[1] Teri Capriotti.Parkinson disease[J]. Home Healthcare Now, 2016, 34(6): 300-307. [2] Alves G, Forsaa EB, Pedersen KF, et al.epidemiology of parkinson's disease[J]. J Neural Transm (Vienna), 2017, 124(8): 901-905. [3] Abeliovich A, Rhinn H.Parkinson's disease: guilt by genetic association[J]. Nature, 2016, 533(7601): 40-41. [4] Henrich MT, Geibl FF, Lee B, et al.A53T-α-synuclein overexpression in murine locus coeruleus induces Parkinson's disease-like pathology in neurons and glia[J]. Acta Neuropathol Commun, 2018, 6(1): 39. [5] Zhou TT, Zhang QS.Effects of bibenzyl compound (20C) from gastrodia elata on MPTP/p-induced mice and mechanism[J]. Chinese Journal of Pharmacovigilance(中国药物警戒), 2020, 17(11): 753-757,772. [6] Zhang QS, Chen Y.Parkinsonian lesion in rat induced by rotenone and its possible mechanism[J]. Chinese Journal of Pharmacovigilance(中国药物警戒), 2017, 14(9): 513-517. [7] Mattammal MB, Haring JH, Chung HD, et al.An endogenous dopaminergic neurotoxin: implication for Parkinson's disease[J]. Neurodegeneration, 1995, 4(3): 271-281. [8] Jackson-Lewis V, Przedborski S.Protocol for the MPTP mouse model of parkinson's disease[J]. Nature Protocols, 2007, 2(1): 141-151. [9] Masato A, Plotegher N, Boassa D, et al.Impaired dopamine metabolism in Parkinson's disease pathogenesis[J]. Molecular Neurodegeneration, 2019, 14(1): 35. [10] Marchitti SA, Deitrich RA, Vasiliou V.Neurotoxicity and metabolism of the catecholamine-derived 3,4-dihydroxyphenylacetaldehyde and 3,4-dihydroxyphenylglycolaldehyde: the role of aldehyde dehydrogenase[J]. Pharmacological Reviews, 2007, 59(2): 125-150. [11] Lima Vanderlei de A, Do Nascimento LA, Eliezer D, et al. Role of Parkinson's disease-linked mutations and N-terminal acetylation on the oligomerization of α-synuclein induced by 3,4-dihydroxyphenylacetaldehyde[J]. ACS Chemical Neuroscience, 2019, 10(1): 690-703. [12] Burke WJ, Li SW, Williams EA, et al.3,4-Dihydroxyphenylacetaldehyde is the toxic dopamine metabolite in vivo: implications for Parkinson's disease pathogenesis[J]. Brain Research, 2003, 989(2): 205-213. [13] Goldstein DS, Sullivan P, Cooney A, et al.Vesicular uptake blockade generates the toxic dopamine metabolite 3,4-dihydroxyphenylacetal- dehyde in PC12 cells: relevance to the pathogenesis of Parkinson's disease[J]. Journal of Neurochemistry, 2012, 123(6): 932-943. [14] Casida JE, Ford B, Jinsmaa Y, et al.Benomyl, aldehyde dehy- drogenase, DOPAL, and the catecholaldehyde hypothesis for the pathogenesis of Parkinson's disease[J]. Chemical Research in Toxicology, 2014, 27(8): 1359-1361. [15] Goldstein DS.The catecholaldehyde hypothesis: where MAO fits in[J]. Journal of Neural Transmission, 2020, 127(2): 169-177. |