Enid T. McKinley, Timothy C. Baranowski, Delali O. Blavo, Candace Cato, Thanh N. Doan, Amy L. Rubinstein
{"title":"mptp对斑马鱼多巴胺能神经元毒性的神经保护作用","authors":"Enid T. McKinley, Timothy C. Baranowski, Delali O. Blavo, Candace Cato, Thanh N. Doan, Amy L. Rubinstein","doi":"10.1016/j.molbrainres.2005.08.014","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Parkinson's disease is characterized by a severe loss of </span>dopaminergic<span><span> neurons resulting in a range of motor deficits. The neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is known to cause a similar loss of dopaminergic neurons in the human midbrain with corresponding Parkinsonian symptoms. Several animal species have also shown sensitivity to MPTP, including primates, mice, goldfish, and, most recently, zebrafish. This study demonstrates that the effect of MPTP on dopaminergic neurons in zebrafish larvae is mediated by the same pathways that have been demonstrated in mammalian species. MPTP-induced </span>neurodegeneration was prevented by co-incubation with either the monoamine oxidase-B (MAO-B) inhibitor </span></span><span>l</span><span>-deprenyl or the dopamine transporter<span> (DAT) inhibitor nomifensine. Furthermore, targeted inactivation of the </span></span><em>DAT</em><span> gene by antisense morpholinos also protected neurons from MPTP damage. Thus, the mechanism for MPTP-induced dopaminergic neuron toxicity in mammals is conserved in zebrafish larvae. Effects on swimming behavior and touch response that result from MPTP damage are partially ameliorated by both </span><span>l</span>-deprenyl and <em>DAT</em> knockdown.</p></div>","PeriodicalId":100932,"journal":{"name":"Molecular Brain Research","volume":"141 2","pages":"Pages 128-137"},"PeriodicalIF":0.0000,"publicationDate":"2005-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.molbrainres.2005.08.014","citationCount":"175","resultStr":"{\"title\":\"Neuroprotection of MPTP-induced toxicity in zebrafish dopaminergic neurons\",\"authors\":\"Enid T. McKinley, Timothy C. Baranowski, Delali O. Blavo, Candace Cato, Thanh N. Doan, Amy L. Rubinstein\",\"doi\":\"10.1016/j.molbrainres.2005.08.014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>Parkinson's disease is characterized by a severe loss of </span>dopaminergic<span><span> neurons resulting in a range of motor deficits. The neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is known to cause a similar loss of dopaminergic neurons in the human midbrain with corresponding Parkinsonian symptoms. Several animal species have also shown sensitivity to MPTP, including primates, mice, goldfish, and, most recently, zebrafish. This study demonstrates that the effect of MPTP on dopaminergic neurons in zebrafish larvae is mediated by the same pathways that have been demonstrated in mammalian species. MPTP-induced </span>neurodegeneration was prevented by co-incubation with either the monoamine oxidase-B (MAO-B) inhibitor </span></span><span>l</span><span>-deprenyl or the dopamine transporter<span> (DAT) inhibitor nomifensine. Furthermore, targeted inactivation of the </span></span><em>DAT</em><span> gene by antisense morpholinos also protected neurons from MPTP damage. Thus, the mechanism for MPTP-induced dopaminergic neuron toxicity in mammals is conserved in zebrafish larvae. Effects on swimming behavior and touch response that result from MPTP damage are partially ameliorated by both </span><span>l</span>-deprenyl and <em>DAT</em> knockdown.</p></div>\",\"PeriodicalId\":100932,\"journal\":{\"name\":\"Molecular Brain Research\",\"volume\":\"141 2\",\"pages\":\"Pages 128-137\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-11-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.molbrainres.2005.08.014\",\"citationCount\":\"175\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Brain Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0169328X05003426\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Brain Research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169328X05003426","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Neuroprotection of MPTP-induced toxicity in zebrafish dopaminergic neurons
Parkinson's disease is characterized by a severe loss of dopaminergic neurons resulting in a range of motor deficits. The neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is known to cause a similar loss of dopaminergic neurons in the human midbrain with corresponding Parkinsonian symptoms. Several animal species have also shown sensitivity to MPTP, including primates, mice, goldfish, and, most recently, zebrafish. This study demonstrates that the effect of MPTP on dopaminergic neurons in zebrafish larvae is mediated by the same pathways that have been demonstrated in mammalian species. MPTP-induced neurodegeneration was prevented by co-incubation with either the monoamine oxidase-B (MAO-B) inhibitor l-deprenyl or the dopamine transporter (DAT) inhibitor nomifensine. Furthermore, targeted inactivation of the DAT gene by antisense morpholinos also protected neurons from MPTP damage. Thus, the mechanism for MPTP-induced dopaminergic neuron toxicity in mammals is conserved in zebrafish larvae. Effects on swimming behavior and touch response that result from MPTP damage are partially ameliorated by both l-deprenyl and DAT knockdown.