Drug Res (Stuttg) 2016; 66(05): 270-274
DOI: 10.1055/s-0035-1569405
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Effects of Uric Acid on the NO Production of HUVECs and its Restoration by Urate Lowering Agents

Authors

  • M. Mishima

    1   Division of Regenerative Medicine and Therapeutics, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Sciences, Tottori University, Yonago, Japan
  • T. Hamada

    2   Department of Regional Medicine, Tottori University Faculty of Medicine, Yonago, Japan
  • N. Maharani

    1   Division of Regenerative Medicine and Therapeutics, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Sciences, Tottori University, Yonago, Japan
  • N. Ikeda

    1   Division of Regenerative Medicine and Therapeutics, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Sciences, Tottori University, Yonago, Japan
  • T. Onohara

    3   Division of Organ Regeneration Surgery, Tottori University Faculty of Medicine, Yonago, Japan
  • T. Notsu

    1   Division of Regenerative Medicine and Therapeutics, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Sciences, Tottori University, Yonago, Japan
  • H. Ninomiya

    4   Department of Biological Regulation, Tottori University Faculty of Medicine, Yonago, Japan
  • S. Miyazaki

    5   Division of Cardiovascular Medicine, Fujii Masao Memorial Hospital, Kurayoshi, Japan
  • E. Mizuta

    6   Department of Cardiovascular Medicine, Sanin Rosai Hospital, Yonago, Japan
  • S. Sugihara

    7   Division of Cardiovascular Medicine Department of Molecular Medicine and Therapeutics, Tottori University Faculty of Medicine, Yonago, Japan
  • M. Kato

    7   Division of Cardiovascular Medicine Department of Molecular Medicine and Therapeutics, Tottori University Faculty of Medicine, Yonago, Japan
  • K. Ogino

    8   Department of Clinical Laboratory, Tottori University Hospital, Yonago, Japan
  • M. Kuwabara

    9   Department of Cardiology, Toranomon Hospital, Tokyo, Japan
  • Y. Hirota

    10   Department of Surgery, Tomimasu Surgical and Primary Care Clinic, Yonago, Japan
  • A. Yoshida

    1   Division of Regenerative Medicine and Therapeutics, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Sciences, Tottori University, Yonago, Japan
  • N. Otani

    11   Department of Pharmacology, Dokkyo Medical College, Tochigi, Japan
  • N. Anzai

    11   Department of Pharmacology, Dokkyo Medical College, Tochigi, Japan
  • I. Hisatome

    1   Division of Regenerative Medicine and Therapeutics, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Sciences, Tottori University, Yonago, Japan
Further Information

Publication History

received 20 May 2015

accepted 29 December 2015

Publication Date:
24 February 2016 (online)

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Abstract

Background: Although urate impaired the endothelial function, its underlying mechanism remains unknown. We hypothesized that urate impaired nitric oxide (NO) production in human umbilical vein endothelial cells (HUVECs) via activation of uric acid transporters (UATs).

Purpose and method: In the present study, we studied effects of urate on NO production and eNOS protein expression in HUVEC cells in the presence and absence of urate lowering agents using molecular biological and biochemical assays.

Results: HUVECs expressed the 4 kinds of UATs, URATv1, ABCG2, MRP4 and MCT9. Exposure to urate at 7 mg/dl for 24 h significantly reduced production of NO. Pretreatment with benzbromarone, losartan or irbesartan normalized NO production. The same exposure resulted in dephosphorylation of endothelial NO synthase (eNOS) in HUVECs. Again pretreatment with benzbromarone, losartan or irbesartan abolished this effect.

Conclusion: Urate reduced NO production by impaired phosphorylation of eNOS in HUVEC via activation of UATs, which could be normalized by urate lowering agents.

Supplementary Material