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Study on the neuroprotective effect of curculigoside on rats with spinal cord injury
- ZHONGGUO YAOFANG Vol. 35, Issue 12, Pages: 1469-1475(2024)
- 作者机构：
1.濮阳医学高等专科学校基础医学部，河南 濮阳 457000
2.郑州大学 第一附属医院神经重症病区，郑州 450052
- 作者简介：
- 基金信息：
DOI：10.6039/j.issn.1001-0408.2024.12.10
CLC： R965Published：30 June 2024，
Received：20 November 2023，
Revised：27 April 2024，
扫 描 看 全 文
刘娜,黄培培,杨静等.仙茅苷对脊髓损伤大鼠的神经保护作用研究 Δ[J].中国药房,2024,35(12):1469-1475.
LIU Na,HUANG Peipei,YANG Jing,et al.Study on the neuroprotective effect of curculigoside on rats with spinal cord injury[J].ZHONGGUO YAOFANG,2024,35(12):1469-1475.
刘娜,黄培培,杨静等.仙茅苷对脊髓损伤大鼠的神经保护作用研究 Δ[J].中国药房,2024,35(12):1469-1475. DOI： 10.6039/j.issn.1001-0408.2024.12.10.
LIU Na,HUANG Peipei,YANG Jing,et al.Study on the neuroprotective effect of curculigoside on rats with spinal cord injury[J].ZHONGGUO YAOFANG,2024,35(12):1469-1475. DOI： 10.6039/j.issn.1001-0408.2024.12.10.
摘要
目的
2
基于人第10号染色体缺失的磷酸酶及张力蛋白同源基因诱导的假定激酶1（PINK1）/E3泛素连接酶Parkin信号通路探讨仙茅苷（CUR）对脊髓损伤（SCI）大鼠的神经保护作用。
方法
2
以雄性SD大鼠为对象，随机选取15只作为假手术组，其余大鼠以脊髓撞击法建立SCI模型并将造模成功的大鼠分为模型组、CUR低剂量组（36 mg/kg CUR，灌胃）、CUR高剂量组（72 mg/kg CUR，灌胃）、CUR高剂量+3-甲基腺嘌呤（3-MA）组（72 mg/kg CUR，灌胃+20 mg/kg自噬抑制剂3-MA，腹腔注射），每组15只。各组大鼠给予相应药液/生理盐水，每天1次，持续28 d。于给药后第14、28天对各组大鼠进行Basso-Beattie-Bresnahan（BBB）评分和Rivlin斜板实验；观察各组大鼠脊髓组织的病理学变化，检测其脊髓组织的细胞凋亡情况、氧化应激因子[丙二醛（MDA）、超氧化物歧化酶（SOD）、谷胱甘肽（GSH）]水平以及脑源性神经营养因子（BDNF）、胶质细胞原纤维酸性蛋白（GFAP）、PINK1、Parkin、p62、微管相关蛋白轻链3（LC3）蛋白的表达水平。
结果
2
与假手术组比较，模型组大鼠脊髓组织可见明显的水肿和出血，并伴有大量炎症细胞浸润，其BBB评分和斜板角度，SOD和GSH水平，BDNF、PINK1、Parkin蛋白的表达水平和LC3Ⅱ/Ⅰ比值均显著降低，脊髓组织的细胞凋亡率、MDA水平和GFAP、p62蛋白的表达水平均显著升高（
P
＜0.05）；与模型组比较，各药物组大鼠脊髓组织水肿、出血、炎症细胞浸润均有所减少，上述各定量指标均显著改善（
P
＜0.05）；3-MA可显著逆转CUR对上述指标的改善作用（
P
＜0.05）。
结论
2
CUR能促进SCI大鼠神经功能和运动功能的恢复，改善其脊髓组织病理损伤并抑制细胞凋亡，上述作用可能与CUR可激活PINK1/Parkin信号通路介导的线粒体自噬有关。
Abstract
OBJECTIVE
2
To investigate the neuroprotective effect of curculigoside （CUR） on rats with spinal cord injury （SCI） based on phosphatase and tensin homologue deleted on chromosome ten gene-induced putative kinase 1 （PINK1）/E3 ubiquitin ligase Parkin signaling pathway.
METHODS
2
Taking male SD rats as subjects， 15 rats were randomly selected as sham operation group； the rest rats were chosen to establish SCI model by spinal cord impact method， and then were divided into model group， CUR low-dose group （36 mg/kg CUR， gavage）， CUR high-dose group （72 mg/kg CUR， gavage） and CUR high-dose+3-methyladenine （3-MA） group （72 mg/kg CUR， gavage+20 mg/kg autophagy inhibitor 3-MA， intraperitoneal injection）， with 15 rats in each group. Rats in each group were given corresponding liquid/normal saline， once a day， for 28 consecutive days. Basso-Beattie-Bresnahan （BBB） score and Rivlin inclined plate experiment were performed on the 14th and 28th day after administration； the pathological changes of spinal cord tissue in rats were observed in each group； the apoptosis of spinal cord tissue， the levels of oxidative stress factors [malondialdehyde （MDA）， superoxide dismutase （SOD）， glutathione （GSH）]， and the protein expressions of brain-derived neurotrophic factor （BDNF）， glial fibrillary acidic protein （GFAP）， PINK1， Parkin， p62 and microtubule-associated protein light chain 3 （LC3） were all determined.
RESULTS
2
Compared with the sham operation group， obvious edema and bleeding in the spinal cord tissue of rats were observed in the model group， accompanied by a large number of inflammatory cell infiltration； BBB score and inclined plate angle， SOD and GSH levels， the protein expressions of BDNF， PINK1 and Parkin， and LC3Ⅱ/Ⅰ ratio were significantly reduced； the apoptosis rate， MDA level， the protein expressions of GFAP and p62 in spinal cord tissue were significantly increased （
P
＜0.05）. Compared with the model group， the edema， bleeding and infiltration of inflammatory cells in the spinal cord tissue of rats were redu
ced in the administration groups， and the above quantitative indicators had been significantly improved （
P
＜0.05）； 3-MA could significantly reverse the improvement effects of the above indexes by CUR （
P
＜0.05）.
CONCLUSIONS
2
CUR can promote the recovery of neurological and motor functions in SCI rats， improve the pathological injury of the spinal cord and inhibit apoptosis， which may be related to mitochondrial autophagy mediated by activating the PINK1/Parkin signaling pathway.
关键词
仙茅苷脊髓损伤神经保护PINK1/Parkin信号通路线粒体自噬
Keywords
spinal cord injuryneuroprotectionPINK1/Parkin signaling pathwaymitochondrial autophagy
references
ZENG H，LIU N，YANG Y Y，et al. Lentivirus-mediated downregulation of α-synuclein reduces neuroinflammation and promotes functional recovery in rats with spinal cord injury[J]. J Neuroinflammation，2019，16（1）：283.
HONG Y R，LEE E H，PARK K S，et al. Ultrasound stimulation improves inflammatory resolution，neuroprotection，and functional recovery after spinal cord injury[J]. Sci Rep，2022，12（1）：3636.
DU Y，CAI X. Therapeutic potential of natural compounds from herbs and nutraceuticals in spinal cord injury：regulation of the mTOR signaling pathway[J]. Biomedecine Pharmacother，2023，163：114905.
李若淳，曾明燕，苏艳丽，等. 仙茅苷对阿尔茨海默病大鼠行为学及海马神经元凋亡的影响[J]. 中国临床药理学杂志，2019，35（7）：654-656，670.
LI R C，ZENG M Y，SU Y L，et al. Effect of curculigoside on the behavior and hippocampal neuronal apoptosis of Alzheimer’s rats[J]. Chin J Clin Pharmacol，2019，35（7）：654-656，670.
LI N，SHU J，YANG X Y，et al. Exosomes derived from M2 microglia cells attenuates neuronal impairment and mitochondrial dysfunction in Alzheimer’s disease through the PINK1/parkin pathway[J]. Front Cell Neurosci，2022，16：874102.
MAO Y Q，DU J Q，CHEN X H，et al. Maltol promotes mitophagy and inhibits oxidative stress via the Nrf2/PINK1/parkin pathway after spinal cord injury[J]. Oxid Med Cell Longev，2022，2022：1337630.
IKEFUAMA E C，KENDZIORSKI G E，ANDERSON K，et al. Improved locomotor recovery in a rat model of spinal cord injury by bioluminescent-optogenetic（BL-OG）stimulation with an enhanced luminopsin[J]. Int J Mol Sci，2022，23（21）：12994.
张驰昊，郑迪，张成，等. 虾青素通过上调PINK1/parkin通路增强线粒体自噬并减轻大鼠对比剂急性肾损伤[J]. 中国病理生理杂志，2022，38（8）：1430-1439.
ZHANG C H，ZHENG D，ZHANG C，et al. Astaxanthin enhances mitophagy through PINK1/parkin pathway to attenuate contrast-induced acute kidney injury in rats[J]. Chin J Pathophysiol，2022，38（8）：1430-1439.
YANG S J，SONG Z J，WANG X C，et al. Curculigoside facilitates fear extinction and prevents depression-like behaviors in a mouse learned helplessness model through increasing hippocampal BDNF[J]. Acta Pharmacol Sin，2019，40（10）：1269-1278.
ABDANIPOUR A，NIKFAR A，NIKBAKHT RAD M，et al. Neuroprotective effect of L-deprenyl on the expression level of the Mst1 gene and inhibition of apoptosis in rat-model spinal cord injury[J]. Iran J Basic Med Sci，2022，25（1）：53-59.
LI X，ZHAN J H，HOU Y，et al. Coenzyme Q10 regulation of apoptosis and oxidative stress in H2O2 induced BMSC death by modulating the Nrf-2/NQO-1 signaling pathway and its application in a model of spinal cord injury[J]. Oxid Med Cell Longev，2019，2019：6493081.
赵曼云，郭蔚虹，张霞. 益母草碱通过调节cAMP/PKA信号通路抑制脊髓损伤大鼠神经细胞凋亡[J]. 中成药，2022，44（7）：2315-2319.
ZHAO M Y，GUO W H，ZHANG X. Leonurine inhibits neuronal apoptosis in rats with spinal cord injury by regulating cAMP/PKA signaling pathway[J]. Chin Tradit Pat Med，2022，44（7）：2315-2319.
LI Z H，WU F R，XU D F，et al. Inhibition of TREM1 reduces inflammation and oxidative stress after spinal cord injury（SCI）associated with HO-1 expressions[J]. Biome-decine Pharmacother，2019，109：2014-2021.
ZHOU K L，CHEN H W，XU H Z，et al. Trehalose augments neuron survival and improves recovery from spinal cord injury via mTOR-independent activation of autophagy[J]. Oxid Med Cell Longev，2021，2021：8898996.
LI R R，CHEN J Z. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy[J]. Oxid Med Cell Longev，2019，2019：9341018.
KANG L，LIU S W，LI J C，et al. The mitochondria-targeted anti-oxidant MitoQ protects against intervertebral disc degeneration by ameliorating mitochondrial dysfunction and redox imbalance[J]. Cell Prolif，2020，53（3）：e12779.
GU C J，LI L W，HUANG Y F，et al. Salidroside ameliorates mitochondria-dependent neuronal apoptosis after spinal cord ischemia-reperfusion injury partially through inhibiting oxidative stress and promoting mitophagy[J]. Oxid Med Cell Longev，2020，2020：3549704.
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