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普瑞巴林在小鼠神经性疼痛样模型中的抗伤害感受和催眠活性。

Antinociceptive and hypnotic activities of pregabalin in a neuropathic pain-like model in mice.

作者信息

Wang Tian-Xiao, Yin Dou, Guo Wei, Liu Yuan-Yuan, Li Ya-Dong, Qu Wei-Min, Han Wu-Jian, Hong Zong-Yuan, Huang Zhi-Li

机构信息

Department of Pharmacology, School of Basic Medical Sciences, Fudan University, Shanghai, China; Department of Pharmacology, Wannan Medical College, Wuhu, China.

Department of Pharmacology, School of Basic Medical Sciences, Fudan University, Shanghai, China; Department of Pharmacology, College of Pharmaceutical Science, Fudan University, Shanghai, China.

出版信息

Pharmacol Biochem Behav. 2015 Aug;135:31-9. doi: 10.1016/j.pbb.2015.05.007. Epub 2015 May 16.

Abstract

To evaluate the antinociceptive and hypnotic effects of pregabalin, we established a neuropathic pain-like model in mice using partial sciatic nerve ligation (PSNL), and examined thermal hyperalgesia, mechanical allodynia, electroencephalogram, rota-rod testing, and c-Fos expression in the anterior cingulate cortex. Gabapentin was used as a reference drug in the study. Pregabalin administered i.g. at 12.5 and 25mg/kg prolonged the duration of thermal latencies by 1.4- and 1.6-fold and increased the mechanical threshold by 2.2- and 3.1-fold 3h after administration, respectively, but did not affect motor coordination in PSNL mice, compared with vehicle control. Pregabalin (12.5 and 25mg/kg) given at 6:30 increased the amount of non-rapid eye movement sleep in a 4-h period by 1.3- and 1.4-fold, respectively, in PSNL mice. However, pregabalin (25mg/kg) given at 20:30 did not alter the sleep pattern in normal mice. Immunohistochemical study showed that PSNL increased c-Fos expression in the neurons of anterior cingulate cortex by 2.1-fold, which could be reversed by pregabalin. These results indicate that pregabalin is an effective treatment for both neuropathic pain and sleep disturbance in PSNL mice.

摘要

为评估普瑞巴林的抗伤害感受和催眠作用,我们通过部分坐骨神经结扎(PSNL)在小鼠中建立了神经性疼痛样模型,并检测了热痛觉过敏、机械性异常疼痛、脑电图、转棒试验以及前扣带回皮质中的c-Fos表达。加巴喷丁用作该研究的对照药物。与赋形剂对照组相比,腹腔注射12.5和25mg/kg的普瑞巴林分别使给药后3小时的热潜伏期延长了1.4倍和1.6倍,机械阈值提高了2.2倍和3.1倍,但对PSNL小鼠的运动协调性无影响。在6:30给予12.5和25mg/kg的普瑞巴林,可使PSNL小鼠在4小时内非快速眼动睡眠量分别增加1.3倍和1.4倍。然而,在20:30给予25mg/kg的普瑞巴林对正常小鼠的睡眠模式无改变。免疫组织化学研究表明,PSNL使前扣带回皮质神经元中的c-Fos表达增加了2.1倍,而普瑞巴林可使其逆转。这些结果表明,普瑞巴林对PSNL小鼠的神经性疼痛和睡眠障碍均有有效治疗作用。

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