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三七皂苷R1通过雌激素受体调节ATF6/Akt信号通路减轻OGD/R所导致的神经元损伤

2017-04-05侯倩伶王岩李英博胡雪莲王莎莉

中国中药杂志 2017年6期
关键词:凋亡

侯倩伶+王岩++李英博++胡雪莲+王莎莉

[摘要]三七皂苷R1(notoginsenoside R1,NGR1)是傳统中药三七的重要活性成分,也是雌激素受体激动剂。因其蕴含抗炎、抗氧化、抗凋亡等多种功能,故在疾病治疗中被普遍运用。为阐明NGR1在缺血缺氧性脑病(hypoxicischemic brain damage,HIBD)中的潜在神经保护作用机制,该研究采用原代皮层神经元建立氧糖剥夺再灌注(oxygenglucose deprivation/reoxygenation,OGD/R)损伤模型,并且给予NGR1及雌激素受体阻断剂ICI182780处理,然后分别采用MTT,LDH和Hochest 33342染色检测神经元存活率、细胞膜完整性和凋亡,Western blot检测抗凋亡通路ATF6α,pAkt,Akt蛋白及凋亡相关蛋白Bax,Cleaved Caspase3的表达。结果显示:神经元在OGD/R损伤后,其细胞存活率明显下降(P<005)、细胞膜相对完整性显著降低(P<005)、细胞凋亡加重(P<005),ATF6α,pAkt表达下调且促凋亡蛋白Bax,Cleaved Caspase3表达增加(P<005)。NGR1处理后能够减轻OGD/R造成的神经元细胞损伤,上调ATF6α表达、促进Akt磷酸化并且减少Bax,Cleaved Caspase3蛋白的表达(P<005),但是,NGR1的这些神经保护性作用能够被雌激素受体阻断剂ICI182780阻断。研究结果证实:NGR1在缺血缺氧情况下对神经元具有保护性作用,该保护作用可能是NGR1通过雌激素受体调控ATF6/Akt信号通路实现的。

[关键词]三七皂苷R1; 原代皮层神经元细胞; 缺血缺氧性脑病; 凋亡; 氧糖剥夺再灌注; ATF6; Akt

[Abstract]Notoginsenoside R1(NGR1),a critical compound in traditional herb Panax notoginseng, is a kind of estrogen receptor agonistIt is reported to exhibit antiapoptotic,antioxidative and antiinflammatory properties activity, so it is widely used for treatment of various diseasesIn order to investigate the potential neuroprotective effect of NGR1 in hypoxicischemic brain damage(HIBD), primary cortical neurons were used in this study to establish oxygenglucose deprivation/reoxygenation(OGD/R) injury models They were treated with NGR1 and estrogen receptor inhibitor ICI182780 respectively, then the neuronal survival, cell membrane integrity and apoptosis were assessed by MTT assay,lactate dehydrogenase test(LDH) and Hoechst 33342 stain respectively, while the protein expression levels of ATF6α,pAkt,Akt,Bax and Cleaved Caspase3 were measured by Western blotting Results indicated that as compared with the blank control group,OGD/R could induce cell injury and apoptosis(P<005), reduce relative integrity of cell membrane(P<005), decrease protein expression of ATF6α,pAkt(P<005), and increase protein expression of Bax and Cleaved Caspase3(P<005) in the primary cortical cells After NGR1 treatment, the expression levels of ATF6α,pAkt were obviously increased, and the expression levels of Bax and Cleaved Caspase3 and the apoptosis of neuron were decreased(P<005) However, these neuroprotective properties of NGR1 against ODG/Rinduced cell damage could be blocked by ICI182780 This finding indicated that NGR1 may protect the primary cortical neurons against OGD/R induced injury,and the mechanism may be associated with accelerating the activation of the ATF6/Akt signaling pathway via estrogen receptors

[Key words]notoginsenoside R1; primary cortical neurons; hypoxicischemic brain damage; apoptosis; oxygenglucose deprivation/reoxygenation; ATF6; Akt

缺血缺氧性脑病(hypoxicischemic brain damage,HIBD)是常见的神经系统疾病,其病理过程包含炎癥反应,兴奋性神经毒性反应以及神经元的凋亡和坏死现象等[12],且神经细胞凋亡在疾病发生过程中占重要作用[3]。三七皂苷R1(notoginsenoside R1,NGR1)是从三七中提取的皂苷类化合物,也是一种天然雌激素受体激动剂,它具有抗凋亡、抗炎、抗氧化、抗内质网应激等多种保护作用[46]。研究发现:NGR1能够以抑制细胞凋亡的方式来对抗缺血再灌注后心肌细胞损伤以及糖尿病肾病中肾小球足细胞损伤[78];可以通过雌激素受体减轻HIBD中的内质网应激,发挥其脑保护功能[9]。但NGR1对抗HIBD中神经元凋亡的报道很少,具体机制也不明确。本研究是为了验证NGR1在HIBD中的保护作用并探讨其相关机制。

1材料和方法

11材料

SpragueDawley(SD)孕鼠(重庆医科大学实验动物中心)。……

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