Up-regulation of heme oxygenase-1 after infarct initiation reduces mortality, infarct size and left ventricular remodeling: experimental evidence and proof of concept

Male Wistar rats were either bred in our local animal husbandry facility or purchased from Harlan Italy s.r.l (Udine, Italy). Animals were housed in an environment with controlled 12 h/12 h light/dark cycle, temperature (21 ± 0.5°C) and relative humidity (55% ± 2%) and fed with 4 RF 18 standard rat diet for long-term maintenance (Mucedola, Milano, Italy). Water was available ad libitum.

Cobalt protoporphyrin (CoPP, Frontier Scientific Inc., Logan, UT, USA), a well-known inducer of HO-1 expression [17, 18] was administered via intra-peritoneal injection. We prepared a 5 mg/ml CoPP stock solution in TRIS buffer (pH 8.0); handling of CoPP solution was performed in the dark due to its sensitivity to light. The injected dose was 5 mg/kg body weight.

In order to preliminarily assess the time course of HO-1 protein synthesis after a single injection of CoPP (5 mg/kg), we monitored cardiac expression of HO-1 protein by Western blot analysis in 10 control rats sacrificed at different times (0, 8, 16, 24 and 48 h) following CoPP administration (n = 2 for each time point) (see details in Additional file 1: S1). The expression of HO-1 protein had increased by 16 h and continued to increase through 48 h (see Additional file 1: Figure S1A). In addition, to exclude that the rise of HO activity in the heart forerun the increase in HO-1 abundance (16 h), we also measured the HO activity in myocardial tissue (Additional file 1: Figure S1B) at 0 and 8 hours following CoPP administration (n = 3 for each time point). No increase in HO activity was observed at 8 h.

Tin mesoporphyrin IX (SnMP, Rockfeller University, New York, NY, USA), an inducer of HO protein synthesis [20], is considered a potent inhibitor of the activity of both preformed and newly synthesized enzyme [21, 22]. SnMP was administered via intra-peritoneal injection at a dose of 8 mg/kg body weight.

A total of 144 male Wistar rats 10–12 weeks old and weighing 310 ± 3 g were used in the study. After thoracotomy, MI was induced by ligation of the left anterior descending coronary artery (LAD) (see details in Additional file 1: S2). Immediately after chest closure rats received an intra-peritoneal injection of either vehicle alone (TRIS buffer, MI group, n = 63) or cobalt protoporphyrin alone (CoPP-treated MI group, n = 40) or CoPP in association with SnMP (CoPP + SnMP group, n = 8). Due to the > 16 h delay of CoPP induced HO-1 up-regulation, the adopted scheme of treatment mimicked the clinical condition of a pharmacological intervention well after initiation of MI. Thereafter, in order to sustain HO-1 over-expression, additional doses of CoPP or vehicle were administered i.p. once a week over a 4-week study period. Sham-operated rats underwent all surgical procedures except LAD ligation and received the same intra-peritoneal treatment with vehicle (Sham group, n = 30). In the CoPP + SnMP group, SnMP was administered i.p. every second day [23].

The number and times of spontaneous deaths during the 4 weeks were carefully recorded. Out of 144 animals, three died during surgery due to irreversible ventricular fibrillation and were not allocated to any group. Thus the remaining 141 are included in the study. At 4 weeks, a total of 117 rats survived and entered the morpho-functional study. Allocation of animals to different groups and procedures is detailed in the Additional file 1: S3 and Additional file 1: Table S1.

ECG was recorded at 2 kHz sampling rate and heart rate was calculated using the Power Lab monitoring system (ML135 PowerLab/8SP) equipped with ML135 Dual Bio Amp and MLA0112 ECG Lead Switch Box (ADI Instruments Ltd., Oxford, UK). ECG recordings were continuously acquired before (basal condition) and during surgery up to 60 min. Arrhythmias were classified according to the Lambeth Conventions [24] and their severity was scored (range 0–5) [25] as detailed in the Additional file 1: S4. Moreover, an extensive ECG analysis was carried out at 4 weeks after infarction as previously described [26]. The ECG parameters studied were: heart rate, frontal QRS axis (Â_QRS) using D1 and AVF leads, and QRS amplitude index (I_QRS), i.e., the sum of positive or negative peak deflections of the QRS complexes in D1, D2 and D3, and QRS duration (T_QRS). ECG at 4 weeks was compared to the basal one.

Echocardiographic studies were performed 4 weeks after infarction with a portable ultrasound system (MyLab 25, Esaote SpA, Genova, Italy) equipped with a high frequency linear transducer (LA523, 12.5 MHz). Under intra-peritoneal anesthesia, as previously described, images were obtained from the left parasternal view. A short-axis 2-dimensional view of the left ventricle (LV) was taken at the level of papillary muscles to obtain M-mode recording. Anterior (infarcted) and posterior (viable) end-diastolic and end-systolic wall thicknesses, systolic wall thickening, and LV internal dimensions were measured following the American Society of Echocardiography guidelines. Parameters were the mean of measurements of three consecutive cardiac cycles. The global LV systolic function was expressed as fractional shortening (FS%).

Plasma samples were assayed to determine the circulating levels of B-type natriuretic peptide (BNP), endothelin-1 [27, 28] and prostaglandin E2 [29], as detailed in the Additional file 1: S5.

Microvascular coronary resistance (CR) was evaluated 4 weeks after surgery in the isolated beating heart in Langendorff configuration. This procedure has been previously described in detail [30].

Briefly, two side-arms in the perfusion line, located close to the heart inlet, allowed switching between two reservoirs set at normal (70 mmHg) and low (30 mmHg) pressure. Coronary flow was continuously measured with a flowmeter (model T106, Transonic System Inc, Ithaca, NY, USA) and by measurement of effluent volume with a calibrated pipette. Coronary resistance was calculated as input pressure divided by coronary flow per gram of myocardial tissue (mmHg*g*min/ml). As in infarcted hearts the injection of Evans blue dye into the aortic root did not color the infarcted tissue at macroscopic morphometry (in the Additional file 1: Figure S2), the weight of perfused myocardium was calculated as the total ventricle weight minus the necrotic myocardium.

After an initial 15-min period of stabilization, not included in the analysis, CR was measured in two alternative protocols, (i) at the onset and at the end of 65 min of 70 mmHg perfusion pressure (ii) at 20 min of low perfusion pressure (30 mmHg) and early after reperfusion at 70 mmHg (peak hyperemia).

Four weeks after surgery, under deep anesthesia, hearts were arrested in diastole by a lethal KCl injection, and left ventricles were weighted and cut in transversal and parallel slices about 2 mm thick. To enhance the contrast between viable and infarcted myocardium, fresh slices were incubated with triphenyltetrazolium chloride 1% solution at 37° for 10 min. Slivers were photographed with a digital camera and the images processed by dedicated image software (MIAO, Myocardial Infarcted Area Outline), which measured the value of the infarcted area in radiants encompassing the pale area and expressed it as a percentage of the entire left ventricle (360°). The thickness of the central infarcted area and of its opposite wall were measured in each animal (see details in Additional file 1: S6).

Next, in each slice, cardiac tissue was divided into four distinct areas, which were frozen and analyzed separately: a) right ventricle wall; b) left ventricle posterior wall, opposite to LAD territory (remote zone); c) border region to LAD area (border zone); d) central zone of the infarcted area.

In addition, the abdomen was incised and four samples from the right and median lobes of the liver were excised and flash-frozen to determine tissue HO activity.

To define the efficacy of CoPP in inducing HO-1 expression, HO activity was determined in rat liver microsomes of each MI group by measuring bilirubin as previously described [31]. Details of the procedure are reported in the Additional file 1: S7.

Heart tissue from different cardiac regions was separately homogenized and blotted on PVDF membrane as detailed in the Additional file 1: S8. The membranes were probed with rabbit anti-HO-1. Rabbit anti β-actin or rabbit anti GAPDH antibodies were used to probe the reference proteins. After incubation with HRP-conjugate secondary antibody enhanced chemiluminescence detection was performed and digital images were acquired for densitometry analysis of the bands by using “open source” program Image J (National Institute of Health, Bethesda MD, USA). Protein-specific bands were normalized to the protein loading staining β-actin or GAPDH.

Possible effect of CoPP on cardiac apoptosis was explored in an especially dedicated additional set of animals (n = 18, 6 sham, 6 untreated MI and 6 CoPP-treated MI rats). Rats were sacrificed at 16 and 24 h, times proved to correspond to the onset-time of HO-1 over-expression (n = 3 for each time in each group). Myocardial tissue homogenates from infarcted, border and remote regions were processed to assay caspase 3 activity (Caspase 3 Colorimetric Assay Kit, AbCam, Cambridge, UK) and to measure BCL-2 levels (custom made rat BCL-W ELISA kit, RayBiotech, Inc, Georgia, USA).

Hearts were arrested in diastole at 4 weeks, ventricles were weighted and fixed in 10% buffered formalin (see details in the Additional file 1: S9). Cardiomyocyte junctions were identified by immunoperoxidase staining, using a polyclonal rabbit anti-connexin 43 (Cx43) primary antibody (AbCam, Cambridge, UK); arterioles and capillaries were labeled with anti-smooth muscle actin (α-SMA) primary antibody (SantaCruz, Dallas, USA) or anti-PECAM 1 (CD31) primary antibody (SantaCruz, Dallas, USA) respectively. Sections were counter-stained with hematoxylin and examined using light microscopy (Olympus BX43) at 10× to 40× original magnification and digitized by a video system (Olympus DP20 camera) interfaced to a computer with dedicated software (CellSens Dimension, Olympus) for image acquisition and morphometric and/or color analysis. Cx43 was quantified as the percent of myocardial area occupied by positive staining (calculated by averaging the values from ten fields at 10× magnification) for each LV area. The density (number/mm²) of arterioles (10–100 μm in diameter) was counted by averaging values from eight fields randomly chosen for each LV area at 20× magnification. The same was done for capillaries density (<10 μm in diameter), except magnification 40×.

All experimental values are expressed as the mean ± standard error of the mean (SEM). On the basis of the Kolmogorov-Smirnov test (p > 0.05), the visual inspection of their histograms, and the normal Q-Q plots we assumed that our data were approximately normally distributed.

All analyses were done with the statistical computer program StatView 5.0 (Abacus Concepts, Berkeley, CA, U.S.A.).

Among the 141 animals who survived the surgical procedure, overall mortality at 4 weeks was 3% in the sham group, 25% in the vehicle MI group, 12% in the CoPP-MI group and 25% in the CoPP + SnPP-MI group (in the Additional file 1: Table S1), with vehicle-MI significantly different from CoPP-treated MI rats (χ² = 3.89, p = 0.048) but not different from CoPP + SnMP MI group (χ² = 0.167, p = 0.6831). A comparison of vehicle vs CoPP MI mortality at 24 h (early) and at 72 h (intermediate mortality) showed that cumulative mortality was similar in the two groups at 24 h (6 vs 5%) but had diverged at 72 h (19 vs 7% respectively, χ² = 6.67, p = 0.0098) supporting the assumption of a ‘late’ biological effect of our pharmacological intervention.

In MI groups severe ventricular arrhythmias occurred 5 to 20 min after coronary occlusion. The average severity score was no different in vehicle when compared to CoPP and CoPP + SnMP MI groups (3.35 ± 0.15, 3.35 ± 0.11, and 3.33 ± 0.10 respectively) suggesting the absence of an apparent anti-arrhythmogenic effect of CoPP in the first 20 min of MI. At 4 weeks, only sporadic arrhythmias were observed, never exceeding a score of 0 in all groups.

QRS morphology, 4 weeks after surgery, showed a difference between sham and vehicle MI animals with a rightward shift (> 90°) of the frontal QRS axis, reduction in QRS amplitude index, and prolongation of QRS interval (Table 1). CoPP treatment significantly decreased the rightward shift with 53% of cases of Â_QRS axis < 90°, preserved QRS amplitude index, partially restored QRS duration. Concurrent SnMP administration cancelled out the CoPP effect and abolished ECG morphological differences relative to the vehicle MI group.

The main echocardiographic parameters are shown in Table 2. LV geometry changed in vehicle MI as the result of a progressive LV remodeling over the 4-week study period post coronary artery ligation. Both LV end-diastolic and end-systolic diameters, as well as HR increased in untreated MI compared to sham-operated animals. Moreover, anterior (infarcted) LV wall thickness was reduced in untreated MI hearts, while the posterior (viable) wall thickness was higher than sham rats and CoPP-MI. In vehicle MI the percentage of systolic thickening (an index of contractility) of the anterior and the posterior walls as well as LV fractional shortening was reduced compared to sham animals. CoPP treatment significantly reduced both end-diastolic and end-systolic diameters of infarcted hearts, blunted both the increase in heart rate and the thinning of the anterior wall and improved systolic thickening of both anterior and posterior walls as well as the fractional shortening compared to untreated MI. Concurrent SnMP administration reversed the CoPP effect, abolishing both the LV geometry and functional changes relative to vehicle MI group (Table 2).

Plasma BNP, ET-1 and PGE₂ concentrations before treatment (basal value) were 18 ± 5 pg/mL, 19 ± 0.5 pg/mL, and 8.1 ± 0.5 ng/mL, respectively. Changes in plasma concentrations of the three markers 4 weeks after surgery in sham-operated as well as in vehicle- or CoPP-treated infarcted rats are shown in Additional file 1: Table S2. Briefly, MI group exhibited an increase in both BNP (p = 0.06) and ET-1 (p < 0.01) plasma concentration levels. CoPP treatment dampened the post-infarct rise of both parameters to levels akin to those of sham-operated animals. Moreover CoPP caused a significant increase in PGE₂ circulating levels in comparison to both sham and MI animals.

Ex vivo measurements of CR are shown in Table 3. Hearts from sham-operated rats perfused at constant pressure exhibited only a small increase in CR detectable over the 65-min study period (p < 0.05). In infarcted animals, coronary resistance values were significantly higher than those in the sham group (p < 0.001 vs sham-operated). The bolus administration of papaverine (50 μg), abolished the increase in resistance in infarcted rats, proving its active nature and ruling out the intervention of extra-vascular compressive forces.

CoPP treatment blunted the increased coronary resistance observed in infarcted rats (p < 0.01 vs untreated MI) (Table 3). Treated animals did not differ from sham-operated ones. In sham-operated hearts, hypotension caused an increase in coronary resistance (paradoxical vasoconstriction, p < 0.01 vs baseline). The return to normal perfusion pressure caused a fall in resistance in the first minute (hyperemic response) below baseline (p < 0.001 vs baseline).

As shown in Table 3, in untreated MI hearts, hypotension induced a marked rise in resistance (p < 0.01 vs sham and CoPP-MI). The return to normal perfusion pressure caused a fall in resistance to a value higher than baseline (p < 0.05 vs baseline). The values of CR were higher than those of sham-operated animals (p < 0.001 vs sham-operated rats).

CoPP-treated MI rats showed basal CR values similar to those of the sham group and lower than those of untreated infarct group (p < 0.01 vs untreated infarct). During transient low-pressure ischemia, CoPP treatment in MI rats largely abolished the vasoconstrictive response to hypotension. At the peak, CR was not significantly different from that of the sham group. Reperfusion produced a drop in CR to a level that was no different from that of the sham-operated group.

Ventricles of MI group had significantly (p < 0.001) higher weights than those of sham-operated animals (Additional file 1: Table S3). CoPP treatment decreased (p < 0.001) the post-infarct gain in ventricle weight.

Figure 1A shows MI size evaluated 4 weeks after MI or sham operation. Sham group showed an insignificant area of LV damage (< 2%), mainly due to tissue trauma during sham operation. Four weeks after MI, infarct size was 35.9 ± 1.6% of LV (p < 0.001 vs sham-operated). Thickness of the core infarcted wall was about 43% of the one in the sham group, whereas opposite wall thickness was about 119%, a value significantly (p < 0.05) higher than in sham animals (Additional file 1: Table S3). CoPP treatment significantly reduced MI size to 23.2 ± 1.3% of LV (p < 0.002 vs untreated MI). Moreover, it reduced thinning of the core infarcted region (66% of sham group) and completely prevented the increase in thickness of the opposite region (101% of sham group).

SnMP resulted in MI size of 33.6 ± 1.5% of LV after 4 weeks (p < 0.001 vs CoPP-MI); thickness of the core infarcted wall was 39% while the opposite wall was 120% compared to the sham group.

CoPP increased HO activity in the liver of infarcted rats 2.1-fold as compared to untreated infarcted rats (24.0 ± 5.0 vs 11.6 ± 1.5 pmol bilirubin * min-1 * mg-1, p < 0.05).

SnMP-treated animals exhibited minimal HO activity (0.1 ± 0.08 pmol bilirubin * min-1 * mg-1, p < 0.001 vs both vehicle and CoPP treated-MI groups).

In sham-operated hearts HO-1 protein levels in different myocardial regions were low (Figure 1B). Conversely, in the untreated MI group 4 weeks after LAD occlusion, HO-1 expression levels were significantly increased in the central zone of the infarcted area. CoPP treatment resulted in an increase of HO-1 protein levels in all regions compared with both sham and untreated MI groups (p < 0.001 vs the other groups). Nonetheless in the CoPP-treated MI group there was a heterogeneous expression of HO-1 protein in the different myocardial regions with the highest levels in the core of the infarcted area (p < 0.05 vs border zone and p < 0.001 vs both LV remote zone and RV). Likewise, HO-1 levels in the border region were about twofold higher than in both remote area and right ventricle (p < 0.05). The relative values of HO-1 expression level in each region of CoPP-treated MI group were: IZ > BZ > RZ = RV.

The addition of SnMP induced a regional pattern and levels of HO-1 expression in each cardiac region akin to those of CoPP alone.

Immunohistochemistry showed a discrete pattern of connexin-43 staining in LV sections of sham-operated rats, predominantly localized to the myocyte-myocyte junction corresponding to intercalated discs. As compared to sham hearts, quantitative analysis of connexin-43 staining showed a significantly decreased Cx43 in untreated MI rats both in the remote region (57% ± 8% of sham, p < 0.001 vs sham group) (Figure 2) and in the border zone (51% ± 10% of sham, p < 0.001 vs sham group) (data not shown). CoPP treatment resulted in a significant conservation of Cx43 expression in the remote region (84% ± 8% of sham, p < 0.001 vs MI vehicle group) and also in the border areas (75% ± 16% of sham, p < 0.02 vs MI vehicle group).

In the SnMP treated group, Cx43 staining was significantly lower in both the remote zone (66% of sham, p < 0.02 vs sham) and in the border zone (63% of sham, p < 0.05 vs sham), similar to untreated MI hearts.

Figure 3 shows the results of morphometric analysis in untreated and in CoPP treated animals. In untreated MI, as compared to the corresponding zones in sham hearts, we observed the increase in arteriolar density in the border zone (140%, p = 0.02) as opposite to the capillary rarefaction in the border (55%, p < 0.001) as well as in the remote zone (79%, p < 0.05). CoPP treatment further increased arteriolar density in the border zone (162%, p < 0.05) and corrected capillary rarefaction partially in the border zone (69%, p < 0.05 vs untreated MI) while completely in the remote zone (86% ns).

Correlation matrix of ECG diagnostic signs, anatomical parameters, indices of LV function, and tissue and humoral biomarkers (Cx43 and BNP respectively) in untreated infarcted animals is shown in Additional file 1: Table S4. Infarct size positively correlated with Â_QRS, indicating that the rightward shift of the frontal axis is a reliable index of anterior infarct size in the animal model used, and with LV enlargement. Remote wall thickness, a marker of LV remodeling, negatively correlated with LV function and Cx43 and positively with BNP. Functional parameters of LV correlated well with ECG diagnostic signs, with Cx43 staining and BNP.

Hearts untreated and CoPP-treated rats sacrificed at 16 and 24 h after MI were tested for caspase 3 activity and BCL-W expression level and compared with sham hearts. (n = 3 for each time in each group). Results did not evidence any significant difference between untreated and CoPP-treated MI rats either in the caspase 3 activity or in the level of BCL-W expression. As the BCL-W level is concerned, a significant increased level of BCL-W at both 16 h (p < 0.05) and 24 h (p < 0.01) was found in the infarct zone irrespective of treatment with respect to sham operated animals.

LAD ligation produced a LV antero-lateral transmural scar, which averaged 35.9 ± 1.6% of the LV 4-weeks after occlusion, confirming previous data [16, 32‐34].

In untreated MI animals the frontal QRS axis (ÂQRS) shifted to the right, QRS amplitude decreased, while QRS duration increased when compared to sham animals. ÂQRS deviation embodies an imbalance in the cardiac electrical field, due to the loss of an electrically active area, towards a direction divergent from infarct location [26, 35, 36]. In contrast, the decrease in QRS amplitude reflects the reduction in viable myocardium that contributes to electrical potential generation as well as to ventricular function [26]. Finally, the increase in QRS duration reflects a delay in electrical propagation through the viable myocardium being generally attributed to the derangement of the intra-ventricular Purkinje conduction system and thought to be responsible for asynchrony of contraction and thus loss of ventricular systolic function [37]. However, in the interpretation of ECG changes it should be considered that gap junctions (clusters of channels constructed from connexins, mainly Cx43) are a major determinant of the electrical propagation and electro-mechanical coupling [38, 39].

In our study Cx43 staining positively correlated with QRS amplitude and negatively with QRS duration. Previous studies have shown decreased QRS amplitude in genetically restricted Cx43 mice [40, 41] and Bacharova et al. have attributed to Cx43 reduction the discrepancy between QRS voltage and LV mass in spontaneously hypertensive rats [42]. Finally, at least two studies have shown a significant prolongation of QRS complex in heterozygous deficient Cx43 mice [38, 43].

Regarding myocardial infarction, decreased Cx43 expression and disorganization of the gap junctions in the border zone [44] or in the peri-infarct zone [45] or in both [15, 46] have been reported. In contrast, information on Cx43 expression and organization in the remote LV region is very scanty. In line with our findings, decreased Cx43 staining in the myocardium far from any scar has been reported in ischemic patients [47] as well as in the remote region of infarcted mouse heart [48]. Unfortunately previous studies did not focus on the relationship of Cx43 with ECG and LV structural and functional changes in MI but rather on the putative arrhythmogenic role of Cx43 [46, 49, 50].

Compared to sham-operated hearts, untreated infarcted hearts had a higher basal resistance that progressively increased during prolonged perfusion, and higher vasoconstrictive response to hypotension. The vasoconstrictive nature of this increase in resistance was confirmed by its reversal by papaverine. The finding of increased basal microvascular resistance is in agreement with the documented hypo-perfusion of the remote viable region in patients with chronic myocardial infarction [51, 52]. In previous ex-vivo experiments, we found a similar increase in coronary resistance in control hearts following L-NAME [30] suggesting impaired endothelial function and reduced NO bioavailability in the surviving myocardium. However, the mechanism(s) underlying the further increase in resistance during hypotension (paradoxical vasoconstriction) in the remote zone of infarcted heart remains to be elucidated, especially in relation to the observed significant increase of circulating ET-1 in MI as opposed to PGE₂.

The preliminary test on the time course of HO-1 over-expression induced by CoPP i.p. injection in a group of normal rats indicated that HO-1 over-expression became apparent 16 h after CoPP administration, and further increased at 24 and at 48 h (Additional file 1: Figure S1). These results augment previous data from Lakkisto et al. showing a 1.5-twofold increase in HO-1 protein at 24 h following a single i.p. injection of CoPP at the same dose we used, which lasted for 1 week [16]. Continuing increase of HO-1 expression at 48 h confirms a previous report suggesting a long-lasting effect of CoPP on HO-1 over-expression [17]. In MI animals we administered CoPP after coronary occlusion, and then once a week for 4 weeks. This treatment schedule pursued the idea of inducing HO-1 expression late after LAD occlusion and sustaining its activation for the 4-week study period. A powerful and prolonged increase in HO-1 expression was evident at 4 weeks in all cardiac regions with the highest level in the infarcted area. Compared to untreated MI, CoPP significantly decreased the rate of spontaneous death beyond 24 h, inferring a beneficial effect of treatment at delayed times only. Compared to untreated MI, CoPP reduced ECG alterations at 4 weeks, according to the decreased size and transmurality of the infarct, as well as to the preserved Cx43 architecture in the remote zone. CoPP treatment improved left ventricular function as assessed in vivo by reduced LV volumes, increased LV fractional shortening and increased systolic thickening of the viable wall. The above were associated in vitro with reduced infarct size, no clear hypertrophy of the remote myocardium, and preservation of the Cx43 staining and its spatial organization in the remote region. SnMP cancelled the beneficial effects of CoPP, abolishing any differences relative to the untreated MI group. This finding focuses on HO activity as very primarily responsible for the improved conditions in the heart after LAD occlusion. CoPP also prevented the increase in heart rate observed in untreated MI. This finding was likely related to the protective effect of CoPP on ventricular function and its limitation of heart failure.

The reduction of infarct size by CoPP post-occlusion administration is of considerable clinical significance. As HO-1 up-regulation conceivably began well beyond the completion of the ischemic necrosis, a process not susceptible to reversibility, one should consider that the infarct size at 4 weeks in untreated animals was the integrated result of ischemic plus non-ischemic myocardial loss taking place late after ischemic necrosis [9]. Moreover, one should consider additional processes moving in the opposite direction, i.e., repairing and regenerative processes limiting final infarct size. Lakkisto and colleagues found that a single injection of CoPP 24 h before LAD ligation was able to increase cell proliferation and tissue repair and decrease the apoptotic loss of cardiomyocytes in the border area during the first few days after MI [16, 53]. This very dynamic scenario of loss and replacement of myocardial tissue makes it reasonable to conceive that the increase in HO activity, although delayed, was able to prevent ‘non-ischemic’ tissue loss, and/or to exalt regeneration of new muscular tissue or both.

Although this study does not allow discrimination between these mechanisms, the higher expression of HO-1 in the infarct area and in the border zone relatively to the other territories, still evident at 4 weeks after the initial event, strongly suggests its role in the healing process of MI. The occurrence of reparative processes sustained by the formation of new vascular structures seems to be supported by the finding of increased density of both arterioles and capillaries in the present study following CoPP.

Moreover, CoPP prevented the increase in CR observed ex vivo in the isolated heart of untreated MI hearts. The effects of CoPP seen here may be partly due to the end-products of heme degradation, bilirubin and carbon monoxide, a powerful vasodilator. In addition, CoPP administration abolished the progressive increase of resistance during prolonged perfusion, in agreement with our previous observations obtained in animal models with critical shortage in both NO production and bioavailability [54‐56].