甘丙肽-芒果苷联合应用在福尔马林诱导的二级机械性痛觉过敏和痛觉过度中的协同作用是通过激活一氧化氮-环鸟苷酸-三磷酸腺苷敏感性钾通道途径介导的。
Synergistic Interaction of a Gabapentin- Mangiferin Combination in Formalin-Induced Secondary Mechanical Allodynia and Hyperalgesia in Rats Is Mediated by Activation of NO-Cyclic GMP-ATP-Sensitive K Channel Pathway.
机构信息
Departamento de Sistemas Biológicos, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana-Xochimilco, Calzada del Hueso 1100, Colonia Villa Quietud, Mexico, D.F, 04960, Mexico.
出版信息
Drug Dev Res. 2017 Dec;78(8):390-402. doi: 10.1002/ddr.21411. Epub 2017 Sep 20.
Preclinical Research Gabapentin is an anticonvulsant used to treat neuropathic pain. Mangiferin is an antioxidant that has antinociceptive and antiallodynic effects in inflammatory and neuropathic pain models. The purpose of this study was to determine the interaction between mangiferin and gabapentin in the development and maintenance of formalin-induced secondary allodynia and hyperalgesia in rats. Gabapentin, mangiferin, or their fixed-dose ratio combination were administrated peripherally. Isobolographic analyses was used to define the nature of the interaction of antiallodynic and/or antihyperalgesic effects of the two compounds. Theoretical ED values for the combination were 74.31 µg/paw and 95.20 µg/paw for pre- and post-treatment, respectively. These values were higher than the experimental ED values, 29.45 µg/paw and 37.73 µg/paw respectively, indicating a synergistic interaction in formalin-induced secondary allodynia and hyperalgesia. The antiallodynic and antihyperalgesic effect induced by the gabapentin/mangiferin combination was blocked by administration of L-NAME, the soluble guanylyl cyclase inhibitor, ODQ and glibenclamide. These data suggest that the gabapentin- mangiferin combination produces a synergistic interaction at the peripheral level. Moreover, the antiallodynic and hyperalgesic effect induced by the combination is mediated via the activation of an NO-cyclic GMP-ATP-sensitive K channel pathway. Drug Dev Res 78 : 390-402, 2017. © 2017 Wiley Periodicals, Inc.
临床前研究 加巴喷丁是一种抗惊厥药,用于治疗神经性疼痛。芒果苷是一种抗氧化剂,在炎症和神经性疼痛模型中具有镇痛和抗痛觉过敏作用。本研究的目的是确定芒果苷和加巴喷丁在福尔马林诱导的继发性触诱发痛和痛觉过敏发展和维持中的相互作用。加巴喷丁、芒果苷或其固定剂量比例组合经外周给药。使用等对数分析来定义两种化合物的抗痛觉过敏和/或抗痛觉作用的相互作用性质。组合的理论 ED 值分别为预处理和后处理时的 74.31 µg/爪和 95.20 µg/爪。这些值高于实验 ED 值,分别为 29.45 µg/爪和 37.73 µg/爪,表明在福尔马林诱导的继发性触诱发痛和痛觉过敏中存在协同相互作用。加巴喷丁/芒果苷组合诱导的抗触诱发痛和抗痛觉过敏作用被 L-NAME、可溶性鸟苷酸环化酶抑制剂、ODQ 和格列本脲阻断。这些数据表明,加巴喷丁-芒果苷组合在外周水平产生协同相互作用。此外,组合诱导的抗触诱发痛和抗痛觉过敏作用是通过激活 NO-环鸟苷酸-ATP 敏感的 K 通道途径介导的。药物开发研究 78:390-402,2017。© 2017 威利期刊公司