Yong Tan, Haijun Yu, Shanquan Sun, Shengwei Gan, Rui Gong, Ke-Jie Mou, Jun Xue, Shiye Xu, Jiangfeng Wu, Lan Ma
{"title":"本木酚通过调节er -线粒体相互作用抑制少突胶质细胞凋亡,对脊髓压缩性损伤后的神经髓鞘具有保护作用。","authors":"Yong Tan, Haijun Yu, Shanquan Sun, Shengwei Gan, Rui Gong, Ke-Jie Mou, Jun Xue, Shiye Xu, Jiangfeng Wu, Lan Ma","doi":"10.1080/10790268.2021.1890878","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the effect of honokiol on demyelination after compressed spinal cord injury (CSCI) and it's possible mechanism.</p><p><strong>Design: </strong>Animal experiment study.</p><p><strong>Setting: </strong>Institute of Neuroscience of Chongqing Medical University.</p><p><strong>Interventions: </strong>Total of 69 Sprague-Dawley (SD) rats were randomly divided into 3 groups: sham group (n=15), honokiol group (n=27) and vehicle group (n=27). After established CSCI model by a custom-made compressor successfully, the rats of sham group were subjected to the limited laminectomy without compression; the rats of honokiol group were subjected to CSCI surgery and intraperitoneal injection of 20 mg/kg honokiol; the rats of vehicle group were subjected to CSCI surgery and intraperitoneal injection of an equivalent volume of saline.<b>Outcome measures:</b> The locomotor function of each group was assessed using the Basso, Beattie and Bresnahan (BBB) rating scale. The pathological changes of myelinated nerve fibers of spinal cord in 3 groups were detected by osmic acid staining and transmission electron microcopy (TME). Immunofluorescence and Western blot were used to research the experessions of active caspase-3, caspase-12, cytochrome C and myelin basic protein (MBP) respectively.</p><p><strong>Results: </strong>In the vehicle group, the rats became paralyzed and spastic after injury, and the myelin sheath became swollen and broken down along with decreased number of myelinated nerve fibers. Western blot analysis manifested that active caspase-3, caspase-12 and cytochrome C began to increase 1 d after injury while the expression of MBP decreased gradually. After intervened with honokiol for 6 days, compared with the vehicle group, the locomotor function and the pathomorphological changes of myelin sheath of the CSCD rats were improved with obviously decreased expression of active caspase-3, caspase-12 and cytochrome C.</p><p><strong>Conclusions: </strong>Honokiol may improve locomotor function and protect neural myelin sheat from demyelination via prevention oligodendrocytes (OLs) apoptosis through mediate endoplasmic reticulum (ER)-mitochondria pathway after CSCI.</p>","PeriodicalId":501560,"journal":{"name":"The Journal of Spinal Cord Medicine","volume":" ","pages":"595-604"},"PeriodicalIF":0.0000,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/10790268.2021.1890878","citationCount":"4","resultStr":"{\"title\":\"Honokiol exerts protective effects on neural myelin sheaths after compressed spinal cord injury by inhibiting oligodendrocyte apoptosis through regulation of ER-mitochondrial interactions.\",\"authors\":\"Yong Tan, Haijun Yu, Shanquan Sun, Shengwei Gan, Rui Gong, Ke-Jie Mou, Jun Xue, Shiye Xu, Jiangfeng Wu, Lan Ma\",\"doi\":\"10.1080/10790268.2021.1890878\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To investigate the effect of honokiol on demyelination after compressed spinal cord injury (CSCI) and it's possible mechanism.</p><p><strong>Design: </strong>Animal experiment study.</p><p><strong>Setting: </strong>Institute of Neuroscience of Chongqing Medical University.</p><p><strong>Interventions: </strong>Total of 69 Sprague-Dawley (SD) rats were randomly divided into 3 groups: sham group (n=15), honokiol group (n=27) and vehicle group (n=27). After established CSCI model by a custom-made compressor successfully, the rats of sham group were subjected to the limited laminectomy without compression; the rats of honokiol group were subjected to CSCI surgery and intraperitoneal injection of 20 mg/kg honokiol; the rats of vehicle group were subjected to CSCI surgery and intraperitoneal injection of an equivalent volume of saline.<b>Outcome measures:</b> The locomotor function of each group was assessed using the Basso, Beattie and Bresnahan (BBB) rating scale. The pathological changes of myelinated nerve fibers of spinal cord in 3 groups were detected by osmic acid staining and transmission electron microcopy (TME). Immunofluorescence and Western blot were used to research the experessions of active caspase-3, caspase-12, cytochrome C and myelin basic protein (MBP) respectively.</p><p><strong>Results: </strong>In the vehicle group, the rats became paralyzed and spastic after injury, and the myelin sheath became swollen and broken down along with decreased number of myelinated nerve fibers. Western blot analysis manifested that active caspase-3, caspase-12 and cytochrome C began to increase 1 d after injury while the expression of MBP decreased gradually. 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引用次数: 4
摘要
目的:探讨厚朴酚对压缩性脊髓损伤(CSCI)后脱髓鞘的影响及其可能的机制。设计:动物实验研究。单位:重庆医科大学神经科学研究所。干预措施:69只SD大鼠随机分为3组:假药组(n=15)、本木酚组(n=27)和载药组(n=27)。假手术组大鼠用特制压气机成功建立CSCI模型后,行无压气机有限椎板切除术;厚朴酚组大鼠行CSCI手术并腹腔注射厚朴酚20 mg/kg;载体组大鼠行CSCI手术,腹腔注射等量生理盐水。结果测量:采用BBB (Basso, Beattie and Bresnahan)评定量表评估各组运动功能。采用锇酸染色和透射电镜(TME)观察3组大鼠脊髓髓鞘神经纤维的病理变化。免疫荧光法和Western blot法分别检测活性caspase-3、caspase-12、细胞色素C和髓鞘碱性蛋白(MBP)的表达。结果:载药组大鼠损伤后出现麻痹、痉挛,髓鞘肿胀破裂,有髓神经纤维数量减少。Western blot分析显示,损伤1 d后活性caspase-3、caspase-12和细胞色素C开始升高,而MBP的表达逐渐下降。与对照药组相比,厚木酚干预CSCD大鼠运动功能和髓鞘病理形态学改变明显改善,活性caspase-3、caspase-12和细胞色素c的表达明显降低。结论:厚木酚可能通过介导内质网(ER)-线粒体通路阻止少突胶质细胞(OLs)凋亡,从而改善CSCD大鼠运动功能,保护髓鞘脱髓鞘。
Honokiol exerts protective effects on neural myelin sheaths after compressed spinal cord injury by inhibiting oligodendrocyte apoptosis through regulation of ER-mitochondrial interactions.
Objective: To investigate the effect of honokiol on demyelination after compressed spinal cord injury (CSCI) and it's possible mechanism.
Design: Animal experiment study.
Setting: Institute of Neuroscience of Chongqing Medical University.
Interventions: Total of 69 Sprague-Dawley (SD) rats were randomly divided into 3 groups: sham group (n=15), honokiol group (n=27) and vehicle group (n=27). After established CSCI model by a custom-made compressor successfully, the rats of sham group were subjected to the limited laminectomy without compression; the rats of honokiol group were subjected to CSCI surgery and intraperitoneal injection of 20 mg/kg honokiol; the rats of vehicle group were subjected to CSCI surgery and intraperitoneal injection of an equivalent volume of saline.Outcome measures: The locomotor function of each group was assessed using the Basso, Beattie and Bresnahan (BBB) rating scale. The pathological changes of myelinated nerve fibers of spinal cord in 3 groups were detected by osmic acid staining and transmission electron microcopy (TME). Immunofluorescence and Western blot were used to research the experessions of active caspase-3, caspase-12, cytochrome C and myelin basic protein (MBP) respectively.
Results: In the vehicle group, the rats became paralyzed and spastic after injury, and the myelin sheath became swollen and broken down along with decreased number of myelinated nerve fibers. Western blot analysis manifested that active caspase-3, caspase-12 and cytochrome C began to increase 1 d after injury while the expression of MBP decreased gradually. After intervened with honokiol for 6 days, compared with the vehicle group, the locomotor function and the pathomorphological changes of myelin sheath of the CSCD rats were improved with obviously decreased expression of active caspase-3, caspase-12 and cytochrome C.
Conclusions: Honokiol may improve locomotor function and protect neural myelin sheat from demyelination via prevention oligodendrocytes (OLs) apoptosis through mediate endoplasmic reticulum (ER)-mitochondria pathway after CSCI.