Rook Jerri M, Hasan Wohaib, McCarson Kenneth E
Department of Pharmacology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
Anesthesiology. 2008 Jul;109(1):130-6. doi: 10.1097/ALN.0b013e31817b5ac3.
Studies have shown that topical administration of exogenous opioid drugs impairs wound healing by inhibiting the peripheral release of neuropeptides, thereby inhibiting neurogenic inflammation. This delay is immediate and peaks during the first days of wound closure. This study examined the effects of topical morphine treatment in a cutaneous wound healing model in the rat.
Full-thickness 4-mm-diameter wounds were placed on the periscapular region of rats that subsequently received twice-daily topical applications of IntraSite Gel (Smith+Nephew, Hull, United Kingdom) alone or gel infused with 5 mm morphine sulfate on days 0-3 or 4-10 postwounding or throughout the time course. Wound tissue was taken on days 1, 3, 5, 8, and 18 postwounding and immunostained for myofibroblast and macrophage markers or stained with hematoxylin and eosin.
Delays in wound closure observed during morphine application on days 0-3 postwounding mimicked those seen in wounds treated with morphine throughout the entire healing process. However, no significant delays in closure were seen in wounds treated with morphine beginning on day 4 postwounding. Treatment of wounds with morphine significantly reduced the number of myofibroblasts and macrophages in the closing wound. In addition, morphine application resulted in decreases in skin thickness and an increase in residual scar tissue in healed skin.
These findings demonstrate the time-dependent and persistent nature of the detrimental effects of topical morphine on cutaneous wound healing. The data identify specific limitations that could be ameliorated to optimize topical opioid administration as an analgesic therapeutic strategy in the treatment of painful cutaneous wounds.
研究表明,局部应用外源性阿片类药物会通过抑制神经肽的外周释放来损害伤口愈合,从而抑制神经源性炎症。这种延迟是即时性的,且在伤口闭合的最初几天达到峰值。本研究在大鼠皮肤伤口愈合模型中检测了局部应用吗啡治疗的效果。
在大鼠肩胛区制作直径4毫米的全层伤口,随后在伤口形成后的第0至3天、第4至10天或整个时间过程中,每天两次局部应用单纯的IntraSite凝胶(英国赫尔的施乐辉公司)或注入5毫米硫酸吗啡的凝胶。在伤口形成后的第1、3、5、8和18天采集伤口组织,对肌成纤维细胞和巨噬细胞标志物进行免疫染色,或用苏木精和伊红染色。
在伤口形成后第0至3天应用吗啡期间观察到的伤口闭合延迟与在整个愈合过程中用吗啡治疗的伤口所见延迟相似。然而,在伤口形成后第4天开始用吗啡治疗的伤口中未观察到明显的闭合延迟。用吗啡治疗伤口显著减少了正在闭合的伤口中肌成纤维细胞和巨噬细胞的数量。此外,应用吗啡导致皮肤厚度降低以及愈合皮肤中残余瘢痕组织增加。
这些发现证明了局部应用吗啡对皮肤伤口愈合的有害影响具有时间依赖性和持续性。数据确定了一些特定的局限性,若加以改善,可优化局部应用阿片类药物作为治疗疼痛性皮肤伤口的镇痛治疗策略。