Large numbers of patients with advanced heart disease undergo anesthesia and surgery each year. Methods of safely anesthetizing these patients are available, but they are frequently associated with delayed emergence and a prolonged period of respiratory depression requiring mechanically assisted ventilation, often in an intensive care setting. The use of the potent inhalation agents in these patients would be ideal from the standpoint of affording a more rapid recovery. However, cardiac contractile depression with these anesthetics can be appreciable and can result in dangerous depression of circulatory function. Antagonism of the depression of cardiac function caused by the potent agents is not readily accomplished with the presently available cardiotonic drugs because of side effects, such as dysrhythmias, associated with their use. It is proposed that a better understanding of the mechanisms which underlie anesthetic-induced negative inotropy will facilitate the development of rational methods for its reversal. The general scientific goals of the presently proposed research are to perform, in isolated, intact, cardiac contractile tissue, a systematic investigation of the effects of general anesthetics on the steps in electromechanical coupling which result in contraction, and to investigate methods for reversing such depression.
Specific aims are to study the effects of anesthetics on the sources of calcium which activate contraction, i.e. on the calcium which is derived via transsarcolemmal influx and via intracellular release from the sarcoplasmic reticulum. Determination of the effect of an anesthetic on a particular source of activator calcium will be accomplished by measuring the anesthetic's effect on contractile performance under conditions which inhibit, or enhance the influence of the particular source of calcium on the activation of contraction. Calcium selective microelectrodes will be used to evaluate the effect of anesthetics on calcium movement (calcium influx) during contraction under these conditions. It is expected that knowledge concerning the differential effects of anesthetics on the calcium will suggest which of the several newly developed positive inotropic agents will be effective in reversing their specific negative inotrophic effects. Studies employing these agents will be performed.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM029527-04A2
Application #
3277182
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1982-05-01
Project End
1991-01-31
Budget Start
1988-02-01
Budget End
1989-01-31
Support Year
4
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Komai, H; Chiou, K Y; Rusy, B F (1996) Lack of inhibition by inhalational anesthetics of myocardial contraction dependent on intracellular sodium activity. Anesthesiology 85:1139-46
Komai, H; Redon, D; Rusy, B F (1995) Procaine enhancement of the rapid cooling contracture and inhibition of the decay of potentiated state in rabbit papillary muscle. J Mol Cell Cardiol 27:2543-50
Komai, H; Rusy, B F (1994) Effects of inhibition of transsarcolemmal calcium influx on content and releasability of calcium stored in sarcoplasmic reticulum of intact myocardium. Adv Pharmacol 31:215-21
Komai, H; Rusy, B F (1994) Effect of thiopental on Ca2+ release from sarcoplasmic reticulum in intact myocardium. Anesthesiology 81:946-52
Komai, H; Rusy, B F (1993) Effects of inhibition of transsarcolemmal calcium influx by nickel on force of postrest contraction and on contracture induced by rapid cooling. Cardiovasc Res 27:801-6
Komai, H; Rusy, B F (1991) Contribution of the known subcellular effects of anesthetics to their negative inotropic effect in intact myocardium. Adv Exp Med Biol 301:115-23
Komai, H; Redon, D; Rusy, B F (1991) Effects of thiopental and halothane on spontaneous contractile activity induced in isolated ventricular muscles of the rabbit. Acta Anaesthesiol Scand 35:373-9
Komai, H; Rusy, B F (1990) Direct effect of halothane and isoflurane on the function of the sarcoplasmic reticulum in intact rabbit atria. Anesthesiology 72:694-8
Rusy, B F; Amuzu, J K; Bosscher, H A et al. (1990) Negative inotropic effect of ketamine in rabbit ventricular muscle. Anesth Analg 71:275-8
Komai, H; Redon, D; Rusy, B F (1989) Effects of isoflurane and halothane on rapid cooling contractures in myocardial tissue. Am J Physiol 257:H1804-11

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