Department of Pharmacological Research, Institute of Bio-active Science, Nippon Zoki Pharmaceutical Co., Ltd., 442-1, Kinashi, Kato, Hyogo, 673-1461, Japan.
Department of Pharmacological Research, Institute of Bio-active Science, Nippon Zoki Pharmaceutical Co., Ltd., 442-1, Kinashi, Kato, Hyogo, 673-1461, Japan.
J Pharmacol Sci. 2024 Sep;156(1):30-37. doi: 10.1016/j.jphs.2024.07.001. Epub 2024 Jul 2.
We aimed to examine the efficacy of combination therapies of Neurotropin® with tramadol and Neurotropin with mirogabalin for neuropathic pain management. A neuropathic pain model (L5 spinal nerve ligation model: L5-SNL) using male Wistar rats was generated through tight ligation of the left fifth lumbar nerve using silk sutures. Mechanical allodynia was assessed using the 50% paw withdrawal threshold. The combined antiallodynic effects were evaluated using isobolographic analyses. Small intestinal transit was evaluated using the charcoal meal test, and motor coordination using the rota-rod test. Neurotropin (50-200 NU/kg, p.o.), tramadol (7.5-60 mg/kg, p.o.), and mirogabalin (3-30 mg/kg, p.o.) showed a dose-dependent antiallodynic effect in L5-SNL rats. The combined antiallodynic effects of Neurotropin and tramadol were additive or synergistic, whereas those of Neurotropin and mirogabalin were additive. Neurotropin (100-400 NU/kg, p.o.) did not affect the small intestinal transit, whereas tramadol (30-100 mg/kg, p.o.) significantly inhibited it. Neurotropin (100-400 NU/kg, p.o.) did not affect the walking time, whereas mirogabalin (10-100 mg/kg, p.o.) significantly decreased it. Neurotropin dose-dependently ameliorated mechanical allodynia in rats, and combination therapy with Neurotropin-tramadol or Neurotropin-mirogabalin may alleviate neuropathic pain without aggravating the adverse effects of tramadol and mirogabalin.
我们旨在研究Neurotropin®与曲马多联合疗法和 Neurotropin 与米罗加巴林联合疗法治疗神经性疼痛的疗效。通过丝线紧密结扎左侧第五腰椎神经,在雄性 Wistar 大鼠中产生神经性疼痛模型(L5 脊神经结扎模型:L5-SNL)。使用 50%足底撤回阈值评估机械性痛觉过敏。使用等对数分析评估联合抗痛觉过敏作用。使用木炭餐试验评估小肠转运,使用转棒试验评估运动协调。Neurotropin(50-200NU/kg,po)、曲马多(7.5-60mg/kg,po)和米罗加巴林(3-30mg/kg,po)在 L5-SNL 大鼠中表现出剂量依赖性抗痛觉过敏作用。Neurotropin 和曲马多的联合抗痛觉过敏作用是相加或协同的,而 Neurotropin 和米罗加巴林的联合抗痛觉过敏作用是相加的。Neurotropin(100-400NU/kg,po)不影响小肠转运,而曲马多(30-100mg/kg,po)显著抑制小肠转运。Neurotropin(100-400NU/kg,po)不影响行走时间,而米罗加巴林(10-100mg/kg,po)显著降低行走时间。Neurotropin 剂量依赖性地改善大鼠的机械性痛觉过敏,Neurotropin-曲马多或 Neurotropin-米罗加巴林联合治疗可能缓解神经性疼痛,而不会加重曲马多和米罗加巴林的不良反应。