1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (BioDeep_00000003465)

 

Secondary id: BioDeep_00001868301

human metabolite blood metabolite


代谢物信息卡片


1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine

化学式: C12H15N (173.1204)
中文名称: 1-甲基-4-苯基-1,2,3,6-四氢吡啶
谱图信息: 最多检出来源 Homo sapiens(blood) 8.76%

分子结构信息

SMILES: CN(C2)CC=C(C2)c(c1)cccc1
InChI: InChI=1S/C12H15N/c1-13-9-7-12(8-10-13)11-5-3-2-4-6-11/h2-7H,8-10H2,1H3

描述信息

D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents
D009676 - Noxae > D009498 - Neurotoxins
KEIO_ID M034

同义名列表

4 个代谢物同义名

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; N-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; MPTP; 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine



数据库引用编号

20 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 11 CASP1, CASP9, HTT, KEAP1, NOS1, NR4A2, PINK1, PPARG, PTEN, SIRT1, SQSTM1
Peripheral membrane protein 1 NOS1
Endosome membrane 1 HTT
Endoplasmic reticulum membrane 2 CD4, DRD1
Cytoplasmic vesicle, autophagosome 1 SQSTM1
Nucleus 11 CASP9, DRD1, HTT, KEAP1, NOS1, NR4A2, PINK1, PPARG, PTEN, SIRT1, SQSTM1
autophagosome 3 HTT, MAP1LC3A, SQSTM1
cytosol 11 CASP1, CASP9, HTT, KEAP1, MAP1LC3A, NOS1, PINK1, PPARG, PTEN, SIRT1, SQSTM1
dendrite 5 DRD2, HTT, PDYN, PENK, SLC18A2
centrosome 1 SLC18A2
nucleoplasm 8 HTT, KEAP1, NOS1, NR4A2, PPARG, PTEN, SIRT1, SQSTM1
RNA polymerase II transcription regulator complex 1 PPARG
Cell membrane 5 CASP1, CD4, DRD1, DRD2, HTT
Lipid-anchor 1 MAP1LC3A
Cell projection, axon 1 SLC18A2
Multi-pass membrane protein 4 DRD1, DRD2, HTT, SLC18A2
Golgi apparatus membrane 1 DRD2
Synapse 4 DRD2, HTT, NOS1, PDYN
glutamatergic synapse 4 DRD1, DRD2, MAP1LC3A, SQSTM1
Golgi apparatus 1 HTT
Golgi membrane 1 DRD2
growth cone 1 PINK1
mitochondrial inner membrane 1 PINK1
neuronal cell body 2 PDYN, PENK
presynaptic membrane 3 DRD1, DRD2, HTT
sarcolemma 1 NOS1
synaptic vesicle 1 SLC18A2
Cytoplasm, cytosol 2 PINK1, SQSTM1
Lysosome 1 SQSTM1
acrosomal vesicle 1 DRD2
plasma membrane 11 CASP1, CD4, DRD1, DRD2, GCG, HTT, NOS1, PDYN, PENK, PTEN, SLC18A2
synaptic vesicle membrane 2 DRD2, SLC18A2
terminal bouton 1 SLC18A2
Membrane 2 PINK1, SLC18A2
apical plasma membrane 1 PTEN
axon 4 DRD2, HTT, PINK1, SLC18A2
extracellular exosome 1 SQSTM1
endoplasmic reticulum 4 HTT, KEAP1, PINK1, SQSTM1
extracellular space 2 ARTN, GCG
perinuclear region of cytoplasm 4 HTT, NOS1, PINK1, PPARG
mitochondrion 5 CASP9, NOS1, PINK1, SIRT1, SQSTM1
protein-containing complex 5 CASP1, CASP9, HTT, NOS1, NR4A2
intracellular membrane-bounded organelle 4 MAP1LC3A, PPARG, SLC18A2, SQSTM1
postsynaptic density 2 NOS1, PTEN
chromatin silencing complex 1 SIRT1
Single-pass type I membrane protein 1 CD4
Secreted 4 ARTN, GCG, PDYN, PENK
extracellular region 5 ARTN, GCG, PDYN, PENK, PTEN
cytoplasmic side of plasma membrane 1 PTEN
Mitochondrion outer membrane 1 PINK1
Single-pass membrane protein 1 PINK1
mitochondrial outer membrane 1 PINK1
hippocampal mossy fiber to CA3 synapse 1 PDYN
transcription regulator complex 1 NR4A2
centriolar satellite 1 KEAP1
ciliary membrane 2 DRD1, DRD2
photoreceptor inner segment 1 NOS1
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 SLC18A2
external side of plasma membrane 1 CD4
dendritic spine 4 DRD1, DRD2, NOS1, PTEN
neuronal dense core vesicle lumen 1 PENK
perikaryon 2 DRD2, PENK
cytoplasmic vesicle 1 SQSTM1
nucleolus 2 CASP1, SIRT1
midbody 1 KEAP1
P-body 1 SQSTM1
Early endosome 2 CD4, HTT
postsynaptic membrane 3 DRD1, DRD2, HTT
Cell membrane, sarcolemma 1 NOS1
Cytoplasm, perinuclear region 1 NOS1
Mitochondrion inner membrane 1 PINK1
heterochromatin 1 SIRT1
Membrane raft 3 CD4, HTT, NOS1
Cell junction, focal adhesion 1 HTT
Cytoplasm, cytoskeleton 1 MAP1LC3A
focal adhesion 1 HTT
microtubule 2 CASP1, MAP1LC3A
GABA-ergic synapse 2 DRD1, DRD2
sarcoplasmic reticulum 1 NOS1
Cell projection, dendritic spine 3 DRD1, NOS1, PTEN
Nucleus, PML body 3 PTEN, SIRT1, SQSTM1
PML body 3 PTEN, SIRT1, SQSTM1
mitochondrial intermembrane space 1 PINK1
lateral plasma membrane 1 DRD2
nuclear speck 1 NR4A2
NLRP3 inflammasome complex 1 CASP1
nuclear inner membrane 1 SIRT1
Cytoplasm, myofibril, sarcomere 1 SQSTM1
Late endosome 3 HTT, MAP1LC3A, SQSTM1
sarcomere 1 SQSTM1
receptor complex 1 PPARG
Cell projection, neuron projection 2 HTT, PTEN
neuron projection 2 HTT, PTEN
cilium 2 DRD1, DRD2
chromatin 4 NR4A2, PINK1, PPARG, SIRT1
Cytoplasmic vesicle, autophagosome membrane 1 MAP1LC3A
autophagosome membrane 1 MAP1LC3A
cell projection 1 PTEN
cell periphery 1 NOS1
cytoskeleton 2 NOS1, PINK1
centriole 1 HTT
actin filament 1 KEAP1
non-motile cilium 2 DRD1, DRD2
sperm midpiece 1 SQSTM1
organelle membrane 1 MAP1LC3A
sperm flagellum 1 DRD2
Cul3-RING ubiquitin ligase complex 1 KEAP1
fibrillar center 1 SIRT1
nuclear envelope 1 SIRT1
Endomembrane system 2 HTT, MAP1LC3A
phagophore assembly site 1 SQSTM1
Cytoplasmic vesicle membrane 1 HTT
cell body fiber 1 PENK
Cell projection, dendrite 2 DRD1, SLC18A2
euchromatin 1 SIRT1
cell body 1 PINK1
secretory granule lumen 1 GCG
secretory granule membrane 1 SLC18A2
endoplasmic reticulum lumen 3 CD4, GCG, PENK
axon terminus 3 DRD2, PDYN, PENK
endocytic vesicle 1 DRD2
Schmidt-Lanterman incisure 1 PTEN
neuronal dense core vesicle 1 PDYN
aggresome 1 SQSTM1
apoptosome 1 CASP9
AIM2 inflammasome complex 1 CASP1
clathrin-coated endocytic vesicle membrane 1 CD4
canonical inflammasome complex 1 CASP1
eNoSc complex 1 SIRT1
rDNA heterochromatin 1 SIRT1
dopaminergic synapse 2 DRD2, SLC18A2
intracellular non-membrane-bounded organelle 1 SQSTM1
Cytoplasmic vesicle, secretory vesicle membrane 1 SLC18A2
Lewy body 2 PINK1, SQSTM1
postsynaptic cytosol 1 HTT
Cell projection, cilium membrane 1 DRD1
Preautophagosomal structure 1 SQSTM1
presynaptic cytosol 1 HTT
astrocyte projection 1 PINK1
Cytoplasmic vesicle, secretory vesicle, chromaffin granule lumen 1 PENK
chromaffin granule lumen 1 PENK
symmetric synapse 1 PENK
synaptic vesicle lumen 1 PENK
[Glucagon-like peptide 1]: Secreted 1 GCG
T cell receptor complex 1 CD4
Autolysosome 2 MAP1LC3A, SQSTM1
inclusion body 3 HTT, KEAP1, SQSTM1
myelin sheath adaxonal region 1 PTEN
[Isoform alpha]: Secreted 1 PTEN
G protein-coupled receptor complex 2 DRD1, DRD2
clathrin-sculpted monoamine transport vesicle membrane 1 SLC18A2
serotonergic synapse 1 HTT
IPAF inflammasome complex 1 CASP1
NLRP1 inflammasome complex 1 CASP1
protease inhibitor complex 1 CASP1
[Huntingtin]: Cytoplasm 1 HTT
[Huntingtin, myristoylated N-terminal fragment]: Cytoplasmic vesicle, autophagosome 1 HTT
caspase complex 1 CASP9
amphisome 1 SQSTM1
[SirtT1 75 kDa fragment]: Cytoplasm 1 SIRT1


文献列表

  • Xian-Zhe Fan, Jia-Qi Song, Xin-Yi Shi, Jin-Fang Zhou, Rui-Juan Yuan, Ting Liu, Xiang-Qian Kong, Ya-Si Huang, Li-Jun Zhang, Hai-Bing Liao. New sesquiterpenoids with neuroprotective effects in vitro and in vivo from the Picrasma chinensis. Fitoterapia. 2024 Jun; 175(?):105908. doi: 10.1016/j.fitote.2024.105908. [PMID: 38479621]
  • Ziliang He, Yeye Hu, Ying Zhang, Jing Xie, Zhiqiang Niu, Guigui Yang, Ji Zhang, Zixuan Zhao, Shuai Wei, Haifeng Wu, Weicheng Hu. Asiaticoside exerts neuroprotection through targeting NLRP3 inflammasome activation. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 May; 127(?):155494. doi: 10.1016/j.phymed.2024.155494. [PMID: 38471370]
  • Wenping Yang, Yongyue Wei, Jin Sun, Caixia Yao, Fen Ai, Haixia Ding. Safranal exerts a neuroprotective effect on Parkinson's disease with suppression of NLRP3 inflammation activation. Molecular biology reports. 2024 Apr; 51(1):593. doi: 10.1007/s11033-024-09537-y. [PMID: 38683404]
  • J Gui, X Sun, S Wen, X Liu, B Qin, M Sang. [Resveratrol protects dopaminergic neurons in a mouse model of Parkinson's disease by regulating the gut-brain axis via inhibiting the TLR4 signaling pathway]. Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 2024 Feb; 44(2):270-279. doi: 10.12122/j.issn.1673-4254.2024.02.09. [PMID: 38501412]
  • Li Liu, Lei Jiang, Jinglan Zhang, Yan Ma, Min Wan, Xueqing Hu, Lian Yang. Imperatorin inhibits oxidative stress injury and neuroinflammation via the PI3K/AKT signaling pathway in the MPTP-induced Parkinson's disease mouse. Neuroreport. 2024 Feb; 35(3):175-184. doi: 10.1097/wnr.0000000000001997. [PMID: 38305108]
  • Jiahua Huang, Xinyue Zhang, Xueping Yang, Qingyun Yv, Fanlong Ye, Sheng Chen, Ying Cui, Linting Gu, Min Zhu, Wenwei Li. Baicalin exerts neuroprotective actions by regulating the Nrf2-NLRP3 axis in toxin-induced models of Parkinson's disease. Chemico-biological interactions. 2024 Jan; 387(?):110820. doi: 10.1016/j.cbi.2023.110820. [PMID: 38016618]
  • Yuan Gao, Jiang Liu, Xiaoyan Wang, Qiang Meng. Vanillin attenuates oxidative stress and neurochemical balance in MPTP-induced Parkinson's disease mice by regulating the TLR-4 inflammatory pathway. Folia neuropathologica. 2024 Jan; ?(?):. doi: 10.5114/fn.2023.131191. [PMID: 38174675]
  • Bo Niu, Minhong Zhao, Xiu'an Gao, Jiangping Xu, Linzhong Yu. TMT-based quantitative proteomics analysis of neuroprotective effects of Forsythoside A on the MPTP-induced Parkinson's disease mouse model. Experimental neurology. 2023 Dec; 373(?):114642. doi: 10.1016/j.expneurol.2023.114642. [PMID: 38056584]
  • Eduarda Monteiro Fidelis, Anne Suely P Savall, Jhuly Dornelles Mello, Caroline Brandão Quines, Antônio Alvenir Comis-Neto, Tuane Bazanella Sampaio, Cristiane Casagrande Denardin, Daiana Silva de Ávila, Suzan Gonçalves Rosa, Simone Pinton. Purple pitanga extract (Eugenia uniflora) attenuates oxidative stress induced by MPTP. Metabolic brain disease. 2023 12; 38(8):2615-2625. doi: 10.1007/s11011-023-01318-z. [PMID: 37921949]
  • Hong-Yan Li, De-Shui Liu, Li-Bo Li, Ying-Bo Zhang, Hai-Ying Dong, Hua Rong, Jing-Yan Zhang, Jun-Ping Wang, Ming Jin, Nan Luo, Xiao-Jie Zhang. Total Glucosides of White Paeony Capsule ameliorates Parkinson's disease-like behavior in MPTP-induced mice model by regulating LRRK2/alpha-synuclein signaling. Journal of ethnopharmacology. 2023 Oct; ?(?):117319. doi: 10.1016/j.jep.2023.117319. [PMID: 37838295]
  • Sai Teja Meka, Sree Lalitha Bojja, Gautam Kumar, Sumit Raosaheb Birangal, C Mallikarjuna Rao. Novel HDAC inhibitors provide neuroprotection in MPTP-induced Parkinson's disease model of rats. European journal of pharmacology. 2023 Sep; 959(?):176067. doi: 10.1016/j.ejphar.2023.176067. [PMID: 37751833]
  • Xinran Guo, Yuhan Wu, Qingqing Wang, Jianbing Zhang, Xueping Sheng, Lanrong Zheng, Yule Wang. Huperzine A injection ameliorates motor and cognitive abnormalities via regulating multiple pathways in a murine model of Parkinson's disease. European journal of pharmacology. 2023 Aug; ?(?):175970. doi: 10.1016/j.ejphar.2023.175970. [PMID: 37549727]
  • Zhengjia Pu, Shuya Liu, Zeming Guo, Xuemei Zhang, Jie Yan, Yong Tang, Hong Xiao, Jieying Gao, Yingli Li, Qunhua Bai. Casein Reactivates Dopaminergic Nerve Injury and Intestinal Inflammation with Disturbing Intestinal Microflora and Fecal Metabolites in a Convalescent Parkinson's Disease Mouse Model. Neuroscience. 2023 08; 524(?):120-136. doi: 10.1016/j.neuroscience.2023.05.014. [PMID: 37321369]
  • Tao Pan, Qi Xiao, Hui-Jie Fan, Lei Xu, Shao-Chen Qin, Li-Xia Yang, Xiao-Ming Jin, Bao-Guo Xiao, Bo Zhang, Cun-Gen Ma, Zhi Chai. Wuzi Yanzong Pill relieves MPTP-induced motor dysfunction and neuron loss by inhibiting NLRP3 inflammasome-mediated neuroinflammation. Metabolic brain disease. 2023 Jul; ?(?):. doi: 10.1007/s11011-023-01266-8. [PMID: 37470879]
  • Ziying Wang, Jinshuai Cui, Dongni Li, Shuzhen Ran, Junqing Huang, Gang Chen. Morin exhibits a neuroprotective effect in MPTP-induced Parkinson's disease model via TFEB/AMPK-mediated mitophagy. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 May; 116(?):154866. doi: 10.1016/j.phymed.2023.154866. [PMID: 37209604]
  • María Dolores García-Fernández, Ane Larrea, Roberto Fernández, Rafael Rodríguez-Puertas, Egoitz Astigarraga, Iván Manuel, Gabriel Barreda-Gómez. Microarrays, Enzymatic Assays, and MALDI-MS for Determining Specific Alterations to Mitochondrial Electron Transport Chain Activity, ROS Formation, and Lipid Composition in a Monkey Model of Parkinson's Disease. International journal of molecular sciences. 2023 Mar; 24(6):. doi: 10.3390/ijms24065470. [PMID: 36982541]
  • Hongwei Cai, Pei Zhang, Tongxia Li, Ming Li, Lijun Zhang, Chi Cui, Jie Lei, Jian Yang, Kun Ren, Jie Ming, Bo Tian. Amygdalo-nigral circuit mediates stress-induced vulnerability to the parkinsonian toxin MPTP. CNS neuroscience & therapeutics. 2023 Mar; ?(?):. doi: 10.1111/cns.14151. [PMID: 36914579]
  • Sarah Martins Presti-Silva, Alice Laschuk Herlinger, Cristina Martins-Silva, Rita Gomes Wanderley Pires. Biochemical and behavioral effects of rosmarinic acid treatment in an animal model of Parkinson's disease induced by MPTP. Behavioural brain research. 2023 Feb; 440(?):114257. doi: 10.1016/j.bbr.2022.114257. [PMID: 36526017]
  • I O Ishola, A K Oloyo, T G Olubodun-Obadun, O D Godswill, S A Omilabu, O O Adeyemi. Neuroprotective potential of plant derived parenchymal stem cells extract on environmental and genetic models of Parkinson disease through attenuation of oxidative stress and neuroinflammation. Metabolic brain disease. 2023 Feb; 38(2):557-571. doi: 10.1007/s11011-022-01120-3. [PMID: 36401682]
  • Wenda Zhu, Yiping Fan, Yanbing Li, Lizhi Peng, Yifang Li, Fengxia Yan, Jiaqiang Zhao, Lei Zhang, Hiroshi Kurihara, Rongrong He, Heru Chen. Hybridization of amantadine with gardenamide A enhances NMDA antagonism and in vivo anti-PD effects. Bioorganic chemistry. 2023 01; 130(?):106223. doi: 10.1016/j.bioorg.2022.106223. [PMID: 36356372]
  • Yiru Ding, Meiyu Zhou, Ruoyin Zheng, Ruijia Ma, Jialin Deng, Wen-Zhi Hao, Lu Wang, Ji-Chun Zhang, Chi-Tang Ho, Jun-Qing Huang. Feruloylated oligosaccharides ameliorate MPTP-induced neurotoxicity in mice by activating ERK/CREB/BDNF/TrkB signalling pathway. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Jan; 108(?):154512. doi: 10.1016/j.phymed.2022.154512. [PMID: 36288652]
  • Adeola Oluwatosin Adedara, Guilherme Wildner, Julia Sepel Loreto, Matheus Mulling Dos Santos, Amos Olalekan Abolaji, Nilda Vargas Barbosa. Kaempferol counteracts toxicity induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in D. melanogaster: An implication of its mitoprotective activity. Neurotoxicology. 2022 Dec; 95(?):23-34. doi: 10.1016/j.neuro.2022.12.008. [PMID: 36592898]
  • Xing-Jie Xu, Tao Pan, Hui-Jie Fan, Xu Wang, Jie-Zhong Yu, Hai-Fei Zhang, Bao-Guo Xiao, Zhen-Yu Li, Bo Zhang, Cun-Gen Ma, Zhi Chai. Neuroprotective effect of hyperoside in MPP+/MPTP -induced dopaminergic neurodegeneration. Metabolic brain disease. 2022 Dec; ?(?):. doi: 10.1007/s11011-022-01153-8. [PMID: 36576692]
  • Derya Cansız, Unsal Veli Ustundag, Ismail Unal, A Ata Alturfan, Ebru Emekli-Alturfan. Morphine attenuates neurotoxic effects of MPTP in zebrafish embryos by regulating oxidant/antioxidant balance and acetylcholinesterase activity. Drug and chemical toxicology. 2022 Nov; 45(6):2439-2447. doi: 10.1080/01480545.2021.1957558. [PMID: 34340603]
  • Samaresh Pal Roy, Sunil Kumar Kadiri, Vipulkumar V Karkar, Srinivasa Rao Konijeti. Antiparkinsonian activity of Tabebuia impetiginosa bark and biochemical analysis of dopamine in rat brain homogenates. Annales pharmaceutiques francaises. 2022 Nov; 80(6):853-863. doi: 10.1016/j.pharma.2022.02.007. [PMID: 35240121]
  • Yuhan Wu, Hao Liu, Yule Wang, Hongda Sheng, Zhilin Chen, Dejin Xun, Huimin Wu, Shun Xiao, Yong Bi, Yi Wang. DiHuangYin decoction protects dopaminergic neurons in a Parkinson's disease model by alleviating peripheral inflammation. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2022 Oct; 105(?):154357. doi: 10.1016/j.phymed.2022.154357. [PMID: 35933898]
  • Urmi Vora, Vivek Kumar Vyas, Pranay Wal, Bhagawati Saxena. Effects of eugenol on the behavioral and pathological progression in the MPTP-induced Parkinson's disease mouse model. Drug discoveries & therapeutics. 2022 Sep; 16(4):154-163. doi: 10.5582/ddt.2022.01026. [PMID: 36002316]
  • Li-Kung Wu, Surbhi Agarwal, Chia-Hua Kuo, Yen-Lun Kung, Cecilia Hsuan Day, Pi-Yu Lin, Shinn-Zong Lin, Dennis Jine-Yuan Hsieh, Chih-Yang Huang, Chien-Yi Chiang. Artemisia Leaf Extract protects against neuron toxicity by TRPML1 activation and promoting autophagy/mitophagy clearance in both in vitro and in vivo models of MPP+/MPTP-induced Parkinson's disease. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2022 Sep; 104(?):154250. doi: 10.1016/j.phymed.2022.154250. [PMID: 35752074]
  • Lei Wang, Xinghong Wu, Ge Yang, Nan Hu, Zijian Zhao, Lei Zhao, Shengyu Li. Cannabidiol Alleviates the Damage to Dopaminergic Neurons in 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Induced Parkinson's Disease Mice Via Regulating Neuronal Apoptosis and Neuroinflammation. Neuroscience. 2022 08; 498(?):64-72. doi: 10.1016/j.neuroscience.2022.06.036. [PMID: 35792194]
  • Francesca Palese, Silvia Pontis, Natalia Realini, Alexa Torrens, Faizy Ahmed, Francesca Assogna, Clelia Pellicano, Paola Bossù, Gianfranco Spalletta, Kim Green, Daniele Piomelli. Targeting NAAA counters dopamine neuron loss and symptom progression in mouse models of parkinsonism. Pharmacological research. 2022 08; 182(?):106338. doi: 10.1016/j.phrs.2022.106338. [PMID: 35781057]
  • José Luis Téllez-Arreola, Ataúlfo Martínez-Torres, Adriana E Flores-Moran, José M Lazaro-Guevara, Argel Estrada-Mondragón. Analysis of the MCTP Amino Acid Sequence Reveals the Conservation of Putative Calcium- and Lipid-Binding Pockets Within the C2 Domains In Silico. Journal of molecular evolution. 2022 08; 90(3-4):271-282. doi: 10.1007/s00239-022-10057-1. [PMID: 35604448]
  • Richard J Smeyne, Jeffrey B Eells, Debotri Chatterjee, Matthew Byrne, Shaw M Akula, Srinivas Sriramula, Dorcas P O'Rourke, Peter Schmidt. COVID-19 Infection Enhances Susceptibility to Oxidative Stress-Induced Parkinsonism. Movement disorders : official journal of the Movement Disorder Society. 2022 Jul; 37(7):1394-1404. doi: 10.1002/mds.29116. [PMID: 35579496]
  • Qingyu Ren, Xin Jiang, Yam Nath Paudel, Xin Gao, Daili Gao, Pengyu Zhang, Wenlong Sheng, Xueliang Shang, Kechun Liu, Xiujun Zhang, Meng Jin. Co-treatment with natural HMGB1 inhibitor Glycyrrhizin exerts neuroprotection and reverses Parkinson's disease like pathology in Zebrafish. Journal of ethnopharmacology. 2022 Jun; 292(?):115234. doi: 10.1016/j.jep.2022.115234. [PMID: 35358621]
  • Xiaojuan Han, Yuan Liu, Yan Dai, Tianshu Xu, Qinghui Hu, Xiaolan Yi, Liangyou Rui, Gang Hu, Jun Hu. Neuronal SH2B1 attenuates apoptosis in an MPTP mouse model of Parkinson's disease via promoting PLIN4 degradation. Redox biology. 2022 06; 52(?):102308. doi: 10.1016/j.redox.2022.102308. [PMID: 35390677]
  • Wei Hang, Hui-Jie Fan, Yan-Rong Li, Qi Xiao, Lu Jia, Li-Juan Song, Yao Gao, Xiao-Ming Jin, Bao-Guo Xiao, Jie-Zhong Yu, Cun-Gen Ma, Zhi Chai. Wuzi Yanzong pill attenuates MPTP-induced Parkinson's Disease via PI3K/Akt signaling pathway. Metabolic brain disease. 2022 06; 37(5):1435-1450. doi: 10.1007/s11011-022-00993-8. [PMID: 35488941]
  • Tingting Zuo, Mo Xie, Meiling Yan, Zengyan Zhang, Tian Tian, Ying Zhu, Lihua Wang, Yanhong Sun. In situ analysis of acupuncture protecting dopaminergic neurons from lipid peroxidative damage in mice of Parkinson's disease. Cell proliferation. 2022 Apr; 55(4):e13213. doi: 10.1111/cpr.13213. [PMID: 35274781]
  • Shan Dongjie, R Samuel Rajendran, Qing Xia, Gaimei She, Pengfei Tu, Yun Zhang, Kechun Liu. Neuroprotective effects of Tongtian oral liquid, a Traditional Chinese Medicine in the Parkinson's disease-induced zebrafish model. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2022 Apr; 148(?):112706. doi: 10.1016/j.biopha.2022.112706. [PMID: 35152046]
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