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阿米替林和布比卡因在炎症动物模型中对坐骨神经阻滞的对侧效应

Contralateral effect of amitriptyline and bupivacaine for sciatic nerve block in an animal model of inflammation.

作者信息

Estebe J-P, Gentili M E, Le Corre P, Leduc C, Moulinoux J-P, Ecoffey C

机构信息

Service d'Anesthésie Réanimation Chirurgicale 2, Laboratoire Optimisation Biopharmaceutique par modulation des passages transmembranaire and Laboratoire GRETAC, University of Rennes 1, Rennes, France.

出版信息

Br J Anaesth. 2004 Nov;93(5):705-9. doi: 10.1093/bja/aeh264. Epub 2004 Sep 17.

Abstract

BACKGROUND

Using a carrageenan inflammation rat model, we evaluated two experimental approaches to prolong sciatic nerve block on contralateral hyperalgesia. Method. We performed ipsilateral sciatic nerve block on the inflamed hind paw with bupivacaine-loaded microspheres suspended in dexamethasone (bupivacaine 12.5 mg) and with amitriptyline (6.25 and 12.5 mg) as ultralong-acting local anaesthetics. Bupivacaine (1.25 mg) was used as long-acting local anaesthetic and saline was used as a control. The sixth group received amitriptyline 6.25 mg intraperitoneally (n=10 for each group).

RESULTS

The duration of ipsilateral nerve block was 2 h for bupivacaine, 7 h for amitriptyline 6.25 mg, 11 h for amitriptyline 12.5 mg and 21 h for bupivacaine-loaded microspheres in suspension with dexamethasone. Whereas contralateral hyperalgesia was not observed during block produced by bupivacaine-loaded microspheres, contralateral hyperalgesia was observed with sciatic nerve block using amitriptyline.

CONCLUSIONS

Because of the differential effect observed on the contralateral side, the mechanism underlying the prolongation of ipsilateral block with amitriptyline may not result only from a prolonged Na(+) channel blockade but might be explained by a local toxic effect or lack of systemic actions.

摘要

背景

我们使用角叉菜胶炎症大鼠模型,评估了两种延长对侧痛觉过敏时坐骨神经阻滞的实验方法。方法:我们用悬浮于地塞米松中的布比卡因微球(布比卡因12.5毫克)以及阿米替林(6.25毫克和12.5毫克)作为超长时效局部麻醉药,对发炎后爪进行同侧坐骨神经阻滞。布比卡因(1.25毫克)用作长效局部麻醉药,生理盐水用作对照。第六组腹腔注射阿米替林6.25毫克(每组n = 10)。

结果

布比卡因同侧神经阻滞持续时间为2小时,阿米替林6.25毫克为7小时,阿米替林12.5毫克为11小时,悬浮于地塞米松中的布比卡因微球为21小时。在布比卡因微球产生的阻滞过程中未观察到对侧痛觉过敏,而使用阿米替林进行坐骨神经阻滞时观察到了对侧痛觉过敏。

结论

由于在对侧观察到不同的效应,阿米替林延长同侧阻滞的潜在机制可能不仅仅是由于延长了钠通道阻滞,还可能是由局部毒性作用或缺乏全身作用来解释。

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