A novel lipoprotein (a) lowering drug, D-47, decreases neointima thickening after vascular injury

  • Nakaya Yutaka
    Department of Nutrition and Metabolism, Institute of Biomedical sciences, Tokushima University Graduate School
  • Fukuda Daiju
    Department of Cardiology, Institute of Biomedical sciences, Tokushima University Graduate School
  • Oyamada Takashi
    Department of Nutrition and Metabolism, Institute of Biomedical sciences, Tokushima University Graduate School
  • Ogawa Kazuo
    Pharmaceutical Science, Tokushima Bunri University
  • Harada Nagakatsu
    Department of Nutrition and Metabolism, Institute of Biomedical sciences, Tokushima University Graduate School
  • Nakagami Hironori
    Department of Clinical Gene Therapy, Graduate School of Medicine, Osaka University
  • Morishita Ryuichi
    Department of Clinical Gene Therapy, Graduate School of Medicine, Osaka University
  • Sata Masataka
    Department of Cardiology, Institute of Biomedical sciences, Tokushima University Graduate School
  • Sakaue Hiroshi
    Department of Nutrition and Metabolism, Institute of Biomedical sciences, Tokushima University Graduate School

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Abstract

<p>Although Lp(a) have been thought to be a cardiovascular risk factor, it is unclear whether lowering Lp(a) levels reduces the risk of cardiovascular diseases. No pharmacological agents which selectively reduce serum Lp(a) levels, and Lp(a) is present in primate but absent in common laboratory animals such as mice and pigs. In the present study we used transgenic mice of human Lp(a) and tested effect a novel Lp(a) lowering drug D-47 on neointima formation after vascular injury. D-47 successfully decreased plasma levels of Lp(a) and possibly inhibited neointima formation in Lp(a) transgenic mice. The results indicate that we can modulate plasma Lp(a) levels by pharmacologic agents and inhibit atherogenic properties of Lp(a) by reducing plasma levels of Lp(a). J. Med. Invest. 64: 64-67, February, 2017</p>

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