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大车前苷对大鼠急性脊髓损伤模型的保护作用机制

The protective mechanism of action of plantamajoside on a rat model of acute spinal cord injury.

作者信息

Hu Hua, Jian Xiaofei

机构信息

Department of Orthopedics, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Jiangan, Wuhan, Hubei 430014, P.R. China.

出版信息

Exp Ther Med. 2021 Apr;21(4):378. doi: 10.3892/etm.2021.9809. Epub 2021 Feb 19.

Abstract

Acute spinal cord injury (ASCI) is a severe traumatic disease of the central nervous system, characterized by a high incidence and high morbidity, for which there are no effective drug therapies in the clinic. A rat model of ASCI was established to study the effects of plantamajoside (PMS) treatment on the expression of apoptotic factors, including caspase-3, caspase-9, poly (ADP-ribose) polymerase (PARP), Bax and Bcl-2. The Allen's weight hit rat ASCI model was used for the present study, and the rats were treated with various concentrations of PMS. The behavior of rats was assessed using the Basso-Beattle-Bresnahan locomotor rating scale (BBB), the histopathologic changes of spinal cord tissue were observed by hematoxylin and eosin staining, the survival of neurons was assessed by TUNEL staining and the expression levels of apoptotic proteins such as caspase-3, caspase-9, PARP, Bcl-2 and Bax was measured using western blot assays and RT-qPCR. It was observed that PMS could reverse the decrease in the BBB score after ASCI, improve the morphological characteristics of the spinal cord, reduce the degree apoptosis and affect the expression of caspase-3, caspase-9, PARP, Bax and Bcl-2 in a concentration dependent manner. In conclusion, PMS protected ASCI rats by inhibiting apoptosis; therefore PMS may be a potential candidate for ASCI therapy.

摘要

急性脊髓损伤(ASCI)是一种严重的中枢神经系统创伤性疾病,具有高发病率和高致残率的特点,临床上尚无有效的药物治疗方法。建立ASCI大鼠模型以研究大车前苷(PMS)治疗对凋亡因子表达的影响,这些凋亡因子包括半胱天冬酶-3、半胱天冬酶-9、聚(ADP-核糖)聚合酶(PARP)、Bax和Bcl-2。本研究采用Allen's重量打击大鼠ASCI模型,用不同浓度的PMS对大鼠进行治疗。使用Basso-Beattle-Bresnahan运动评分量表(BBB)评估大鼠的行为,通过苏木精-伊红染色观察脊髓组织的组织病理学变化,通过TUNEL染色评估神经元的存活情况,并使用蛋白质免疫印迹法和逆转录-定量聚合酶链反应(RT-qPCR)检测半胱天冬酶-3、半胱天冬酶-9、PARP、Bcl-2和Bax等凋亡蛋白的表达水平。观察到PMS可以逆转ASCI后BBB评分的下降,改善脊髓的形态特征,降低凋亡程度,并以浓度依赖的方式影响半胱天冬酶-3、半胱天冬酶-9、PARP、Bax和Bcl-2的表达。总之,PMS通过抑制凋亡对ASCI大鼠起到保护作用;因此,PMS可能是ASCI治疗的一个潜在候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47ff/7918247/44ac8c4ecefe/etm-21-04-09809-g00.jpg

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