Metformin overdose causes platelet mitochondrial dysfunction in humans
© Protti et al.; licensee BioMed Central Ltd. 2012
Received: 11 June 2012
Accepted: 31 August 2012
Published: 3 October 2012
We have recently demonstrated that metformin intoxication causes mitochondrial dysfunction in several porcine tissues, including platelets. The aim of the present work was to clarify whether it also causes mitochondrial dysfunction (and secondary lactate overproduction) in human platelets, in vitro and ex vivo.
Human platelets were incubated for 72 hours with saline or increasing doses of metformin (in vitro experiments). Lactate production, respiratory chain complex activities (spectrophotometry), mitochondrial membrane potential (flow-cytometry after staining with JC-1) and oxygen consumption (Clark-type electrode) were then measured. Platelets were also obtained from ten patients with lactic acidosis (arterial pH 6.97 ± 0.18 and lactate 16 ± 7 mmol/L) due to accidental metformin intoxication (serum drug level 32 ± 14 mg/L) and ten healthy volunteers of similar sex and age. Respiratory chain complex activities were measured as above (ex vivo experiments).
In vitro, metformin dose-dependently increased lactate production (P < 0.001), decreased respiratory chain complex I activity (P = 0.009), mitochondrial membrane potential (P = 0.003) and oxygen consumption (P < 0.001) of human platelets. Ex vivo, platelets taken from intoxicated patients had significantly lower complex I (P = 0.045) and complex IV (P < 0.001) activity compared to controls.
Depending on dose, metformin can cause mitochondrial dysfunction and lactate overproduction in human platelets in vitro and, possibly, in vivo.
Metformin is the drug of choice for adults with type 2 diabetes . It is the seventh most frequently prescribed generic drug in the US (fifty-nine million prescriptions in 2011)  and is currently taken by almost two per cent of the Italian population .
Metformin is a safe drug  but lactic acidosis can develop rarely, especially when renal failure leads to accidental intoxication [5–7]. Sixty-six similar cases have been reported to the Poison Control Centre of Pavia, Italy, over the last five years, resulting in seventeen deaths (Dr. Sarah Vecchio, unpublished data). Since metformin use is constantly increasing (4% to 8% rise in prescriptions per year in the US and Italy) [2, 3], related episodes of lactic acidosis will possibly become less uncommon .
The pathogenesis of lactic acidosis during metformin therapy remains poorly understood, particularly when no other major risk factors (such as hypoxia, tissue hypoperfusion or liver failure) can be identified . Nonetheless, growing evidence suggests that metformin intoxication may directly induce lactic acidosis , possibly by altering liver lactate metabolism. In fact, metformin readily accumulates in hepatocytes that express the Organic Cation Transporter (OCT) 1  and dose-dependently inhibits their mitochondrial respiration [12–15]. Therefore, metformin intoxication may either increase liver lactate production or decrease clearance (along with gluconeogenesis) [13, 16]. The fact that OCT-1 knock-out mice do not develop lactic acidosis in response to (non severe) metformin overdose does support this model .
However, we have recently noted that animals  and humans  with lactic acidosis due to severe metformin overdose have a 30% to 60% decrease in their global oxygen consumption. This finding can hardly be explained solely by the inhibition of hepatic respiration. Moreover, metformin-intoxicated pigs have clear signs of mitochondrial dysfunction not just in the liver, but also in the heart, kidney, skeletal muscle and platelets . Others have observed, usually in vitro, that metformin overdose can alter mitochondrial activity in several other tissues including animal cerebral cortex , pancreatic beta cells , neutrophils  and oocytes  and human endothelial , carcinoma-derived (KB)  and adrenal  cells. If extra-hepatic lactate production also globally increases (while hepatic lactate clearance decreases), then lactic acidosis will easily develop.
The aim of the present work was to clarify whether metformin intoxication alters the mitochondrial function of human platelets, taken as an example of extra-hepatic tissue. We decided to work with these cells after observing that, in pigs, metformin overdose similarly inhibits the mitochondrial activity of platelets and other more vital, but less accessible, organs .
Materials and methods
The effects of metformin on human platelet mitochondria were first investigated in vitro and then ex vivo. Informed consent was always obtained. The study was approved by the Ethics Committee of the Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico (Milan, Italy) and registered with ClinicalTrials.gov (NCT 00942123).
Platelet-rich-plasma (PRP) was obtained from whole blood of healthy donors, anticoagulated with citrate-phosphate-dextrose and then centrifuged (1000 g for 10 min). Final platelet concentration was 389 ± 55 × 109/L and total leukocyte count was 24 ± 22 × 106/L. It was incubated for 72 hours with saline (NaCl 154 mmol/L) or metformin (Sigma Aldrich, St. Louis, MO, USA) diluted in saline at a final concentration of 1.66 mg/L (0.01 mmol/L; therapeutic dose), 166 mg/L (1 mmol/L; toxic dose) or 16,600 mg/L (100 mmol/L; factitiously and extremely high dose), while stored at room temperature in a plastic bag permeable to air (plasma oxygen tension was always > 100 mmHg (13.3 kPa)). At the end of the incubation, plasma pH, bicarbonate, and glucose levels were measured with a blood gas analyzer (ABL 800 Flex, Radiometer GmbH, Willich, Germany) and platelets counted with a hemocytometer. Platelet respiratory chain complex activities, mitochondrial membrane potential and oxygen consumption were assessed as reported below.
In a second set of experiments, PRP was similarly incubated with saline or metformin (16,600 mg/L) but plasma pH, lactate and platelet mitochondrial membrane potential were measured every 24 hours, up to 72 hours (rather than just at 72 hours).
In a third set, PRP was incubated for 72 hours with lactic acid (30% in water) (Sigma Aldrich) or metformin (16,600 mg/L) plus sodium bicarbonate. Lactic acid was added to PRP every 24 hours so as to reach the same lactate level as the samples incubated with metformin (16,600 mg/L). Sodium bicarbonate was added every 24 hours to PRP already treated with metformin (16,600 mg/L) to maintain bicarbonate at the same level as the samples incubated with saline. Plasma pH, lactate levels and platelet oxygen consumption were measured at 72 hours.
Finally, we incubated human red blood cells, instead of platelets, with saline or metformin (16,600 mg/L) and measured pH and lactate levels every 24 hours, up to 72 hours.
We enrolled ten consecutive patients admitted since 2008 to one Hospital in Milan (Italy) with lactic acidosis (arterial pH < 7.30 and lactate concentration > 5 mmol/L), serum metformin concentration > 10 mg/L (therapeutic level is < 4 mg/L) and no other primary explanation for lactic acidosis (such as, for instance, overt respiratory, heart or liver failure). Exclusion criteria were pre-existing mitochondrial disease and hemoglobin < 8 g/dl (< 10 g/dl in the case of ischemic cardiomyopathy). Platelet mitochondrial function was studied within 48 hours of diagnosis. Blood was anticoagulated with ethylenediamine tetraacetic acid (EDTA) (30 ml) (for measuring platelet mitochondrial respiratory chain complex activities, always done) or citrate (20 ml) (for measuring platelet mitochondrial membrane potential, only performed since the beginning of 2010). It was then sedimented and centrifuged (2,500 g for 10 min) and PRP collected for further analysis (see below). Ten healthy volunteers (similar in sex and age to intoxicated patients) acted as controls.
Mitochondrial respiratory chain complex enzyme activities
PRP (either from in vitro or ex vivo experiments) was washed with distilled water, centrifuged at 5,000 g for 10 min (14,500 g from the second cycle on) and then washed again with PBS until a clear platelet pellet could be stored at -80°C (two or three cycles were usually required). At the time of analysis, the platelet pellet was diluted in buffer (KCl 120 mM, HEPES 20 mM, MgCl2 5 mM and EGTA 1 mM; pH 7.2, 300 to 400 μl), sonicated (two cycles at 60 W for 10 seconds) and centrifuged (750 g for 10 min) while kept at 4°C. Supernatant was then analyzed using spectrophotometry (at 30°C). We measured the activity of respiratory chain NADH-ubiquinone 1 reductase (complex I), succinate-cytochrome c reductase (complex II+III) and cytochrome c oxidase (complex IV) and expressed it relative to that of citrate synthase (a marker of mitochondrial density) . Proteins were measured using Lowry's method.
Mitochondrial membrane potential
Platelets were diluted in plasma at 100,000/μl and kept for 30 min at 37°C in the dark with a cationic and lipophilic dye, named JC-1, that emits a green fluorescence in its native (monomeric) form. If mitochondria are normally polarized (that is, their inner milieu is negatively charged), JC-1 will accumulate into them forming dimers that emit orange, rather than green, fluorescence. This will not occur if mitochondria are not normally polarized. The ratio of normally polarized and abnormally depolarized mitochondria can then be measured as the ratio between orange and green fluorescence with flow-cytometry (JC-1 fluorescence ratio: FL2/FL1) .
Platelet oxygen consumption
Platelets were resuspended in Tyrode's solution enriched with 5 mM EDTA and 1 μM prostaglandin E1 (final concentration 1 to 1.5 × 109/ml). One ml of this suspension was transferred into a sealed chamber connected to a Clark-type electrode, and maintained at 37°C (Rank Brothers, Bottisham, UK). Oxygen consumption was recorded as the rate of decrease in oxygen tension within the chamber over the first 180 seconds (ADC-16; Pico Technology, St. Neots, UK). The results were corrected for spontaneous drift (oxygen used by the electrode itself) and platelet count (measured with a hemocytometer) .
Platelets were fixed with 2.5% glutaraldehyde in PBS (pH 7.4), post-fixed in 1% osmium tetroxide and then embedded in Epon. Ultra-thin sections were counterstained with uranyl acetate and lead citrate. Mitochondrial morphology was assessed using ZEISS EM-109.
Sample size was only calculated for experiments performed ex vivo. Based on preliminary in vitro observations, we planned to demonstrate a 30% difference in the activity of the mitochondrial respiratory chain complex I between healthy subjects and metformin-intoxicated patients (ex vivo experiments). Accordingly, ten individuals had to be included in each group (power 0.80 and alpha level 0.05).
Results are presented as mean and standard deviation (SD). Normally distributed data (Shapiro-Wilcoxon test) were analyzed using t test, one-way, one-way repeated measures or two-way repeated measures analysis of variance (ANOVA; post-hoc comparisons with the Holm-Sidak method). Non-normally distributed data were first transformed in ranks and then similarly analyzed. Correlation between variables was expressed as R2 (linear regression analysis). A P value < 0.05 was considered statistically significant (SigmaPlot version 11.0, Jandel Scientific Software, San Jose, CA, USA).
In contrast to platelets, a very high dose of metformin did not increase lactate production of human red blood cells compared to saline (P = 0.927) [see Additional File 4].
The effects of metformin intoxication on human platelets were also assessed ex vivo. Ten patients (70 ± 5 years; women 60%) with drug accumulation (serum metformin level 32 ± 14 mg/L) and lactic acidosis (arterial pH 6.97 ± 0.18 and lactate 16 ± 7 mmol/L) were enrolled. Intoxication was always accidental and associated with renal failure (creatininemia 8.9 ± 2.5 mg/dl, urea 215 ± 72 mg/dl and oligo-anuria) and continued drug intake. Possible precipitating factors were dehydration (a few days history of vomiting and diarrhea was reported in eight cases), use of potentially nephrotoxic drugs (four cases), urinary tract infection (one case) and/or complicated prostatic surgery (one case). Treatment included hemodialysis (nine cases) or continuous renal replacement therapy (one case), mechanical ventilation (two cases), catecholamines (four cases) and admission to ICU (five cases). All patients survived to hospital discharge.
This study demonstrates that, depending on dose (and time), metformin can cause mitochondrial dysfunction and lactate overproduction in human platelets.
In fact, human platelets incubated with a high (toxic) dose of metformin had progressively lower complex I activity, mitochondrial membrane potential and oxygen consumption and higher lactate production than those incubated with saline. These changes occurred independently from hypoxia and differences in platelet count and mitochondrial density. Human platelets incubated with a low (therapeutic) dose of metformin behaved as those incubated with saline. This finding is consistent with the observation that metformin does not significantly increase the incidence of lactic acidosis, compared to other antidiabetic drugs , unless it accumulates.
When lactic acid was used instead of metformin to induce severe lactic acidosis, human platelet oxygen consumption never significantly declined. Conversely, when sodium bicarbonate was used to mitigate metformin-induced acidosis, human platelet oxygen consumption never returned to normal. Therefore, human platelet respiration diminishes during metformin-induced lactic acidosis because of drug accumulation, rather than (lactic) acidosis. Accordingly, healthy pigs infused with a large dose of metformin consume less oxygen than sham controls, whereas those infused with lactic acid do not (despite similar severity of lactic acidosis) .
When human red blood cells (that lack mitochondria) were used instead of platelets, an extremely high dose of metformin did not alter cellular metabolism. Thus, it may be concluded that metformin can cause lactate overproduction by specifically altering mitochondrial function, in human platelets as well as in mouse pancreatic ß and connective tissue cells [20, 29], rat hepatocytes and skeletal muscle [12, 13, 30] and human intestine .
Aside from dose, metformin toxicity also depended on the duration of incubation. Slow drug diffusion into cells, due to inherent lipophilicity, is the most likely explanation. For this reason, patients who acutely ingest large doses of metformin may initially have very high serum drug levels but no, or only mild, lactic acidosis. In contrast, those who inadvertently get intoxicated over a few days may have relatively low serum drug levels (but still above therapeutic limits) and extremely severe lactic acidosis .
Our in vitro findings were, at least partially, replicated ex vivo. In fact, platelets taken from metformin-intoxicated patients had clear signs of mitochondrial dysfunction, including inhibition of complex I and IV and a lower proportion of normally polarized mitochondria (although this was only occasionally measured).
On average, patients with metformin intoxication had a 20% decrease in platelet complex I activity. We initially expected a larger effect, based on our in vitro experiments in which a 30%, or even larger, decrease was observed. However, the effects of metformin on mitochondria likely depend on dose, in vivo just as in vitro. Patients enrolled in this present study had an average serum drug level of 32 ± 14 mg/L, much lower than that of severely intoxicated patients (61 ± 25 mg/L in our previous series) . in vitro, metformin was added to plasma to obtain an initial (toxic) concentration of 166 mg/L, or higher. Even if final drug levels were probably lower, due to cellular uptake , they likely exceeded 32 ± 14 mg/L. In other words, overdose severity was high (or very high) in vitro, but only moderate in vivo. We cannot exclude that a 24- to 48-hour delay in evaluating platelet mitochondrial function further contributed to diminish our capacity to detect early larger alterations.
The constant decrease in platelet complex IV activity was totally unexpected, as it never occurred in vitro, not even at the highest drug dose. Underlying mechanisms were not specifically investigated so that we can only speculate on them. Only some of the patients received sedation, catecholamines and/or mechanical ventilation, so that these factors likely had no major role. Conversely, all patients had undergone renal replacement therapy by the time their platelet mitochondrial function was assessed. Whether renal failure per se or extra-corporeal support can inhibit human platelet complex IV is currently unknown.
All patients enrolled in this study had a favourable outcome, despite signs of mitochondrial inhibition in platelets (and possibly other tissues). This may suggest that prognosis does not depend on the effects of metformin on the respiratory chain. However, it may also indicate that the rate of survival will be unexpectedly high if mitochondrial dysfunction is due to a compound that can be easily removed from the body (using renal replacement therapy, for instance) .
Severe metformin overdose can alter mitochondrial function and increase lactate production of human platelets, in vitro and, possibly, ex vivo. If analogue changes also occur in other organs, they will likely contribute to the pathogenesis of metformin-induced lactic acidosis.
In pigs, severe metformin intoxication causes mitochondrial dysfunction in platelets as well as in other more vital organs, including the heart, kidney and skeletal muscle.
Human platelets exposed to a toxic dose of metformin, either in vitro or in vivo, have clear signs of mitochondrial dysfunction.
If mitochondrial dysfunction is a generalized phenomenon even in humans, it will likely contribute to the development of lactic acidosis (possibly by augmenting tissue lactate production).
analysis of variance
ethylenediamine tetraacetic acid
ethylene glycol tetraacetic acid
hydroxyl ethyl piperazine ethane sulfonic acid
nicotinamide adenine dinucleotide
organic cation transporter
phosphate buffered saline
Preliminary results have been presented in abstract form at the 21st SMART Symposium (Italy, 2010) and 31st ISICEM Symposium (Belgium, 2011).
This study was supported in part by an Italian grant provided by Fondazione Fiera di Milano for Translational and Competitive Research (2007, Luciano Gattinoni).
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