Ahrens J, Leffler A
Klinik für Anästhesiologie und Intensivmedizin, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, 30625, Hannover, Deutschland.
Anaesthesist. 2014 May;63(5):376-86. doi: 10.1007/s00101-014-2302-2.
Local anesthetics (LA) are broadly used in all disciplines and it could be considered that relatively little is reflected on the mechanisms of action of this old substance group. However, several molecular mechanisms of LAs mediating wanted and unwanted effects remain to be explored. Furthermore, the number of indications for application of LAs seems to be expanding. The local anesthetic effect of LAs is primarily mediated by a potent inhibition of voltage-gated sodium channels. However, this effect is due to much more than the interaction of LAs with one single molecule. Most recent studies indicated that the development of selective local anesthetics might be possible and LAs also interact with several other membrane molecules. Although the relevance of these effects is still unclear, they might play a role in systemic analgesia, tissue protection and anti-inflammatory effects of LA. The therapeutic index of systemically applied LA is very narrow. Systemic application is formally not permitted because the impending systemic toxicity is still a life-threatening complication. Although the cardiac and central nervous toxicity at least partly result from an unselective block of neuronal and cardiac sodium channels, preclinical studies suggest the involvement of several mechanisms. A local LA toxicity is less clinically impressive; however, all LAs induce a significant tissue toxicity for which the underlying mechanisms have been partly identified. This review reports on recent findings on mechanisms and on the clinical relevance of some LA-induced effects which are of relevance for anesthesiological activities.
局部麻醉药(LA)广泛应用于各个学科,人们可能认为对这类古老药物的作用机制的研究相对较少。然而,局部麻醉药介导预期和非预期效应的几种分子机制仍有待探索。此外,局部麻醉药的应用适应证数量似乎正在增加。局部麻醉药的局部麻醉作用主要通过对电压门控钠通道的强力抑制来介导。然而,这种作用不仅仅是局部麻醉药与单个分子相互作用的结果。最近的研究表明,开发选择性局部麻醉药或许是可行的,并且局部麻醉药还与其他几种膜分子相互作用。尽管这些作用的相关性仍不明确,但它们可能在局部麻醉药的全身镇痛、组织保护和抗炎作用中发挥作用。全身应用局部麻醉药的治疗指数非常窄。由于潜在的全身毒性仍然是一种危及生命的并发症,所以正式不允许全身应用。尽管心脏和中枢神经毒性至少部分是由对神经元和心脏钠通道的非选择性阻断引起的,但临床前研究表明涉及多种机制。局部局部麻醉药毒性在临床上的影响较小;然而,所有局部麻醉药都会引起显著的组织毒性,其潜在机制已部分明确。本综述报道了一些与麻醉学活动相关的局部麻醉药诱导效应的机制和临床相关性的最新研究结果。