Güneş Yasemin, Mert Tufan, Dağlioğlu Y Kenan, Ozbek Hayri, Günay Ismail, Ozcengiz Dilek, Işik Geylan
Cukurova University Faculty of Medicine, Department of Anesthesiology, Adana, Turkey.
Agri. 2005 Jan;17(1):33-8.
Abnormal impulses in peripheral nerves play a critical role in neuropathic pain syndromes. The voltage-gated Na+ channels that underlie the action potential are main targets for clinically useful drugs in the pain therapy. Systemic tramadol has been shown to have clinical efficacy against some forms of neuropathic pain. Therefore, we investigated the mechanisms of action of tramadol by an in vitro model by sucrose-gap technique. Tramadol produced concentration-dependent and frequency-dependent decrements in CAP amplitude. Also, injured nerves were more sensitive to tramadol. Tramadol decreased the amplitude of the delayed depolarization and the hyperpolarizing afterpotentials. In conclusion, blocking potencies of small concentration tramadol on the delayed depolarization and hyperpolarizing afterpotential in regeneration period may be contributed for understanding of the action mechanisms of tramadol on neuropathic pain therapy.
外周神经中的异常冲动在神经性疼痛综合征中起关键作用。构成动作电位基础的电压门控钠通道是疼痛治疗中临床常用药物的主要靶点。已证明全身性曲马多对某些形式的神经性疼痛具有临床疗效。因此,我们通过蔗糖间隙技术的体外模型研究了曲马多的作用机制。曲马多使复合动作电位(CAP)幅度产生浓度依赖性和频率依赖性降低。此外,受损神经对曲马多更敏感。曲马多降低了延迟去极化的幅度和超极化后电位。总之,小浓度曲马多对再生期延迟去极化和超极化后电位的阻断作用可能有助于理解曲马多在神经性疼痛治疗中的作用机制。