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The serine-threonine kinase Akt/PKB mediates stimuli from different classes of cardiomyocyte receptors, including the growth hormone/insulin like growth factor and the β-adrenergic receptors. Whereas the growth-promoting and antiapoptotic properties of Akt activation are well established, little is known about the effects of Akt on myocardial contractility, intracellular calcium (Ca2+) handling, oxygen consumption, and β-adrenergic pathway. To this aim, Sprague–Dawley rats were subjected to a wild-type Akt in vivo adenoviral gene transfer using a catheter-based technique combined with aortopulmonary crossclamping. Left ventricular (LV) contractility and intracellular Ca2+ handling were evaluated in an isolated isovolumic buffer-perfused, aequorin-loaded whole heart preparations 10 days after the surgery. The Ca2+–force relationship was obtained under steady-state conditions in tetanized muscles. No significant hypertrophy was detected in adenovirus with wild-type Akt (Ad.Akt) versus controls rats (LV-to-body weight ratio 2.6±0.2 versus 2.7±0.1 mg/g, controls versus Ad.Akt, P, NS). LV contractility, measured as developed pressure, increased by 41% in Ad.Akt. This was accounted for by both more systolic Ca2+ available to the contractile machinery (+19% versus controls) and by enhanced myofilament Ca2+ responsiveness, documented by an increased maximal Ca2+-activated pressure (+19% versus controls) and a shift to the left of the Ca2+–force relationship. Such increased contractility was paralleled by a slight increase of myocardial oxygen consumption (14%), while titrated dose of dobutamine providing similar inotropic effect augmented oxygen consumption by 39% (P<0.01). Phospholamban, calsequestrin, and ryanodine receptor LV mRNA and protein content were not different among the study groups, while sarcoplasmic reticulum Ca2+ ATPase protein levels were significantly increased in Ad.Akt rats. β-Adrenergic receptor density, affinity, kinase-1 levels, and adenylyl cyclase activity were similar in the three animal groups. In conclusion, our results support an important role for Akt/PKB in the regulation of myocardial contractility and mechanoenergetics.
Akt (or protein kinase B) is a serine threonine kinase, which mediates signals from different classes of receptors. Particularly, it is activated by receptors endowed with intrinsic tyrosin kinase (e.g. insulin growth factor (IGF)-1 or insulin receptor), seven-membrane G-protein-coupled receptors (e.g. β-adrenergic receptor), gp130-dependent cytokines (e.g. interleukin-6), and estrogens.1–4 Akt phosphorylation occurs primarily through phosphoinositide 3-kinase (PI3K) activation, translocating the kinase to the membrane.4 The relevant downstream effectors of Akt are less clear, but include glycogen synthase kinase 3 (GSK-3), tuberus sclerosis complex 1–2, and members of the apoptotic cascade. The principal and most extensively investigated physiological actions of Akt consist of growth activation and apoptosis inhibition, both consistently documented in many systems.4–9 However, it appears that Akt may also be involved in the regulation of myocardial contractility. A recently generated transgenic mouse with cardiac-restricted overexpression of constitutively active Akt, the E40K, exhibited a phenotype characterized not only by cardiomyocyte hypertrophy but also by a remarkable increase of myocardial contractility.10 In this model of enhanced Akt activity, there is a marked upregulation of myocardial sarcoplasmic reticulum Ca2+ ATPase (SERCA-2) protein, and an increase of Ca2+ transients and channel currents.11 However, the consequences of a transient elevation of Akt myocardial signaling on contractility and Ca2+ handling, particularly on Ca2+ responsiveness of the myofilaments in the normal myocardium, independent of the confounding effects of cardiac growth in vivo, are unknown. Equally unexplored are the mechanoenergetics responses to Akt overexpression that appear particularly relevant in view of the proposed therapeutic use of Akt in ischemia–reperfusion injury and heart failure.
Therefore, to address these issues, adenoviral gene transfer with Akt was performed in rats using a catheter-based technique coupled with aortopulmonary cross-clamping and coronary retroperfusion. At 10 days after gene transfer, hearts were harvested, aequorin-loaded and buffer-perfused in an isolated isovolumic Langendorff apparatus. Specifically, experiments were designed to address the following questions:
Notably, experiments were performed only 10 days after gene transfer, to avoid the occurrence of significant cardiac growth in vivo.
We and others have previously demonstrated that the catheter-based aortopulmonary crossclamping with retrograde coronary perfusion yields stable, uniform, and efficient cardiac infection.12–14 Immunohistochemistry analysis of cross-sectional myocardial slices sampled each millimeter with anti-hemoagglutinin (HA) monoclonal antibody showed that approximately 70% of cardiomyocytes were positive (Figure 1, panels a and b). Moreover, tissue histology analysis demonstrated a uniform distribution of the adenoviral infection with adenovirus with wild-type Akt (Ad.Akt) throughout the myocardium. No differences were noticed between the apical and the remaining area, where the aequorin macroinjection was performed. Control sections obtained by omitting the primary antibody showed no immuno-reaction (Figure 1, panels c and d). In the Ad.GFP-injected hearts, cardiomyocytes showed a similar percentage of infection and signal distribution compared with Ad.Akt group (Figure 1, panel g), but viral expression is also evident in the liver and kidney (Figure 1, panels h and i).
We then explored whether the adenoviral-mediated gene transfer of Akt resulted in increased protein expression and activation. Indeed, in the left ventricles exposed to the virus, we observed an increase in both the total amount and the phosphorylated Akt and phosphorylated GSK-3 (Figure 2). Accordingly, Akt activity assessed in vitro by GSK-3-GST fusion protein phosphorylation was significantly higher in the left ventricles exposed to the gene transfer (Figure 2).
Infected cardiac tissue displayed a slight inflammatory response with no evidence of tissue disruption nor increase of collagen deposition as assessed by picrosirius red staining. On the whole, left ventricular (LV) architecture appeared similar among the three study groups (Figure 1, panels e and f).
Rats with myocardial Akt overexpression displayed no signs of cardiac growth, as documented by similar histological cardiomyocyte diameter among the study groups (17.42±3 versus 16.05±2.3 μm Ad.HA, 17±4 μm Ad.GFP and 16.58±2.5 μm controls). Lack of myocardial hypertrophy was further confirmed by echocardiography. Specifically, LV-to-body weight (BW) ratio was 2.7±0.2, 2.6±0.3, 2.6±0.5, and 2.7±0.3 mg/g, in Ad.Akt, adenovirus tagged with the HA epitope (Ad.HA), Ad.GFP, and controls, respectively. LV systolic function, as assessed by endocardial fractional shortening, was increased by 20% in Ad.Akt rats compared with Ad.HA, Ad.GFP, and control saline-treated animals (45±3 versus 38±2, 38±4, and 39±3%, respectively, P<0.05).
Myocardial infection with Ad.HA and with Ad.GFP had no effects on cardiac function, as shown by the mechanical twitches similar to those of control rats (Table 1). On the contrary, Ad.Akt hearts displayed a significant increase of contractility. As a prototype, developed pressure was 41% higher than in controls rats, solely due to an increase in systolic pressure. Despite a longer mechanical twitch, diastolic function was not significantly altered by Ad.Akt, as shown by similar tau values in the four groups, which accurately measures LV relaxation, and by higher peak negative dP/dt (Table 1). The subcellular mechanisms of the inotropic effects of Ad.Akt were investigated in aequorin-loaded whole heart preparations in which [Ca2+]i transients and the corresponding pressure tracings were simultaneously recorded. Figure 3 shows a typical [Ca2+]i transient and the corresponding LV pressure tracing at baseline perfusate Ca2+ in the three study groups. The first relevant finding was the association of increased developed pressure with a larger amplitude of the [Ca2+]i transient, which averaged 19%, in the absence of changes of diastolic [Ca2+]i. The time course of the transient was slightly but not significantly prolonged after Ad.Akt. Tau of the [Ca2+]i transient, which has been shown to reflect mostly the uptake of calcium by the sarcoplasmic reticulum,15 was not significantly changed in Ad.Akt hearts, supporting the stance that the relaxation phase is not impaired by elevated myocardial Akt signaling. Since the magnitude of contractility change upon Akt adenoviral infection could not be explained only by increased Ca2+ available to the myofilament, a change in myofilament Ca2+ responsiveness was suggested. Indeed, maximal Ca2+-activated pressure under tetanic conditions was significantly increased by 19%; the Ca2+-concentration–response relationship was slightly shifted to the left, with EC50 values decreased by approximately 10% (Table 2). Figure 4 shows a representative tracing of intracellular Ca2+ and of corresponding pressure recorded under steady-state tetanic conditions in control and Ad.Akt-perfused hearts.
Myocardial oxygen consumption was evaluated as MVO2. Dobutamine doses titrated to achieve a similar positive inotropic effect in isolated hearts caused an increase in MVO2 in Ad.Akt hearts, which was significantly smaller than that observed in control hearts (14 versus 39%, respectively, P<0.01) (Figure 5). This difference remained even after adjusting for heart rate (32 versus 12%, P<0.01).
To determine whether nitric oxide (NO) is involved in Akt-mediated positive inotropism, 12 additional rats were divided into the three study groups, and employed for additional perfusion studies. Specifically, four additional heart per each group were perfused with buffer plus the nonselective nitric oxide synthase (NOS) inhibitor, l-NAME (50 μM). In the control and HA groups, the 50 l-NAME infusion induced a rapid 8.2±2% increase of coronary perfusion pressure, while LV developed pressure and +dP/dt remained unchanged (112±5 versus 112±4 mmHg in control, and 115±6 versus 115±4 mmHg in Ad.HA, baseline and postinfusion values, respectively). In the Ad.Akt group, l-NAME application to the perfusate similarly increased coronary perfusion pressure by 9±4%, without affecting LV systolic and diastolic pressure. Thus, in this model system, NO does not appear to be involved in the increased contractility induced by Akt adenoviral gene transfer.
To gain further insight into the mechanisms of Akt-induced augmented contractility, we measured mRNA and protein LV content of four major calcium-regulating proteins including SERCA-2, which has been previously shown to be increased in Akt-overexpressing mice,11 phospholamban, which is an important modulator of SERCA-2 activity, calsequestrin, an important SR Ca2+ buffer, and ryanodine receptor. Western blotting analysis revealed that LV protein levels of SERCA-2 (Figure 6) were significantly increased in Ad.Akt hearts compared with controls and Ad.HA (155±11 and 104±9% of control values in Ad.Akt and Ad.HA groups, respectively, P<0.01), while phospholamban, ryanodine receptor, and calsequestrin levels were similar among the study groups (Figure 6).
No significant differences were detected with regard to the expression of the calcium-regulatory proteins mRNAs, as showed by Northern blot analysis (Figure 7).
No differences were found among the study groups in β-adrenergic receptor density and affinity and β-adrenergic receptor kinase 1 protein content (Figure 8). Therefore, neither downregulation of β-adrenergic receptor density nor alterations at the level of receptor coupling were present in conditions of elevated myocardial Akt signaling.
The current study demonstrates that Akt adenoviral gene transfer in normal hearts increases contractility. Such Akt-induced inotropic effects are independent of cardiac hypertrophy, and are secondary to both an increment of Ca2+ activator available to the contractile apparatus and to an augmented myofilament responsiveness to Ca2+. Moreover, when compared with a typical inotropic stimulus such as that induced by dobutamine, the oxygen cost of pressure development is remarkably lower in Akt-infected hearts, indicating improved mechanical efficiency. Finally, while β-adrenergic receptor activation status is not affected by Akt activation, SERCA-2 protein level is significantly increased by 155% of control values, which may in part account for the observed changes in contractility. Upregulation of SERCA-2 appears mediated post-transcriptionally and is not associated with changes of myocardial mRNA and protein content of phospholamban, ryanodine receptor, and calsequestrin.
We provide the first evidence that the inotropic effect secondary to Akt activation, previously described only in chronic models of Akt overexpression, is independent of myocardial hypertrophy. Moreover, such contractile changes occur without significant impairment of diastolic function, at variance with other Ca2+ sensitizers.16,17 As to the subcellular mechanisms underlying such positive inotropic effects, the contractile state of the muscle can be altered by several mechanisms: ‘upstream’ mechanisms, (1) altering the amplitude or time course of the [Ca2+]i transient, (2) altering the affinity of troponin C for Ca2+, or downstream mechanisms such as (3) altering the response of the myofilaments to a given level of occupancy of the calcium binding sites on troponin C.16,17 Viewed from this perspective, the changes of the Ca2+ transients observed in our study include a combination of such mechanisms. In fact, the amplitude of the transients was significantly increased compared to baseline. On the other hand, the increase in maximal Ca2+-activated force observed in Ad.Akt rats speaks in favor of downstream mechanisms, that is, changes of myofilament kinetics after Ca2+ binding to troponin C.
In this regard, recent studies addressing the possibility that Akt mediates physiological hypertrophy have reported that controlled interval training increases cardiomyocyte contractility through a combination of higher myofilament Ca2+ sensitivity coupled with enhanced Ca2+ handling and increased SERCA-2 levels.18–19
Another distinct feature of Akt-positive inotropic action is that the increase in the amplitude of the mechanical twitch is accomplished without significant impairment of the myocardial relaxation, as shown by the similar tau values of the mechanical twitch in the four animal groups. This is further supported by the observation that intracellular Ca2+ decline is not different from controls, as shown by similar values of tau of the Ca2+ transients in Ad-Akt-infected hearts. On the other hand, tau of the Ca2+ transient has been proposed to depend primarily upon sarcoplasmic reticulum Ca2+ ATPase, the sarcolemma Na+/Ca2+ exchanger, and buffering of Ca2+ by intracellular proteins, and its prolongation often precedes and causes abnormal myocardial relaxation.15 These findings are at variance with other pure myofilament Ca2+ sensitizers, whose action is almost invariably associated with variable degrees of myocardial relaxation impairment and slowed intra-cellular Ca2+ decline.16,17
A final interesting finding is the relatively low oxygen cost of pressure development induced by Akt activation. This may be explained by the Ca2+-sensitizing effect, insofar as the reduction in the amounts of Ca2+ required to activate the myofilaments also lowers energy requirement for Ca2+ transport. Interestingly, also heart rate does not increase following elevated myocardial Akt signaling, which may further lower oxygen cost of pressure development compared with other inotropic agents inducing tachycardia. The use of sympathomimethic agents such as dobutamine or isoproterenol typically leads to a remarkable raise of MVO2 due to both heart rate and per beat MVO2 increase.20 On the other hand, the decline of MVO2 upon administration of vasodilators such as nitroprusside or inhibitors of phosphodiesterase III that elevate cAMP and combine vasodilating and inotropic effects is not due to direct myocardial effect but is rather secondary to the vasodilation.21
To date no study has addressed the mechanisms of enhanced cardiac function induced by elevated myocar-dial Akt signaling without the confounding impact of LV hypertrophy. Our data are congruent with the data obtained by Kim et al.11 in conditions of remarkable myocardial hypertrophy (heart weight-to-body weight ratio in transgenic+60% versus wild-type animals), insofar as the magnitude of augmented myocyte contractile function (+74% transgenic versus wild-type animals) could not be solely explained by the 57% increase of Fura-2 Ca2+ transients, but pointed to an increase of Ca2+ responsiveness of the myofilaments as a potential underlying mechanism. However, steady-state calcium concentration response were not obtained by Kim et al. Consistent is also the observation that Akt increases contractility without impairing myocardial relaxation. The differences concerning the magnitude of contractility increase, the level of SERCA-2 upregulation, can be explained by more prolonged myocardial exposure to higher levels of Akt overexpression, by the concomitant presence of cardiac hypertrophy, and by the different type of the Akt transgene, which in that study is a constitutively active form of Akt-1, while here we used the wild-type one. The IGF signaling pathway activates Akt through PI3K.4 The growth-promoting and anti-apoptotic properties of IGF-1 activation are indeed partly mediated by Akt activation.4,6 It has been proposed that myocardial Akt activation may also be involved in the structural and functional changes observed after long-term exposure to GH excess, as typically occurs in the acromegaly.5,22 In the same model system, we have previously shown an increase of contractility averaging 20% following acute application of graded concentration of IGF-1 in the perfusate, mostly due to augmented Ca2+ responsiveness of the myofilaments.23 Although it is difficult to compare the acute application of IGF-1 on isolated muscle preparations with increased Akt signaling due to in vivo gene transfer, it is possible that part of the IGF-1 effects on contractility may be mediated by Akt, although there are differences in the magnitude of contractility increase.
It therefore appears that Akt acts through different pathways known to affect myocardial mechanics, which is perfectly congruent with its critical position downstream of receptors with intrinsic tyrosin kinase activity (growth factors such as IGF-1 or insulin), IL6 family receptors, and seven-transmembrane G-protein-coupled receptors (β-receptors).1–4 Moreover, the recent demonstration of a direct SERCA-2 upregulation in Akt-overexpressing mice11 is in part supported by our data demonstrating a significant increase of SERCA-2 protein in Ad.Akt-infected rats. This finding, which was also observed in rats following exogenous GH administration,24 provides potential molecular underpinnings for the contractility and Ca2+ handling changes observed in the current study. In fact, SERCA-2 overexpression is known to increase Ca2+ transport and cardiac function, and is mainly characterized by increased systolic Ca2+ levels, shorter transients, enhanced contractility with accelerated rates of contraction and relaxation, and no evidence of diastolic Ca2+ overload consistent with the enhanced capacity of the SR to sequester calcium.25,26 The mechanisms of SERCA-2 are likely complex, but do not involve significant changes of phospholamban, calsequestrin, and ryanodine receptor protein and transcripts levels, confirming previous data obtained in Akt-overexpressing mice.11 However, the possibility of a change in the extent of phospholamban phosphorylation and its effect on SERCA-2 cannot be excluded. The increase of SERCA-2 in our model system is mediated by post-transcriptional mechanism, since SERCA-2 mRNA was not different among the three study groups. Further research in needed to clarify whether elevated myocardial Akt signaling is associated with enhanced translation or stability of SERCA-2.
Akt activation increases contractility with a combined mechanism of increase [Ca2+]i, and by sensitizing the myofilaments to Ca2+, with marginal increase of myocar-dial oxygen consumption. The reduced oxygen consumption required for Ca2+ transport in turn limits the threat of arrhythmias, and may blunt Ca2+-dependent transcriptional and translational mechanisms leading to hypertrophy and failure. Coupled with the well-established antiapoptotic and growth-promoting properties displayed by Akt in several model systems, the observed remarkable positive inotropic effects opens new scenarios regarding clinical heart disease. Indeed, changes in the activation status of Akt have been recently reported in experimental diabetic cardiomyopathy27 and human heart failure,28 thus painting Akt as a target for novel therapeutic strategies. To support this view, recent studies have demonstrated beneficial effects following elevated myocardial Akt signaling in experimental heart failure.29
We used replication-defective adenoviral vectors encoding for the human AKT1 wild-type gene included in a frame HA epitope 3′-tag (A.-AKT) under the control of the cytomegalovirus promoter, and as a control, a similar adenoviral vector encoding for the HA epitope.30,31 A small group of five animals (Ad.GFP) was injected with a similar adenoviral vector encoding for the reporter GFP fusion protein.
Sprague–Dawley male rats (Charles River, Italy, body weight (BW), 210–250 g) were randomized into three groups (n=11 in each group +4 for l-NAME experiments and +5 injected with GFP, see below): saline treatment (sham), Ad.HA, and Ad.Akt.31 The viral delivery procedure has been described previously in detail.12 Briefly, rats were anesthetized with a mixture of ketamine hydrochloride (Sigma, 50 mg/kg BW) and xylazine (Sigma, 10 mg/kg BW) and then orally intubated and ventilated. The animals were subsequently cooled with ice bags and their temperature monitored with a thermistor catheter. A method based on that reported by Hajjar et al.13 and subsequently modified by Ikeda et al.14 was used to deliver the viral construct. When the animal's temperature reached 30°C, an anterior thoracotomy was performed, the heart was exteriorized, and a 7.0 suture placed on the apex of the left ventricle. A 22 G catheter containing 200 μl of viral solution of 1 × 1012 PFU was then gently introduced into the left ventricle. The aortic root and pulmonary artery were identified and the catheter advanced through the left ventricle into the aortic root. The aorta and pulmonary artery were clamped gently, distal to the site of the catheter and the viral solution injected. The period of total occlusion (time for viral injection and the postinjection period) lasted 30 s, allowing the solution to circulate down the coronary arteries. Then, the aortic and pulmonary clamps and the catheter were removed, the pneumothorax evacuated, and the chest closed. Animals were transferred back to their cages where they were allowed to recover. The same procedure was followed for sham-operated rats, but the catheter was filled with saline.
Transthoracic echocardiograms were performed in all surviving animals, according to previously described methods,32 with a SONOS 5500 electronic system equipped with a 7 or 12 MHz probe (Agilent Technologies, MA, USA). All measurements, performed with an off-line analysis system by one observer who was blinded to prior results, were based on the average of three to six consecutive cardiac cycles.
Rats were killed and the isolated hearts were placed in a isovolumic, buffer-perfused preparation according to the Langendorff technique, as described previously.23,33 Briefly, the rats were anesthetized with ether, followed by an injection of 200 IU heparin in the femoral vein. After 1 min, the thorax was opened and the heart quickly removed and put into ice-cold Krebs–Henseleit solution (vide infra), weighed, and mounted on a cannula inserted into the ascending aorta. Retrograde aortic perfusion of the coronary arteries was performed within 30 s after the thoracotomy via a constant flow of 10 ml/min/g heart weight. Pressure was monitored by a Statham P23Db transducer. Cardiac temperature was set at 25°C, measured by a temperature probe inserted into the right ventricle. The composition of the perfusate was as follows (mM): NaCl 118, KCl 4.7, KH2PO4 1.2, CaCl2 2, MgCl2 1.2, NaHCO3 23, dextrose 5.5, and saturated with a 95% O2–5% CO2 gas mixture to a pH of 7.4±0.2. LV pressure was measured using a fluid-filled latex balloon inserted into the left ventricle via the mitral valve. After an equilibration period of 15–30 min at 25°C, the temperature was gradually increased to 361C and the hearts were paced at 3.5 Hz. Measurements of LV function were obtained when the preparation achieved a steady state after instrumentation (approximately 15 min); the balloon volume was inflated to achieve a diastolic pressure of 2–4 mmHg in all the animal groups.
The digital signal of the LV pressure tracing was further analyzed using customized software to obtain the following parameters: peak LV–systolic pressure, LV end–diastolic pressure, LV developed pressure, time to peak pressure, time from peak systolic pressure to 90% of relaxation, time constant of exponential pressure decay using the variable asymptote method, or tau, and maximum and minimum values of the first pressure derivative with respect to time. Every parameter was measured three times for each experimental point and was then averaged.
Aequorin loading was performed as described previously.23,33 Briefly, 3–5 μl of an aequorin containing solution (1 μg/ml) was macroinjected into the interstitium of the inferoapical region of the LV. The heart was then positioned in an organ bath with the aequorin-loaded area of the LV directed toward the cathode of a photomultiplier (model 9635QA, Thorn-EMI, Gencom Inc.) and submerged in Krebs–Henseleit solution. At 5–10 min after loading, which was performed under Ca2+-free conditions, CaCl2 was gradually added to the coronary perfusate up to a total Ca2+ concentration of 1 mmol/l. The experimental protocol was started 5–10 min after a steady state of the mechanical parameters was reached.
Aequorin light signals were recorded on a four-channel recorder in parallel with the LV pressure and coronary perfusion pressure tracings and were digitized as described above for the LV pressure tracings. At each step of perfusate Ca2+, 30–60 light transients were wave averaged, and values were converted into intracellular Ca2+ concentrations using the method of fractional luminescence as described previously.23,33 At the end of each experiment, the heart was perfused with a solution containing 20 mmol/l Ca2+ and 5% Triton X-100 to lyse the aequorin-loaded cells and expose all of the remaining aequorin to Ca2+. This resulted in an instantaneous burst of light, subsequently declining to baseline within 10–20 min. The area under the curve was integrated to obtain a value for Lmax. The ratio of the light versus Lmax is the fractional luminescence, which was converted into intracellular Ca2+ concentrations by the use of a calibration curve derived in vitro. The wave-averaged signals were analyzed for peak systolic Ca2+, diastolic Ca2+, time to peak light, time from peak light to 50% of light decay, and time constant of exponential light decay, tau, using the variable asymptote method.
The response of the myofilament apparatus to Ca2+ consists of two terms: the myofilament Ca2+ sensitivity, which describes the affinity of the contractile apparatus for [Ca2+]i over the ranges of contractile responsiveness to [Ca2+]i (the EC50 of the Ca2+-concentration–response relationship), and the maximal Ca2+ activated force, which determines the amplitude of the contractile response.16,17 Both components were evaluated in the isolated whole heart by steady-state pressure–Ca2+ relations obtained by eliciting tetanus with rapid pacing after exposure to ryanodine, according to a previously described technique.23,33 Ryanodine 10−7 m (Calbiochem, San Diego, CA, USA) was added to the perfusate to inhibit sarcoplasmic reticulum function. Typically, LV function declined gradually reaching a new steady state after about 20 min. Tetanus was then elicited by 4 s of high-frequency electrical stimulation (15 Hz) with a pulse width of 50 ms at 1.5–2.0 times the threshold. Tetanic pressures peaked after approximately 2 s, and tetanic light signals reached a plateau after 2–3 s. Tetanic responses at 0.5, 1.0, 2.0, 4.0, and 6.0 mM [Ca2+] with repeated and averaged (3–5 tetani) measurements for peak tetanic pressure and light signals at each Ca2+ level were assessed. Sensitivity (EC50) and maximal Ca2+-activated pressure of the calcium concentration–response relationship were obtained as described previously,23,33 plotting peak tetanic pressure against peak systolic calcium.
In another series of experiments, l-NAME 50 μM was added to perfusate in control, Ad.HA, and Ad.Akt (four animals per each group) after the equilibration period, and all the above-mentioned parameters were monitored continuously, with 3–5 averaged measurements.
Coronary flow was determined by collecting coronary effluent for 60 s. Perfusate PO2 between the aortic perfusate with a blood gas analyzer (model ABL 510, Radiometer); arteriovenous oxygen difference was calculated from the difference in PO2 between the aortic perfusate and the coronary venous effluent, assuming a solubility of 0.023 ml O2 per milliliter of perfusate at 760 mmHg, and was expressed as micromoles per millimiter. Myocardial oxygen consumption was calculated as the product of arteriovenous oxygen difference and coronary flow and expressed as micromoles per minute per gram of left ventricle.34 Each sample was assayed twice.
After recording baseline mechanical parameters, dobutamine was added to the perfusate in increasing steps starting from a concentration of 10−8 m until reaching the same level of inotropic stimulation of Ad.Akt rats expressed as +dP/dt/developed pressure. Heart rate, inotropic, and lusitropic parameters of function (peak positive, peak negative dP/dt normalized to developed pressure, and time to 90% of relaxation) were recorded before and during continuous perfusion with dobuta-mine35 with three averaged measurements for each step.
Formalin-fixed and paraffin-embedded myocardial sections were stained with hematoxylin–eosin (general morphology) or with picrosirius red (collagen content) or were immunostained to evaluate adenoviral expression. The morphometric analyses were carried out on sections sampled each millimeter, from myocardial apex to base; a total of 40 fields each millimeter were evaluated.
Immunohistochemistry was performed with anti-HA antibody (Sigma, 1:50) followed by ABC (avidin–biotin complex) kit (Pierce) and diaminobenzidine (Pierce) chromogen as peroxidase substrate. Collagen content was expressed as the mean percentage of picrosirius red-stained tissue areas divided by total tissue area in the same field; percentage of infected cardiomyocytes was expressed as the mean percentage of immunopositive myocytes with respect to total myocyte number in the same field. Two researchers blinded for the experimental protocols carried out all measurements independently.
Left ventricles were homogenated in RIPA-SDS buffer (50 mm Tris-HCl (pH 7.5), 150 mm NaCl, 1% NP-40, 0.25%, deoxycholate, 9.4 mg/50 ml sodium orthovana-date, 20% sodium dodecyl sulfate). Equal amount of protein from clarified homogenates were resolved by PAGE and transferred to nitrocellulose filter as described previously.30 Total Akt, serine 473-phosphorylated Akt, phosphorylated GSK-3 and ERK2 were visualized by specific antibodies (Cell Signaling), followed by incubation with an anti-rabbit horseradish peroxidase (HRP)-conjugated secondary antibody (Santacruz Biotechnology) and standard chemiluminescence (Renaissance, NEN).
Akt kinase activity was analyzed as described previously.30 LV extracts were incubated 2 h with immobilized Akt monoclonal antibody. After an extensive washing, the kinase reaction was performed at 30°C for 30 min in the presence of 200 μM cold ATP and GSK-3 substrate. Phosphorylation of GSK-3 was measured by Western blot by using phospho-GSK-3α/β (Ser-21/9) antibody. Autoradiographies were digitalized and quantified using Image Quant software (Molecular Dynamics) using ERK2 as loading control. Each sample was run in duplicate and two to three Western blotting were performed.
For the analysis of calcium-regulatory proteins, cardiac tissue was quickly snap frozen in nitrogen and then homogenated as described in detail by Callies et al.36 Proteins were separated with discontinuous PAGE with 4 and 17% acrylamide and transferred to polyvinylidene difluoride membranes; transfer efficiency was verified by Ponceau S staining of the protein bands. Membranes were incubated with antibodies against against SERCA-2a (1:1500, Affinity Bioreagents), phospholamban (1:2000, Upstate Biotech.), and calsequestrin (1:2000, Upstate Biotech), which was detected for control. Immunoblots were then detected, enhanced, and evaluated as described above.
Three independent Western blots were performed for each antibody36 and each sample was run in duplicate.
Cardiac RNA was extracted as described by Chomczynski et al.,37 separated on 1.2% agarose-formaldehyde gel and Northern blotted as described previously.38 Probes for SERCA-2, phospholamban, ryanodine receptor calsequestrin (from rabbit heart), and glyceralde-hyde-3 phosphate dehydrogenase (GAPDH) were 523, 2090, 535, 2400, and 428 bp, respectively.
Quantitative evaluation of each specific autoradio-gram was approached by normalizing the scanned densitometric intensity to the hybridization signal obtained with GAPDH from the same lane. The size of hybridized messengers was estimated using the 28S rRNA band as standard. Every probe was assayed in duplicate and two to three Northern Blotting were performed.
Receptor binding on myocardial membranes was performed as previously described using the nonselective βAR ligand [125I]-cyanopindolol.39 Competition binding isotherms in sarcolemmal membranes was performed as described previously39 in triplicate with 12 varying concentration of isoproterenol (10−12–10−4 M). Assays were conduced at 37°C for 60 min and then filtered over glass fiber membranes (Skatron), washed, and counted in a γ counter. Competition curves were analyzed by nonlinear least-squares curve fit (Graph Pad Prism).
Immunodetection of left ventricle levels of β-adreno-receptor kinase-1 was performed on detergent-solubilized extracts by Western blot technique, using a polyclonal antibody (SC 562, Santacruz Biotechnology) and an HRP-conjugated goat anti-rabbit secondary antibody and visualized by chemiluminescence (Renaissance, NEN) on autoradiographic sheets. Blots were therefore digitalized and quantified by Image Quant software, as described previously.39 Each assay was repeated twice and each sample was examined in duplicate.
Data are reported as mean±s.e.m. Between-group comparisons of echocardiographic indexes were performed using a two-way ANOVA with repeated measure in one factor (time), followed by Neumann–Keuls test. One-way ANOVA was employed for the other comparisons, also followed by Neumann–Keuls test. Percent differences of MVO2 among the groups were compared using nonparametric tests. A P-value of <0.05 was considered significant.
This work was supported in part by grants from the Italian National Institute of Health, The Italian Ministy of Education (MIUR), and Adriano Buzzati-Traverso Foundation.
Presented in part at the Annual La Jolla-Kyoto-Horizons on heart failure, La Jolla, CA, December 16–19, 2002.