Gadolinium decreases inflammation related to myocardial ischemia and reperfusion injury
© Strande et al; licensee BioMed Central Ltd. 2009
Received: 3 August 2009
Accepted: 10 December 2009
Published: 10 December 2009
The lanthanide cation, gadolinium (GdCl3) protects the myocardium against infarction following ischemia and reperfusion. Neutrophils and macrophages are the main leukocytes responsible for infarct expansion after reperfusion. GdCl3 interferes with macrophage and neutrophil function in the liver by decreasing macrophage secretion of inflammatory cytokines and neutrophil infiltration. We hypothesized that GdCl3 protects against ischemia and reperfusion injury by decreasing inflammation. We determined the impact of GdCl3 treatment for reperfusion injury on 1) circulating monoctye and neutrophil counts, 2) secretion of inflammatory cytokines, and 3) influx of monocytes and neutrophils into the myocardium.
Rats (n = 3-6/gp) were treated with saline or GdCl3 (20 μmol/kg) 15 min prior to a 30 min period of regional ischemia and 120 min reperfusion. Sham rats were not subject to ischemia. Blood was collected either after 30 min ischemia or 120 min reperfusion and hearts were harvested at 120 min reperfusion for tissue analysis. Blood was analyzed for leukocytes counts and cytokines. Tissue was analyzed for cytokines and markers of neutrophil and monocyte infiltration by measuring myeloperoxidase (MPO) and α-naphthyl acetate esterase (ANAE).
GdCl3 did not affect the number of circulating neutrophils prior to ischemia. Two hours reperfusion resulted in a 2- and 3- fold increase in circulating monocytes and neutrophils, respectively. GdCl3 decreased the number of circulating monocytes and neutrophils during reperfusion to levels below those present prior to ischemia. Furthermore, after 120 min of reperfusion, GdCl3 decreased ANAE and MPO activity in the myocardium by 1.9-fold and 6.5-fold respectively. GdCl3 decreased MPO activity to levels below those measured in the Sham group. Serum levels of the major neutrophil chemoattractant cytokine, IL-8 were increased from pre-ischemic levels during ischemia and reperfusion in both control and GdCl3 treated rats. Likewise, IL-8 levels increased throughout the 3 hour time period in the Sham group. There was no difference in IL-8 detected in the myocardium after 120 min reperfusion between groups. In contrast, after 120 min reperfusion GdCl3 decreased the myocardial tissue levels of macrophage secreted cytokines, GM-CSF and IL-1.
GdCl3 treatment prior to ischemia and reperfusion injury decreased circulating monocytes and neutrophils, macrophage secreted cytokines, and leukocyte infiltration into injured myocardium. These results suggest GdCl3 decreased monoctye and neutrophil migration and activation and may be a novel treatment for inflammation during ischemia and reperfusion.
The lanthanide cation, gadolinium (GdCl3) protects the myocardium against infarction following ischemia and reperfusion (IR) in vivo , although this preconditioning is not observed in a buffer perfused, isolated heart model of acute reperfusion injury (unpublished observation). This discrepancy suggests that GdCl3-induced cardioprotection is dependent upon factors found only in vivo, such as blood cells, proteins or hormones among others.
Inflammatory cells are important in the pathophysiological response to injury associated with IR. While crucial to healing, the influx of inflammatory cells, specifically macrophages and neutrophils, results in tissue injury beyond that caused by ischemia alone. Many studies have focused on the acute myocardial inflammatory reaction as a mediator of ischemia-reperfusion injury . Monocytes and other leukocytes infiltrate the area at risk soon after the onset of ischemia. Activated macrophages secrete cytokines that promote tissue damage and recruit neutrophils . Accordingly, the influx of neutrophils into ischemic tissue increases tissue necrosis by releasing proteolytic enzymes and reactive oxygen species and expands the zone of infarction .
Strategies aimed at reducing the levels of inflammatory cytokines  or the infiltration of leukocytes  attenuate myocardial damage associated with reperfusion. Evidence suggests that GdCl3 interferes with macrophage and neutrophil function in the liver by decreasing macrophage secretion of inflammatory cytokines and toxic oxygen radicals  and by inhibiting neutrophil infiltration . The role GdCl3 plays in monocyte and neutrophil infiltration during myocardial ischemia and reperfusion is unknown. Accordingly, this study tests the hypothesis that GdCl3 modulates leukocyte function either directly by interfering with migration or indirectly by decreasing the generation of inflammatory cytokines and chemokines, thereby decreasing the signal that triggers leukocytes to infiltrate into the injured tissue.
Male Sprague Dawley rats at 8 weeks of age (250-300 g) were used in this study and received humane care in compliance with the "Guide for the Care and Use of Laboratory Animals" published by the US National Institutes of Health (NIH Publication No. 85-23, revised 1996). This project was granted approval by the local IACUC review board.
Instrumentation, ischemia-reperfusion protocol and GdCl3 treatment
Rats were anesthetized with 20-40 mg/kg intraperitoneal sodium pentobarbital. The right jugular vein was cannulated for delivery of saline solution. A catheter was inserted in the left femoral artery to measure both blood pressure and heart rate and to withdraw blood. Pressure and rate measurements were monitored using a Gould PE50 or PE23 pressure transducer connected to a Grass model 7 polygraph. The rats were intubated with a 14-gauge catheter and ventilated at 38-45 breaths/min (Harvard Apparatus, model 683; South Natick, MA) with supplemental oxygen. Atelectasis was prevented by maintaining a positive end-expiratory pressure of 5-10 mm H2O. Arterial pH, pCO2 and pO2 were monitored with an AVL 995 pH/blood gas analyzer, and normal values were maintained by adjusting respiratory rate, tidal volume and/or oxygen flow. Body temperature was maintained between 35 and 37°C using a heating pad.
A left thoracotomy was performed, the pericardium was opened and the left coronary artery was identified. A ligature (6-0 Prolene) was passed around the proximal segment of the left coronary artery, and the ends of the suture were threaded through a propylene tube to form a snare. Regional left ventricular ischemia was induced by tightening the snare for 30 min. Coronary artery occlusion was confirmed by epicardial cyanosis and a decrease in blood pressure. Reperfusion was achieved by releasing the snare and was confirmed by a marked hyperemic response of the myocardium. The heart was reperfused for 120 min then excised and assessed for extent of tissue injury.
Myocardial Tissue Myeloperoxidase Activity Assay
Myeloperoxidase (MPO) activity was assayed as a measure of neutrophil activity in hearts using a modified protocol . The heart was homogenized in 50 mM potassium phosphate buffer (pH 6.0) and centrifuged. The pellet was washed twice in 5 mM potassium phosphate buffer. After washing, the pellets were resuspended in extraction buffer (50 mM potassium phosphate buffer (pH 6.0) containing 0.5% hexadecyltrimethyl ammoniumbromide), followed by three rounds of freeze-thawing. The suspension was incubated at 4°C for 20 minutes and then centrifuged at 13,000 rpm at 4°C for 15 minutes. The supernatant (100 μL) was mixed with 100 μL of reaction buffer (50 mM potassium phosphate buffer (pH 6.0) containing 0.6 mg/mL O-dianisidine dihydrochloride and 0.03% hydrogen peroxide). Absorbance was measured at 450 nm after 5 minutes of incubation. After normalization for protein concentration, the MPO content was expressed as units of MPO activity per milligram of protein.
Myocardial Tissue α-Naphthyl Acetate Esterase Assay
The activity of α-naphthyl acetate esterase (ANAE), a marker enzyme of monocytes and macrophages was detected using a previous published protocol . In brief, frozen specimens from Sham, Sham + GdCl3, Control and GdCl3 groups were separately homogenized in ice-cold 0.25 mol/L sucrose (1:5; weight to volume) for 2 × 5 seconds. The samples were centrifuged at 10,000 g for 10 min at 4°C. The supernatant was further sonicated for 90 seconds in ice, centrifuged at 105,000 g for 90 minutes at 4°C, and assayed for protein. An equivalent of 25 mg of supernatant protein for each sample and 5 mL of 200 mmol/L α-naphthyl acetate (Sigma-Aldrich, St. Louis, MO), dissolved in 95% ethanol to give a final concentration of 0.5 mmol/L, was added to a final volume of 2 mL of saline solution. Blanks received no substrate. After 10 minutes of incubation at 37°C, the reaction was stopped by adding 116 mL of 12.5% w/v sodium dodecyl sulfate solution. Subsequently, 5 mL of 200 mmol/L α-naphthyl acetate was added to the blanks. Finally, 30 mL of fast red solution (10 mg/mL distilled water; Fast Red B, Sigma-Aldrich, St. Louis, MO) was added to the sample, followed by an incubation period of 15 minutes at room temperature. Optical density absorption at 490 nm was used to estimate the metabolism of α-naphthyl acetate to α-naphthol. Alpha-naphthyl acetate esterase activity was estimated as absorption at 490 nm per 25 mg of protein.
Blood was collected either 30 min after ischemia or 120 min after reperfusion. Plasma was separated by centrifuging the sample at 14,000 rpm × 10 min at 4°C and frozen at -80°C until analysis. Left ventricular free wall tissue homogenates were processed and quantiated using methods described previously . Interleukin (IL)-8 levels were determined using an IL-8 (Rat cytokine-induced neutrophil chemoattractant (CINC)-1) enzyme-linked immunoassay kit from R&D Systems (Minneapolis, MN) according to the manufacture's instructions. CINC-2, CINC-3, granulocyte monocyte colony stimulating factor (GM-CSF), Interferon (INF)-γ, IL-1α, IL-1β, IL-4, IL-6, IL-10, Monocyte chemotactic protein (MCP)-1, Macrophage inflammatory protein (MIP)-3A, and Tumor necrosis factor (TNF)- α tissue levels were determined using RayBio® Rat Cytokine Antibody Array 1 (Norcross, GA) according to the manufacture's instructions. Each dot on the immunoblot representing a cytokine was quantitated using ImageJ 1.37v software.
Data are reported as mean ± SEM. Statistical analyses were performed by the Student's t test for paired values and a one-way Analysis of Variance (ANOVA) for differences between treatment groups. If significant, a Newman-Keuls multiple comparison test was used to perform pair wise comparisons. Data were considered significant at a p < 0.05. Statistics were performed using WINKS SDA Software (Texasoft, Cedar Hill, TX).
GdCl3 Attenuates IR-induced Increases in Circulating Monocytes and Neutrophils
Macrophage Infiltration in Myocardium
Neutrophil Infiltration in Myocardium
GdCl3 Modulation of Cytokine Levels
The important finding in this study is that a single treatment of GdCl3 prior to ischemia decreased the numbers of circulating monocytes and neutrophils following reperfusion and reduced infiltration of these leukocytes into the injured myocardium. In addition, GdCl3 decreased production of cytokines that are typically secreted by monocytes. These finding are associated with GdCl3-mediated reduction in infarct size after ischemia and reperfusion .
The early phase of myocardial infarction is associated with tissue infiltration of circulating leukocytes in response to chemotactic factors . As the leukocytes infiltration the tissue and become activated, they release more cytokines thereby recruiting further leukocytes to the injured area. Activated leukocytes within the tissue cause further tissue injury by releasing reactive oxygen species and proteases and cause capillary plugging leading further tissue hypoxia. Inhibiting neutrophil infiltration using anti-neutrophil antibodies , neutrophil depleting antimetabolites  or neutrophil filters  have been successful in limiting myocardial infarct size. We have shown that GdCl3 is also a potent monocyte and neutrophil depleting compound as it prevents these leukocytes from circulating and infiltrating into the myocardium.
Gadolinium is known to modulate inflammatory responses by liver macrophages (Kupfer cells) [7, 16]. Gadolinium causes a 70% reduction in the phagocytosis of radiolabeled bacteria , and GdCl3 has been shown to prevent the release of both inflammatory cytokines and toxic oxygen radicals such as superoxide anion produced by activated Kupffer cells [18, 19]. Gadolinium also upregulates secretion of TNF-α from Kupfer cells in response to endotoxemia.
In the present study, GdCl3 treatment pre-ischemia was associated with attenuation of the IR-induced increases in circulating monocytes and neutrophils, and it decreased circulating monocytes in animals not exposed to IR. The selective action of GdCl3 on monocytes is based on the fact that this compound is readily dissolved in normal saline; however, when it is injected into the bloodstream, it rapidly aggregates into relatively large colloidal particles at neutral pH. The particles of GdCl3 are taken up exclusively by circulating phagocytic mononuclear cells of a monocyte lineage (CD11b+, CD13+, and CD14+) [20, 21]. Once inside the cell and after exceeding the threshold concentration, GdCl3 causes cell apoptosis . The GdCl3 aggragates are not expected to cross the endothelial barrier and thus would not be taken up by resident tissue phagocytic cells.
This decrease in circulating leukocytes was not associated with any changes in the levels of the major monocyte chemoattractants, MCP-1 and the neutrophil chemoattractants IL-8/CINC-1, CINC-2, and CINC-3 suggesting that GdCl3 modulates leukocyte trafficking to the heart via some other, as yet undefined mechanism following myocardial IR. Interleukin-8/CINC-1 serum levels increased over baseline levels during ischemia and reperfusion. Interestingly, there was a similar increase in serum levels at the corresponding time points in the Sham group. Although the Sham animals do not undergo LAD occlusion, they still receive a tracheostomy and a thoracotomy. These two invasive surgical procedures may be enough to induce an inflammatory response in these rats.
Gadolinium triggered an increase of TNF-α levels in the myocardium after 120 min reperfusion (Figure 6B). TNF-α is a potent cytokine which is elevated in a variety of inflammatory conditions. Endogenous TNF-α has been correlated with the deterioration of myocardial performance, while blockade of TNF-α with a neutralizing antibody preserves myocardial function after IR . Somewhat paradoxically, exogenously added TNF-α is protective during ischemia and reperfusion through mechanisms which involve the JAK/STAT3 pathway, KATP channels and the mitochondrial permeability transition pore [24, 25]. This protective effect of TNF-α may be related to our previous data, which showed that GdCl3-induced cardioprotection is dependent upon the activation of JAK-STAT3 and KATP channels .
We have previously shown that GdCl3 given 24-72 hours prior to the index ischemic event is also able to attenuate reperfusion injury as determined by infarct size . Interesting, in that study even though GdCl3 was intravenously administered to the rats in vivo, infarct size was determined in isolated buffer perfused hearts subject to IR injury. Since the isolated heart model of IR does not have circulating blood components, the infarcts are not likely solely caused by the inflammatory response. However, it still could be possible that GdCl3-mediated up-regulation of TNF-α in the myocardium could be part of the mechanism of GdCl3-mediated delayed cardioprotection. TNF-α was not measured in the delayed cardioprotection studies but this hypothesis forms the basis of further studies.
Gadolinium also attenuated IR-induced expression of the macrophage-secreted cytokines GM-CSF and IL-1 in this study, suggesting that attracted monocytes may not be differentiating into activated macrophages. Treatment with GdCl3 also did not significantly alter levels of INF-γ and MIP-3 which are activators of macrophage function. In support, we observed a decrease in ANAE activity in the myocardium which suggests decreased infiltration and activation of monocytes into the myocardium. Similarly, we observed decreased MPO activity in the myocardial tissue which suggests a decrease of neutrophil infiltration into the myocardium although the levels of circulating and tissue IL-8/CINC-1 are not modified by GdCl3 treatment. This suggests that GdCl3 may be inhibiting leukocyte chemotaxis and in essence "paralyzing" the monocytes and neutrophils at their storage locations. Swirski et al. have recently identified the splenic subcapsular red pulp as the reservoir for monocytes . From their splenic reservoirs, the monocytes are deployed to inflammatory sites such as the infarcted myocardium . The reservoir of neutrophils is yet to be verified but the neutrophils are thought to reside in the post-capillary venule sites in the periphery such as the bone marrow . Although previous studies have shown that GdCl3 does not affect the migration of neutrophils , inhibition of monocyte migration has not been reported.
One limitation of this study is that we did not study the in vitro migration of isolated monocytes or neutrophils treated with GdCl3. However, the decrease in monocytes and neutrophils into the circulation after GdCl3 treatment indicates that the leukocytes are either not migrating from their reservoirs or are being scavenged prior to the 120 min reperfusion time point.
In summary, a single dose of GdCl3 when given prior to ischemia and reperfusion decreased circulating monocytes and neutrophils as well as decreased the infiltration of these leukocytes into the myocardium. Furthermore, this was not associated with a change in tissue levels of the major monocyte chemoattractant MCP-1 or neutrophil chemoattractant IL-8/CINC-1 but was associated with an up-regulation of TNF-α.
List of abbreviations
Ischemia and Reperfusion
cytokine-induced neutrophil chemoattractant
monocyte colony stimulating factor
monocyte chemotactic protein
macrophage inflammatory protein
tumor necrosis factor
Analysis of Variance.
This study was supported in part by National Institutes of Health Grant HL54075 to J.E.B. J.L.S. was supported by National Institutes of Health Training Grant HL07792 (awarded to the Medical College of Wisconsin).
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