Cells (Mar 2020)

Inhibition of Gastrin-Releasing Peptide Attenuates Phosphate-Induced Vascular Calcification

  • Hyun-Joo Park,
  • Yeon Kim,
  • Mi-Kyoung Kim,
  • Jae Joon Hwang,
  • Hyung Joon Kim,
  • Soo-Kyung Bae,
  • Moon-Kyoung Bae

DOI
https://doi.org/10.3390/cells9030737
Journal volume & issue
Vol. 9, no. 3
p. 737

Abstract

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Vascular calcification is the pathological deposition of calcium/phosphate in the vascular system and is closely associated with cardiovascular morbidity and mortality. Here, we investigated the role of gastrin-releasing peptide (GRP) in phosphate-induced vascular calcification and its potential regulatory mechanism. We found that the silencing of GRP gene and treatment with the GRP receptor antagonist, RC-3095, attenuated the inorganic phosphate-induced calcification of vascular smooth muscle cells (VSMCs). This attenuation was caused by inhibiting phenotype change, apoptosis and matrix vesicle release in VSMCs. Moreover, the treatment with RC-3095 effectively ameliorated phosphate-induced calcium deposition in rat aortas ex vivo and aortas of chronic kidney disease in mice in vivo. Therefore, the regulation of the GRP-GRP receptor axis may be a potential strategy for treatment of diseases associated with excessive vascular calcification.

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