• DocumentCode
    2740152
  • Title

    Effects of Interleukin-2 on the Mechanical Restitution and Post-rest Contraction in Rat Ventricular Papillary Muscle

  • Author

    Lin, G.-H. ; Ru, H.-L. ; Wu, P.-L. ; Cao, C.-M. ; Xia, Q.

  • Author_Institution
    Department of Physiology, Hangzhou Normal College Medical School
  • Volume
    2
  • fYear
    2004
  • fDate
    1-5 Sept. 2004
  • Firstpage
    3628
  • Lastpage
    3631
  • Abstract
    To determine whether application of interleukin-2 (IL-2) alters function of sarcoplasmic reticulum (SR), we measured mechanical restitution and post-rest potentiation (PRP) in isolated rat papillary muscles. Mechanical restitution curves were constructed by interpolating extrasystoles at different test intervals following a train of steady state beats. In control group, the maximal PRP was reached after 60-120s of rest and the maximal potentiation factor was 2.36 ± 0.23. IL-2 at 200 U/ml decreased the steady-state force of contraction to 56.4 ± 7.2% of pre-drug control. But the time constant of recovery of steady-state force was not altered after IL-2. IL-2 decreased PRP at all intervals, shifted the potentiation curve parallel to lower values. But the potentiation was enhanced when compared with pre-rest control value in the presence of IL-2. In papillary muscle treated with IL-2, the onset of maximal PRP was delayed and the potentiation factor after 300s was 4.72 ± 0.58 times that at the steady-state. Recirculation fraction of calcium calculated from the decay of PRP was 0.78 ± 0.09 in control and 0.59 ± 0.08 after IL-2 treatment. We conclude that IL-2 decreases the function of SR, which suggests that an impaired function of SR may contribute to the negative inotropic effect of IL-2.
  • Keywords
    Heart; Inotropy; Interleukin-2; Calcium; Cardiac disease; Cardiology; Force control; Heart; Mechanical variables measurement; Muscles; Steady-state; Strontium; Testing;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology Society, 2004. IEMBS '04. 26th Annual International Conference of the IEEE
  • Print_ISBN
    0-7803-8439-3
  • Type

    conf

  • DOI
    10.1109/IEMBS.2004.1404020
  • Filename
    1404020