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L-DOPA and Its Receptor GPR143: Implications for Pathogenesis and Therapy in Parkinson's Disease

期刊

FRONTIERS IN PHARMACOLOGY
卷 10, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2019.01119

关键词

L-DOPA; neurotransmitter; G protein-coupled receptor; Parkinson's disease; dopamine; Lewy bodies

资金

  1. Japanese SRF Grand for Biomedical Research [1565]
  2. Uehara Memorial Foundation [201320161, 201720339, 201810115]
  3. fund for Creation of Innovation Centers for Advanced Interdisciplinary Research Areas Program in the Project for Developing Innovation Systems from MEXT [42890001]
  4. Japanese government (MEXT) [8513]
  5. [15H04687]
  6. [18H02580]
  7. [18K14923]
  8. [18K06896]
  9. [19K16375]

向作者/读者索取更多资源

L-3,4-Dihydroxyphenylalanine (l-DOPA) is the most effective therapeutic agent for Parkinson's disease (PD). l-DOPA is traditionally believed to be an inert amino acid that exerts actions and effectiveness in PD through its conversion to dopamine. In contrast to this generally accepted idea, l-DOPA is proposed to be a neurotransmitter. Recently, GPR143 (OA1), the gene product of ocular albinism 1 was identified as a receptor candidate for L-DOPA. GPR143 is widely expressed in the central and peripheral nervous system. GPR143 immunoreactivity was colocalized with phosphorylated alpha-synuclein in Lewy bodies in PD brains. GPR143 may contribute to the therapeutic effectiveness of l-DOPA and might be related to pathogenesis of PD.

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