Abstract | BACKGROUND: We examined effects of phosphodiesterase type III inhibition on regional myocardial metabolism and global left ventricular function, during ischemia, in the presence of beta-blockade. METHODS: Twenty-three pigs were randomized and studied to completion in four groups: C, did not receive drugs; M, received 50 microg/kg milrinone; E, received esmolol (150 microg/kg/min); E+M, received both. The left anterior descending artery (LADa) was then occluded for 15 min, followed by a 60-min reperfusion. Left ventricular (LV) function data obtained included LV pressures, cardiac output (CO), slope of end-systolic pressure-volume relationship (Emax), and dP/dT. Blood lactate concentrations were obtained from the aorta, LADa, and vein at baseline, end of occlusion, and during early (5 min) and late (1 h) reperfusion. RESULTS: During ischemia, occlusion produced significant depression in LV dP/dT, Emax and concomitant elevation of LVEDP that persisted over early reperfusion in groups not treated with milrinone. After ischemia, measurements of CO were higher, with lower LVEDP and SVR; LV dP/dT and the Emax were higher, with lower LVEDP in the E+M group vs. the E group. Ischemic region lactate extraction during ischemia was better with E group vs. C group. Esmolol without or with milrinone was associated with nonsignificant lactate ischemic production during early reperfusion from baseline values. CONCLUSION: We demonstrated that the pre-emptive administration of milrinone before ischemia was associated with less ischemic hemodynamic effects, without worsening the ischemic metabolic process. The combination E+M diminished ischemic metabolic impairment, and preserved left ventricular function and baseline hemodynamics.
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Authors | A Sidi, J D Muehlschlegel, D S Kirby, E B Lobato |
Journal | Acta anaesthesiologica Scandinavica
(Acta Anaesthesiol Scand)
Vol. 52
Issue 3
Pg. 397-405
(Mar 2008)
ISSN: 1399-6576 [Electronic] England |
PMID | 18269389
(Publication Type: Journal Article)
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Chemical References |
- Adrenergic beta-Antagonists
- Cardiotonic Agents
- Propanolamines
- Lactic Acid
- Milrinone
- esmolol
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Topics |
- Adrenergic beta-Antagonists
(pharmacology)
- Animals
- Blood Pressure
(drug effects)
- Cardiac Output
(drug effects)
- Cardiotonic Agents
(pharmacology)
- Coronary Stenosis
(complications)
- Disease Models, Animal
- Heart Rate
(drug effects)
- Lactic Acid
(metabolism)
- Milrinone
(pharmacology)
- Myocardial Reperfusion
- Myocardial Stunning
(drug therapy, etiology, metabolism)
- Propanolamines
(pharmacology)
- Random Allocation
- Swine
- Time Factors
- Vascular Resistance
(drug effects)
- Ventricular Dysfunction, Left
(drug therapy, etiology)
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