Metabolic Behaviors of Aconitum Alkaloids in Different Concentrations of Aconiti Lateralis Radix Praeparata and Effects of Aconitine in Healthy Human and Long QT Syndrome Cardiomyocytes

Aconiti Lateralis Radix Praeparata (Fu Zi) is the processed lateral root of Aconitum carmichaelii Debx, which is widely used in emergency clinics. Poisoning incidents and adverse reactions occur with the improper intake of Fu Zi. Metabolic characteristics of aconitum alkaloids of Fu Zi may vary, and the effects of Fu Zi in healthy and Long QT syndrome (LQTS) patients is unknown. In this experiment, 24 Sprague Dawley rats were randomly divided into three groups: 2.0, 1.0, and 0.5 g/kg dose groups, and blood samples were collected after the oral administration of Fu Zi extract. We used an ultra-high performance liquid chromatography-tandem mass spectrometry system to detect the concentrations of six aconitum alkaloids. Cell toxicity, calcium imaging, and patch-clamp recordings of human induced pluripotent stem cells-cardiomyocytes (hiPSC-CMs) of aconitine in healthy and LQTS were observed. We found that the AUC(0–48h), Cmax, and t1/2 of the six compounds increased with the multiplicative dosages; those in the high group were significantly higher than those in the low group. Aconitine concentration-dependently decreased the amplitude, which has no significant effect on the cell index of normal hiPSC-CMs. Aconitine at 5.0 μM decreased the cell index between 5–30 min for LQTS hiPSC-CMs. Meanwhile, aconitine significantly increased the frequency of calcium transients in LQTS at 5 μM. Aconitine significantly shortened the action potential duration of human cardiomyocytes in both normal and LQTS groups. These results show metabolic behaviors of aconitum alkaloids in different concentrations of Fu Zi and effects of aconitine in healthy and LQTS patients.


Introduction
Traditional Chinese Medicine (TCM) is now practiced in many countries, such as the United States, Canada, and Europe [1], and it has been proposed to possess great potential to improve people's health and wellness [2,3]. Aconitum carmichaelii Debx of the genus Aconitum L. (Ranunculaceae) is an example of TCM that has been used for 2000 years. Aconiti Lateralis Radix Praeparata (Fu Zi) is the processed lateral root of Aconitum carmichaelii Debx (Figure 1) [4][5][6][7]. The active aconitum alkaloids in Fu Zi encompass diester-diterpene alkaloids (DDAs): aconitine (AC), hypaconitine (HA), mesaconitine (MA), and monoester-diterpene alkaloids (MDAs), which include benzoylaconine (BAC),  Thus, the present study aims to establish an ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the simultaneous determination of six aconitum alkaloids in rat plasma, to obtain valuable pharmacokinetic data, and to compare different effects of AC on normal and LQTS hiPSCs.

Selectivity
The selectivity of the method was determined by comparing the chromatograms of blank, spiked, and experiment plasma samples after the dosing of Fu Zi extracts. The retention time of AC, HA, MA, BAC, BHA, and BMA was 2.16, 2.18, 2.08, 2.03, 2.01, and 1.93 min, respectively, which demonstrated that there was no endogenous interference at the same retention times (Figure 3).  Thus, the present study aims to establish an ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the simultaneous determination of six aconitum alkaloids in rat plasma, to obtain valuable pharmacokinetic data, and to compare different effects of AC on normal and LQTS hiPSCs.

Selectivity
The selectivity of the method was determined by comparing the chromatograms of blank, spiked, and experiment plasma samples after the dosing of Fu Zi extracts. The retention time of AC, HA, MA, BAC, BHA, and BMA was 2.16, 2.18, 2.08, 2.03, 2.01, and 1.93 min, respectively, which demonstrated that there was no endogenous interference at the same retention times (Figure 3). The selectivity of the method was determined by comparing the chromatograms of blank, spiked, and experiment plasma samples after the dosing of Fu Zi extracts. The retention time of AC, HA, MA, BAC, BHA, and BMA was 2.16, 2.18, 2.08, 2.03, 2.01, and 1.93 min, respectively, which demonstrated that there was no endogenous interference at the same retention times (Figure 3).

Sensitivity and Linearity
The sensitivity was defined by the six spiked samples at a lower limit of quantitation (LLOQ) concentration. The signal-to-noise ratio of limit of detection (LOD) was above three. The linearity was accessed by peak areas of seven points on the optimal calibration curve and established by the weighted least squares linear regression. The calibration

Sensitivity and Linearity
The sensitivity was defined by the six spiked samples at a lower limit of quantitation (LLOQ) concentration. The signal-to-noise ratio of limit of detection (LOD) was above three. The linearity was accessed by peak areas of seven points on the optimal calibration curve and established by the weighted least squares linear regression. The calibration equations, linear ranges, coefficients, LLOQ, and LOD were measured and calculated (Table 1).  Table 2). The data indicated that the methods had an optimal accuracy and reproducibility of the method. The RE of the six compounds at different conditions varied from 12.2-11.4% and the RSDs ranged from 2.9-13.1% (Table 3). The samples were stable at different storage conditions, such as at room temperature for 4 h, at the autosampler for 10 h, at −20 • C for 1 week, and after three freeze-thaw cycles.

Extraction Recovery and Matrix Effect
The extraction recovery of the six compounds ranged from 67.7 ± 4.0 to 101.1 ± 5.5%, and the matrix effects varied from 67.6 ± 8.8 to 100.3 ± 6.9%. In addition, the RSDs ranged from 4.5% to 9.4% for extraction recovery and 6.1% to 14.0% for matrix effect, which fulfilled the criteria (Table 4). These results demonstrated that the approach of protein precipitation was acceptable, and the peaks of the endogenous matrix had no effect on the quantification of the six compounds.

Pharmacokinetic Study
When applied to the pharmacokinetic assessment, the validated method was suitable for the quantification of the six compounds in SD rat plasma at different oral doses of 2.0 g/kg, 1.0 g/kg, and 0.5 g/kg of Fu Zi extracts. The mean plasma concentrationtime profiles of the six compounds were tested (Figure 4), and the main pharmacokinetic parameters were calculated (Table 5). Briefly, the AUC (0-48h) , C max , and t 1/2 of the six compounds increased with the multiplicative dosages; those in the high group were significantly higher than those in the low group. The plasma concentrations of BHA in the low group were below LLOQ at most of the time points. Table 5. The main pharmacokinetic parameters of the six compounds in SD rat plasma at different oral doses of 0.5 g/kg, 1.0 g/kg and 2.0 g/kg of Fu Zi extracts (mean ± SD, n = 8).   Table 5. The main pharmacokinetic parameters of the six compounds in SD rat plasma at different oral doses of 0.5 g/kg, 1.0 g/kg and 2.0 g/kg of Fu Zi extracts (mean ± SD, n = 8).

Cell Toxicity of AC on Normal and LQTS hiPSC-CMs
AC, MA, and HA have a similar structure and function, and because most researchers of the prior Fu Zi toxicity-effect studies selected AC as the representative component, cell toxicity of AC on normal and LQTS hiPSC-CMs. were also examined.
None of the three concentrations (0.05, 0.5, and 5 µM) AC caused cardiomyocyte death during the 48 h observation period ( Figure 5A,E). The contraction frequency was slightly higher and the contraction force was slightly lower than the control group ( Figure 5B,D,F,H). The concentration of 0.5 µM increased cell frequency and decreased cell contractility ( Figure 5B,C,F,G). ers of the prior Fu Zi toxicity-effect studies selected AC as the representative component, cell toxicity of AC on normal and LQTS hiPSC-CMs. were also examined.
None of the three concentrations (0.05, 0.5, and 5 μM) AC caused cardiomyocyte death during the 48 h observation period ( Figure 5A,E). The contraction frequency was slightly higher and the contraction force was slightly lower than the control group ( Figure  5B,D,F,H). The concentration of 0.5 μM increased cell frequency and decreased cell contractility ( Figure 5B,C,F,G).
Molecules 2022, 27, x FOR PEER REVIEW 10 of 23 Figure 5. High-throughput analysis of AC toxicity in hiPSC-CMs from control or LQT syndrome. (A) Cell index of normal hiPSC-CMs exposed to AC; (B) Cell beat amplitude of normal hiPSC-CMs exposed to AC; (C) Cell beat frequency of normal hiPSC-CMs exposed to AC; (D) Cell beat rate of normal hiPSC-CMs exposed to AC; (E) Cell index of LQT syndrome hiPSC-CMs exposed to AC; (F) Cell beat amplitude of LQT syndrome hiPSC-CMs exposed to AC; (G) Cell beat frequency of LQT syndrome hiPSC-CMs exposed to AC; (H) Cell beat rate of LQT syndrome hiPSC-CMs exposed to AC.
Cell contractility was significantly reduced at 5 μM concentration and was very weak within 6 h after treatment. Cell beat rate of normal hiPSC-CMs exposed to AC (0.5 μM) was faster after 12 h, while cell beat frequency of LQT syndrome hiPSC-CMs (AC 0.5 μM) continued to 6 h.
Effects of AC on LQT myocardial cells. None of the three concentrations caused sig- (A) Cell index of normal hiPSC-CMs exposed to AC; (B) Cell beat amplitude of normal hiPSC-CMs exposed to AC; (C) Cell beat frequency of normal hiPSC-CMs exposed to AC; (D) Cell beat rate of normal hiPSC-CMs exposed to AC; (E) Cell index of LQT syndrome hiPSC-CMs exposed to AC; (F) Cell beat amplitude of LQT syndrome hiPSC-CMs exposed to AC; (G) Cell beat frequency of LQT syndrome hiPSC-CMs exposed to AC; (H) Cell beat rate of LQT syndrome hiPSC-CMs exposed to AC.
Cell contractility was significantly reduced at 5 µM concentration and was very weak within 6 h after treatment. Cell beat rate of normal hiPSC-CMs exposed to AC (0.5 µM) was faster after 12 h, while cell beat frequency of LQT syndrome hiPSC-CMs (AC 0.5 µM) continued to 6 h.
Effects of AC on LQT myocardial cells. None of the three concentrations caused significant myocardial cell death during the 48 h observation period. The concentration of 0.05 µM had a significant effect on the cells, which showed higher contraction frequency and lower contraction force than the control group. The cell frequency and contractility were significantly increased at the 0.5 µM concentration. The cell contractility decreased to zero with the 5 µM concentration, and it was very weak within 30 h after treatment with AC.

Effects of AC on Calcium Transients in Normal and LQT Syndrome hiPSC-CMs
Compared with the control group, the detected AC had no significant effect on the amplitude and frequency of calcium transient in normal hiPSC-CMs, but it could significantly increase the frequency of calcium transient in cardiomyocytes of LQTS at 5 μM ( Figure 8).

Effects of AC on Calcium Transients in Normal and LQT Syndrome hiPSC-CMs
Compared with the control group, the detected AC had no significant effect on the amplitude and frequency of calcium transient in normal hiPSC-CMs, but it could significantly increase the frequency of calcium transient in cardiomyocytes of LQTS at 5 µM (Figure 8).

Effects of AC on L-Type Calcium Current in Normal and LQTS hiPSC-CMs
The peak value of L-type calcium current of human cardiomyocytes in normal and LQT groups was significantly decreased by 0.05-5 μM AC, with IC50 > 5 μM with no concentration dependence. A stronger ICa,L blocking was noted (Figure 9). The effects of AC on ICa,L (L-type calcium channel) currents in normal and LQTS hiPSC-CMs were validated

Effects of AC on L-Type Calcium Current in Normal and LQTS hiPSC-CMs
The peak value of L-type calcium current of human cardiomyocytes in normal and LQT groups was significantly decreased by 0.05-5 µM AC, with IC 50 > 5 µM with no concentration dependence. A stronger I Ca,L blocking was noted (Figure 9). The effects of AC on I Ca,L (L-type calcium channel) currents in normal and LQTS hiPSC-CMs were validated in the heterologous expression systems. Using a HEKA EPC-10 patch-clamp system, the effects of AC (0.05-5µM) on I Ca,L were measured in normal and LQTS hiPSC-CMs. AC showed a mild blockage with IC 50 of 27.51 µM and 27.23 µM for normal and LQTS hiPSC-CMs, respectively.

Effects of AC on L-Type Calcium Current in Normal and LQTS hiPSC-CMs
The peak value of L-type calcium current of human cardiomyocytes in normal and LQT groups was significantly decreased by 0.05-5 μM AC, with IC50 > 5 μM with no concentration dependence. A stronger ICa,L blocking was noted (Figure 9). The effects of AC on ICa,L (L-type calcium channel) currents in normal and LQTS hiPSC-CMs were validated in the heterologous expression systems. Using a HEKA EPC-10 patch-clamp system, the effects of AC (0.05-5μM) on ICa,L were measured in normal and LQTS hiPSC-CMs. AC showed a mild blockage with IC50 of 27.51 μM and 27.23 μM for normal and LQTS hiPSC-CMs, respectively.

Discussion
Considering the complex components and the different doses of Fu Zi in prescriptions, multiple components must be analyzed to ensure that Fu Zi is used safely in therapeutic treatments. A rapid and accurate method for the determination of three types of DDAs (AC, HA, and MA) was established previously [26]. That study suggested that Panax ginseng (P. ginseng) could inhibit the metabolism of DDAs in vivo. Our group has developed a new method to simultaneously detect the concentration of six aconitum alkaloids in rat plasma in 5 min. The calibration curves of each component range from 0.1 to 10 ng/mL. The method has reliable performance on the selectivity, linearity, accuracy, precision, stability, extraction recovery, and matrix effects [27], which conform to the guidelines of the National Medical Products Administration for bioanalytical assay validation. Therefore, the method could be applied to pharmacokinetic study.
In our previous work, we suggested that calcium disorder and calcium transient were observed in myocardial cells induced by AC at high doses (1-10 µmol/L), while the low doses (5-20 nmol/L) of AC could improve mitochondrial energy metabolism. These data all indicate that Fu Zi has the trend of high-dose toxicity and low-dose effect. AC, HA, and MA can be hydrolyzed to BAC, BHA, and BMA. In Figure 3, two peaks of BAC, BHA, and BMA were observed in the chromatograms. After a literature review and comparison, the phenomenon of two peaks may be caused by the hydrolysis of AC, HA, and MA by the action of the cytochrome P450 enzyme. In our previous study, we systematically studied the cytochrome P450 (CYP 450) enzyme subtypes of metabolizing AC, HA, and MA. CYP3A4 was found to be the main subtype for alkaloid (AC, HA, and MA) metabolism in vivo, and the activity of CYP3A4 is affected by the combined action of multiple alkaloids [28]. Hence, the number of various alkaloids in the body at different doses is the key to their toxicity effects.
Toxic cardiovascular effects, including arrhythmia, lower heart rate, and blood pressure, were observed after we orally administered 0.4 mg/kg of AC in rats, and these effects were not found in the low-dose (0.1 mg/kg) group [29]. The patients who experienced acute poisoning by Fu Zi ingestion presented with excessive salivation, arrhythmia, pre-mature ventricular contraction, and shallow breathing [30,31]. In the pharmacodynamics pre-experiments, we found that a high dose of Fu Zi (5 g/kg/d) had obvious toxicity to normal mice but could partially restore the heart function of myocardial ischemia mice and improve the myocardial fibrosis of mice. Large doses of Fu Zi significantly enhanced the formation of autophagosomes in normal mice, but they partially inhibited the formation of autophagosomes and promoted the fusion of autophagosomes and lysosomes after the occurrence of myocardial ischemia. Compared with the poisoning symptoms of salivation and arrhythmia in the high-dose group, the rats in the low-and middle-dose groups acted normally in this study, which was similar to the clinical symptoms of Fu Zi high dose with toxicity while low dose with treatment. Six alkaloids in the low-dose group were eliminated within 48 h, while there was still limited residue in the high-dose group at 48 h. It was found that the pharmacokinetic parameters of three MDAs were similar [32], with small C max, T max , and greater t 1/2 indicating that the three MDAs can be absorbed rapidly and are difficult to be metabolized or excreted. However, the low C max indicated that the bioavailability of the MDAs will be very low, and their absorption may be inhibited by some transport proteins. By incubating three MDAs in rat liver microsome, which cannot be metabolized in vivo. The CYP3A4 enzyme unit may be the key element for metabolizing the MDAs. Researchers also found that P-gp inhibits the absorption of MDAs by using a Caco-2 transwell model. The pharmacokinetic characteristics of different doses of Fu Zi extracts in SD rats may be related to the binding mechanism of the main components of Fu Zi and transporter in vivo.
It was found that intestinal metabolic profiles of the DDAs varied more than the MDAs. No glucuronide metabolites were detected, which agreed with the human liver microsome (HLM) metabolism [33]. Similarly, we observed bimodal phenomena in the plasma concentration-time curves of the six aconitum alkaloids, which was consistent with previous reports.
LQTS mutations can cause syncope and sudden death by prolonging the cardiac action potential (AP). Researchers found that myocytes carrying an LQT2 mutation (HERG-A422T), APS, and [Ca 2+ ] i transients were prolonged in parallel, compared with the normal groups. LQTS models are difficult to replicate in drug evaluation studies [34], but hiPSCs make it possible to rapidly detect the toxicity or efficiency of compounds in vitro for LQTS patients. Rather than using drug-induced LQTS rat models, human LQTS cardiomyocytes come from clinical patients, which are completely consistent with the pathogenesis of patients. The importance of applying human cardiomyocyte models for evaluating the effects of various drugs has been receiving unprecedented attention. A variety of research on the mechanism of arrhythmia in human cardiomyocytes compared to that from other animals, particularly rodents, reveals the intra-species variations in cardiac electrophysiology.
Early studies have shown that AC can improve arrhythmia in patients by affecting calcium channels, but whether AC will accelerate the deterioration of LQTS mutations has not yet been reported. In our preliminary experiment, several dose groups were set up with AC concentrations ranging from 0.05-0.5 µM, which would not cause death but the doses of AC are cytotoxic. The present work suggested that 0.05-0.5 µM concentrations did not cause significant myocardial cell death during the 48 h observation period. The concentration of 0.05 µM had a significant effect on the cells, which showed higher contraction frequency and lower contraction force than the control group. The cell frequency and contractility were significantly increased at the 0.5 µM concentration. The cell contractility decreased to zero using the 5 µM concentration, and it was very weak within 30 h after treatment of AC ( Figure 5). This does not imply that AC is more toxic on LQTS than normal because the LQTS cardiomyocytes also lose a substantial amount of contractility over time. The beat rate is accelerated earlier due to the effect of AC (0.5 µM) on patients with LQTS cardiomyocytes, as compared with normal hiPSC-CMs; however, it is still not clear why the cell index did not change even though the amplitude and beating rate were reduced by AC (5 µM). Compared with the normal control, the AC had no significant effect on the amplitude and frequency of calcium transient in normal hiPSC-CMs, but it could significantly increase the frequency of calcium transient in cardiomyocytes of LQTS at 5 µM (Figure 8). This explains why the fluctuation anomaly appears earlier in LQTS cardiomyocytes as compared with AC in normal hiPSC-CMs.
We further detected the effect of AC on L-type calcium current in both normal hiPSC-CMs and LQTS hiPSC-CMs, and it showed similar blockage, which suggested that L-type calcium current may not be the major target on the effect of AC on LQTS. This study has some limitations. First, we did not examine diverse types of LQTS mutations. Second, Na + channels and K + channels were not involved in the experiment. Therefore, we encourage additional studies examining diverse types of LQTS mutations, and these studies should supplement the data of other ion channels. In addition, although KCNQ1, KCNH2 (K + channels), and the SCN5A (Na + channel) also play important roles in LQTS, we only observed the effect of AC on the L-type Ca channel alone in LQTS hiPSC-CMs; therefore, K + channels, such as KCNQ1 and KCNH2, and Na + channels, such as SCN5A, must be observed in further studies.
In summary, there are still some deficiencies in our study despite the use of eight rats in each group. The plasma concentrations at some points on the drug concentration-time curves showed a large deviation, which may be due to individual differences in the drug resistance of the rats or an insufficient sample size. Nevertheless, research on this type of disease model is more practical and meaningful, so we will conduct a pharmacokinetic study of Fu Zi extracts in rats with heart failure in the future. Moreover, the effects of Fu Zi in healthy and LQTS cardiomyocytes may be caused by various alkaloids, such as HA and MA, so we will examine the results of other alkaloids in our upcoming work. The results of the present study show the parameters of six aconitum alkaloids in Fu Zi at multiple doses for the first time, which could provide support for the safe clinical application of Fu Zi. Moreover, for the first time we compared the effects of AC in normal and LQT-hiPSC-CMs, which may provide data for the basic research of drugs containing AC.

Materials and Instruments
The standard compounds (purity ≥ 98%) of AC ( The UPLC-MS/MS system consisted of a Waters ACQUITY I-Class UPLC system connected to a Waters (Milford, MA, USA) Xevo TQ-S triple quadrupole mass spectrometer with a degasser, a binary pump, flow-through-needle sample manager, a column oven with temperature control, and a cooling autosampler.

Preparation of Fu Zi Extracts
Fu Zi (200 g) was taken and broken by a pulverizer to the size of 0.5-1.0 cm. The broken Fu Zi was soaked in 1.6 L distilled water and boiled for 0.5 h. The filtrate was collected and the previous step was repeated for the filtered residue. The mixed filtrates were precipitated with 60% ethanol, and then centrifuged (2000× g, 10 min) [22]. The supernatant was decompressed and concentrated to a final density of 2.0 g/mL by the amount of the crude drugs. The final concentration of ethanol in Fu Zi extracts before administration was below 0.5%. The extract was subsequently kept at −20 • C for oral administration to rats. The contents of AC, HA, MA, BAC, BHA, BMA in Fu Zi extracts were detected to be 0.140, 0.475, 0.525, 0.910, 0.234, and 0.571 mg/g by UPLC-MS/MS, respectively.
The detection was quantified by a triple quadrupole mass spectrometer that was set as multiple reactive monitoring (MRM) in the electrospray positive ionization mode (ESI+). The correlative parameters were as follows: capillary voltage: 3 kV; desolvation gas flow: 800 L·h −1 ; cone gas flow: 150 L·h −1 ; source temperature: 150 • C; desolvation temperature: 500 • C. Quantitative parameters are listed in Table 6.

Preparation of Calibration Standards and Quality Control Samples
The stock solutions of the six alkaloids were prepared in methanol at the concentration of 2.0 mg/mL individually. Then working and quality control solutions were obtained by serial dilution of the stock solutions with 50% acetonitrile. All solutions were stored at −20 • C.
The standard curves of the six alkaloids were in the linear range from 0.1 to 10 ng/mL (0.1, 0.25, 0.5, 1.0, 2.5, 5.0, and 10 ng/mL). The QC samples were prepared by adding the corresponding level of QC working solutions to the blank plasma, consisting of low-QC (0.2 ng/mL), mid-QC (2 ng/mL), and high-QC (8 ng/mL) samples. To obtain the plasma matrix samples with a serial of concentrations, 10 µL of a 10-fold concentration of the calibrators was added to 90 µL of blank plasma from SD rats. Standards curves and QC samples were prepared for every validation assay and sample test.

Pre-Treatment of Plasma Samples
The method of liquid-liquid extraction was utilized [23]. An amount of 100 µL of plasma samples from rats after oral administration of Fu Zi extracts was precipitated with 300 µL of 50% acetonitrile plus 50% methanol, vortexed for 1.0 min and centrifuged at a speed of 12,000× g at 4 • C for 10 min. The supernatant was transferred to another 1.5 mL centrifuge tube, dried with a stream of nitrogen at 40 • C, redissolved in 50 µL methanol and centrifuged at 12,000× g for 10 min. Then, the supernatant was pipetted out into the autosampler vials and analyzed by UPLC-MS/MS system.

Method Validation
To ensure that there were no endogenous compounds, the selectivity of the six alkaloids was determined by comparing the chromatograms of blank plasma samples, spiked plasma samples, and plasma samples after oral administration of Fu Zi extracts.
The calibration curves at a range from 0.1 to 10 ng/mL were evaluated by least-square regression using 1/x 2 as a weighting factor. The quality control samples, including low-QC (0.2 ng/mL), mid-QC (2 ng/mL), and high-QC (8 ng/mL) samples, were prepared from another stock solution independently. The LLOQ signal-to-noise ratio was above 10 and the deviation did not exceed 20%.
The accuracy and precision were determined by LLOQ and QC samples at high, middle, and low concentrations (each for six replicate analyses) in intra-day and inter-day batches. The inter-day accuracy and precision should be assessed by three batches for at least 2 days. The accuracy [RE (%)] and precision [RSD (%)] for QC samples were required within ±15%, while for LLOQ samples, they were less than 20%.
The stability was assessed by analyzing the QC samples at high and low concentrations under different storage conditions: at room temperature for 4 h, in the autosampler after preparation for 10 h, after three freeze-thaw cycles and at −20 • C for 1 week, respectively. The RE (%) comparing the standard curve on the detection day was required to be within ± 15% in the stability test.
The matrix effect was calculated by comparing the difference of response between samples of 50% methanol and the supernatant of precipitated blank plasma with the addition of high, middle, and low QC samples, respectively. The extraction recovery was assessed by comparing the difference of peak areas between samples of 50% methanol and blank plasma with the addition of QC samples at high, middle, and low QC samples. Both RSD (%) of each QC sample should be less than 15%.

Animals and Treatments
24 Sprague Dawley rats (half male and female, weight 180-220 g) were purchased from Beijing Weitong Lihua Biotechnology Co.Ltd. (Beijing, China). The license number of experimental animal production was SCXK (Jing) 2016-0006. The animals were maintained under a standard laboratory condition (humidity: 40-70%, room temperature: 20-26 • C, relative humidity: 45-65%, 12 h dark-light cycle) and fed separately. All animal experiments were conducted according to the Guide for the Care and Use of Laboratory Animals (National Research Council of the USA, 1996) and approved by the Institutional Animal Care and Use Committee (IACUC-DWZX-2020-776). After 5 days of acclimation, the rats were fasted for 12 h but provided with water freely before the experiments. The rats were randomly divided into 3 groups: high (2.0 g/kg), middle (1.0 g/kg), and low (0.5 g/kg) dose groups. The Fu Zi extracts was administered to each rat intragastrically. An equivalent of 0.20 mL blood samples were collected from the fossa orbitalis vein into 1.5 mL heparinized centrifuge tubes at the designated time points after dosing: 0.08, 0.25, 0.5, 1, 2, 4, 8, 12, 24, and 48 h. The plasma samples were pipetted out into another 1.5 mL centrifuge tubes after being centrifuged at 5000× g for 10 min and then stored at −20 • C until further analysis.

Impedance Beating Recordings
The cardiomyocytes were seeded on Nanion CardioExcyte 96 Sensor Plates (NSP-96, Nanion Technologies, Munich, Germany) after 0.1% gelatin coating for 1 h. The initial volume was 200 µL per well and contained approximately 100 million cells. After seeding, the NSP-96 and CardioExcyte 96 were returned to the incubator. All cells were replaced with fresh medium 200 µL per well every 48 h and tested after 168 h. Cellular index, beat rate, base impedance and beat amplitude were monitored in this experiment.

Ca 2+ Imaging
Dissociated day 30-33 post-differentiation hiPSC-CMs (healthy and LQT specific patient) were reseeded Matrigel-coated plate in HELP4004 (HELP) and were treated with 5 µM Fluo-3 AM and 0.02% Pluronic (Life Technologies) in DMEM/F12 (Gibco) for 60 min at 37 • C. Cells were washed with DMEM/F12 without fluorochrome solution afterwards for 30 min, replaced the solution with Tyrode's solution. Ca 2+ imaging was conducted using Olympus IX71 confocal microscope (Olympus IX71, Tokyo, Japan) and analyzed using Olympus imaging software. Ca 2+ spontaneous transients were obtained using a single cell line scan mode at 37 • C.

Patch-Clamp Recordings of hiPSCs
Standard patch-clamp techniques were used to record action potentials, and L-type calcium currents. Composition of intracellular fluid and extracellular fluid were shown in Tables 7 and 8, respectively. The signal was amplified using an HEKA EPC-10 patch-clamp amplifier (HEKA, Electronics, Ludwigshafen, Germany) and low-pass filtered at 5 kHz. Patch pipettes were fabricated from glass capillaries using a Sutter P-97 microelectrode puller (Novato, CA, USA) and the tips were heat polished with a microforge (NARISHIGE MF-900) to gain a resistance of 2-5 MΩ. Data acquisition was achieved using HEKA Patchmaster (V2x73.2). Data analysis and fit were performed using Clamfit and Graphpad Prism 6.0. The experiment was conducted at 37 • C. One cell can test one or more drugs, or multiple concentrations of the same drug but needs to be rinsed with extracellular fluid between each test. Nifedipine (Sigma) was used as a positive control to ensure cell quality. External solution containing 0.1% DMSO was applied as vehicle to establish the baseline.
Recording was done at a temperature-controlled room of 35-37 degrees Celsius.

Compound Solutions in Drug Assay
Isoproterenol, nifedipine, and AC were purchased from Sigma-Aldrich, which were resolved in DMSO (Sigma-Aldrich, D2650). Drug compounds final concentration were AC (0.05, 0.5,5 µM), nifedipine (1 µM), isoproterenol (3 µM), respectively. Dilutions were prepared within 60 min of treatment. All the compound solutions were subjected to regular 10 min ultrasound and oscillations to ensure that compounds were completely dissolved. Equal amounts of DMSO (0.1%) were used as the vehicle controls.

Statistical Analysis
The data were acquired by Mass Hunter Workstation Software from Waters (UNIFI). Microsoft Office Excel and the SPSS software (Version 13.0) was used for data analysis. The data below the LLOQ were regarded as zero in summary statistics. The pharmacokinetic parameters were calculated by DAS pharmacokinetic program (Version 2.0) and all analyzed by non-compartmental method. The figures were displayed and processed by GraphPad prisms ware (Version 5.01). All data were presented as mean ± SD. One-way analysis of variance was used to detect significant differences between the high, middle, and low dose groups. Statistical analysis was determined by paired or unpaired Student's t-test (two tail) for comparison between two groups. Unless otherwise specified, statistically significant differences defined by * p < 0.05 or ** p < 0.01 or *** p < 0.001.

Conclusions
A rapid, sensitive, and reproducible method to simultaneously detect the concentration of AC, HA, MA, BAC, BHA, and BMA in biological samples has been developed, validated, and then employed successfully. The pharmacokinetic characteristics of six aconitum alkaloids after oral administration of Fu Zi extracts in SD rats have shown significant differences between the high-and low-dose group. AC had no significant effect on the amplitude and frequency of calcium transient in normal hiPSC-CMs, but it could significantly increase the frequency of calcium transient in cardiomyocytes of LQTS at 5 µM. The six aconitum alkaloids in the high group could be more quickly absorbed, more slowly eliminated, and more widely distributed. The pharmacokinetics data could provide valuable information for the safe application and clinical treatment of Fu Zi.

Informed Consent Statement:
The animal study protocol was approved by Institutional Animal Care and Use Committee (IACUC-DWZX-2020-776).

Data Availability Statement:
The data used to support the findings of this study are available from the corresponding author upon request.