Feedback control of multiple hemodynamic variables with multiple cardiovascular drugs

Annu Int Conf IEEE Eng Med Biol Soc. 2009:2009:2030-2. doi: 10.1109/IEMBS.2009.5334417.

Abstract

The ultimate goal of disease treatment is to control the biological system beyond the native regulation to combat pathological process. To maximize the advantage of drugs, we attempted to pharmacologically control the biological system at will, e.g., control multiple hemodynamic variables with multiple cardiovascular drugs. A comprehensive physiological cardiovascular model enabled us to evaluate cardiovascular properties (pump function, vascular resistance, and blood volume) and the feedback control of these properties. In 12 dogs, with dobutamine (5+/-3 mug.kg(-1).min(-1)), nitroprusside (4+/-2 mug.kg(-1).min(-1)), dextran (2+/-2 ml.kg(-1)), and furosemide (10 mg in one, 20 mg in one), rapid, sufficient and stable control of pump function, vascular resistance and blood volume resulted in similarly quick and stable control of blood pressure, cardiac output and left atrial pressure in 5+/-7, 7+/-5, and 12+/-10 minutes, respectively. These variables remained stable for 60 minutes (RMS 4+/-3 mmHg, 5+/-2 ml.min(-1).kg(-1), 0.8+/-0.6 mmHg, respectively).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Blood Pressure / drug effects*
  • Blood Volume / drug effects*
  • Cardiac Output / drug effects*
  • Cardiovascular Physiological Phenomena / drug effects
  • Dextrans / pharmacology
  • Dobutamine / pharmacology*
  • Dogs
  • Functional Laterality
  • Furosemide / pharmacology
  • Heart Atria / drug effects
  • Hemodynamics / drug effects
  • Hemodynamics / physiology*
  • Kinetics

Substances

  • Adrenergic beta-Agonists
  • Dextrans
  • Dobutamine
  • Furosemide