Calikoglu Cagatay, Aytekin Hikmet, Akgül Osman, Akgül Mehmet Hüseyin, Gezen Ahmet Ferruh, Akyuz Feyzullah, Cakir Murteza
Department of Neurosurgery, Atatürk University, Faculty of Medicine, Erzurum, Turkey.
Department of Neurosurgery, Private Anadolu Hostpital, Zonguldak, Turkey.
Med Sci Monit. 2015 Mar 18;21:813-20. doi: 10.12659/MSM.893887.
In this study we aimed to explore the effects of pregabalin on a traumatic brain injury model in rats.
This study included 40 adult male Sprague-Dawley rats randomized into 4 groups, each of which contained equal numbers of animals. The control group had no head trauma and thus was not treated. The trauma group had head trauma but was not treated. The pregabalin group had no head trauma but was treated by pregabalin. The trauma + pregabalin group had head trauma treated with pregabalin. The biopsy samples taken from the study animals were histopathologically examined for the presence of edema, inflammation, and neuronal damage.
All animals in the trauma group had edema, inflammation, and neuronal damage. Four subjects in the control group, 6 in the pregabalin group, and 4 in the trauma + pregabalin group had edema; inflammation was present in 1 subject in the control group, 3 subjects in the pregabalin group, and 3 subjects in the trauma + pregabalin group; neuronal damage existed in 1 subject in the control group, 1 subject in the pregabalin group, and 6 subjects in the trauma+pregabalin group. The trauma group had significantly higher edema and neuronal damage scores than the other groups. Similarly, inflammation was significantly more prevalent in the trauma group than the control and trauma+pregabalin groups.
The results of the present study indicated anti-edema, anti-inflammatory, and neuroprotective effects of pregabalin in an experimental head trauma model in rats. Pregabalin may thus be beneficial in humans with acute TBI by relieving concomitant edema and inflammation.
在本研究中,我们旨在探讨普瑞巴林对大鼠创伤性脑损伤模型的影响。
本研究纳入40只成年雄性Sprague-Dawley大鼠,随机分为4组,每组动物数量相等。对照组无头部创伤,因此未接受治疗。创伤组有头部创伤但未接受治疗。普瑞巴林组无头部创伤但接受普瑞巴林治疗。创伤+普瑞巴林组有头部创伤并接受普瑞巴林治疗。对研究动物采集的活检样本进行组织病理学检查,以确定是否存在水肿、炎症和神经元损伤。
创伤组所有动物均出现水肿、炎症和神经元损伤。对照组有4只动物、普瑞巴林组有6只动物、创伤+普瑞巴林组有4只动物出现水肿;对照组有1只动物、普瑞巴林组有3只动物、创伤+普瑞巴林组有3只动物存在炎症;对照组有1只动物、普瑞巴林组有1只动物、创伤+普瑞巴林组有6只动物存在神经元损伤。创伤组的水肿和神经元损伤评分显著高于其他组。同样,创伤组的炎症发生率显著高于对照组和创伤+普瑞巴林组。
本研究结果表明,普瑞巴林在大鼠实验性头部创伤模型中具有抗水肿、抗炎和神经保护作用。因此,普瑞巴林可能通过减轻伴随的水肿和炎症,对急性创伤性脑损伤患者有益。