ナカムラ フミオ
Nakamura Fumio
中村 史雄 所属 医学部 医学科 職種 教授・基幹分野長 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | L-DOPA sensitizes vasomotor tone by modulating the vascular alpha1-adrenergic receptor. |
掲載誌名 | 正式名:JCI insight 略 称:JCI Insight ISSNコード:(2379-3708)2379-3708(Linking) |
掲載区分 | 国外 |
巻・号・頁 | 2(18),pp.e90903 |
著者・共著者 | Masukawa Daiki†, Koga Motokazu, Sezaki Anna, Nakao Yuka, Kamikubo Yuji, Hashimoto Tatsuo, Okuyama-Oki Yuki, Aladeokin Aderemi Caleb, Nakamura Fumio, Yokoyama Utako, Wakui Hiromichi, Ichinose Hiroshi, Sakurai Takashi, Umemura Satoshi, Tamura Koichi, Ishikawa Yoshihiro, Goshima Yoshio* |
発行年月 | 2017/09 |
概要 | Blood pressure is regulated by extrinsic factors including noradrenaline, the sympathetic neurotransmitter that controls cardiovascular functions through adrenergic receptors. However, the fine-tuning system of noradrenaline signaling is relatively unknown. We here show that l-3,4-dihydroxyphenylalanine (L-DOPA), a precursor of catecholamines, sensitizes the vascular adrenergic receptor alpha1 (ADRA1) through activation of L-DOPA receptor GPR143. In WT mice, intravenous infusion of the ADRA1 agonist phenylephrine induced a transient elevation of blood pressure. This response was attenuated in Gpr143 gene-deficient (Gpr143-/y) mice. Specific knockout of Gpr143 in vascular smooth muscle cells (VSMCs) also showed a similar phenotype, indicating that L-DOPA directly modulates ADRA1 signaling in the VSMCs. L-DOPA at nanomolar concentrations alone produced no effect on the VSMCs, but it enhanced phenylephrine-induced vasoconstriction and intracellular Ca2+ responses. Phenylephrine also augmented the phosphorylation of extracellular signal-regulated kinases in cultured VSMCs from WT but not Gpr143-/y mice. In WT mice, blood pressure increased during the transition from light-rest to dark-active phases. This elevation was not observed in Gpr143-/y mice. Taken together, our findings provide evidence for L-DOPA/GPR143 signaling that exerts precursor control of sympathetic neurotransmission through sensitizing vascular ADRA1. |
DOI | 10.1172/jci.insight.90903 |
PMID | 28931752 |