Sun Zhonglei, Liu Yingfu, Kong Xianbin, Wang Renjie, Xu Yunqiang, Shang Chongzhi, Huo Jingrui, Huang Mengqiang, Zhao Fei, Bian Kefeng, Zhang Sai, Tu Yue, Chen Xuyi
Tianjin Key Laboratory of Neurotrauma Repair, Institute of Traumatic Brain Injury and Neuroscience, Center for Neurology and Neurosurgery, Affiliated Hospital of the Logistics University of the Chinese People's Armed Police Force, Tianjin, China.
Jinzhou Medical University, Jinzhou, China.
Cell Physiol Biochem. 2018;47(2):617-629. doi: 10.1159/000490017. Epub 2018 May 22.
BACKGROUND/AIMS: Current therapies for spinal cord injury (SCI) have limited efficacy, and identifying a therapeutic target is a pressing need. Sarcoplasmic/endoplasmic reticulum Ca2+ ATPase 2 (SERCA2) plays an important role in regulating calcium homeostasis, which has been shown to inhibit apoptosis. Exendin-4 has been shown to inhibit the apoptosis of nerve cells in SCI, which can also improve SERCA2 expression. In this study, we sought to determine whether exendin-4 plays a protective role in a rat model of SCI via SERCA2.
To investigate the effects of exendin-4 on SCI, a rat model of SCI was induced by a modified version of Allen's method. Spinal cord tissue sections from rats and western blot analysis were used to examine SERCA2 expression after treatment with the long-acting glucagon-like peptide 1 receptor exendin-4 or the SERCA2 antagonist 5(6)-carboxyfluorescein diacetate N-succinimidyl ester (CE). Locomotor function was evaluated using the Basso Beattie Bresnahan locomotor rating scale and slanting board test.
Cell apoptosis was increased with CE treatment and decreased with exendin-4 treatment. Upregulation of SERCA2 in female rats with SCI resulted in an improvement of motor function scores and histological changes.
These findings suggest that exendin-4 plays a protective role in a rat model of SCI through SERCA2 via inhibition of apoptosis. Existing drugs targeting SERCA2 may be an effective therapeutic strategy for the treatment of SCI.
背景/目的:目前脊髓损伤(SCI)的治疗方法疗效有限,确定治疗靶点迫在眉睫。肌浆网/内质网Ca2+ATP酶2(SERCA2)在调节钙稳态中起重要作用,已证明其可抑制细胞凋亡。艾塞那肽-4已被证明可抑制SCI中神经细胞的凋亡,还可提高SERCA2表达。在本研究中,我们试图确定艾塞那肽-4是否通过SERCA2在大鼠SCI模型中发挥保护作用。
为研究艾塞那肽-4对SCI的影响,采用改良的艾伦法诱导大鼠SCI模型。用长效胰高血糖素样肽1受体激动剂艾塞那肽-4或SERCA2拮抗剂5(6)-羧基荧光素二乙酸N-琥珀酰亚胺酯(CE)处理后,通过大鼠脊髓组织切片和蛋白质印迹分析检测SERCA2表达。使用Basso Beattie Bresnahan运动评分量表和斜板试验评估运动功能。
CE处理增加细胞凋亡,艾塞那肽-4处理减少细胞凋亡。SCI雌性大鼠中SERCA2的上调导致运动功能评分改善和组织学变化。
这些发现表明,艾塞那肽-4通过SERCA2抑制细胞凋亡,在大鼠SCI模型中发挥保护作用。现有的靶向SERCA2的药物可能是治疗SCI的有效治疗策略。