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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Antiallodynic and antihyperalgesic activity of 3-[4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-dihydrofuran-2-one compared to pregabalin in chemotherapy-induced neuropathic pain in mice
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Antiallodynic and antihyperalgesic activity of 3-[4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-dihydrofuran-2-one compared to pregabalin in chemotherapy-induced neuropathic pain in mice

机译:与普瑞巴林相比,3- [4-(3-三氟甲基-苯基)-哌嗪-1-基]-二氢呋喃-2-酮的抗痛觉过敏和抗痛觉过敏活性对化疗所致的小鼠神经性疼痛

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Background: Anticancer drugs - oxaliplatin (OXPT) and paclitaxel (PACLI) cause painful peripheral neuropathy activating Transient Receptor Potential (TRP) channels. Here we investigated the influence of 3-[4-(3-trifluoromethyl-phenyl)-piperazin-l-yl]-dihydrofuran-2-one (LPP1) and pregabalin on nociceptive thresholds in neuropathic pain models elicited by these drugs. Pharmacokinetics of LPP1 and its ability to attenuate neurogenic pain caused by TRP agonists: capsaicin and allyl isothiocyanate (AITC) were also investigated. Methods: Antiallodynic and antihyperalgesic effects of intraperitoneally administered LPP1 and pregabalin were tested in the von Frey, hot plate and cold water tests. The influence of LPP1 on locomotor activity and motor coordination was assessed using actimeters and rotarod. Serum and tissue concentrations of LPP1 were measured using the HPLC method with fluorimetric detection.
机译:背景:抗癌药-奥沙利铂(OXPT)和紫杉醇(PACLI)引起痛苦的周围神经病变,激活了瞬态受体电位(TRP)通道。在这里,我们研究了3- [4-(3-三氟甲基-苯基)-哌嗪-1-基]-二氢呋喃-2-酮(LPP1)和普瑞巴林对这些药物引起的神经性疼痛模型中伤害阈值的影响。还研究了LPP1的药代动力学及其减轻TRP激动剂辣椒素和异硫氰酸烯丙酯(AITC)引起的神经源性疼痛的能力。方法:在冯·弗雷,热板和冷水试验中,对腹腔注射LPP1和普瑞巴林的镇痛和抗痛觉过敏作用进行了测试。 LPP1对自发活动和运动协调的影响是使用辐射计和旋转仪评估的。 LPP1的血清和组织浓度使用HPLC方法和荧光检测法进行测量。

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