Metformin attenuates ventilator-induced lung injury
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Diabetic patients may develop acute lung injury less often than non-diabetics; a fact that could be partially ascribed to the usage of antidiabetic drugs, including metformin. Metformin exhibits pleiotropic properties which make it potentially beneficial against lung injury. We hypothesized that pretreatment with metformin preserves alveolar capillary permeability and, thus, prevents ventilator-induced lung injury.
Twenty-four rabbits were randomly assigned to pretreatment with metformin (250 mg/Kg body weight/day per os) or no medication for two days. Explanted lungs were perfused at constant flow rate (300 mL/min) and ventilated with injurious (peak airway pressure 23 cmH2O, tidal volume ≈17 mL/Kg) or protective (peak airway pressure 11 cmH2O, tidal volume ≈7 mL/Kg) settings for 1 hour. Alveolar capillary permeability was assessed by ultrafiltration coefficient, total protein concentration in bronchoalveolar lavage fluid (BALF) and angiotensin-converting enzyme (ACE) activity in BALF.
High-pressure ventilation of the ex-vivo lung preparation resulted in increased microvascular permeability, edema formation and microhemorrhage compared to protective ventilation. Compared to no medication, pretreatment with metformin was associated with a 2.9-fold reduction in ultrafiltration coefficient, a 2.5-fold reduction in pulmonary edema formation, lower protein concentration in BALF, lower ACE activity in BALF, and fewer histological lesions upon challenge of the lung preparation with injurious ventilation. In contrast, no differences regarding pulmonary artery pressure and BALF total cell number were noted. Administration of metformin did not impact on outcomes of lungs subjected to protective ventilation.
Pretreatment with metformin preserves alveolar capillary permeability and, thus, decreases the severity of ventilator-induced lung injury in this model.
KeywordsMetformin Continuous Positive Airway Pressure Acute Lung Injury Pulmonary Arterial Pressure Lung Preparation
acute lung injury
acute respiratory distress syndrome
bronchoalveolar lavage fluid
continuous positive airway pressure
high pressure-no metformin
high pressure-metformin pretreatment
low pressure-no metformin
low pressure-metformin pretreatment
arterial carbon dioxide tension
arterial oxygen tension
positive end-expiratory pressure
ventilator-induced lung injury.
Despite its firmly established role as a fundamental life-support modality for critically ill patients, mechanical ventilation (MV) may elicit ventilator-induced lung injury (VILI), which is characterized by alveolar edema and hemorrhage. Recognized mechanisms of VILI include alveolar over-distention by high tidal volumes (volutrauma) and cyclic opening and closing of alveoli (atelectrauma), which operate in concert to trigger inflammatory processes (biotrauma), oxidant/antioxidant imbalance, intra-alveolar coagulation and disturbances in surfactant function [1, 2].
Clarification of the above pathophysiologic mechanisms serves a basis for the discovery of effective pharmacological therapies against VILI, which currently is mainly prevented through the limitation of the mechanical insult to the lung parenchyma (that is, through the implementation of protective ventilation) . Such pharmacological therapies could be novel agents, for example, sphingosine 1-phosphate , or drugs already in clinical use. Our research group contributed to the idea that established drugs may indeed be beneficial when they are re-used for indications other than their initial indication, a concept which we call the drug recycle concept; indeed, we reported that pretreatment with atorvastatin attenuates VILI . Reduced cost, clinician familiarity and known undesired effects profile are obvious advantages of using drugs with proven efficacy for a different indication.
Such a popular established drug is metformin (N',N'-dimethylbiguanide), which enjoys a long-standing recognition in the setting of type 2 diabetes mellitus. Metformin recently emerged as a potential adjunct in the management of patients with cancer [6, 7, 8]; a fact indicating that it may also have effects other than its antihyperglycemic ones. Indeed, there is growing (albeit still limited) evidence that metformin might exhibit pleiotropic properties, including anti-angiogenic , anti-inflammatory , antioxidant  and endothelial barrier-enhancing . Some of the above properties might make metformin a potential candidate for protection against VILI as well.
Interestingly, several clinical studies point out that diabetic patients develop acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) less frequently than non-diabetics [13, 14, 15]; a benefit that could be partially ascribed to the usage of antidiabetic therapies, such as metformin . This evidence (derived from observational studies) [13, 14, 15] along with the known pleiotropic effects of metformin (derived from experimental studies) [9, 10, 11, 12] generated the research idea that it could indeed prevent lung injury. Thus, we endeavored to test the hypothesis that pretreatment with metformin preserves pulmonary vascular permeability, and therefore, confers protection against VILI in non-diabetic animals.
Materials and methods
Animal care and pretreatment
A previously described isolated rabbit lung model was implemented . Male New Zealand white rabbits (approximately 3 kg) were used for these experiments, which were conducted in accordance with the 160/1991 Council Directive of European Union. All experimentation was approved by the Institutional Review Board of the Attikon Hospital and by the Veterinary Directorate of the Prefecture of Athens.
Experiment animals were given metformin (250 mg/kg body weight/day per os in drinking water) or no medication, 48 hours and 24 hours before surgery.
Detailed information is available in Additional file 1.
Description of the circuit
The perfusate consisted of 350 mL of Krebs-Henseleit solution (to which 5% bovine serum albumin was added) plus 40 mL of autologous blood (serving as a marker for capillary rupture) to achieve a total volume of 390 mL.
The perfusion circuit consisted sequentially of the left atrium cannula, a venous plastic tubing with its free distal end open to atmosphere, the venous reservoir collecting the perfusate from the venous plastic tubing, a digital rotary pump and an arterial plastic tubing leading consequently to a water bath, a bubble trap and finally to the pulmonary artery cannula and the lungs.
Initial hemodynamic and ventilation settings
As previously described , each heart-lung preparation was connected to a ventilator and the lungs were initially recruited with continuous positive airway pressure (CPAP) of 20 cmH2O. Then, each preparation was ventilated with pressure-control ventilation (PCV) at peak inspiratory pressure of 11 cmH2O, positive end-expiratory pressure (PEEP) of 3 cmH2O, respiratory rate of 15 breaths/minute, inspiration:expiration ratio of 0.5 and fraction of inspired oxygen of 0.21, while the blood flow increased gradually to 300 mL/minute. Heart-lung preparations were maintained in these conditions (that is, constant perfusion with 300 mL/minute and mechanical ventilation with PCV 11:3) for the next 16 minutes and were subsequently switched to CPAP 5 cmH2O to measure the ultrafiltration coefficient (Kf,c) [17, 18].
Group allocation and ventilation/perfusion protocol
After measurement of the baseline Kf,c, each lung preparation was randomly allocated to be ventilated with PCV at peak inspiratory pressures of 23 cmH2O (high pressure, HiP) or 11 cmH2O (low pressure, LoP) for 60 minutes. Four experimental groups of lung preparations were set: high pressure metformin pretreatment (HiP-Met); high pressure no metformin (HiP-C); low pressure metformin pretreatment (LoP-Met) and low pressure no metformin (LoP-C). Experiments were not performed in a blinded manner.
Post-ventilation protocol measurements
After the completion of the ventilation protocol and the measurement of the final Kf,c, the blood flow and ventilation were stopped. The following variables were considered as outcomes for our study:
ΔKf,c (that is, final Kf,c - baseline Kf,c) was the change in Kf,c before and after the institution of the 60-minute ventilation protocol. ΔKf,c indicated pulmonary capillary permeability alterations. Weight gain was the weight of the heart-lung preparation at 20, 40 and 60 minutes minus its weight after 1 minute of the ventilation protocol. Given that the weight of the heart could not change during the ventilation, this variable reflected the change in lung weight and, eventually, it served as a surrogate for formation of pulmonary edema. Changes in pulmonary artery pressure (mean, inspiratory and expiratory) were defined as the pulmonary arterial pressure at 20, 40 and 60 minutes minus the pulmonary arterial pressure after 1 minute of the ventilation protocol. Changes in tidal volume were defined as the tidal volume at 20, 40 and 60 minutes minus the tidal volume after 1 minute of the ventilation protocol. Total protein concentration in bronchoalveolar lavage fluid (BALF) was measured, as previously described .
Angiotensin-converting enzyme (ACE) activity in BALF was measured following incubation of BALF with ACE substrate hippuryl-histidine-leucine and using a previously described fluorometric assay . Increased levels of ACE activity in BALF indicated diffusion of this enzyme into the alveolar spaces and, thus, served as a marker of pulmonary microvascular barrier disruption .
The total cell number in BALF was calculated using a hemocytometer.
GraphPad Prism 5 (La Jolla, CA, USA) was used for statistical analyses. Data were summarized as means ± standard deviation. One way analysis of variance was used to determine the statistical significance of between-group differences. Statistically significant results (P < 0.05) were further examined by post hoc analysis using the Student Newman-Keuls test. For outcomes such as BALF protein, BALF ACE activity, BALF total cell number and histology, where data from four animals per group were available, data were summarized as medians (range) and compared using the non-parametric Kruskal-Wallis test.
Of the thirty-two animals sacrificed for this experiment, eight animals were omitted before the measurement of the baseline Kf,c according to prespecified exclusion criteria. Thus, lung preparations from twenty-four rabbits (specifically, seven animals per HiP group and five animals per LoP group) were used.
Characteristics of the compared groups at baseline.
Animal weight, kg
3.2 ± 0.2
3.4 ± 0.2
3.3 ± 0.4
3.0 ± 0.3
Serum glucose, mg/dL
179 ± 44
182 ± 91
152 ± 93
144 ± 59
Initial lung weight, g
24.1 ± 2.4
24.4 ± 2.3
23.8 ± 2.5
20.6 ± 2.7
Ischemic time, minutes
34.6 ± 5.5
39.0 ± 7.1
39.0 ± 6.8
34.4 ± 4.9
Before the beginning of 60-minute ventilation
20.4 ± 3.5
24.8 ± 7.5*
16.8 ± 3.1*
16.7 ± 4.0*
24.9 ± 3.8
30.8 ± 8.4
22.5 ± 4.4
22.0 ± 4.4
18.4 ± 3.7
21.4 ± 6.7*
13.9 ± 2.7*
12.9 ± 2.2*
7.5 ± 1.8
7.0 ± 0.6
6.3 ± 0.4
6.8 ± 0.6
At the beginning of 60-minute ventilation:
7.33 ± 0.17
7.27 ± 0.09
7.32 ± 0.11
7.33 ± 0.07
161 ± 9**
154 ± 9
147 ± 2**
147 ± 8
44.7 ± 19.9
47.2 ± 6.6
44.8 ± 5.4
44.7 ± 7.3
35.9 ± 0.5
35.2 ± 0.8
36.2 ± 0.8
35.6 ± 0.5
Pulmonary capillary permeability (Kf,c)
Among lungs ventilated at the higher peak inspiratory pressure/higher tidal volume, pretreatment with metformin compared to no pretreatment was associated with lower final Kf,c (HiP-Met 0.267 ± 0.205 vs. HiP-C 0.881 ± 0.605) (Figure 1) and lower ΔΚf,c (HiP-Met 0.023 ± 0.266 vs. HiP-C 0.672 ± 0.613).
Pulmonary edema formation (weight gain)
Among lungs ventilated at the higher peak inspiratory pressure/higher tidal volume, those with, as opposed to those without metformin pretreatment, sustained less weight gain at 20 minutes (HiP-Met 1.01 ± 0.47 g vs. HiP-C 3.32 ± 3.02 g), 40 minutes (HiP-Met 1.76 ± 1.18 g vs. HiP-C 5.96 ± 4.01 g) and 60 minutes (HiP-Met 2.91 ± 2.38 g vs. HiP-C 7.35 ± 4.32 g) of mechanical ventilation (Figure 2). This was also the case after adjustment of weight gain for initial lung weight.
Changes in pulmonary arterial pressure
There was no difference between the compared groups in increase in mean pulmonary arterial pressure at any time of ventilation. This was also the case for the expiratory and the inspiratory pulmonary pressure.
Changes in tidal volume
Gross examination of the lungs
After the end of injurious ventilation, we noticed more edema and more hemorrhagic spots on the surface of the lungs exposed in injurious (HiP) compared to protective (LoP) ventilation. Among the HiP groups, on gross observation there was less edema and fewer hemorrhagic spots on the lungs of animals with metformin pretreatment (HiP-Met group) as opposed to those without (HiP-C group).
Protein concentration in BALF
ACE activity in BALF
Total cell number in BALF
There was no difference between the compared groups in the total cell number in BALF.
The findings of the present study suggest that pretreatment with metformin prevented increases in pulmonary microvascular permeability in response to injurious mechanical ventilation, thus attenuating VILI in terms of edema formation and histology.
One may wonder if this beneficial effect of metformin against VILI could be attributed to the modification of the serum glucose level of treated animals rather than the metformin itself. The evidence (albeit controversial) that hyperglycemia promotes ALI might justify this notion [13, 22]. However, serum glucose levels did not differ in the groups compared in our study. This was congruent with the results of other experiments that also showed that administration of metformin in non-diabetic animals did not alter their glycemic status . Similarly, administration of metformin does not influence serum glucose in humans who are not suffering from diabetes mellitus . Thus, metformin appears to prevent VILI by a mechanism other than its antihyperglycemic action.
By measuring the pulmonary microvascular filtration coefficient Kf,c, an accurate marker of pulmonary microvascular permeability [24, 25], in addition to BALF protein and ACE activity levels, we observed that metformin prevented the rise in endothelial permeability upon challenge of the isolated lung preparation with excessive airway pressure, indicating a direct barrier-stabilizing effect of the drug. In line with our results, other investigators have advocated that metformin restores pulmonary endothelial function after injurious stimuli other than over-distention, such as hypoxia, through activation of adenosine monophosphate-activated protein kinase . Interestingly, beneficial effects of metformin on the endothelial function of organs other than lung were repeatedly reported [26, 27], indicating that metformin might act similarly on the pulmonary vascular endothelium as well, hence justifying further research in the field.
Agard and colleagues reported that metformin exhibits vasodilatory effects and therefore, it protects against experimental pulmonary hypertension . This finding , in conjunction with evidence regarding the impact of pulmonary hypertension (combined with high airway pressure) on the development of lung injury , could lead to the claim that mitigation of VILI in our study could take place through improvements in hemodynamics. However, we found no difference between the metformin (HiP-Met) and the no metformin (HiP-C) groups in pulmonary arterial pressure at any time of injurious ventilation, and given the constant-flow conditions and pulmonary venous pressure of our system, no differences in pulmonary vascular resistance can be expected between the groups. Thus, the putative vasodilatory effects of metformin (as indicated by the determination of pulmonary arterial pressure in the HiP groups) appear not to contribute to the attenuation of lung injury under the present experimental conditions.
Likewise, other pleiotropic effects of metformin, such as anti-inflammatory effects , may also not participate in its benefit against VILI in the present study. Our experimental protocol had a negligible amount of leucocytes in the perfusate and a short duration of injurious ventilation, so there was not enough time for inflammatory pathways to be activated. Indeed, we found no difference between the compared groups in terms of the BALF total cell number and infiltration of alveolar spaces by neutrophils. Thus, in our model of VILI (in which mechanical phenomena rather than inflammation are the major determinants of injury), it seems unlikely that a drug could provide benefit by acting as an anti-inflammatory agent.
A comment on our results of the changes in tidal volume during the 60-minute ventilation period may be worthwhile (Figure 3). Indeed, we observed an increase in the tidal volume in lungs ventilated at the higher peak inspiratory pressure/higher tidal volume (HiP groups) during the early phases of injurious ventilation, which (given the applied PCV mode of ventilation) could be translated into an increase in compliance (Figure 3). This increase in compliance after the initiation of high pressure ventilation is a consistent finding in our ex-vivo experiments [5, 20, 21]. On the other hand, as depicted in Figure 3, during the last 20 minutes of the injurious ventilation, lungs in the HiP-C, but not the HiP-Met group, sustained a decrease in tidal volume (and thus, in compliance). This could be explained by the formation of pulmonary lung edema in the HiP-C group as VILI proceeded.
Careful combing of the literature may reveal several (indirect) indications that usage of metformin might prevent ALI. Specifically, during the last few years, there is accumulating clinical evidence that a medical history of diabetes mellitus predicts reduced susceptibility to ALI/ARDS in patients at risk. Indeed, at least three large cohorts of patients with risk factors for ALI/ARDS (namely sepsis/septic shock, trauma and massive transfusion) inferred that there is a protective association between diabetes and ALI/ARDS, even after adjustment for potential confounders [13, 14, 15]. In a relevant review, it was assumed that diabetes may merely be a confounder and instead other factors related to the management of diabetic patients, such as antihyperglycemic therapies, may account for the observed protection of such patients ; the lack of firm evidence that acute hyperglycemia (a cardinal feature of diabetes) alone modulates ALI makes this assumption reasonable [13, 29]. Metformin is a very commonly prescribed anti-diabetic medication; thus, it may mediate the relative protection of diabetic patients against the development of ALI.
Our isolated lung model, albeit well-established for the research of VILI, entails unavoidable limitations. First, it is an ex-vivo model, which means that lungs do not interact with other organs or the lymphatic or the nervous system. However, this model provides us with the ability to accurately measure the Kf,c and, thereby, to reliably assess the improvements in alveolar capillary permeability achieved by the administration of metformin [24, 25]. In addition, it allows us to continuously monitor the formation of edema, and pulmonary arterial pressure over time.
Second, although our ex-vivo rabbit lung model provided us with the ability to make an intriguing observation (namely, metformin preserves alveolar capillary permeability despite injurious ventilation), it could not allow us to gain a mechanistic insight into how metformin affords this benefit. For example, we were unable to examine whether metformin protects through inhibition of the mitochondrial function and oxidative burst of leukocytes . There is evidence that metformin induces a hypometabolic state , which in turn might be beneficial against injury . Additional in-vivo animal studies are justified, focusing on the mechanism through which metformin prevents VILI.
Third, our choice to administer a dose of metformin as high as 250 mg/kg/day and not to check for actual drug intake might be questioned. Rare reports that metformin is associated with lactic acidosis, which is surprisingly of good prognosis , might justify this criticism. However, the risk for lactic acidosis due to metformin seems to be overestimated according to a recent relevant meta-analysis . Given that we did not measure pH and lactate concentration in the blood of rabbits before sacrificing them, we could not preclude subclinical lactic acidosis. However, we did not observe any apparent adverse event after administration of the drug. Similarly, several other investigators who gave the same dosage of metformin (250 mg/kg) did not notice any toxicity [10, 35].
Fourth, data on several outcomes (namely BALF protein, BALF ACE activity, BALF total cell number and histology) were derived from only four animals per group. In an attempt to address this concern, we treated these data conservatively; specifically, we summarized them as the median and the range and compared these using non-parametric tests. Finally, we noticed that our HiP-C group sustained less injury than in our previous study . However, given that all groups (HiP-Met, HiP-C, LoP-Met and LoP-C) in the present study were compared during the same time period and under the same experimental conditions (that is, without the use of historical controls), this could not affect the robustness of our results.
The findings of the present study demonstrate that pretreatment with the widely used antidiabetic agent metformin protects against VILI under the present experimental conditions. These results expand our knowledge regarding the non-antidiabetic effects of metformin and may be of clinical value. Should these results be replicated in an in-vivo animal model of VILI, they might provide a rationale for carrying out observational studies that will examine the relationship between administration of metformin and development of ALI/ARDS. The fact that metformin is inexpensive and already widely used may make execution of such trials feasible.
Oral administration of metformin does not cause hypoglycemia or other apparent adverse events in non-diabetic rabbits.
Administration of metformin decreases the severity of VILI.
For excellent technical assistance and advice, the authors would like to thank Zoe Kollia and Dr Panagiotis Zacharatos. This study was supported by the Thorax Foundation, Athens, Greece and by a grant of Hellenic Thoracic Society to IIS (Grant number 11470).
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