Bisphenol-a (BPA) is a high volume production chemical – with more than 8 million pounds produced worldwide each year. BPA is commonly used in the manufacturing of polycarbonate plastics, polyvinyl chloride plastics, resins, and thermal printing applications1. Humans are unintentionally exposed to bisphenols through contact with consumer products and/or medical devices, which leach BPA under normal conditions of use. Consequently, widespread and continuous exposure to bisphenols can occur through dietary intake, inhalation, dermal or intravenous exposure. Indeed, biomonitoring studies suggest that >90% of the general population is exposed to detectable levels of BPA through environmental exposure1,2. In comparison, intensive care patients are often exposed to extraordinarily high BPA concentrations due to medical procedures that employ BPA-containing plastic products (i.e., nasogastric tube, cardiopulmonary bypass or extracorporeal membrane oxygenation circuits, intravenous tubing, catheters)3,4,5. Once inside the body, BPA is biologically active – exerting widespread effects through endocrine disruption, genomic and non-genomic mechanisms6,7,8.

Recent studies have shown that BPA exposure negatively impacts cardiac electrophysiology and excitation-contraction coupling, using adult rodent models9,10,11,12. Our laboratory previously reported a linear dose-response relationship between acute BPA exposure (15 min) and impaired electrical and mechanical function, using excised Langendorff-perfused hearts from adult Sprague-Dawley rats9,10. Specifically, increasing BPA concentrations resulted in prolonged atrioventricular conduction time, slowed epicardial conduction velocity, decreased left ventricular developed pressure and reduced cardiac contractility (10−9–10−4M)9,10. Similarly, Pant et al. showed that increasing concentrations of BPA causes a negative inotropic and chronotropic effect on adult atrial preparations11. BPA exposure has also been linked to an increase in the incidence of arrhythmias and spontaneous aftercontractions in isolated adult cardiomyocytes, which may be attributed to calcium leak from the sarcoplasmic reticulum (SR)12. The effects of BPA on individual processes of calcium handling (i.e., L-type calcium current, SR calcium uptake, calcium spark frequency) were previously shown to have a monotonic dose response relationship in adult cells13.

Epidemiological studies have also shown a correlation between BPA exposure and cardiovascular pathologies, including an increased risk of hypertension, angina, myocardial infarction and reduced heart rate variability14,15,16,17,18,19,20,21,22,23. These associations are worrisome to the general public – but even more concerning for vulnerable populations who are exposed to exceedingly high BPA concentrations (i.e., intensive care patients, industrial workers)3,4,5,24,25,26 or those who are developmentally susceptible to chemical exposures (i.e., developing fetus, children)27. Indeed, young children with an underdeveloped metabolic system can be exposed to chemical contaminants for longer periods of time, due to slowed chemical processing and elimination. As examples, biomonitoring studies have reported maximal BPA concentrations of 0.1–0.4 × 10−5M in neonatal intensive care patients3,4. Taken together, neonatal and pediatric intensive care patients are at the greatest risk for bisphenol exposure – yet, the impact of BPA on pediatric cardiac function is unknown.

Previous studies have highlighted the link between BPA and altered cardiac functionality; although, to date, these studies have been limited to adult models. Yet, significant developmental differences exist between the immature and adult heart, including: ion channel expression and localization, development of the t-tubule system, and maturation of the excitation-contraction machinery. Developmental differences in the calcium-handling machinery of pediatric hearts could precipitate an exaggerated response to BPA chemical exposure. Based on our previously published data9,10, we sought to further examine the linear dose response relationship between BPA and impaired cardiac function. Specifically, we investigated the sensitivity of neonatal cardiomyocytes to BPA exposure by monitoring automaticity, excitability, intracellular calcium handling – and examined the reversibility of such effects.


Acute BPA exposure does not negatively influence neonatal cardiomyocyte viability

Patient contact with BPA-containing medical products can result in urinary concentrations that reach micromolar levels3,4,5,28,29. In vitro exposure to similar concentrations has been shown to induce cytotoxicity in multiple cell types, including pancreatic islet cells, monocytes and hepatocytes30,31,32. Such an impact on cardiomyocyte viability would also effect cell structure, metabolism and/or intracellular ATP production – and impede basal cardiomyocyte functionality. With this in mind, the effect of BPA treatment on cardiomyocyte viability was assessed prior to performing secondary phenotypic testing. Cardiac cells were loaded with either a metabolic indicator dye or dual-labeled to measure cell membrane integrity (Fig. 1A). No significant difference in cell viability was observed between control and BPA-supplemented cardiomyocytes (30 min) using either assay, even at maximal concentrations (10−5–10−4M, Fig. 1B).

Figure 1
figure 1

Acute BPA exposure does not impair cardiomyocyte viability. Cardiac cell viability was assessed following 30-min exposure to vehicle control or increasing concentrations of BPA. (A) Confluent monolayer of neonatal cardiomyocytes labeled with calcein-AM (white) and ethidium homodimer-1 (blue) to assess cell viability via membrane integrity (100 μm scale). (B) Cell viability measured via membrane integrity (left, as described above) and via metabolic capacity (right, resazurin-based assay). au = arbitrary units, ns = not significantly different, *p ≤ 0.05, n = 4.

Acute BPA exposure reduces cardiomyocyte automaticity and excitability

Confluent neonatal cardiomyocyte monolayers undergo phase synchronization and exhibit coordinated spontaneous beating or automaticity in culture. The intrinsic spontaneous beating rate (SBR) of cardiomyocytes is determined by a balance between inward and outward currents33,34,35 and calcium oscillations (e.g., “calcium clock”)36. Therefore, alterations in SBR can serve as a sensitive, yet cumulative index, of cardiac health and excitability. Previous studies have shown a causal relationship between BPA dose and slowed SBR, in adult rat atrial preparations11 and isolated adult rat whole hearts10. Acute BPA exposure (15 min) reduced SBR in neonatal cardiomyocyte monolayers, albeit only at high concentrations (Fig. 2B). The intrinsic SBR decreased by 50.0% in 10−5M and 64.3% in 10−4M BPA-treated samples, compared with control. We also observed a decrease in cardiomyocyte excitability in the presence of BPA (Fig. 2D). The threshold voltage required to externally pace cardiac cells increased to 14.3 ± 2.3 V in 10−8M, 14.6 ± 3.2 V in 10−5M, and 41.3 ± 10.2 in 10−4M BPA-treated samples compared with 10.9 ± 0.9 V control. Such an effect on electrical excitability could be related to the antagonistic effect of BPA on voltage gated sodium currents37,38, modifications in calcium handling, and/or alterations in cell membrane resistance between neighboring cells.

Figure 2
figure 2

Acute BPA exposure decreases the spontaneous beating rate and cardiac excitability, and increases beat rate variability. Cardiomyocyte spontaneous beating rate was monitored following 15-min exposure to either vehicle control or BPA-supplemented media. (A) Representative example traces of neonatal cardiomyocytes under control conditions, or media supplemented with 10−8M BPA. (B,C) Mean spontaneous beating frequency (Hz) and beat rate variability measurements (SD of interbeat interval). (D) Minimum threshold voltage required for excitation via field stimulation. AUF = arbitrary units of fluorescence, F1 = peak fluorescence amplitude, F0 = baseline fluorescence. *p ≤ 0.05, n ≥ 4.

Acute BPA exposure increases beat rate variability

Isolated cardiomyocytes exhibit beat rate variability (BRV) that reflects intrinsic cardiac regulatory mechanisms, including ion channel current, intracellular calcium handling, and cell coupling34,39,40,41,42. Similar to SBR measurements, BRV has been used as a cumulative index to assess cardiac safety, which can be influenced by a variety of proteins involved in excitation-contraction coupling43. Greater variance in the interbeat interval is commonly observed in poorly coupled cardiac networks or in the presence of drugs that hinder calcium handling34. Neonatal cardiomyocyte monolayers exhibited a regular rhythmic beating pattern under control conditions (Fig. 2A). In comparison, acute BPA exposure (15 min) increased the BRV by +179% and +189% in 10−8M and 10−5M BPA-treated samples, respectively (Fig. 2A,C). BRV also increased at the highest BPA concentration tested (10−4M), although the mean value was influenced by an exaggerated decrease in SBR (Fig. 2B) which resulted in complete cessation of automaticity in 57% of samples (data not shown).

Acute BPA exposure alters intracellular calcium handling

Calcium is a vital regulator of cardiac automaticity, beat rate variability, contraction and relaxation33,44,45. We previously reported that BPA exposure can alter calcium handling in adult rat hearts, resulting in impaired mechanical function and decreased cardiac contractility9. Although, structural differences (i.e., rudimentary t-tubules and calcium release units)46 lead to variations in the calcium handling of immature cardiomyocytes (e.g., less pronounced calcium-induced calcium release) compared with adult cells. Calcium transients were recorded from neonatal cardiomyocytes loaded with Fluo-4AM, which exhibits an increase in fluorescence upon binding to calcium ions during systole (Fig. 3). Neonatal cardiomyocytes were externally paced, at room temperature, to negate rate dependent differences in calcium kinetics. Figure 3 shows a decrease in the peak CaT amplitude across all BPA doses tested, ranging from 18.12 to 25.45% compared with control. Such a reduction in CaT amplitude suggests a decrease in SR calcium loading, as previously described47,48. Importantly, the latter was not attributed to nonspecific fluorescence decay, since calcium transient amplitudes decreased by 0.9 ± 0.7% during repeated imaging under control conditions (basal vs 20 min recording).

Figure 3
figure 3

Acute BPA exposure reduces calcium transient amplitudes. (A) Representative CaT recorded from neonatal cardiomyocytes under control conditions, and following supplementation with 10−8M BPA. Cardiac monolayers were paced at 0.2 Hz using field stimulation. (B) Representative images show the fluorescence intensity of Fluo-4AM corresponding to diastolic (baseline) and systolic intracellular calcium (peak). (C) Mean CaT amplitude measured by fluorescent calcium indicator dye (Fluo4-AM), F1 = peak fluorescence amplitude, F0 = baseline fluorescence, *p ≤ 0.05, n ≥ 15.

Pace-induced CaT were recorded, normalized (Fig. 4A), and temporal attributes of calcium handling were quantified. BPA-treatment slowed the time to peak (90% upstroke time), and CaT upstroke velocity beginning at low nanomolar concentrations (Fig. 4). The upstroke time increased from 65.1 ± 2.9 msec in control samples to 83.1 + 7.7 msec in 10−9M BPA and 164.7 + 28 msec in 10−4M BPA-treated samples (Fig. 4A–C). We also observed modest prolongation of CaD30 (duration from activation to 30% relaxation time) from 281.6 ± 11.1 msec in control samples to 317 ± 29.5 msec in 10−9M BPA and 415.2 ± 27.7 msec in 10−4M BPA-treated samples (Fig. 4D). Taken together, these results suggest that calcium release and reuptake to the sarcoplasmic reticulum can be hindered in BPA-treated samples.

Figure 4
figure 4

Acute BPA exposure slows intracellular calcium handling. (A) CaT (amplitude normalized) recorded from neonatal cardiomyocyte monolayer under control conditions, and after supplementation with 10−8M BPA. (BE) CaT parameters measured under external pacing, including (B) upstroke velocity, (C) upstroke time, (D) 30% CaT duration (CaD30) and (E) 80% CaT duration (CaD80). s = seconds, ns = not significantly different, AUF = arbitrary units fluorescence, *p ≤ 0.05, n ≥ 10.

BPA increases the incidence of calcium transient alternans and alters restitution

Cardiac cells display mechanical restitution, whereby a period of time is required after each contraction before another contraction of the sample amplitude can be elicited45. Consequently, underlying changes in cardiac refractoriness may go unnoticed at slower beating rates, but become identifiable as the beating frequency is increased. Neonatal cardiomyocytes were subjected to pacing frequencies that increased stepwise (Fig. 5A), and cell refractoriness was measured by the incidence and magnitude of CaT alternans. An alternans ratio was calculated to gauge the severity of alternans, or alternating large and small amplitudes [1-(small CaT/large CaT)]49,50. At the fastest pacing rate tested (3 Hz), acute BPA treatment increased the magnitude of beat-to-beat CaT alternans across all concentrations tested (Fig. 5B). Whereas substantial lengthening of refractoriness resulted in skipped beats at higher BPA concentrations (Fig. 5C,D). Acute BPA exposure decreased the maximum calcium cycling frequency to 1.8 Hz in 10−5M BPA and 0.6 Hz in 10−4M BPA, compared with 2.7 Hz in control samples (Fig. 5A,C). Cardiac refractoriness was evident at pacing rates >1 Hz, where the 1:1 capture rate decreased due to skipped or dropped beats at increasing BPA concentrations (Fig. 5D, 2 Hz pacing rate). These data suggest that BPA decreases the threshold for pacing-induced alternans and lengthens the refractoriness of calcium release. The latter may be attributed to changes in SR calcium release and/or calcium reuptake51, which leads to calcium instabilities.

Figure 5
figure 5

Acute BPA exposure promotes calcium transient alternans and impairs the rate of calcium cycling. (A) Pace-induced CaT recorded at multiple pacing frequencies (1–3 Hz) under control conditions, or following BPA-exposure. Representative example depicts CaT alternans with alternating long (L) and short (S) duration times following exposure to 10−8M (inset). Higher BPA concentrations (10−5M) slow calcium cycling, resulting in loss of capture at faster pacing rates. (B) Magnitude of CaT alternans expressed as a ratio [1-(CaT small/CaT large)]. (C) Maximum calcium cycling frequency. (D) Loss of 1:1 capture (2 Hz external pacing frequency). *p ≤ 0.05, n ≥ 8.

BPA-induced alterations in calcium handling are partially reversible

Human pharmacokinetic studies suggest that BPA is rapidly metabolized, with a half-life of a few hours52,53,54. With this in mind, we aimed to determine whether the effects of BPA on calcium handling were reversible. CaT were recorded from neonatal cardiomyocytes under control conditions, following acute 15 min exposure to maximal concentrations of BPA (10−4M) and again after 1 hr wash out (Fig. 6). CaT amplitude decreased by −29.2% and CaT duration increased by +62.9% after exposure to 10−4M BPA, compared with control. Following wash out, calcium handling parameters partially recovered, but remained significantly different from baseline control recordings. CaT amplitude remained −13.4% lower (Fig. 6A) and CaT duration remained +23.8% longer (Fig. 6B) in wash out samples, compared with baseline control recordings.

Figure 6
figure 6

Reversibility of BPA-induced changes in calcium handling. (A) CaT amplitude is diminished following 15-min exposure to 10−4M BPA (left panel); this effect is partially reversible when 10−4M BPA is washed out (middle panel, right panel). (B) Normalized calcium signals shown prolonged CaT upstroke time and duration time following 15-min exposure to 10−4M BPA (left panel); CaT duration effects are partially negated following 1-hr wash out. F1 = peak fluorescence amplitude, F0 = baseline fluorescence, ns = not significantly different, *p ≤ 0.05, n ≥ 6.


Significant developmental differences exist between the immature and adult heart, including: ion channel expression and localization, development of the t-tubule system, and maturation of the excitation-contraction machinery. Calcium handling also matures dramatically during development – calcium oscillations first serve a pacemaker function (“calcium clock”)36,55, whereas later, action potential-driven calcium-induced calcium release becomes essential for synchronized muscle contraction46. Indeed, inefficient excitation-contraction coupling is observed in myocytes with rudimentary t-tubules and reduced coupling between L-type calcium channels and ryanodine receptors46. Such an immature phenotype can increase the propensity for arrhythmias, reduce calcium transient amplitude, and diminish contractile force56. These unique characteristics can impede the extrapolation of BPA cardiotoxicity data between adult9,10,12,57,58 and pediatric experimental studies.

Although pediatric populations may be more vulnerable to endocrine disrupting chemicals (“window of vulnerability”27,59,60) – the effect of BPA exposure on immature heart cells is unknown. To address this knowledge gap, we examined the impact of BPA exposure on excitation-contraction coupling in neonatal cardiomyocytes. The current study investigated a wide range of BPA doses that mimic environmental, clinical and supraphysiological exposure levels (10−9–10−4M). In the presented study, acute (15 min) BPA exposure slowed the SBR, increased BRV, and diminished cardiac cell excitability at nanomolar concentrations. We also detected significant, although modest, changes in calcium transient kinetics at slow pacing rates – which were coupled with an increased propensity for calcium transient alternans and prolonged refractoriness at faster pacing rates. Importantly, the observed effects on calcium handling were at least partially reversible. The presented study supports our previous finding that BPA exposure can impact cardiac electrical and mechanical function9,10, and highlights the importance of addressing pediatric heart vulnerability to endocrine-disrupting chemicals.

Spontaneous beating rate, beat rate variability and excitability

Although isolated adult cardiomyocytes are quiescent, neonatal cardiomyocytes exhibit spontaneous synchronized beating that can serve as a sensitive and cumulative index of cardiac health and excitability. In the presented study, we observed slowing of the SBR and an increase in BRV following BPA-treatment of neonatal myocytes. In vivo measurements of heart rate variability can be influenced by extracardiac factors (i.e., autonomic, endocrine), whereas BRV in the neonatal myocyte model reflects the intrinsic properties of cardiac tissue (i.e., ion channel current, intracellular calcium handling, gap junction intercellular communication)34,42. Indeed, alterations in the BRV of isolated cardiomyocytes has previously been reported in poorly coupled cell networks, in the presence of drugs that hinder calcium handling, or following funny current inhibition34,41. Whereas slowing of the SBR may be attributed to a disturbance in spontaneous calcium oscillations (e.g., calcium leak from SR)61, and outward calcium/inward sodium flux via the sodium-calcium exchanger46,62,63. This finding concurs with published studies noting a negative chronotropic response to BPA-treatment in isolated adult atrial preparations11 and excised whole hearts10. We also observed a decrease in cell excitability following BPA-treatment, which may be related to the antagonistic effect of BPA on voltage gated sodium currents37,38, activation of potassium channels64, modifications in calcium handling, and/or alterations in cell membrane resistance between neighboring cells. Indeed, BPA-treatment has been shown to influence gap junction functionality65,66,67, although these studies have not yet been confirmed in a cardiac model.

Calcium handling, calcium transient alternans and refractoriness

Alterations in calcium cycling will also influence excitation-contraction coupling – the process linking electrical excitation to contraction. Liang, et al. previously reported that BPA exposure inhibited L-type calcium channel current and modified the calcium release/reuptake kinetics of the SR in adult myocytes13. The authors noted an increase in the propensity for spontaneous aftercontractions in adult cardiac cells and arrhythmias in adult animals, which was attributed to calcium leak from the SR12,68. In the current study, we observed modest slowing of calcium cycling kinetics (upstroke, upstroke velocity, CaD30) that coincided with an increased propensity for alternans and skipped beats. Calcium transient alternans can result from an imbalance between calcium release (e.g., ryanodine receptor69) and reuptake (e.g. SR calcium ATPase, SERCA), and/or an increase in ryanodine receptor refractoriness70, which leads to calcium instabilities. Importantly, intracellular calcium alternans have been linked to action potential alternans, t-wave alternans and re-entrant arrhythmias71,72,73. Additional studies are needed to ascertain whether BPA exposure increases the propensity for electrical alternans.

In the present study, we also observed a decrease in the CaT amplitude of BPA-treated samples, indicating a reduction in the amount of calcium released from the SR with each contraction. Given the relationship between intracellular calcium concentration, myofilament sensitivity, and contractile force – diminished calcium release would explain the negative inotropic response observed in atrial and whole heart preparations9,11. Diminished CaT amplitudes are also observed in situations of reduced SERCA activity and/or diminished ryanodine receptor synchronization74,75. Given the immediate effects of BPA, post-translational modifications of key calcium handling proteins (e.g. phospholamban, ryanodine) and/or interference with ion channel current (e.g. L-type calcium channel) may explain our observations.

Reversibility of cardiac effects

In the presented study, we showed that the effects of high-dose BPA exposure (10−4M; acute 15-min) on calcium handling are partially reversible. This finding coincides with previously published studies showing that the effects of BPA on ion channel functionality are likely reversible – and presents important insight for human risk assessment. Deutschmann, et al. showed that BPA (10−5–10−4M) is a potent blocker of voltage gated calcium channels, but noted that current inhibition was almost fully reversible in cardiac myocytes76. Similarly, Wang, et al. noted the rapid inhibitory effects of BPA on voltage-gated sodium channels in neurons; this inhibitor effect was concentration-dependent (2–12 × 10−5M) and mostly reversible after a short wash out period38. BPA treatment has also been shown to inhibit gap junction intercellular communication and the outward current of connexin hemichannels, although the reversibility of these effects may be cell or connexin-isoform specific (connexin-43 vs connexin-46)65,66,67. Finally, Asano, et al. reported that BPA-treatment (10−6–10−4M) reversibly activates Maxi-K channels in coronary smooth muscle cells64. It is unclear whether similar results translate to the human myocardium65,66.


The scope of the current study was limited to the effect of acute (15 min) BPA exposure on neonatal rat cardiomyocytes. We hypothesize that the quick, partially-reversible action of BPA is likely due to ion channel interactions, as described in other cell types, and/or post-translational modifications of key calcium-handling proteins. Additional studies are needed to fully interrogate the underlying mechanisms of bisphenol chemicals, which are likely multifactorial and may differ entirely in instances of longer-term exposure. Our previous findings reported a linear dose-response relationship between BPA and whole heart physiology; therefore, our current study included a range of BPA concentrations that covered environmental (10−9–10−8M), maximal clinical (10−5M) and supraphysiological exposure levels (10−4M). The latter allowed our group to show that phenotypic changes were not solely attributed to cardiomyocyte death and were partially reversible, even at extraordinarily high concentrations. Nevertheless, we cannot rule out alternative cardiac outcomes at different exposure levels, since BPA may exert a non-monotonic dose-response77,78. Finally, the current study was limited to neonatal cell preparations from newborn rats (1 day old, male and female mixed litter), which prevented the examination of sex-specific cardiac effects in response to BPA exposure. Since BPA is estrogenic12, additional studies are warranted to determine whether the observed effects on cardiac physiology are exacerbated in females.


Plastics have revolutionized medical device technology, transformed hematological care and transfusion medicine, and facilitated modern cardiology procedures. Despite these benefits, the ubiquitous nature of plastics has also raised concerns pertaining to human health risks – particularly in sensitive pediatric populations. For the first time, we have shown that a commonly used plastic chemical (BPA) can have an immediate effect on neonatal cardiomyocyte beating rate, intracellular calcium handling, and the incidence of alternans. Our data suggests that incidental BPA exposure may precipitate secondary adverse effects on contractile performance and/or electrical alternans, both of which are dependent on intracellular calcium homeostasis. Additional studies are necessary to determine the effects of bisphenol exposure on pediatric whole heart physiology and the impact of prolonged exposure, which may more closely mimic clinical exposure. Given the elevated risk of BPA exposure in intensive care settings, our data highlights the importance of incentivizing the development, manufacturing, and clinical adoption of alternative biomaterials to improve patient safety.

Materials and Methods


Animal protocols were approved by the Institutional Animal Care and Use Committee of the Children’s Research Institute, and followed the National Institutes of Health’s Guide for the Care and Use of Laboratory Animals. Neonatal rat cardiomyocytes were isolated from 1 day old Sprague-Dawley rats (male and female, mixed litter) by an enzymatic digestion protocol, as previously described79,80. Cells were plated on laminin-coated coverglass (105 cells/cm2), and maintained under standard cell culture conditions in Dulbecco-modified minimum essential medium supplemented with 5% Fetal bovine serum, 10 U/ml penicillin, and 1 μg/ml streptomycin (Thermo Fisher Scientific). Three days after plating, neonatal rat cardiomyocytes formed a confluent monolayer and exhibited strong synchronized contractions. Cardiac cells were used thereafter for subsequent experiments, as previously described48,80,81.

Experimental Protocol

An analytical standard of bisphenol-a (≥99% purity, Sigma Aldrich) was dissolved in 100% ethanol to provide a 500 mM stock solution. The stock solution was then diluted in Tyrode salt solution (Sigma Aldrich) to obtain final working concentrations of 10−9–10−4M BPA. The highest possible ethanol concentration was used as vehicle control (0.001%). Cardiomyocytes were incubated with BPA-supplemented media for 15 minutes for all live-cell recordings.

Cell viability measurements

Confluent adherent cardiomyocytes were exposed to maximum BPA concentrations (10−5–10−4M) for 30 min and cell viability was quantified. A live/dead viability dye-based assay (Thermo Fisher Scientific) was used to visualize and quantify cell membrane integrity in live (calcein-AM, 495 nm excitation/517 nm emission) versus dead cells (ethidium homodimer-1, 517 nm excitation/617 nm emission). Widefield fluorescent images were acquired from (4) different fields of view, per coverslip, using a Nikon TiE microscope system equipped with a scMOS camera (Andor Zyla 4.2 plus) and deconvolution software (Nikon Elements, NVIDIA GPU). Relative viability was measured by the total cell area corresponding to the live (calcein-AM) or dead (ethidium homodimer-1) labeling, which was quantitated by fluorescent histogram profiles. In a second set of experiments, a resazurin assay was used to measure cell viability based on metabolic capacity (PrestoBlue, Thermo Fisher Scientific). Relative viability was measured as the difference between absorbance at 600 nm and 570 nm, which corresponds to conversion of resazurin to resorufin by live metabolically active cells.

Live imaging of calcium transients (CaT)

Confluent layers of cardiomyocytes were loaded for 40 min at room temperature with 10 μM Fluo-4AM (Thermo Fisher Scientific), a fluorescent calcium indicator, and then washed in dye-free Tyrode salt solution47,80. Cell monolayers were then exposed to vehicle control or BPA-supplemented Tyrode media for 15 min at room temperature. Spontaneous (37 °C) and pace-induced calcium transients (CaT) were acquired using a Nikon TiE microscope system (23 °C), equipped with 470 nm excitation LED (SpectraX, Lumencor), 505–530 nm emission filter, and Andor iXon 860 EMCCD camera (~170 fps, 128 × 128). Cardiac monolayers were paced using field stimulation (monophasic, 5 msec pulses, 1.5 × threshold voltage, 0.2–3 Hz frequency; Grass Technologies).

Analysis of beat rate variability and calcium kinetics

The following parameters were determined from raw CaT signals: amplitude (F1/F0), upstroke time (duration from activation to 90% of maximum amplitude), upstroke velocity (Δfluorescence/s), 30% and 80% CaT duration time (duration from activation to 30% or 80% reuptake time)47,48. The beginning of the CaT upstroke was defined by the initial deflection from baseline (max d2F/dt2). Calcium alternans were induced by increasing the pacing frequency, stepwise from 0.2 Hz to 3 Hz. The calcium alternan ratio was calculated as [1-(CaT small/CaT large)], where CaT small and CaT large are the corresponding fluorescence amplitudes from a pair of alternating calcium transients49,50. Resultant values range from 0 (no alternans) to 1 (maximum alternans). Beat rate variability (BRV) was calculated as the standard deviation of the interbeat interval.

Statistical Analysis

All values are expressed as mean + SEM, with p < 0.05 considered statistically significant, denoted with an asterisk (*). Lowest observed adverse effect level was determined within a treatment group using ANOVA followed by posthoc multiple comparisons testing (individual coverslips) or multiple paired Student t-tests (two-tailed; baseline control vs treated), as previously described (Prism, Graphpad Software Inc)9,82. Representative traces and images are shown.