Prevention of Vascular Calcification by Polyphosphates and Nucleotides
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- Villa-Bellosta Ricardo
- Laboratory of Molecular Toxicology, University of Zaragoza
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- Sorribas Víctor
- Laboratory of Molecular Toxicology, University of Zaragoza
書誌事項
- タイトル別名
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- – Role of ATP –
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説明
Background: In recent decades, the prevention of vascular calcification (VC) by pyrophosphate (PPi), bisphosphonates, and polyphosphates has been extensively reported. However, the possibility of direct inhibition of calcium phosphate deposition (CPD) by nucleoside-associated polyphosphates has not been addressed. We analyzed the role of ATP as an inhibitor of calcification in 2 ways: by characterizing the extracellular hydrolysis of ATP as source of PPi in the aorta, and by demonstrating the ability of ATP to prevent CPD by acting as a polyphosphate. Methods and Results: In our study, both PPi and ATP hydrolysis in the rat aorta was kinetically characterized, thereby resulting in apparent Michaelis-Menten constants of 179 and 435μmol/l, respectively, with the corresponding maximal velocities of 55.1 and 6,177nmol·g–1·min–1. According to these kinetic parameters, the theoretical PPi concentration in the aortic wall was 0.4–3.5μmol/L (for an ATP concentration range of 0.1–1.0μmol/L). In addition, we showed that nonhydrolyzable molecules are more efficient as CPD inhibitors than endogenous compounds, in accordance with the IC50 values: 1.2–2.4μmol/L for bisphosphonates vs. 8.8μmol/L for PPi, and 0.5–1.5μmol/L for nonhydrolyzable ATP analogs vs. 3.2μmol/L for ATP. Conclusions: Extracellular ATP can play an important role in the prevention of VC, not only as the source of PPi but also as a direct inhibitor of CPD. (Circ J 2013; 77: 2145–2151)<br>
収録刊行物
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- Circulation Journal
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Circulation Journal 77 (8), 2145-2151, 2013
一般社団法人 日本循環器学会
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詳細情報 詳細情報について
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- CRID
- 1390001205102778496
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- NII論文ID
- 10031178687
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- NII書誌ID
- AA11591968
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- COI
- 1:CAS:528:DC%2BC3sXhsVSltbjE
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- ISSN
- 13474820
- 13469843
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- PubMed
- 23595088
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可