)同时经皮注射丁卡因(一种新型长效麻醉剂)或利多卡因来实现阻滞。

结果

未进行神经阻滞的角叉菜胶引起了严重的原发性(注射爪)和继发性(对侧爪和尾巴)痛觉过敏,持续3至5天。在角叉菜胶注射前进行丁卡因神经阻滞可完全预防原发性和继发性痛觉过敏。在角叉菜胶注射5小时后进行丁卡因阻滞可逆转继发性痛觉过敏,并预防晚期(≥24小时)原发性和继发性痛觉过敏的发展。角叉菜胶注射前后进行的神经阻滞对爪部水肿和温度没有显著影响。

结论

延长的神经阻滞(12至16小时)可预防持续较长时间(3至5天)的炎症性痛觉过敏的发展。不仅损伤前阻滞可预防晚期痛觉过敏,在痛觉过敏已经充分形成时进行的损伤后阻滞也可预防。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验