1-Methyl-4-phenylpyridinium stereotactic infusion completely and specifically ablated the nigrostriatal dopaminergic pathway in rhesus macaque

Complete and specific ablation of a single dopaminergic (DA) pathway is a critical step to distinguish the roles of DA pathways in vivo. However, this kind of technique has not been reported in non-human primates. This study aimed to establish a lesioning method with a complete and specific ablation...

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Veröffentlicht in:PloS one 2015-05, Vol.10 (5), p.e0127953-e0127953
Hauptverfasser: Lei, Xiaoguang, Li, Hao, Huang, Baihui, Rizak, Joshua, Li, Ling, Xu, Liqi, Huang, Tianzhuang, Liu, Li, Wu, Jing, Lü, Longbao, Wang, Zhengbo, Hu, Yingzhou, Le, Weidong, Deng, Xingli, Li, Jiali, Yao, Yonggang, Xu, Lin, Hu, Xintian, Zhang, Baorong
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container_issue 5
container_start_page e0127953
container_title PloS one
container_volume 10
creator Lei, Xiaoguang
Li, Hao
Huang, Baihui
Rizak, Joshua
Li, Ling
Xu, Liqi
Huang, Tianzhuang
Liu, Li
Wu, Jing
Lü, Longbao
Wang, Zhengbo
Hu, Yingzhou
Le, Weidong
Deng, Xingli
Li, Jiali
Yao, Yonggang
Xu, Lin
Hu, Xintian
Zhang, Baorong
description Complete and specific ablation of a single dopaminergic (DA) pathway is a critical step to distinguish the roles of DA pathways in vivo. However, this kind of technique has not been reported in non-human primates. This study aimed to establish a lesioning method with a complete and specific ablation. A carefully designed infusion route based on a MRI stereotactic technique was developed to deliver the highly selective dopaminergic toxin 1-methyl-4-phenylpyridinium (MPP+) unilaterally into multiple sites of compact part of substantia nigra (SNc) and striatum in monkeys. The nigrostriatal DA pathway was selected because lesioning of this pathway may induce symptoms that are suitable for evaluation. The pathological, behavioral, neuropharmacological, and clinical laboratorial data were collected to evaluate the lesioning effects. Pathological examination revealed a complete ablation of tyrosine hydroxylase positive (TH+) neurons in the SNc, while preserving intact TH+ neurons in the ventral tegmental area (VTA) nearby. TH+ projections in the striatum were also unilaterally lost. The monkeys displayed stable (>28 weeks) rotations and symptoms which were expected with loss of DA neurons in the SNc, with rest tremor being an exception. No item implied the presence of a severe side effect caused by the operation or the intracerebral MPP+ infusion. The results suggested that rest tremor may not directly rely on the nigrostriatal pathway. Taken together, in addition to providing a specific nigrostriatal DA lesioned model, this method, combined with brain stimulation or other techniques, can be applied as a powerful tool for the complete lesion of any desired DA pathway in order to study its specific functions in the brain.
doi_str_mv 10.1371/journal.pone.0127953
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blood</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson's disease</topic><topic>Primates</topic><topic>Respiration - drug effects</topic><topic>Rotation</topic><topic>Stereotaxic Techniques</topic><topic>Substantia nigra</topic><topic>Substantia Nigra - drug effects</topic><topic>Substantia Nigra - pathology</topic><topic>Toxins</topic><topic>Tremor</topic><topic>Tyrosine</topic><topic>Tyrosine 3-monooxygenase</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><topic>Ventral tegmentum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lei, Xiaoguang</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Huang, Baihui</creatorcontrib><creatorcontrib>Rizak, Joshua</creatorcontrib><creatorcontrib>Li, Ling</creatorcontrib><creatorcontrib>Xu, Liqi</creatorcontrib><creatorcontrib>Huang, Tianzhuang</creatorcontrib><creatorcontrib>Liu, Li</creatorcontrib><creatorcontrib>Wu, Jing</creatorcontrib><creatorcontrib>Lü, Longbao</creatorcontrib><creatorcontrib>Wang, Zhengbo</creatorcontrib><creatorcontrib>Hu, Yingzhou</creatorcontrib><creatorcontrib>Le, Weidong</creatorcontrib><creatorcontrib>Deng, Xingli</creatorcontrib><creatorcontrib>Li, Jiali</creatorcontrib><creatorcontrib>Yao, Yonggang</creatorcontrib><creatorcontrib>Xu, Lin</creatorcontrib><creatorcontrib>Hu, Xintian</creatorcontrib><creatorcontrib>Zhang, Baorong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lei, Xiaoguang</au><au>Li, Hao</au><au>Huang, Baihui</au><au>Rizak, Joshua</au><au>Li, Ling</au><au>Xu, Liqi</au><au>Huang, Tianzhuang</au><au>Liu, Li</au><au>Wu, Jing</au><au>Lü, Longbao</au><au>Wang, Zhengbo</au><au>Hu, Yingzhou</au><au>Le, Weidong</au><au>Deng, Xingli</au><au>Li, Jiali</au><au>Yao, Yonggang</au><au>Xu, Lin</au><au>Hu, Xintian</au><au>Zhang, Baorong</au><au>Li, Xiao-Jiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1-Methyl-4-phenylpyridinium stereotactic infusion completely and specifically ablated the nigrostriatal dopaminergic pathway in rhesus macaque</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-05-26</date><risdate>2015</risdate><volume>10</volume><issue>5</issue><spage>e0127953</spage><epage>e0127953</epage><pages>e0127953-e0127953</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Complete and specific ablation of a single dopaminergic (DA) pathway is a critical step to distinguish the roles of DA pathways in vivo. However, this kind of technique has not been reported in non-human primates. This study aimed to establish a lesioning method with a complete and specific ablation. A carefully designed infusion route based on a MRI stereotactic technique was developed to deliver the highly selective dopaminergic toxin 1-methyl-4-phenylpyridinium (MPP+) unilaterally into multiple sites of compact part of substantia nigra (SNc) and striatum in monkeys. The nigrostriatal DA pathway was selected because lesioning of this pathway may induce symptoms that are suitable for evaluation. The pathological, behavioral, neuropharmacological, and clinical laboratorial data were collected to evaluate the lesioning effects. Pathological examination revealed a complete ablation of tyrosine hydroxylase positive (TH+) neurons in the SNc, while preserving intact TH+ neurons in the ventral tegmental area (VTA) nearby. TH+ projections in the striatum were also unilaterally lost. The monkeys displayed stable (&gt;28 weeks) rotations and symptoms which were expected with loss of DA neurons in the SNc, with rest tremor being an exception. No item implied the presence of a severe side effect caused by the operation or the intracerebral MPP+ infusion. The results suggested that rest tremor may not directly rely on the nigrostriatal pathway. Taken together, in addition to providing a specific nigrostriatal DA lesioned model, this method, combined with brain stimulation or other techniques, can be applied as a powerful tool for the complete lesion of any desired DA pathway in order to study its specific functions in the brain.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26010745</pmid><doi>10.1371/journal.pone.0127953</doi><oa>free_for_read</oa></addata></record>
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1932-6203
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subjects 1-Methyl-4-phenylpyridinium - administration & dosage
1-Methyl-4-phenylpyridinium - pharmacology
1-Methyl-4-phenylpyridinium - therapeutic use
Ablation
Animals
Behavior, Animal
Body Weight - drug effects
Brain
Cell Count
Corpus Striatum - pathology
Dopamine receptors
Dopaminergic Neurons - drug effects
Dopaminergic Neurons - pathology
Enterprise zones
Five year plans
Hematologic Tests
Hydroxylase
In vivo methods and tests
Macaca mulatta
Magnetic resonance imaging
Male
Market economies
Monkeys
MPP
Neostriatum
Neural Pathways - drug effects
Neural Pathways - pathology
Neurons
NMR
Nuclear magnetic resonance
Parkinson Disease - blood
Parkinson Disease - drug therapy
Parkinson's disease
Primates
Respiration - drug effects
Rotation
Stereotaxic Techniques
Substantia nigra
Substantia Nigra - drug effects
Substantia Nigra - pathology
Toxins
Tremor
Tyrosine
Tyrosine 3-monooxygenase
Tyrosine 3-Monooxygenase - metabolism
Ventral tegmentum
title 1-Methyl-4-phenylpyridinium stereotactic infusion completely and specifically ablated the nigrostriatal dopaminergic pathway in rhesus macaque
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