• DocumentCode
    386590
  • Title

    Changes in the structure and biosynthetic activity of porcine heart valve leaflets under elevated pressure

  • Author

    Xing, Yun ; Yoganathan, Ajit P.

  • Author_Institution
    Sch. of Chem. Eng., Georgia Inst. of Technol., Atlanta, GA, USA
  • Volume
    1
  • fYear
    2002
  • fDate
    2002
  • Firstpage
    837
  • Abstract
    Fresh porcine heart aortic valves were harvested and cultured for 48 hrs under different pressure conditions. Techniques including routine H&E, Movat´s staining, a SMC actin immunohistochemistry, and 3H-proline radiolabeling were performed. Results showed that the three-layered structure became less distinct after incubation; this was true for both control and pressure groups. The number of α-SMC actin immunoreactive cells decreased in both elevated pressure and control groups; however, the pulsatile pressure group generally retained significantly more actin than control. Elevated pressure leaded to increased protein synthesis; this increase was proportional to the magnitude of applied pressure. Movat´s staining showed less dense collagen in control than in the pressure group. Cell morphology was also different: the pressure group had a higher percentage of elongated cells, and most cells attach well to surrounding matrix; while in the control group, cells are more tended to be rounded and detached from matrix.
  • Keywords
    cardiology; cellular biophysics; haemodynamics; proteins; pulsatile flow; α-SMC actin immunoreactive cells; 48 h; 3H-proline radiolabeling; H; Movat´s staining; SMC actin immunohistochemistry; biosynthetic activity; cell morphology; cellular attachment; elevated pressure; elongated cells; incubation; porcine heart valve leaflets; three-layered structure; Amino acids; Biomedical engineering; Chemical engineering; Heart valves; Hypertension; Immune system; Pressure control; Shape control; Sliding mode control; Stress;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology, 2002. 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society EMBS/BMES Conference, 2002. Proceedings of the Second Joint
  • ISSN
    1094-687X
  • Print_ISBN
    0-7803-7612-9
  • Type

    conf

  • DOI
    10.1109/IEMBS.2002.1137101
  • Filename
    1137101