Sonja Lj Joksimovic, Nathan Lamborn, Vesna Jevtovic-Todorovic, Slobodan M Todorovic
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引用次数: 0
Abstract
Our previous studies have implicated CaV3.2 isoform of T-type Ca2+ channels (T-channels) in the development of postsurgical pain. We have also previously established that different T-channel antagonists can alleviate in vivo postsurgical pain. Here we investigated the analgesic potential of another T-channel blocker and endogenous antioxidant molecule, α-lipoic acid (ALA), in a postsurgical pain model in rats. Our in vivo results suggest that single and repetitive intraperitoneal injections of ALA after surgery or preemptively, significantly reduced evoked mechanical hyperalgesia following surgical paw incision. Furthermore, repeated preemptive systemic injections of ALA effectively alleviated spontaneous postsurgical pain as determined by dynamic weight-bearing testing. We expect that our preclinical study may lead to further investigation of analgesic properties and mechanisms of analgesic action of ALA in patients undergoing surgery.
我们之前的研究表明,T 型 Ca2+ 通道(T-通道)的 CaV3.2 同工型与手术后疼痛的发生有关。我们也曾证实不同的 T 型通道拮抗剂可以减轻体内手术后疼痛。在此,我们研究了另一种 T 通道阻滞剂和内源性抗氧化分子 α-硫辛酸(ALA)在大鼠手术后疼痛模型中的镇痛潜力。我们的体内研究结果表明,在手术后或先发制人地单次和重复腹腔注射 ALA 能显著减轻手术爪切口后诱发的机械性痛觉减退。此外,根据动态负重测试的结果,反复先发制人地全身注射 ALA 能有效减轻手术后的自发性疼痛。我们希望我们的临床前研究能进一步研究 ALA 对手术患者的镇痛特性和机制。