Alebouyeh Mahmoud Reza, Imani Farnad, Rahimzadeh Poupak, Faiz Seyyed Hamid Reza
Department of Anesthesiology and Pain Medicine, Rasoul-Akram Medical Center, Tehran University of Medical Sciences, Tehran, IR Iran.
Department of Anesthesiology, Rasoul-Akram Medical Center, Tehran University of Medical Sciences, Tehran, IR Iran.
Anesth Pain Med. 2011 Jul;1(1):15-9. doi: 10.5812/kowsar.22287523.1511. Epub 2011 Jul 1.
Tricyclic antidepressants (TCAs) are commonly used orally for treating chronic pain states, such as neuropathic pain. TCAs produce analgesia by various mechanisms, including sodium channels, N-methyl-d-aspartate receptors, biogenic amines, opioids, inflammatory mediators, and substance P. Studies have shown that intrathecal tricyclic administration effectively attenuates pain and thermal hyperalgesia in inflammatory and neuropathic pain in rats.
The aim of this study was to evaluate the effect of two tertiary TCAs in sensory and motor block. We also used bupivacaine as a strong local anesthetic for the control group.
In a double-blind randomized controlled trial in an animal lab, intrathecal injection of drugs was performed in 30 Wistar male rats. We divided the subjects into 3 groups: group 1: 90 µL Doxepine (50 mM), group 2: 90 µl amitriptyline (60 mM). and group 3: 90 µL bupivacaine (23 mM). Then sensory, motor, and proprioceptive changes were measured at 1, 2, 3, 4, 6, and 12 hours by one examiner.
In Groups 1 and 2, a total of 3 rats died. After adjusting the concentrations, amitriptyline had a similar potency but a longer duration of spinal blockade of motor, proprioception, and nociception than did bupivacaine (p < 0.05), whereas doxepin had a reasonable but lower efficacy and shorter duration of spinal blockade than did bupivacaine (p < 0.05). The full recovery time for Group 2 was significantly longer.
It seems that tertiary amine drugs such as amitriptyline and doxepin had reasonable potencies of spinal blockade when compared to bupivacaine. However, amitriptyline had a more potent and long-acting spinal anesthetic effect. Amitriptyline may turn out to be a clinically valuable local anesthetic.
三环类抗抑郁药(TCAs)通常口服用于治疗慢性疼痛状态,如神经性疼痛。三环类抗抑郁药通过多种机制产生镇痛作用,包括钠通道、N-甲基-D-天冬氨酸受体、生物胺、阿片类药物、炎症介质和P物质。研究表明,鞘内注射三环类药物可有效减轻大鼠炎症性和神经性疼痛中的疼痛和热痛觉过敏。
本研究旨在评估两种叔胺类三环类抗抑郁药在感觉和运动阻滞方面的效果。我们还使用布比卡因作为对照组的强效局部麻醉剂。
在动物实验室进行的一项双盲随机对照试验中,对30只雄性Wistar大鼠进行鞘内注射药物。我们将受试者分为3组:第1组:90微升多塞平(50毫摩尔),第2组:90微升阿米替林(60毫摩尔),第3组:90微升布比卡因(23毫摩尔)。然后由一名检查者在1、2、3、4、6和12小时测量感觉、运动和本体感觉变化。
在第1组和第2组中,共有3只大鼠死亡。调整浓度后,阿米替林的效力与布比卡因相似,但在运动、本体感觉和伤害感受的脊髓阻滞持续时间比布比卡因更长(p < 0.05),而多塞平的疗效合理但低于布比卡因,脊髓阻滞持续时间比布比卡因短(p < 0.05)。第2组的完全恢复时间明显更长。
与布比卡因相比,阿米替林和多塞平之类的叔胺类药物似乎具有合理的脊髓阻滞效力。然而,阿米替林具有更强效和长效的脊髓麻醉作用。阿米替林可能会成为一种具有临床价值的局部麻醉剂。