Barnet Caryn S, Louis David N, Kohane Daniel S
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts; Department of Pathology and Neurosurgical Service, and Pediatric Intensive Care Unit, Massachusetts General Hospital and Harvard Medical School, Boston Massachusetts.
Anesth Analg. 2005 Dec;101(6):1838-1843. doi: 10.1213/01.ANE.0000184129.50312.C1.
Neurotoxicity has been reported with tricyclic antidepressants (TCAs) used as local anesthetics. We examined the hypothesis that TCAs cause tissue injury, particularly myotoxicity, as occurs with many local anesthetics. Animals were given sciatic nerve injections with 0-80 mM doxepin, amitriptyline, or bupivacaine (1.5 mL for histological studies, 0.3 mL for neurobehavioral studies). Four days after injection, the TCAs caused ischemic tissue injury. Subcutaneous tissue showed expansion and hardening, with hemorrhage and adhesion to overlying skin. Muscle was diffusely pale. Histopathology showed coagulative necrosis of muscle and surrounding soft tissues, with thrombus formation in vasculature near affected areas. These findings were much reduced with bupivacaine. TCA-injected and bupivacaine-injected animals also developed characteristic local anesthetic myotoxicity. Amitriptyline proved less potent than bupivacaine as a local anesthetic: the concentrations required to provide 100 min of nerve block were 20 mM and 3 mM, respectively. Some animals receiving large concentrations of amitriptyline developed spontaneous recrudescence of nerve blockade or had irreversible nerve blockade, both of which may reflect nerve injury. Neither finding occurred in animals injected with bupivacaine. TCAs do not appear to offer any advantages over conventional local anesthetics and do appear to risk substantially increased toxicity.
有报道称,用作局部麻醉剂的三环类抗抑郁药(TCA)具有神经毒性。我们检验了一种假设,即TCA会像许多局部麻醉剂那样导致组织损伤,尤其是肌毒性。给动物的坐骨神经注射0 - 80 mM的多塞平、阿米替林或布比卡因(组织学研究用1.5 mL,神经行为学研究用0.3 mL)。注射后四天,TCA导致了缺血性组织损伤。皮下组织出现肿胀和硬化,伴有出血以及与上方皮肤粘连。肌肉弥漫性苍白。组织病理学显示肌肉和周围软组织发生凝固性坏死,在受影响区域附近的血管中形成血栓。布比卡因导致的这些表现要轻得多。注射TCA和布比卡因的动物也出现了典型的局部麻醉剂肌毒性。作为局部麻醉剂,阿米替林的效力被证明低于布比卡因:提供100分钟神经阻滞所需的浓度分别为20 mM和3 mM。一些接受高浓度阿米替林注射的动物出现了神经阻滞的自发复发或不可逆的神经阻滞,这两者都可能反映神经损伤。注射布比卡因的动物未出现这两种情况。与传统局部麻醉剂相比,TCA似乎没有任何优势,而且其毒性风险似乎大幅增加。