10 results on '"Wang, Ya‐Li"'
Search Results
2. Circadian Rhythms Disruption
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Huang, Guo-Dong, Wang, Ya-Li, and Liu, Chun-Feng, editor
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- 2020
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3. <bold>Uncaria rhynchophylla</bold> Ameliorates Parkinson’s Disease by Inhibiting HSP90 Expression: Insights from Quantitative Proteomics.
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Lan, Yu-Long, Zhou, Jun-Jun, Liu, Jing, Huo, Xiao-Kui, Wang, Ya-Li, Liang, Jia-Hao, Zhao, Jian-Chao, Sun, Cheng-Peng, Yu, Zhen-Long, Fang, Lin-Lin, Tian, Xiang-Ge, Feng, Lei, Ning, Jing, Zhang, Bao-Jing, Wang, Chao, Zhao, Xin-Yu, and Ma, Xiao-Chi
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CHINESE medicine ,PARKINSON'S disease ,PROTEOMICS ,CENTRAL nervous system ,FLOW cytometry ,BIOINFORMATICS - Abstract
Background/Aims: Uncaria rhynchophylla, known as “Gou-teng”, is a traditional Chinese medicine (TCM) used to extinguish wind, clear heat, arrest convulsions, and pacify the liver. Although U. rhynchophylla has a long history of being often used to treat central nervous system (CNS) diseases, its efficacy and potential mechanism are still uncertain. This study investigated neuroprotective effect and the underlying mechanism of U. rhynchophylla extract (URE) in MPP+ -induced SH-SY5Y cells and MPTP-induced mice.Methods: MPP+ -induced SH-SY5Y cells and MPTP-induced mice were used to established Parkinson’s disease (PD) models. Quantitative proteomics and bioinformatics were used to uncover proteomics changes of URE. Western blotting was used to validate main differentially expressed proteins and test HSP90 client proteins (apoptosis-related, autophagy-related, MAPKs, PI3K, and AKT proteins). Flow cytometry and JC-1 staining assay were further used to confirm the effect of URE on MPP+ -induced apoptosis in SH-SY5Y cells. Gait analysis was used to detect the behavioral changes in MPTP-induced mice. The levels of dopamine (DA) and their metabolites were examined in striatum (STR) by HPLC-EC. The positive expression of tyrosine hydroxylase (TH) was detected by immunohischemical staining and Western blotting.Results: URE dose-dependently increased the cell viability in MPP+ -induced SH-SY5Y cells. Quantitative proteomics and bioinformatics results confirmed that HSP90 was an important differentially expressed protein of URE. URE inhibited the expression of HSP90, which further reversed MPP+ -induced cell apoptosis and autophagy by increasing the expressions of Bcl-2, Cyclin D1, p-ERK, p-PI3K p85, PI3K p110α, p-AKT, and LC3-I and decreasing cleaved caspase 3, Bax, p-JNK, p-p38, and LC3-II. URE also markedly decreased the apoptotic ratio and elevated mitochondrial transmembrane potential (DΨm ). Furthermore, URE treatment ameliorated behavioral impairments, increased the contents of DA and its metabolites and elevated the positive expressions of TH in SN and STR as well as the TH protein.Conclusions: URE possessed the neuroprotective effect in vivo and in vitro, regulated MAPK and PI3K-AKT signal pathways, and inhibited the expression of HSP90. U. rhynchophylla has potentials as therapeutic agent in PD treatment. [ABSTRACT FROM AUTHOR]- Published
- 2018
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4. Impaired CBS-H2S signaling axis contributes to MPTP-induced neurodegeneration in a mouse model of Parkinson’s disease.
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Yuan, Yu-Qing, Wang, Ya-Li, Yuan, Bao-Shi, Yuan, Xin, Hou, Xiao-Ou, Bian, Jin-Song, Liu, Chun-Feng, and Hu, Li-Fang
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HYDROGEN sulfide , *NEURODEGENERATION , *PARKINSON'S disease , *OXIDATIVE stress , *SYNTHASES - Abstract
Hydrogen sulfide (H 2 S), a novel neuromodulator, is linked to the pathogenesis of several neurodegenerative disorders. Exogenous application of H 2 S exerts neuroprotection via anti-inflammation and anti-oxidative stress in animal and cellular models of Parkinson’s disease (PD). However, the role of endogenous H 2 S and the contribution of its various synthases in PD remain unclear. In the present study, we found a decline of plasma and striatal sulfide level in 1-methy-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced PD mouse model. Interestingly, among the three H 2 S generating enzymes, only cystathionine β-synthase (CBS) expression was largely reduced in the striatum of MPTP-treated mice. The in vitro study confirmed a significant decrease of CBS expression in 1-methyl-4-phenylpyridinium (MPP + )-stimulated astrocytes and microglia, but not in neurons or SH-SY5Y dopaminergic cells. Striatal CBS overexpression, elicited by stereotaxic delivery with Cbs gene using recombinant adeno-associated-virus ( rAAV-Cbs ), successfully enhanced the sulfide level in the striatum and partially rescued the MPTP-induced dopaminergic neurotoxicity in the midbrain. Specifically, striatal CBS overexpression alleviated the motor deficits and dopaminergic neuron losses in the nigro-striatal pathway, with a concomitant inhibition of glial activation in MPTP-treated mice. Furthermore, compared to rAAV-Vector , rAAV-Cbs injection reduced the aberrant accumulation of nitric oxide and 3-nitrotyrosine (an indicator of protein nitration) in the striatum of MPTP-treated mice. Notably, it also attenuated the increase of nitrated α-synuclein level in MPTP mice. The in vitro study demonstrated that lentivirus-mediated CBS overexpression elevated the sulfide generation in glial cells. Moreover, glial CBS overexpression offered protection to midbrain dopaminergic neurons through repressing nitric oxide overproduction in both glial and neuronal cells induced by MPP + . Taken together, our data suggest that impaired CBS-H 2 S axis may contribute to the pathogenesis of PD, and that modulation of this axis may become a novel therapeutic approach for PD. [ABSTRACT FROM AUTHOR]
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- 2018
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5. Identifying the hub gene and immune infiltration of Parkinson's disease using bioinformatical methods.
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Liu, Si-Han, Wang, Ya-Li, Jiang, Shu-Min, Wan, Xiao-Jie, Yan, Jia-Hui, and Liu, Chun-Feng
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PARKINSON'S disease , *IMMUNE checkpoint proteins , *GENE ontology , *PROGRAMMED cell death 1 receptors , *T helper cells , *GENE regulatory networks , *RECEIVER operating characteristic curves , *INTERLEUKIN-21 - Abstract
[Display omitted] • SLC18A2, SYNGR3 and CALB1 were identified as the potential biomarkers in PD by bioinformatics analysis. • Dendritic cells (DCs) and activated dendritic cells (aDCs) had significant higher infiltration in PD. • CD27, CEACAM1, and CTLA4 had negative correlation with the expression of SLC18A2, SYNGR3 and CALB1. • The expression of SCL18A2 and SYNGR3 were down-regulated in clinical peripheral blood samples of PD. Parkinson's disease (PD) is a common neurodegenerative disorder that affects 1%–2% of the population over 60 years old. Immune response dysfunction in the brain contributes to the occurrence and development of PD. This study aimed to uncover the potential diagnostic genes for PD and characterize the immune cell infiltrates. We downloaded the microarray data of patients with PD samples from the Gene Expression Omnibus (GEO) database. Weighted Gene Co-Expression Network Analysis (WGCNA) was used to identify the modules linked to PD in the GSE20163 dataset. Meanwhile, differentially expressed genes (DEGs) between the healthy control samples and PD samples were also identified. Then the PD-related genes were integrated based on the genes in the key module and DEGs. Functional enrichment analysis was used to explore the molecular mechanisms of these PD-related genes. Protein-protein interaction (PPI) network and least absolute shrinkage and selection operator (LASSO) analysis were used to further screen candidate genes for PD. Gene set enrichment analysis (GSEA) was applied to explore the biological functions of these candidate genes. The infiltration of immune cells was detected by single-sample gene set enrichment analysis (ssGSEA) algorithm in the GSE20163 dataset, and Pearson analysis was used to investigate the correlation of candidate genes with immune cells and immune checkpoint proteins. The expression of candidate genes in clinical samples was verified by qPCR. Altogether, we found a unique gene module related to PD, where 109 DEGs were identified in the GSE20163 dataset. Following these results, we screened 68 genes associated with PD. Gene Expression Omnibus (GEO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses suggested that these genes were markedly enriched in the pathway of synthesis and transport of neurons. Three candidate genes (SLC18A2, CALB1, and SYNGR3) were further identified in PD patients through PPI network and LASSO analysis. The receiver operating characteristic (ROC) curve indicated that the three candidate genes had a good performance in distinguishing the PD samples from healthy control samples. The proportions of the aDC, DC, NK CD56dim cells, and follicular helper T cells (TFH) were obviously different between the healthy control and PD samples. Moreover, CTLA4, LAG3, CEACAM1, and CD27 were highly expressed in the PD group. GSEA analysis for candidate genes revealed that they were all closely related to the neurogenic disease. Additionally, the three candidate genes were all strongly correlated with the above immune cells and immune checkpoint proteins. The qPCR results validated the expression differences of SLC18A2 and SYNGR3 in the clinical PD and control samples. The three candidate genes may be a useful tool for diagnosing PD patients. These findings provide a reference for exploring new therapeutic targets and strategies for PD treatment. [ABSTRACT FROM AUTHOR]
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- 2022
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6. REM sleep without atonia and vestibular-evoked myogenic potentials: clinical brainstem dysfunction in early-stage Parkinson's disease and isolated REM sleep behavior disorder.
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Xie, Wei-ye, Shen, Yun, Chen, Ying, Zhuang, Sheng, Wang, Ya-li, Jin, Hong, Li, Han-xing, Yan, Jia-hui, Li, Ying, Mao, Cheng-jie, Dai, Yong-ping, and Liu, Chun-feng
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RAPID eye movement sleep , *PARKINSON'S disease , *SLEEP disorders , *BRAIN stem , *EYE movements , *RESEARCH , *RESEARCH methodology , *EVALUATION research , *MUSCLE hypotonia , *COMPARATIVE studies , *PARASOMNIAS - Abstract
Objective: To determine whether the onset of rapid eye movement (REM) sleep behavior disorder (RBD) is associated with changes in brainstem neuronal pathway dysfunction as reflected by vestibular-evoked myogenic potentials (VEMPs) and to evaluate associations between VEMPs and REM sleep without atonia (RSWA) in patients with early-stage Parkinson's disease (PD) and isolated RBD (iRBD).Methods: Eighty-two early-stage PD patients, 40 iRBD patients, and 41 healthy control individuals underwent one-night video-polysomnography (vPSG) and VEMPs examination. We compared cervical (cVEMP), ocular (oVEMP), and masseter (mVEMP) VEMP parameters among PD with RBD (PD + RBD), PD without RBD (PD-RBD), iRBD, and control groups and analyzed correlations between VEMPs and RSWA in PD and iRBD groups.Results: The PD + RBD group showed delays in bilateral cVEMP (Lp13, Ln23, Rn23: all p < 0.05) and oVEMP (Ln10, Rn10, Rp15: all p < 0.05) peak latencies compared with the PD-RBD group. Total cVEMP scores were higher in the PD + RBD group than in the iRBD group (p = 0.033). In PD patients, phasic RSWA was correlated with total cVEMP scores (p = 0.003), and tonic RSWA was correlated with left oVEMP scores (p = 0.013).Conclusions: Brainstem neurophysiology as evidenced by altered VEMPs in patients with PD and iRBD could reflect disease evolvement. Moreover, VEMPs alterations may vary depending on the presence of RBD in PD patients. The associations between altered RSWA and VEMP parameters highlight the meaningfulness of detecting brainstem dysfunction in early-stage PD. [ABSTRACT FROM AUTHOR]- Published
- 2022
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7. Correlations between retinal nerve fiber layer thickness and cognitive progression in Parkinson's disease: A longitudinal study.
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Zhang, Jin-ru, Cao, Yu-lan, Li, Kai, Wang, Fen, Wang, Ya-li, Wu, Jia-jing, Pei, Shao-fang, Chen, Jing, Mao, Cheng-jie, and Liu, Chun-feng
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PARKINSON'S disease , *VISUAL fields , *LONGITUDINAL method , *OPTICAL coherence tomography , *MONTREAL Cognitive Assessment , *ALZHEIMER'S disease , *NERVE fibers , *PARKINSON'S disease diagnosis , *DISEASE progression , *EXECUTIVE function , *MEMORY , *RESEARCH , *RETINA , *RESEARCH methodology , *MEDICAL cooperation , *EVALUATION research , *COMPARATIVE studies , *DISEASE complications - Abstract
Background: Retinal abnormalities measured by optical coherence tomography (OCT) have been detected in both Parkinson's disease (PD) and Alzheimer's disease (AD). Cognitive impairment is not only found in AD, but 75-90% of PD patients will also develop dementia in the late stage of disease. We assessed whether baseline retinal nerve fiber layer (RNFL) thickness predicted worsening of cognitive status over time and the correlation between RNFL thickness and the detailed impaired cognitive domains in PD.Methods: RNFL thickness was measured using high-definition OCT in 78 non-dementia PD patients. Clinical and cognitive assessments were performed at baseline and at 3.61 ± 0.65 years follow-up. Linear mixed-effects models were used to examine associations between RNFL thickness and the changes in cognitive test scores, after adjusting for age, sex, disease duration and education.Results: Analysis of outcomes according to baseline RNFL tertiles showed worse performance in global cognitive tests, delayed memory, and executive functions in patients with a thin RNFL. During follow-up, greater cognitive deterioration was found in thin RNFL tertile patients. Lower baseline average RNFL thickness was associated with greater annualized decline in Mini-Mental State Examination and Montreal Cognitive Assessment.Conclusion: The correlation between RNFL thickness and cognitive dysfunction suggests that OCT may be useful for predicting cognitive dysfunction in PD patients. [ABSTRACT FROM AUTHOR]- Published
- 2021
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8. Nicotine improved the olfactory impairment in MPTP-induced mouse model of Parkinson's disease.
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Yang, Jing, Lv, Dong-Jun, Li, Ling-Xi, Wang, Ya-Li, Qi, Di, Chen, Jing, Mao, Cheng-Jie, Wang, Fen, Liu, Yi, Hu, Li-Fang, and Liu, Chun-Feng
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PARKINSON'S disease , *NICOTINE , *DOPAMINERGIC neurons , *OLFACTORY bulb , *OLFACTOMETRY , *INVERSE relationships (Mathematics) - Abstract
• Cholinergic damage in the OB might contribute to the olfactory dysfunction. • Nicotine could improve the olfactory impairment in MPTP-treated mice. • Nicotine enchance choline acetyltransferase activity in the OB of MPTP-treated mice. Olfactory impairment is an early feature of patients with Parkinson's disease (PD). Retrospective epidemiological studies reported lower scores on the University of Pennsylvania Smell Identification Test (UPSIT) in non-smokers than smokers with PD and showed an inverse correlation between susceptibility to PD and a person's history of smoking. But the mechanisms by which cigarettes affect olfaction in PD are not fully understood. So we investigated the effect of nicotine on the olfactory function in 1-methyl-4-phenyl-1, 2, 3, 6 tetrahydropyridine (MPTP)-treated mice. We observed that nicotine improved locomotor activity and protection against dopaminergic neuron loss in the midbrain in MPTP-treated mice. Compared to controls, MPTP-treated mice showed a deficit of odor discrimination and odor detection, which were alleviated by nicotine treatment. But no significant changes were found in olfactory memory in MPTP-treated mice. Moreover, we detected a marked decrease of Choline acetyltransferase (ChAT) expression in the olfactory bulb (OB) in MPTP-treated mice, which was also attenuated by nicotine administration. In addition, nicotine ameliorated the loss of cholinergic neurons and dopaminergic innervation in the horizontal limb of the diagonal band (HDB), which is the primary origin of cholinergic input to the OB. Our results suggested that nicotine could improve the olfactory impairment by protecting cholinergic systems in the OB of MPTP-treated mice. And nicotine protection of cholinergic systems in the OB is relevant to attenuating dopaminergic neuron loss in the midbrain and HDB. [ABSTRACT FROM AUTHOR]
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- 2019
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9. AMPK S-sulfuration contributes to H2S donors-induced AMPK phosphorylation and autophagy activation in dopaminergic cells.
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Hou, Xiao-Ou, Tu, Hai-Yue, Qian, Hai-Chun, Li, Qian, Yang, Ya-Ping, Xu, Guo-Qiang, Wang, Fen, Liu, Chun-Feng, Wang, Ya-Li, and Hu, Li-Fang
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AUTOPHAGY , *LYSOSOMES , *PHOSPHORYLATION , *DOPAMINERGIC neurons , *PARKINSON'S disease , *PROTEIN kinases , *HYDROGEN sulfide , *ADENOSINES - Abstract
Hydrogen sulfide (H 2 S) serves as a neuromodulator and regulator of neuroinflammation. It is reported to be therapeutic for Parkinson's disease (PD) animal and cellular models. However, whether it affects α-synuclein accumulation in dopaminergic cells, the key pathological feature in PD, is poorly understood. In this study we reported that exogenous H 2 S donors NaHS and GYY4137 (GYY) enhanced the autophagy activity, as indicated by the increases of autophagy marker LC3-II expression and LC3 dots formation even during lysosome inhibition in dopaminergic cell lines and HEK293 cells. The enhancement of H 2 S donors on autophagic flux was mediated by adenosine 5′-monophosphate-activated protein kinase (AMPK)-dependent mammalian target of rapamycin (mTOR) inhibition, as H 2 S donors activated AMPK but reduced the mTOR activity and H 2 S donors-induced LC3-II increase was diminished by mTOR activator. Moreover, point mutation of Cys302 into alanine (C302A) in AMPKα2 subunit abolished the AMPK activation and mTOR inhibition, as well as autophagic flux increase elicited by NaHS. Interestingly, NaHS triggered AMPK S -sulfuration, which was not observed in AMPK C302A -transfected cells. Further, NaHS was able to attenuate α-synuclein accumulation in a cellular model induced by dopamine oxidized metabolite 3, 4-dihydroxyphenylacetaldehyde (DOPAL), and this effect was interfered by autophagy inhibitor wortmannin and also eliminated in AMPK Cys302A-transfected cells. In sum, the findings identified a role of Cys302 S -sulfuration in AMPK activation induced by exogenous H 2 S and demonstrated that H 2 S donors could enhance the autophagic flux via AMPK-mTOR signaling and thus reduce α-synuclein accumulation in vitro. • H 2 S enhanced the autophagic flux in dopaminergic cells. • AMPK-mTOR signaling mediated the effect of H 2 S on autophagy. • H 2 S triggered AMPK S -sulfuration at Cys302. • AMPK S -sulfuration contributed to H 2 S-induced autophagy activation. • H 2 S donor attenuated α-syn aggregation in vitro by activating AMPK-dependent autophagy. [ABSTRACT FROM AUTHOR]
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- 2021
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10. Expression of autophagy related genes in peripheral blood cells in Parkinson's disease.
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Tu, Hai-Yue, Gu, Yong-Quan, Li, Xia, Pei, Shao-Fang, Hu, Li-Fang, and Wang, Ya-Li
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PARKINSON'S disease , *BLOOD cells , *AUTOPHAGY , *DOPAMINERGIC neurons , *BIOLOGICAL rhythms , *CIRCADIAN rhythms - Abstract
• This study aimed to investigate whether the rhythm of autophagy is altered in PD. • BECN1 and LAMP2 levels were decreased in patients with PD. • The rhythm of autophagy in PD is not consistent with that in the Control group. Parkinson's disease (PD) is the second most common neurodegenerative disorder and affects dopaminergic neurons. Autophagy often shows a circadian rhythm pattern under physiological conditions across 24 h. Abnormal autophagy and circadian dysfunction are two characteristics of PD. Whether the rhythm of autophagy is altered in PD has not yet been reported. Therefore, in this study, we collected peripheral blood samples at 6:00 h and 18:00 h from PD patients and age-matched controls, and analyzed the mRNA expressions of ULK1 , BECN1 , LAMP2 , AMPK, and SNCA using real-time quantitative PCR. Blood samples analysis found that BECN1 and LAMP2 levels were decreased in patients with PD. Simultaneously, the rhythm of autophagy in PD is not consistent with that in the Control group, which may be a manifestation of the abnormal biological rhythm of PD. [ABSTRACT FROM AUTHOR]
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- 2021
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