Effects of salidroside on OGD/R-induced autophagy and apoptosis of hippocampal neurons by regulating the MAPK/ERK/mTOR signaling pathway
10.11855/j.issn.0577-7402.1815.2025.0528
- VernacularTitle:红景天苷调节MAPK/ERK/mTOR信号通路对OGD/R诱导的海马神经元自噬和凋亡的影响
- Author:
Chao TANG
1
;
Yan-Qun CAO
;
Chao-Liang CHEN
;
Ju-Xiang ZHOU
Author Information
1. 邵阳学院普爱医学院,湖南邵阳 422000
- Keywords:
salidroside;
oxygen-glucose deprivation/reperfusion;
mitogen-activated protein kinase;
hippocampal neurons;
autophagy;
apoptosis
- From:
Medical Journal of Chinese People's Liberation Army
2025;50(8):1008-1014
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effects of Rhodiola salidroside on regulating the mitogen-activated protein kinase(MAPK)/extracellular signal-regulated kinase(ERK)/mammalian target of rapamycin(mTOR)signaling pathway and explore its impact on hippocampal neuron autophagy and apoptosis induced by oxygen-glucose deprivation/reperfusion(OGD/R).Methods The mouse hippocampal neuronal cell line HT22 was cultured in vitro and randomly divided into control group,OGD/R group,salidroside group,tert-butylhydroquinone(TBHQ)group,and salidroside+TBHQgroup.Except for control group,cell models were established by OGD/R induction in other groups.Cells in corresponding groups were treated with Rhodiola salidroside(500 μmol/L)and/or MAPK activator TBHQ(50 μmol/L)for 24 h.The lactate dehydrogenase(LDH)release rates were measured,cell apoptosis was detected by flow cytometry,and cell viability was assessed by MTT assay.Acridine orange(AO)staining was used to detect autophagy.Enzyme-linked immunosorbent assay(ELISA)was used to measure the expression levels of inflammatory cytokines including interleukins(IL)-6,IL-8,and IL-17,and tumor necrosis factor-α(TNF-α).Western blotting was performed to detect the expression levels of proteins related to apoptosis,autophagy,and the MAPK/ERK/mTOR signaling pathway.Results Salidroside(500 μmol/L)significantly enhanced the viability of OGD/R-induced HT22 cells(P<0.05),without obvious effect on the viability of normally cultured HT22 cells(P>0.05).Compared with control group,OGD/R group showed significantly increased LDH release rates,apoptosis rates,autophagosome formation rates,levels of IL-6,IL-8,IL-17 and TNF-α,expressions of Bcl-2-associated X protein(Bax),Cleaved Caspase-3,Caspase-3 and Beclin-1 protein,ratios of microtubule-associated protein 1 light chain 3(LC3)-Ⅱ/LC3-Ⅰ,phosphorylation(p)-p38 MAPK/p38 MAPK,and p-ERK1/2/ERK1/2(P<0.05),while cell viability and p-mTOR/mTOR ratio were significantly decreased(P<0.05).Compared with OGD/R group,salidroside group had significantly reduced LDH release rates,apoptosis rates,autophagosome formation rates,levels of IL-6,IL-8,IL-17,and TNF-α,expressions of Bax,Cleaved Caspase-3,Caspase-3,Beclin-1 protein,and ratios of LC3-Ⅱ/LC3-Ⅰ ratio,p-p38 MAPK/p38 MAPK,and p-ERK1/2/ERK1/2(P<0.05),while cell viability and p-mTOR/mTOR ratio were significantly increased(P<0.05).The change of indicators in TBHQgroup showed an opposite trend to those in salidroside(P<0.05).Compared with salidroside group,salidroside+TBHQgroup had significantly increased LDH release rates,apoptosis rates,autophagosome formation rates,levels of IL-6,IL-8,IL-17 and TNF-α,expressions of Bax,Cleaved Caspase-3,Caspase-3,Beclin-1 protein,and ratios of LC3-Ⅱ/LC3-Ⅰ,p-p38 MAPK/p38 MAPK,and p-ERK1/2/ERK1/2(P<0.05),while cell viability and p-mTOR/mTOR ratio were significantly decreased(P<0.05).Conclusion Salidroside may inhibit OGD/R-induced hippocampal neuron autophagy and apoptosis by blocking the activation and transmission of MAPK/ERK/mTOR signaling pathway.