The role of adenosine in extended myocardial preservation with the University of Wisconsin solution
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1 The role of adenosine in extended myocardial preservation with the University of Wisconsin solution The purpose of this study was to determine the role that adenosine plays in enhanced myocardial preservation during cold storage with the University of Wisconsin solution. Hearts from adult rabbits were flushed with University of Wisconsin solution with or without adenosine and stored at 4 0 C for 24 hours. Interstitial fluid purine levels during the period of cold storage were estimated with cardiac microdialysis probes. In a second series of experiments hearts were flushed with University of Wisconsin solution with or without adenosine or St. Thomas' Hospital cardioplegic solution and stored for 18 hours (4 0 q. Functional recovery was assessed by reperfusing the hearts on a Langendorff apparatus (100 cm H20) for 45 minutes with Krebs-Henseleit buffer. During cold storage dialysate adenosine concentrations in hearts flushed with University of Wisconsin solution were 20- to 40-fold greater than adenosine levels in hearts flushed without adenosine. Mter 45 minutes of reperfusion hearts preserved with University of Wisconsin solution exhibited a rate-pressure product of 11,098 ± 576 mm Hg/min, significantly greater than that for hearts flushed with University of Wisconsin solution minus adenosine (8106 ± 780 mm Hg/min) and St. Thomas' Hospital solution (7317 ± 768 mm Hg/min). These results suggest that adenosine plays a major role in enhanced myocardial preservation with the University of Wisconsin solution, possibly by maintaining elevated interstitial fluid adenosine levels during the period of cold storage. (J THORAC CARDIOV ASC SURG 1994;107: ) Robert D. Lasley, PhD, and Robert M. Mentzer, Jr., MD, Madison, Wis. EIOnged cold-storage organ preservation for transplantation is characterized by high-energy phosphate depletion, intracellular acidosis, cell swelling, and interstitial edema. The University of Wisconsin (UW) preservation solution was developed to minimize these deleterious aspects of cold storage I and has successfully extended preservation times of the liver, kidney, and pancreas. 2-4 The UW solution, in addition to having an intracellular- From the Department of Surgery, University of Wisconsin School of Medicine, Madison, Wis. Supported by a grant to Dr. Lasley from the American Heart Association, Wisconsin Affiliate, and to Dr. Mentzer (ROI HL-34579) from the National Institutes of Health. Received for publication May 25, Accepted for publication Sept. 8, Address for reprints: Robert D. Lasley, PhD, Department of Surgery, University of Wisconsin School of Medicine, H4-383 Clinical Sciences Center, 600 Highland Ave., Madison, WI by Mosby-Year Book, Inc /94 $ /1/51647 based electrolyte composition, contains many constituents designed to reduce ischemic and reperfusion injury. Raffinose, lactobionic acid, and hydroxyethyl starch were added to reduce cellular and interstitial edema. Glutathione and allopurinol were included to reduce injury mediated by oxygen free radicals. Another component of the UW solution is the purine nucleoside adenosine, which was added to stimulate adenosine triphosphate repletion via the purine salvage pathway. Adenosine has been shown to have a beneficial effect on the normothermic ischemic myocardium, reducing both irreversible and reversible injury.5-10 Although the exact mechanism by which adenosine exerts this cardioprotective effect is not known it appears to be mediated via the interaction of adenosine with specific membrane-bound adenosine Al receptors located on the cardiac myocytes. ll This hypothesis is supported by the observations that the cardioprotective effect of adenosine is mimicked by adenosine Al receptor agonists and blocked by adenosine Al receptor antagonists. 8,9 In 1356
2 The Journal of Thoracic and Volume 107, Number 5 Lasley and Mentzer addition, augmentation of endogenous myocardial adenosine levels in the interstitial fluid (ISF) is associated with improved postischemic regional function. 12 There are few studies on the cardioprotective effects or metabolism of adenosine during hypothermic conditions, especially at temperatures used during cold-storage organ preservation (4 C). The purpose of this study was to assess ISF purine levels during prolonged cold storage with UW solution and to determine whether adenosine exerts a cardioprotective effect during these extreme hypothermic conditions. Materials and methods All animals in this study received humane care according to the guidelines set forth by the National Society for Medical Research and the "Guide for the Care and Use of Laboratory Animals" prepared by the National Academy of Sciences and prepared by the Institute of Laboratory Animal Resources and published by the National Institutes of Health (NIH Publication No , revised 1985). Adult New Zealand White rabbits (2 to 4 kg) were anesthetized with sodium pentobarbital (40 mg/kg) and heparinized (1000 units/kg). The hearts were rapidly excised and immediately placed in ice-cold saline to produce cardiac arrest. Metabolic studies. In series I experiments the hearts (n = 5 per group) were immediately flushed with 40 ml cold (4 C) UW solution or UW solution minus adenosine (UW - ADO) at a perfusion pressure of 100 cm H20. When adenosine was omitted from UW solution, adenine (5 mmol/l) was added to maintain constant osmolarity. A dialysis fiber with a I cm exposed window was then inserted into the left ventricular free wall to estimate cardiac ISF purine levels during the period of cold storage. The heart was placed into a small dish filled with the same flush solution and transferred to a cold room (4 C). The dialysis fiber was perfused with Krebs-Henseleit buffer at a r ate of 2 JIl/min, and sample collection times were 10 minutes. The samples were diluted with distilled H20 containing sodium azide and frozen at -70 C until analysis. Samples were collected over a 24-hour period at the following times after probe insertion: 20, 40, 60, and 90 minutes and 2, 3, 4, 5,6,7,10,18, and 24 hours. In addition, in hearts flushed with standard UW solution a sample of pulmonary effluent was collected to measure nucleoside levels. Functional studies. In series 2 experiments the effects of different cold-storage solutions on function after preservation were assessed. Rabbit hearts were excised, arrested in cold saline, and flushed with 40 ml (4 C; 100 em H 20 perfusion pressure) of either standard UW solution, UW-ADO, or St. Thomas' Hospital cardioplegic solution (n = 6 to 7 per group). The compositions of UW solution and St. Thomas' Hospital solution are shown in Table I. When adenosine was omitted from the UW solution, adenine (5 mmol/l) was added to maintain constant osmolarity. After 18 hours of cold storage in a small bag filled with the flush solution and stored in ice, the hearts were reperfused at a constant perfusion pressure of 100 cm H20 on a Langendorff apparatus with Krebs-Henseleit buffer. The reperfusion function of preserved hearts was compared with the function of freshly excised rabbit hearts (non preserved controls). The Krebs-Henseleit buffer consisted of (in millimoles per liter) NaC1118, KCI4.7, MgS04 1.2, KH2P , CaCh Table I. Composition of heart preservation solutions UW solution St. Thomas' Hospital solution Composition Concentration Composition Concentration KH 2 Po mmol/ L NaCI mmoljl MgS mmol/ L KCl 16.0mmol/ L K l actobionate mmol/l MgCIz 16.0 mmol/ L Raffinose 30.0 mmol/ L each 1.2 mmol/ L Penta starch 50.0 gm / L N ahc03 10.Ommol/ L Glutathione 3.0mmol/ L O smolarity 290mOsm/ L Allopurinol 1.0 mmol/ L ph 7.8 Adenosine 5.0mmol/ L Insulin 40.0 U/L Osmolarity 320mOsm/L ph 7.4 UW solution also contains Na+ 30 mmol/ L (from NaOH). When adenosine was omitted from the UW solution, adenine (5 mmol/ L) was substituted to maintain constant osmolarity. 1.25, NaHC , and glucose The perfusate was filtered (0.45 Jim); bubbled with 95% oxygen and 5% carbon dioxide resulting in a ph 7.35 to 7.45, carbon dioxide tension 35 to 40 mm Hg, and oxygen tension 560 to 620 mm Hg; and maintained at 37 C in a constant temperature reservoir. Myocardial temperature was maintained at 37 C by submersing the heart in a water-jacketed chamber filled with Krebs-Henseleit buffer. Left ventricular developed pressure (L VDP) was measured with a fluid-filled latex balloon, connected via a polyethylene caifieter to a pressure transducer (model P23XL, Gould, Inc., Cleveland, Ohio). The balloon catheter was inserted into the left ventricle via the left atrium and inflated to yield an end-diastolic pressure of 10 mm Hg. The hearts were allowed to beat spontaneously and left ventricular function was assessed by measuring heart rate and L VDP and calculating rate-pressure product. Coronary flow rate was measured by timed collections of effluent overflow from the heart bath. The hearts were reperfused for 45 minutes at which time a 125 Jig bolus of dobutamine was injected into the aortic cannula to assess contractile reserve. Cardiac microdialysis. Cardiac microdialysis is essentially a modification of microdialysis techniques established in the early 1980s and currently used extensively in the brain to measure metabolites in the ISFP The cardiac microdialysis technique as used in our laboratory has been described in detail. 14, 15 In brief, it involves the implantation of a small hollow dialysis fiber within the myocardial tissue and the continuous perfusion of the dialysis fiber with Krebs-Henseleit buffer. Diffusion occurs between the ISF surrounding the fiber and the fluid within the dialysis fiber. Adenosine and other molecules present in the ISF therefore enter the dialysis fiber and can be collected in the effiuent. The concentration of a compound in the effiuent (termed the dialysate concentration) is representative of the intramyocardial ISF concentration of that substance. The in vitro percent recovery of the dialysis fibers was determined by placing fibers (1.0 cm window, n = 6) into a small chamber filled with Krebs-Henseleit buffer supplemented with adenosine 10 JImol/ L and maintained at 4 0 C. The fibers were perfused with cold Krebs-Henseleit buffer at a flow rate of 2.0 JIl/min, then stored and analyzed by a method similar to that used for biologic samples.
3 1358 Lasley and Mentzer The Journal of Thoracic and CardiovaS"Cular Surgery May (f) z o 150 ~ 0:::!z 125 w ()~ 6~100 ()~ Adenosine.-. Inosine Hypoxanthine PRESERVATION TIME (hr) Fig. 1. Dialysate purine levels during 24 hours of cold storage in hearts (n = 5) flushed with UW solution. Dialysis fibers 1 cm in length were perfused with Krebs-Henseleit buffer at flow rate of 2.0,ul/min. Samples were collected over lo-minute period. All values are significantly greater than corresponding values in Fig. 2. Table II. Hemodynamic parameters of control and I8-hour cold-stored hearts 15 Minutes' RP 30 Minutes' RP 45 Minutes' RP HR LVDP CF HR LVDP CF HR LVDP CF (beats/min) (mmhg) (ml/min) (beats/min) (mmhg) (ml/min) (beats/min) (mmhg) (ml/min) Control 177 ± 7 82 ± ± ± 7 88 ± ± ± 6 88 ± ± 6.2 UW 205 ± ± 6* 49.7 ± ± ± 5* 49.2 ± ± 6 62 ± 4* 49.0 ± 4.2 UW-ADO 190 ± ± 5*t 41.3 ± 2.2* 174 ± ± 5*t 43.7 ± 2.3' 168 ± 9 49 ± 4*t 44.0 ± 2.6* STS 129 ± 12*t 28 ± 3*t 35.1 ± 3.3* 148 ± ± 4*t 37.4 ± 3.6* 173 ± ± 5*t 38.1 ± 3.6* Data are expressed as means plus or minus standard error of the mean. RP, Reperfusion; HR, heart rate; CF, coronary flow; STS, St. Thomas' Hospital solution. N :2: 5 per group. p < 0.05 versus control. tp < 0.05 versus UW. Biochemical analysis. Adenosine, inosine, and hypoxanthine in pulmonary effluent and dialysate samples were analyzed by high-performance liquid chromatography (HPLC; Waters Chromatography Division of Millipore, Marlborough, Mass.). Samples were injected onto a C-lS reverse phase analytical column (Supelcosil C-IS, Bellafonte, Pa.) and eluted via a step gradient method over a period of 20 minutes. The initial buffer consisted of 100 mmol/l KH2P04 plus 1 % methanol (ph 5.3) and the second buffer consisted of 50% methanol and 50% water. Peaks of interest were determined by absorbance at 254 nm and identified by comparison of retention times to known external standards. Peak quantification was determined by peak area using the Maxima data acquisition system (Waters Chromatography). All reagents for the preservation and perfusion solutions were analytical grade. All solutions were made the day of the experiment. Reagents for HPLC were HPLC grade. Statistical analysis. All results are expressed as mean plus or minus the standard error of the mean. Differences between dialysate purine levels in UW and UW - ADO hearts were analyzed by one-tailed Student's t test. Postpreservation functional data were analyzed by a one-way analysis of variance with statistical significance between the groups determined by Duncan's test. A p value of less than 0.05 was considered statistically significant. Results Metabolic studies. In hearts preserved with standard UW solution pulmonary effluent concentrations of adenosine, inosine, and hypoxanthine at the end of the flush were 4.51 ± 0.14 mmol/l, 0.13 ± 0.04 mmol/l, and 0.05 ± 0.02 mmol/l, respectively. Dialysate purine levels in hearts flushed and cold-stored in standard UW solution are shown in Fig. 1. The in vitro percent recovery of the dialysis fibers used in this study was 25% ± 3%. During the first collection period dialysate adenosine, inosine, and hypoxanthine levels were ± 38.5 /-Lmol/L, 50.5 ± 8.5 /-Lmol/L, and 4.2 ± 0.7 /-Lmol/L, respectively. Adenosine levels progressively decreased to 40.8 ± 4.0 /-Lmol/L after 10 hours and remained stable thereafter. Inosine levels peaked at 4 hours of cold storage (64.7 ± 9.2 /-Lmol/L) and decreased to 42.4 ± 4.5
4 The Journal of Thoracic and Volume 107, Number 5 Lasley and Mentzer (J) z 20 o i= «Cl:: f- ~ 15 o~ z::2' oct 0'-./ W 10 ~ (J) ~ 3 5 o 0-0 Adenosine.-. Inosine Hypoxanthine i ~ PRESERVATION TIME (hr) Fig. 2. Dialysate purine levels during 24 hours of cold storage in hearts (n = 5) flushed with UW -ADO. Adenine (5 mmol/l) was added to UW solution to maintain constant osmolarity. MmoljL at 24 hours. Dialysate hypoxanthine concentrations steadily increased-to 11.0 ± 1.4 MmoljL during cold storage. Fig. 2 illustrates the dialysate purine levels during the pyriod of cold storage in hearts flushed with UW - ADO. Dialysate adenosine levels were highest (5.6 ± 3.0 Mmolj L) during the first collection period and progressively decreased throughout 24 hours to a value of 0.10 ± 0.04 MmoljL. Inosine levels peaked between 60 and 90 minutes of cold storage (20.0 ± 1.4 and 19.6 ± 1.7 MmoljL, respectively) and decreased to 8.1 ± 0.4 MmoljL after 24 hours. Hypoxanthine levels were initially 2.1 ± 0.5 MmoljL and gradually increased to 5.4 ± 0.6 MmoljL after 24 hours. Dialysate purine concentrations in UW - ADO hearts were significantly lower (p < 0.05) at all time points than corresponding values in UW hearts. Functional studies. Hemodynamic variables during 45 minutes of perfusion for fresh control hearts and hearts stored for 18 hours are shown in Table II. There were no differences in heart rates among the groups except for hearts preserved with St. Thomas' Hospital solution, which exhibited significantly lower heart rates after 15 minutes of reperfusion. All preserved hearts exhibited significantly decreased values of L VDP compared with those in fresh control hearts. However, hearts preserved with UW solution displayed significantly greater L VDP values throughout reperfusion compared with those in hearts preserved with UW - ADO and St. Thomas' Hospital solution. Hearts preserved with St. Thomas' Hospital solution also exhibited significantly reduced coronary flow values compared with those of UW-preserved hearts. Rate-pressure product (heart rate X L VDP) values for control and 18-hour preserved hearts are shown in Fig. 3. Fresh control hearts exhibited a rate-pressure product of 14,581 ± 526 mm Hgjmin at 15 minutes of perfusion, and function remained stable throughout the remainder ~f the perfusion period. Hearts preserved with UW solution displayed a significantly greater rate-pressure product (9157 ± 911 mm Hgjmin) at 15 minutes of reperfusion compared with that in hearts preserved with UW-ADO (5168 ± 775 mm Hgjmin) and hearts preserved with St. Thomas' Hospital solution (3754 ± 774 mm Hgjmin). This superior reperfusion function in hearts preserved with UW solution persisted throughout the reperfusion period. After 45 minutes of reperfusion mean functional recovery of UW-preserved hearts was 74% that of fresh control hearts, whereas functional recovery was 54% and 49% in hearts preserved with UW - ADO and St. Thomas' Hospital solution, respectively. Contractile reserve, as determined by the increase in rate-pressure product with dobutamine, in control and preserved hearts after 45 minutes of perfusion is shown in Fig. 4. All groups responded equivalently to inotropic stimulation with an approximately twofold (range 2.1 to 2.6) increase in rate-pressure product. Cold-stored hearts exhibited decreased function with dobutamine compared with fresh control hearts (39,260 ± 3271 mm Hgjmin). However, rate-pressure product in UW-preserved hearts (25,575 ± 1943 mm Hgjmin) was significantly greater than that in hearts preserved with UW - ADO (16,983 ± 1398 mm Hgjmin) and St. Thomas' Hospital solution (18,418 ± 1650 mm Hgjmin).
5 1360 Lasley and Mentzer The Journal of Thoracic and May 1994 T Q ? T RPP (xl0-3 ) Nonpreserved Control.-. UW 6-6 UW - ADO A-A STS ' , , ,-, TIME OF REPERFUSION (min) Fig. 3. Effects of 18 hours of cold storage with UW, UW-ADO, and 8t. Thomas' Hospital (STS) solutions on rate-pressure product (RPP) of isolated perfused hearts. Rate-pressure product of fresh control hearts is shown for comparison. Asterisk indicates p < 0.05 versus UW group CJ 45 min RP _ 125 j.ig Dobutamine RPP (x 10-3 ) n -=- * n * Conlrol UW UW-ADO STS Fig. 4. Effect of dobutamine (125 Ilg bolus) on rate-pressure product (RPP) after 18 hours of cold storage with UW, UW - ADO, and 81. Thomas' Hospital (STS) solutions. Rate-pressure product of fresh control hearts is shown for comparison. Asterisk indicates p < 0.05 versus UW hearts. RP, Reperfusion. Discussion The results of this study indicate that adenosine exerts a cardioprotective effect during cold-storage preservation of the heart with UW solution. Hearts preserved with UW solution exhibited greater reperfusion function after 18 hours of cold storage than hearts preserved with UW - ADO and St. Thomas' Hospital cardioplegic solution. Estimates of ISF purine levels with the cardiac microdialysis technique indicated that enhanced reperfusion function with UW solution preservation was associated with augmented ISF adenosine levels during cold storage. Numerous studies have compared UW preservation solution with other crystalloid preservation solutions, most commonly St. Thomas' Hospital cardioplegic solution The majority of these studies, conducted in rat, pig, and canine hearts, concluded that UW solution provided superior myocardial preservation, 16-18,20,21 consistent with the results obtained in this study in the rabbit heart. The UW solution has also been shown to provide superior cardiac preservation compared with the modified Collins', Stanford, and Bretschneider's cardioplegic solutions, which have low sodium and low chloride electrolyte compositions in addition to glucose or mannitol, or both, added as impermeants. 16, The superior preservation with UW solution is presumably a result of its intracellu-
6 The Journal of Thoracic and Volume 107, Number 5 Lasley and Mentzer I 361 lar-based electrolyte composition and inclusion of lactobionate, raffinose, and hydroxyethyl starch. The low-sodium, high-potassium formulation of UW solution presumably retards cell swelling by reducing the electrochemical gradients of these ions. Lactobionate, raffinose, and hydroxyethyl starch were added as impermeants to reduce interstitial edema. Recently Ko and associates 26 reported that the intracellular-based electrolyte composition and inclusion of hydroxyethyl starch appeared to be important components of UW solution, but raffinose could be omitted and chloride substituted for lactobionate with little if any effects on postpreservation function. The results of this study indicate that adenosine also plays a significant role in enhanced preservation with UW solution. Rabbit hearts cold-stored for 18 hours with UW solution exhibited significantly greater reperfusion function than hearts preserved with UW - ADO and St. Thomas' Hospital solution. Adenosine was originally added to UW solution to accelerate adenosine triphosphate resynthesis via stimulation of the purine salvage pathway, I and adenosine administration has been reported to stimulate postischemic adenine nucleotide pool repletion. 27, 28 However, recently obtained results suggest that the beneficial effect of adenosine on reperfusion function after normothermic ischemia is independent of its effects as an adenine nucleotide precursor. 9, II In addition, it is currently recognized that total myocardial adenosine triphosphate content does not correlate well with postischemic recovery of left ventricular function. 29,30 Consistent with these findings, the majority of myocardial preservation studies with UW solution have reported no beneficial effect on myocardial adenosine triphosphate content. 16, 18-20,24,31 Current evidence indicates that adenosine exerts its cardioprotective effect via interaction with membranebound adenosine Al receptors located on the cardiac myocytes. This hypothesis is supported by the observation that the cardioprotective effect of adenosine is mimicked by adenosine Al receptor agonists and blocked by adenosine Al receptor antagonists, whereas adenosine A2 receptor antagonists have no beneficial effect We did not test the efficacy of adenosine Al receptor agonists or antagonists in this model, but the results obtained in this study with the cardiac microdialysis technique are consistent with this hypothesis. Cardiac microdialysis samples the ISF compartment, which is in direct contact with the myocytes, thus the concentration of adenosine in the ISF determines the effective concentration of adenosine at the Al receptor. Although this is the first study that documents an association between increased ISF adenosine levels during cold-storage preservation and enhanced reperfusion ventricular function, there is other evidence to support this hypothesis. The nucleoside transport inhibitor R has been shown to increase survivability and in vitro left ventricular function in canine hearts subjected to 24 hours of cold storage. 32, 33 Nucleoside transport inhibitors increase interstitial adenosine concentration by diminishing the cellular uptake of adenosine, thereby reducing its metabolism. In addition, Dorheim and associates l2 reported that treatment with the adenosine deaminase inhibitor erythro-9-(2-hydroxy-3-nonyi) adenine augmented endogenous ISF adenosine levels during coronary artery occlusion in the dog and improved postischemic regional ventricular function. It must be pointed out that the dialysate purine measurements reported here, although representative of myocardial ISF, provide only an estimate of true ISF concentration. Because of tissue trauma during probe implantation dialysate adenosine levels are initially elevated, but rapidly decrease and stabilize within 60 to 90 minutes. 12, 14 Thus the dialysate levels during the first hour of cold storage in the UW-ADO hearts may actually overestimate ISF purine levels. Under the conditions used in this study (1 cm dialysis window, 2 ttl/min perfusion rate, 4 0 C) in vitro percent recovery is 25%. Actual percent recovery in situ may be even less, especially with prolonged implantation (24 hours) of the fiber. Despite the limitations of cardiac microdialysis, several conclusions can be drawn from the dialysis purine measurements in this study. Inclusion of adenosine in the UW solution elevated dialysate adenosine levels during cold storage fold compared with levels in hearts flushed and stored in UW-ADO. These results suggest that ISF adenosine concentration was significantly augmented during storage with UW solution. A comparison of purine levels in the pulmonary effluent (during the UW solution flush) and the first dialysate sample (20 minutes after probe insertion) revealed significant metabolism of adenosine as it crosses the coronary endothelium, even at 4 0 C. These results are consistent with previously published reports of extensive metabolism of adenosine as it traverses the coronary endothelium. 34, 35 The beneficial effect of adenosine observed in these studies was demonstrated in Krebs-perfused, nonejecting hearts. Obviously more extensive in vivo studies are needed to determine whether adenosine provides a similar cardioprotective effect in clinically relevant myocardial preservation models. Despite these limitations, the results of this study suggest that UW solution provides superior myocardial preservation compared with st. Thomas' Hospital cardioplegia solution. Functional and metabolic results obtained with omission of adenosine
7 1362 Lasley and Mentzer The Journal of ThoraciC and May 1994 from UW solution support the hypothesis that adenosine plays a major role in prolonged cold-storage myocardial preservation possibly via interaction with myocardial adenosine Al receptors. We thank Mr. Timothy L. Beard, Mr. Gregory M. Anderson, and Mr. Patrick A. Konyn for their expert technical assistance. REFERENCES I. Belzer FO, Southard lh. Principles of solid-organ preservation by cold storage. Transplantation 1988;45: lamieson NV, Sundberg R, Lindal S, et al. Preservation of the canine liver for hours using simple cold storage with UW solution. Transplantation 1988;46: Ploeg Rl, Goossens D, McAnulty lf, Southard lh, Belzer FO. Successful 72-hour cold storage of the dog kidney with UW solution. Transplantation 1988;46: Wahlberg la, Love RA, Landegard L, Southard lh, Belzer FO. 72-hour preservation of the canine pancreas. Transplantation 1987;43: Wyatt DA, Ely SW, Lasley RD, et al. Purine-enriched asanguineous cardioplegia retards adenosine triphosphate degradation during ischemia and improves postischemic ventricular function. 1 THORAC CARDIOVASC SURG 1989;97: Schubert T, Vetter H, Owen P, Reichart B, Opie LH. Adenosine cardioplegia: adenosine versus potassium cardioplegia-effects on cardiac arrest and postischemic recovery in the isolated rat heart. 1 THORAC CARDIOV ASC SURG 1989;98: Bolling SF, Bies LE, Gallagher KP, Bove EL. Enhanced myocardial protection with adenosine. Ann Thorac Surg 1989;47: Lasley RD, Rhee lw, Van Wylen DGL, Mentzer RM lr. Adenosine Al receptor mediated protection of the globally ischemic isolated rat heart. 1 Mol Cell CardioI1990;22: Lasley RD, Mentzer RM lr. Adenosine improves the recovery of postischemic myocardial function via an adenosine Al receptor mechanism. Am 1 Physiol 1992; 263:HI Thornton ld, Liu GS, Olsson RA, Downey 1M. Intravenous pretreatment with AI-selective adenosine analogues protects the heart against infarction. Circulation 1992; 85: II. Mentzer RM, Bunger R, Lasley RD. Adenosine enhanced preservation of myocardial function and energetics: possible involvement of the adenosine A I receptor system. Cardiovasc Re.s 1993;27: Dorheim T A, Hoffman A, Van Wylen DGL, Mentzer RM lr. Enhanced interstitial fluid adenosine attenuates myocardial stunning. 1 Surg 1991;110: Benveniste H, Huttemeier PC. Microdialysis-theory and application. Prog NeurobioI1990;35:195-21O. 14. Van Wylen DGL, Willis 1, Sohdi 1, Weiss Rl, Lasley RD, Mentzer RM lr. Cardiac microdialysis to estimate interstitial adenosine and coronary blood flow. Am 1 Physiol 1990;258:HI Van Wylen DGL, Schmit TJ, Lasley RD, Gingell RL, Mentzer RM lr. Cardiac microdialysis in isolated rat hearts: interstitial purine metabolites during ischemia. Am 1 PhysioI1992;262:HI Swanson DK, Pasaoglu I, Berkoff HA, Southard la, Hegge 10. Improved heart preservation with UW preservation solution. 1 Heart Transplant 1988;7: Ledingham SlM, Katayama 0, Lachno DR, Yacoub M. Prolonged cardiac preservation: evaluation of the University of Wisconsin preservation solution by comparison with the St. Thomas' Hospital cardioplegic solutions in the rat. Circulation 1990;82(Suppl):IV Yeh T, Hanan SA, 10hnson DE, et al. Superior myocardial preservation with modified UW solution after prolonged ischemia in the rat heart. Ann Thorac Surg 1990;49: Tian G, Smith KE, Biro GP, et al. A comparison of UW cold storage solution and st. Thomas' solution II: a 31p NMR and functional study of isolated porcine hearts. 1 Heart Lung Transplant 1991;10: Karck M, Vivi A, Tassini M, et al. The effectiveness of University of Wisconsin solution on prolonged myocardial protection as assessed by phosphorus 31-nuc1ear magnetic resonance spectroscopy and functional recovery. 1 THORAC CARDIOV ASC SURG 1992;104: Mankad PS, Severs Nl, Lachno DR, Rothery S, Yacoub MH. Superior qualities of University of Wisconsin solution for ex vivo preservation of the pig heart. 1 THORAC CARDIOVASC SURG 1992;104: Naka Y, Shirakura R, Matsuda H, et al. Canine heartlung transplantation after 24-hour hypothermic preservation. Eur 1 Cardiothorac Surg 1990;4: Okouchi Y, Shimizu K, Yamaguchi A, Kamada N. Effectiveness of modified University of Wisconsin solution for heart preservation as assessed in heterotopic rat heart transplant model. 1 THORAC CARDIOVASC SURG 1990; 99: Galifianes M, Murashita T, Hearse Dl. Long-term hypothermic storage of the mammalian heart for transplantation: a comparison of three cardioplegic solutions. 1 Heart Lung Transplant 1992;11 : Gott lp, Chih P, Dorsey LMA, Cheung EH, Hatcher CR, Guyton RA. Cardioplegia for transplantation: failure of extracellular solution compared with Stanford or UW solution. Ann Thorac Surg 1990;50: Ko W, Zelano la, Lazenby WD, Isom OW, Krieger KH. Compositional analysis of a modified University of Wisconsin solution for extended myocardial preservation: a study of the left ventricular pressure-volume relation. 1 THORAC CARDIOVASC SURG 1992;86: Reibel DK, Rovetto Ml. Myocardial adenosine salvage rates and restoration of A TP content following ischemia. Am 1 PhysioI1979;237:H Ambrosio G, lacobus WE, Mitchell MC, Litt MR, Becker LC. Effects of ATP precursors on ATP and free
8 The Journal of Thoracic and Volume 107, Number 5 Lasley and Mentzer 1363 ADP content and functional recovery of postischemic hearts. Am J Physiol1989;256:H Neely JR, Grotyohann LW. Role of glycolytic products in damage to ischemic myocardium: dissociation of adenosine triphosphate levels and recovery of function of reperfused ischemic hearts. Circ Res 1984;55: Mallet RT, Hartman DA, Bunger R. Glucose requirement for postischemic recovery of perfused working heart. Eur J Biochem 1990;188: MollhoffT, Sukehiro S, Van Aken H, Flameng W. Longterm preservation of baboon hearts: effects of hypothermic ischemic and cardioplegic arrest on high-energy phosphate content. Circulation 1 990;82(Suppl):IV Flameng W, Sukehiro S, Mollhoff T, Van Belle H, Jans- sen P. A new concept oflong-term donor heart preservation: nucleoside transport inhibition. J Heart Lung Transplant 1991;10: Masuda M, Chen C-C, MollhoffT, Van Belle H, Flameng W. Effects of nucleoside transport inhibition on long-term ex vivo preservation of canine hearts. J THoRAC CAROIO VASC SURG 1992;104: Nees S, Herzog V, Becker BF, BOCk M, Des Rosiers C, Gerlach E. The coronary endothelium: a highly active metabolic barrier for adenosine. Basic Res Cardiol 1985;80: Heller LJ, Mohrman DE. Estimates of interstitial adenosine from surface exudates of isolated rat hearts. J Mol Cell Cardiol 1988;20: Bound volumes available to subscribers Bound volumes of THE JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY are available to subscribers (only) for the 1994 issues from the Publisher, at a cost of $82.50 for domestic, $ for Canadian, and $ for international subscribers for Vol. 107 (January-June) and Vol. 108 (July-December). Shipping charges are included. Each bound volume contains a subject and author index and all advertising is removed. Copies are shipped within 60 days after publication of the last issue of the volume. The binding is durable buckram with the JOURNAL name, volume number, and year stamped in gold on the spine. Payment must accompany all orders. Contact Mosby-Year Book, Inc., Subscription Services, Westline Industrial Drive, St. Louis, Missouri , USA; phone 1(800) or (314) Subscriptions Diust be in force to qualify. Boond volumes are not available in place of a regular JOURNAL subscription.
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