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首页> 外文期刊>Cellular Physiology and Biochemistry >Local Delivery of β-Elemene Improves Locomotor Functional Recovery by Alleviating Endoplasmic Reticulum Stress and Reducing Neuronal Apoptosis in Rats with Spinal Cord Injury
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Local Delivery of β-Elemene Improves Locomotor Functional Recovery by Alleviating Endoplasmic Reticulum Stress and Reducing Neuronal Apoptosis in Rats with Spinal Cord Injury

机译:β-榄香烯的局部递送通过减轻内质网应激和减少脊髓损伤大鼠的神经元凋亡来改善运动功能恢复。

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Background/Aims Spinal cord injury (SCI) is a serious global problem that leads to permanent motor and sensory deficits. This study explores the anti-apoptotic and neuroprotective effects of the natural extract β-elemene in vitro and in a rat model of SCI. Methods CCK-8 assay was used to evaluate cell viability and lactate dehydrogenase assay was used to evaluate cytotoxicity. A model of cell injury was established using cobalt chloride. Apoptosis was evaluated using a fluorescence-activated cell sorting assay of annexin V-FITC and propidium iodide staining. A rat SCI model was created via the modified Allen’s method and Basso, Beattie, and Bresnahan (BBB) scores were used to assess locomotor function. Inflammatory responses were assessed via enzyme-linked immunosorbent assay (ELISA). Apoptotic and surviving neurons in the ventral horn were respectively observed via terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining and Nissl staining. Western blotting was used to measure protein expression. Results β-elemene (20 μg/ml) promoted cell viability by activating phosphorylation of the PI3K-AKT-mTOR pathway. β-elemene reduced CoCl2-induced cellular death and apoptosis by suppressing the expression levels of CHOP, cleaved-caspase 12, 78-kilodalton glucose-regulated protein, cleaved-caspase 3, and the Bax/Bcl-2 ratio. In the rat model of SCI, Nissl and TUNEL staining showed that β-elemene promoted motor neuron survival and reduced neuronal apoptosis in the spinal cord ventral horn. BBB scores showed that β-elemene significantly promoted locomotor behavioral recovery after SCI. In addition, β-elemene reduced the ELISA-detected secretion of interleukin (IL)-6 and IL-1β. Conclusion β-elemene reduces neuronal apoptosis by alleviating endoplasmic reticulum stress in vitro and in vivo. In addition, β-elemene promotes locomotor function recovery and tissue repair in SCI rats. Thus, our study provides a novel encouraging strategy for the potential treatment of β-elemene in SCI patients.
机译:背景/目的脊髓损伤(SCI)是一个严重的全球性问题,会导致永久性的运动和感觉缺陷。这项研究探讨了天然提取物β-榄香烯在体外和SCI大鼠模型中的抗凋亡和神经保护作用。方法采用CCK-8检测细胞活力,乳酸脱氢酶检测细胞毒性。使用氯化钴建立了细胞损伤模型。使用膜联蛋白V-FITC的荧光激活细胞分选测定法和碘化丙啶染色评估凋亡。通过改良的艾伦(Allen)方法创建了大鼠SCI模型,并使用了Basso,Beattie和Bresnahan(BBB)评分来评估运动功能。通过酶联免疫吸附测定(ELISA)评估炎症反应。通过末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)染色和尼氏染色观察腹角的凋亡和存活神经元。蛋白质印迹用于测量蛋白质表达。结果β-榄香烯(20μg/ ml)通过激活PI3K-AKT-mTOR途径的磷酸化来促进细胞活力。 β-榄香烯通过抑制CHOP,裂解半胱天冬酶12、78千达尔顿葡萄糖调节蛋白,裂解半胱天冬酶3和Bax / Bcl-2的表达水平,降低了CoCl2诱导的细胞死亡和细胞凋亡。在SCI大鼠模型中,Nissl和TUNEL染色显示β-榄香烯能促进运动神经元存活并减少脊髓腹角的神经元凋亡。 BBB评分显示,β-榄香烯显着促进脊髓损伤后运动行为的恢复。此外,β-榄香烯减少了ELISA检测到的白介素(IL)-6和IL-1β的分泌。结论β-榄香烯可通过减轻体内外网状内质网应激来减轻神经元凋亡。此外,β-榄香烯促进SCI大鼠运动功能恢复和组织修复。因此,我们的研究为SCI患者中的β-榄香烯的潜在治疗提供了一种新颖的令人鼓舞的策略。

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