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阿片类药物诱导的痛觉过敏随丙泊酚输注而改变。

Opioid induced hyperalgesia altered with propofol infusion.

作者信息

Kaye Alan D, Chung Keun Sam, Vadivelu Nalini, Cantemir Catalin, Urman Richard D, Manchikanti Laxmaiah

机构信息

Department of Anesthesiology, LSU School of Medicine, New Orleans, LA.

出版信息

Pain Physician. 2014 Mar-Apr;17(2):E225-8.

Abstract

Propofol is a common induction agent that is utilized worldwide in the field of anesthesiology. In recent years, its potential therapeutic role in a variety of patient states has been demonstrated. Controversy exists regarding Propofol mediated analgesic and antihyperalgesic properties. Recent studies have suggested a variety of different mechanisms of action, including modulation of N-Methyl-D- Aspartate receptors and the endocannabinoid system. The N-Methyl-D- Aspartate receptor is part of a larger family of glutamate receptors and is an important mediator of excitatory neurotransmission. In the case presented, the pain experienced by the patient was not well-controlled, in spite of increasing doses of opioids, potentially due to superimposed opioid induced hyperalgesia. In the present case, we demonstrate a cycle of opioid induced hyperalgesia which was successfully affected with a Propofol infusion. Controversial reports exist in animal studies on the analgesic properties of Propofol. Randomized controlled studies in animal models studying the effect of Propofol on pain sensation have shown that Propofol possesses an analgesic effect. This clinical case demonstrates that Propofol could possibly have antihyperalgesic effects on opioid induced hyperalgesia caused by high-doses of chronic opioids and worsened by fentanyl. We postulate that a probable mechanism of complete pain relief after the procedure could be the inhibition of activity of the N-Methyl-D- Aspartate receptor by Propofol because it was the only agent the patient received during the procedure, causing a break of the cycle of opioid induced hyperalgesia. Additional research is required to clarify Propofol mediated or modulated analgesic properties in humans.

摘要

丙泊酚是一种常用的诱导麻醉剂,在全球麻醉学领域广泛应用。近年来,其在多种患者状态下的潜在治疗作用已得到证实。关于丙泊酚介导的镇痛和抗痛觉过敏特性存在争议。近期研究提出了多种不同的作用机制,包括对N-甲基-D-天冬氨酸受体和内源性大麻素系统的调节。N-甲基-D-天冬氨酸受体是谷氨酸受体大家族的一部分,是兴奋性神经传递的重要介质。在本病例中,尽管增加了阿片类药物的剂量,但患者所经历的疼痛仍未得到有效控制,这可能是由于叠加的阿片类药物诱导的痛觉过敏所致。在本病例中,我们展示了一个阿片类药物诱导的痛觉过敏循环,通过输注丙泊酚成功得到改善。动物研究中关于丙泊酚镇痛特性的报道存在争议。在动物模型中研究丙泊酚对痛觉影响的随机对照研究表明,丙泊酚具有镇痛作用。该临床病例表明,丙泊酚可能对高剂量慢性阿片类药物引起并因芬太尼而加重的阿片类药物诱导的痛觉过敏具有抗痛觉过敏作用。我们推测,术后疼痛完全缓解的可能机制是丙泊酚抑制了N-甲基-D-天冬氨酸受体的活性,因为它是患者在手术过程中接受的唯一药物,从而打破了阿片类药物诱导的痛觉过敏循环。需要进一步的研究来阐明丙泊酚在人类中的介导或调节的镇痛特性。

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