Previous work in the anesthetized dog has demonstrated that following coronary ligation in the chronically (2-3 weeks) sympathetomized heart, infarct size is dramatically less than in controls. This anti-infarction effect is not evident immediately after sympathectomy, but results strongly suggest that the action is attributable to time dependent reductions in both myocardial oxygen requirement and coronary collateral resistances. To further explore this effect and its underlying causes, the proposed work is an extension of 5 previously funded studies. Studies proposed are as follows: (1) Study 6 will use the nitro-blue tetrazolium method to examine the anti-infarction effect after longer periods of cardiac sympathectomy (4-12 weeks). The results will provide further insight into the time-dependency of the effect. (2) Study 7 will use retrograde flow techniques in the isolated heart to examine the changes in collateral resistances after longer periods of sympathectomy (4-12 weeks). If as previously suggested, the collateral circulation undergoes a structural development after sympathectomy, the changes in resistance should be progressive. (3) Study 8 will extend previous work to a more physiological preparation--the chronically instrumented conscious dog. Following 2-12 weeks of sympathectomy, changes in myocardial contractile function (LVP, uP/dP max, segmental shortening) and in collateral function (peripheral coronary pressure, microsphere perfusion) during 2-min coronary occlusions will be assessed in the conscious animal and compared to controls. (4) Study 9 will examine the effect of chronic sympathectomy (2-12 weeks) on myocardial oxygen and blood flow requirements in the conscious dog. At rest and during standardized exercise, indices of cardiac performance (LVP, dP/dt max, TTI, segmental shortening, heart rate, rate-pressure product) will be monitored and related to MVO2 and blood flow. The results of these studies will tremendously expand our understanding of the long-term effects of cardiac sympathectomy, especially during myocardial ischemic insult.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL029232-04
Application #
3340351
Study Section
Cardiovascular Study Section (CVA)
Project Start
1982-01-01
Project End
1988-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
4
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Texas College of Osteopathic Medicine
Department
Type
Schools of Osteopathy
DUNS #
City
Fort Worth
State
TX
Country
United States
Zip Code
76107
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Gwirtz, P A (1995) Coronary alpha 1-constrictor tone during renovascular hypertension. Circulation 92:1576-81
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Tsuchida, A; Liu, Y; Liu, G S et al. (1994) alpha 1-adrenergic agonists precondition rabbit ischemic myocardium independent of adenosine by direct activation of protein kinase C. Circ Res 75:576-85
Quist, E E; Lee, S C; Vasan, R et al. (1994) Chronic sympathectomy of canine cardiac ventricles affects Gs-adenylyl cyclase coupling and muscarinic receptor density. J Cardiovasc Pharmacol 23:936-43
Brandt, M A; Jones, C E; Gwirtz, P A (1993) Augmented coronary blood flow response to intracoronary norepinephrine after ventricular sympathectomy. Coron Artery Dis 4:101-7
Thornton, J D; Daly, J F; Cohen, M V et al. (1993) Catecholamines can induce adenosine receptor-mediated protection of the myocardium but do not participate in ischemic preconditioning in the rabbit. Circ Res 73:649-55
Gwirtz, P A; Dodd-O, J M; Downey, H F et al. (1992) Effects of a coronary alpha 1-constriction on transmural left ventricular flow and contractile function. Am J Physiol 262:H965-72

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