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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Pharmacol.</journal-id>
<journal-title>Frontiers in Pharmacology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pharmacol.</abbrev-journal-title>
<issn pub-type="epub">1663-9812</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1372973</article-id>
<article-id pub-id-type="doi">10.3389/fphar.2024.1372973</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Pharmacology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Inhibitory effect of aloperine on transient outward potassium currents in rat cardiac myocytes</article-title>
<alt-title alt-title-type="left-running-head">Dong and Li</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fphar.2024.1372973">10.3389/fphar.2024.1372973</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Dong</surname>
<given-names>Xiao-Na</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>&#x2020;</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1802110/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/funding-acquisition/"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/software/"/>
<role content-type="https://credit.niso.org/contributor-roles/validation/"/>
<role content-type="https://credit.niso.org/contributor-roles/visualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author" corresp="yes" equal-contrib="yes">
<name>
<surname>Li</surname>
<given-names>Meng-Ting</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>&#x2020;</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Clinical Medical College</institution>, <institution>Yangzhou University</institution>, <addr-line>Yangzhou</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Baoying County Traditional Chinese Medicine Hospital</institution>, <addr-line>Yangzhou</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/527652/overview">Martin Hennenberg</ext-link>, University Hospital, LMU Munich, Germany</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1296304/overview">Ru Huang</ext-link>, First Affiliated Hospital of Guangzhou Medical University, China</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1105506/overview">Muhammad Naveed</ext-link>, University of Szeged, Hungary</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Meng-Ting Li, <email>mengtingli1026@163.com</email>
</corresp>
<fn fn-type="equal" id="fn001">
<label>
<sup>&#x2020;</sup>
</label>
<p>These authors have contributed equally to this work and share first authorship</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>28</day>
<month>03</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1372973</elocation-id>
<history>
<date date-type="received">
<day>19</day>
<month>01</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>19</day>
<month>03</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2024 Dong and Li.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Dong and Li</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec>
<title>Objective:</title>
<p>Aloperine (ALO) is an effective quinolizidine alkaloid. Previous research has demonstrated its antiarrhythmic effect by inhibiting voltage-gated sodium currents in rat ventricular myocytes. This study explored its effect on transient outward potassium currents (I<sub>to</sub>) in rat atrial myocytes to identify potential targets in the context of ion channel currents.</p>
</sec>
<sec>
<title>Methods:</title>
<p>The I<sub>to</sub> characteristics in rat atrial myocytes were recorded using a whole-cell patch-clamp technique. Molecular docking was performed to validate ligand-protein binding interactions.</p>
</sec>
<sec>
<title>Results:</title>
<p>ALO at concentrations of 3 and 10&#xa0;&#x3bc;M significantly reduced I<sub>to</sub> current densities. Gating kinetics analysis revealed ALO&#x2019;s ability to slow I<sub>to</sub> activation, hasten inactivation, and prolong transition from inactive to resting state. Molecular docking revealed that ALO could stably bind to <italic>KCND2</italic>.</p>
</sec>
<sec>
<title>Conclusion:</title>
<p>ALO may inhibit I<sub>to</sub> by slowing the activation process, accelerating inactivation, and delaying the recovery time after inactivation, potentially preventing acetylcholine-induced AF.</p>
</sec>
</abstract>
<kwd-group>
<kwd>aloperine</kwd>
<kwd>transient outward potassium current</kwd>
<kwd>whole-cell patch-clamp</kwd>
<kwd>atrial fibrillation</kwd>
<kwd>molecular docking</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Cardiovascular and Smooth Muscle Pharmacology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Cardiac arrhythmias refer to any deviation from the normal heart rhythm. Atrial fibrillation (AF) is a global health problem, and its significant impact on disability and mortality has made it a focal point of research in the field of cardiac arrhythmias. Animal models are key in the study of AF pathogenesis, which can be similarized to AF in humans with similar natural onset of the disease.</p>
<p>Recently, monomeric compounds extracted from traditional Chinese herbal medicines for the treatment of cardiovascular diseases have attracted substantial attention due to their high efficiency and safety (<xref ref-type="bibr" rid="B29">Xu and Yang, 2009</xref>). <italic>Sophora alopecuroides</italic> L., a perennial shrub, harbors several active components such as quinolizidine alkaloids, flavonoids, and flavone stilbenes. These compounds have shown efficacy in treating acute dysentery and ameliorating specific cardiovascular conditions (<xref ref-type="bibr" rid="B12">Li Y. et al., 2020</xref>; <xref ref-type="bibr" rid="B26">Wang et al., 2020</xref>; <xref ref-type="bibr" rid="B33">Zhou et al., 2020</xref>). Among these compounds, aloperine (ALO), a quinolizidine alkaloid, has gained attention from researchers worldwide (<xref ref-type="bibr" rid="B25">Wang et al., 2015</xref>; <xref ref-type="bibr" rid="B13">Lv et al., 2020</xref>; <xref ref-type="bibr" rid="B30">Ye et al., 2020</xref>). Studies have revealed ALO&#x2019;s potential in enhancing cardiac function, particularly in conditions such as ischemia-reperfusion and coronary artery microembolization (<xref ref-type="bibr" rid="B16">Mao et al., 2019</xref>). Moreover, ALO can reduce lipid peroxidation and ventricular remodeling in rats with atherosclerosis-induced myocardial hypertrophy (<xref ref-type="bibr" rid="B10">Li W. et al., 2020</xref>).</p>
<p>Evidence suggests that ion channels of cardiac myocytes are key to understanding the mechanisms of cardiac dysfunction and arrhythmia (<xref ref-type="bibr" rid="B21">Thiel et al., 1997</xref>). Previous research has demonstrated antiarrhythmic effect of ALO by inhibiting voltage-gated sodium currents in rat ventricular myocytes in a concentration-dependent manner (<xref ref-type="bibr" rid="B9">Li et al., 2021</xref>). Voltage-dependent potassium (Kv) channels play crucial role in repolarizing cell membranes and modulating membrane excitability, with various subtypes in the heart that are associated with diseases (<xref ref-type="bibr" rid="B14">MacKinnon, 1995</xref>). Among these, Kv4.2 (encoded by <italic>KCND2</italic>) and Kv4.3 (encoded by <italic>KCND3</italic>) act as pore-forming subunits responsible for generating the transient outward K<sup>&#x2b;</sup> current (I<sub>to</sub>) (<xref ref-type="bibr" rid="B4">Drum et al., 2016</xref>; <xref ref-type="bibr" rid="B32">Zhang et al., 2021</xref>). I<sub>to</sub> constitutes a six transmembrane segmented (S1&#x2013;S6) ion channel involved in mediating the transient outward K<sup>&#x2b;</sup> current. In general, variations in its current amplitude and dynamic characteristics may affect several normal physiological functions of the heart, such as the contractile function and impulse conduction process to potentially cause arrhythmias (<xref ref-type="bibr" rid="B28">Workman et al., 2001</xref>). Amiodarone, a commonly prescribed medication for arrhythmia, exerts its effects by inhibiting potassium channels, which results in prolonging the third phase of the action potential in the heart&#x2019;s conduction system cells (<xref ref-type="bibr" rid="B34">Zimetbaum, 2007</xref>; <xref ref-type="bibr" rid="B8">Lei et al., 2018</xref>).</p>
<p>Multiple mechanisms have been hypothesized to contribute to AF development <italic>via</italic> structural and electrical remodeling of the atrial tissue. Several factors, including multiple wavelets and increased focal autoregulation in the atria, have been intensively investigated, and their importance during this process has been confirmed (<xref ref-type="bibr" rid="B20">Sagris et al., 2021</xref>). Variations in the electrical remodeling of cardiac ion channels are associated with AF. Early and delayed afterdepolarizations may underlie the ectopic activity that triggers AF (<xref ref-type="bibr" rid="B3">Brundel et al., 2022</xref>). Since the phase 0 depolarization generated by the fast sodium channel is rapid and of short duration, it has minimal impact on the tricuspid effective refractory period (ERP). Therefore, the shortening of the ERP occurs primarily during the repolarization phase, particularly in phases 2 and 3. The physiological structures within the atrium, including the pulmonary vein muscle cuffs, valves, superior and inferior vena cava inlets, and coronary sinuses, could all be the anatomical basis for fold formation.</p>
<p>Manville et al. demonstrated that ALO relaxes blood vessels by activating the Kv7.5 vascular-expressed potassium channel (<xref ref-type="bibr" rid="B15">Manville et al., 2019</xref>). However, the effect of ALO on cardiac Kv channels remains unclear. Kv4 channels represent the primary subtypes of transient outward currents, characterized by rapid activation and inactivation. They play a crucial role in shaping the morphology of myocardial action potential (AP).</p>
<p>In this study, we investigated the impact of ALO on I<sub>to</sub> in rat atrial myocytes <italic>in vitro</italic> and assessed its influence on acetylcholine-induced arrhythmias <italic>in vivo</italic>. Molecular docking was performed to validate ligand-protein binding interactions. This provides a preliminary theoretical and practical basis for the further development and utilization of this drug and its analog compounds.</p>
</sec>
<sec sec-type="materials|methods" id="s2">
<title>2 Materials and methods</title>
<sec id="s2-1">
<title>2.1 Animals</title>
<p>Male and female SD rats (190&#x2013;200&#xa0;g) were procured from Yangzhou University Comparative Medical Center (SCXK [Su] 2017-0044). The rats were caged in a thermoregulated room at 23&#xb0;C &#xb1; 2&#xb0;C with a relative humidity of 55% &#xb1; 5%. Animal protocols were conducted according to the guidelines of the Institutional Animal Care and Ethics Committee of Yangzhou University, which are aligned with international standards for research ethics and integrity. All experimental procedures were approved by the institution.</p>
</sec>
<sec id="s2-2">
<title>2.2 Drugs and reagents</title>
<p>Aconitine and ALO were provided by Chengdu EFA Biotechnology Co., Ltd. (Chengdu, China). Collagenase type II (batch number: 44N15308B) and bovine serum albumin (BSA, batch number: 8398F) were purchased from Worthington Co. (NJ, United States) and ICN (CA, United States). CsCl (batch number: 101368097), TEA.Cl (batch number: 101394223), taurine (batch number: 101282014T), MgATP (batch number: 1001571838), and HEPES (batch number: 1001621577) were acquired from Sigma-Aldrich (St. Louis, MO, United States). Heparin sodium (batch number: 301A028) and glucose (batch number: 405A096) were obtained from Solarbio Company (Beijing, China). Egtazic acid (EGTA, batch number: 101257840) and tetrodotoxin (TTX, batch number: AF02) were purchased from Sigma-Fluka Company (St. Louis, MO, United States) and AFFIX Company (Kfar Yona, Israel), respectively. All other reagents were of analytical grade.</p>
</sec>
<sec id="s2-3">
<title>2.3 Single cell isolation</title>
<p>Isolation of single atrial myocytes from SD rat hearts was performed as previously described (<xref ref-type="bibr" rid="B6">Guinamard et al., 2014</xref>). Briefly, the animals were heparinized (2000 IU/kg, i.p.) for 10&#xa0;min and then anesthetized with 2% sodium pentobarbital solution (40&#xa0;mg/kg, i.p.). Following successful anesthesia, the animals were placed in the supine position to open the chest. The heart was cut and then cleaned in Ca<sup>2&#x2b;</sup>-free Tyrode&#x2019;s solution containing the following compounds (in mM): HEPES 5.0, glucose 10.0, NaH<sub>2</sub>PO<sub>4</sub> 0.33, MgCl<sub>2</sub> 1.0, KCl 5.4, and NaCl 135 (pH adjusted to 7.3 with NaOH). Excess tissue was trimmed to ligate the aorta into the Langendorff perfusion device. The calcium-saturated Tyrode&#x2019;s solution was obtained by adding CaCl<sub>2</sub> (1.8&#xa0;mM) to the Ca<sup>2&#x2b;</sup>-free Tyrode&#x2019;s solution to resuscitate the cardiac tissue for 30&#xa0;s and to remove the remaining blood. Residual blood from the heart was washed away after 5&#xa0;min of continuous perfusion with Ca<sup>2&#x2b;</sup>-free Tyrode&#x2019;s solution. The hearts were then digested with Ca<sup>2&#x2b;</sup>-free Tyrode&#x2019;s solution containing taurine (0.4&#xa0;g/L), BSA (1&#xa0;g/L), and type II collagenase (0.4&#xa0;g/L) for 20&#xa0;min until the heart became enlarged and soft, and the effluent became viscous and turbid. Temperature was maintained at 37&#xb0;C during perfusion with 95% O<sub>2</sub> and 5% CO<sub>2</sub>. The atrial tissue was cut and filtered using a 100-mesh filter to obtain individual atrial myocytes, and the cell suspension was washed three times with Krebs solution containing (in mM): EGTA 1.0, KCl 25.0, KOH 89.0, glucose 11.0, taurine 10.0, L-glutamic acid 70.0, NaH<sub>2</sub>PO<sub>4</sub> 10.0, and HEPES 5.0 (pH adjusted to 7.4 with KOH) for 10&#xa0;min to discard the supernatant. The cells were maintained at room temperature (23&#xb0;C &#xb1; 2&#xb0;C) for 30&#xa0;min in the dark and then stored in Krebs solution at 4&#xb0;C.</p>
</sec>
<sec id="s2-4">
<title>2.4 Whole-cell patch-clamp recording</title>
<p>Cell suspensions were transferred to a Petri dish containing the bath solution for recording I<sub>to</sub> with Ca<sup>2&#x2b;</sup>-saturated Tyrode&#x2019;s solution. Once the cells adhered to the dish, those exhibiting favorable characteristics (elongated shape, smooth edges, intact, distinct striations, strong stereoscopic sense, and absence of contraction) were chosen for subsequent experiments under an IX73 Inverted Microscope (OLYMPUS Company, Nagano, Japan). Glass microelectrodes were constructed with borosilicate glass electrodes (1.50&#xa0;mm outer diameter, 1.14&#xa0;mm inner diameter) from Wuhan Microprobe Co., Ltd. (Wuhan, China) using a P-97 microelectrode puller (Sutter Co, California, United States). The pipette solution used for recording I<sub>to</sub> included had a resistance of 1&#x2013;3&#xa0;M&#x3a9; and was comprised of the following (in mM): KCl 40.0, K-Asparate 106.0, MgCl<sub>2</sub> 1.0, EGTA 10.0, HEPES 5.0, and K<sub>2</sub>ATP 5.0 (pH adjusted to 7.3 with KOH). The EPC-10 USB/Patchmaster Single Channel Patch Clamp Amplifier (HEKA, Reuttlingen, Germany) and MP-225 Micromanipulator System (Sutter Co, California, United States) were used to record the whole-cell currents. Patchmaster software was utilized for the voltage clamp protocol generation, data acquisition, and current traces analysis. All of the experiments were conducted at room temperature (22&#xb0;C&#x2013;25&#xb0;C).</p>
</sec>
<sec id="s2-5">
<title>2.5 Establishment of an <italic>in vivo</italic> model of AF</title>
<p>Twenty-four SD rats were randomly assigned to four groups that included control (<italic>n</italic> &#x3d; 6), model (<italic>n</italic> &#x3d; 6), amiodarone (<italic>n</italic> &#x3d; 6), and 10&#xa0;mg ALO (<italic>n</italic> &#x3d; 6). The rat tails were soaked in 40&#xb0;C warm water for approximately 3&#xa0;min to soften the corneal layer and facilitate puncture. In addition to the control group, the other three groups of rat tails were disinfected with 75% ethanol solution, and a mixture of calcium chloride (10&#xa0;mg/mL) and acetylcholine (66&#xa0;&#x3bc;g/mL) was injected into the tail vein (1&#xa0;mL/kg&#xb7;d) for 10&#xa0;days to establish an AF model. The rats in the control group were intraperitoneally injected with an equal dose of a 0.9% NaCl solution. From the fourth day of modeling, rats in the amiodarone group and the ALO group were intravenously injected with a mixture of CaCl<sub>2</sub>-Ach solution 1&#xa0;hour before, receiving intravenous injections of amiodarone at a dose of 15&#xa0;mg/kg and ALO at a dose of 10&#xa0;mg/kg once daily for 7 consecutive days. The control group and model group rats were intravenously injected with an equal volume of 0.9% NaCl solution via the tail vein. The rats were injected intraperitoneally with 10% chloral hydrate solution (0.38&#xa0;g/kg) for anesthesia. The RM6240 Biological Data Acquisition and Analysis System (Chengdu Instrument Factory, Chengdu, China) was utilized for analyzing electrocardiograms (ECGs) from standard limb lead II.</p>
</sec>
<sec id="s2-6">
<title>2.6 Molecular docking</title>
<p>The crystal structures of <italic>KCND2</italic> (PDB ID: 1NN7 Chain A), KCND3 (PDB ID: 2I2R Chain A), and <italic>KCNIP4</italic> (predicted protein crystal structure generated by AlphaFold2) were acquired from the RCSB PDB database or AlphaFold2. The acquired protein crystals were processed using the Protein Preparation Wizard module in Schr&#xf6;dinger software. The 2D sdf structure files of ALO and amiodarone obtained from the PubChem database (<ext-link ext-link-type="uri" xlink:href="https://pubchem.ncbi.nlm.nih.gov/">https://pubchem.ncbi.nlm.nih.gov/</ext-link>) were processed using the LigPrep module in the Schr&#xf6;dinger software to generate their respective 3D chiral conformations. The SiteMap module in the Schr&#xf6;dinger software was employed to predict the optimal binding sites between the ligand and protein. Thereafter, the Receptor Grid Generation module in the Schr&#xf6;dinger software was used to set the most appropriate enclosing box to wrap the predicted binding sites perfectly, and the active sites of the three proteins were obtained on this basis. Molecular docking (with the highest precision, XP docking) was performed on the two ligand compounds and the active sites of three proteins. The interaction of the ligand and the active sites of the protein was analyzed through the MM-GBSA calculation. MM-GBSA dG Bind can approximately represent the binding free energy between ligands and proteins.</p>
</sec>
<sec id="s2-7">
<title>2.7 Data analysis</title>
<p>Data are presented as mean &#xb1; standard deviation (SD). Curve fitting was performed using GraphPad Prism 6 software (Axon Instruments). The experimental data were analyzed using Origin 7.0 (Microcal Software, Northampton, MA, United States). Statistical significance was assessed using SPSS 25.0 (SPSS, Inc., Chicago, IL, United States). The <italic>t</italic>-test was employed for comparing two groups, whereas analysis of variance (ANOVA) was utilized for comparing multiple groups. A value for <italic>P</italic> of less than 0.05 was considered to be statistically significance. The study is explorative in character, and as such, <italic>p</italic>-values need to be considered as descriptive and provisional.</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>3 Results</title>
<sec id="s3-1">
<title>3.1 Effect of ALO on peak I<sub>to</sub> in atrial myocytes</title>
<p>To examine the impact of ALO on peak I<sub>to</sub>, a single square-wave stimulus of 70&#xa0;mV for 300&#xa0;ms at a holding potential of &#x2212;80&#xa0;mV was administered in the voltage clamp mode to elicit an outward current. As presented in <xref ref-type="fig" rid="F1">Figure 1A</xref>, the current was almost completely suppressed by 2&#xa0;&#x3bc;M 4-aminopyridine (4-AP), an I<sub>to</sub>-specific blocker, and it was partially restored by removing 4-AP. The current induced in this stimulation mode was I<sub>to</sub>. Subsequently, 10&#xa0;&#x3bc;M ALO was perfused to inhibit I<sub>to</sub>; however, the inhibitory effect was not as significant as that of 4-AP. I<sub>to</sub> induced by ALO at various concentrations is depicted in <xref ref-type="fig" rid="F1">Figure 1B</xref>. We noted that 1&#xa0;&#x3bc;M ALO elicited no significant alterations compared to the control group, whereas treatments with 3 and 10&#xa0;&#x3bc;M ALO resulted in a reduction relative to the control group. This observation suggests that 3 and 10&#xa0;&#x3bc;M ALO can inhibit transient outward potassium channels. Moreover, the current density was slightly higher than that of the control group when the concentration was &#x3e;30&#xa0;&#x3bc;M. An increase in I<sub>to</sub> is the mechanism that causes Brugada syndrome and early repolarization syndrome. Nevertheless, excessive inhibition or an increase in I<sub>to</sub> may induce abnormal changes in the channel, ultimately resulting in cardiovascular disease. ALO at 3 and 10&#xa0;&#x3bc;M moderately affected I<sub>to</sub> and alleviated the abnormal function and expression of I<sub>to</sub> in the diseased hearts. Therefore, 3 and 10&#xa0;&#x3bc;M ALO were used for subsequent experiments. As presented in <xref ref-type="table" rid="T1">Table 1</xref>, the peak current is displayed as the current density (pA/pF). At 70&#xa0;mV depolarization voltage, the concentration of ALO at 1, 3, and 10&#xa0;&#x3bc;M suppressed I<sub>to</sub> and reduced the current by 3.03% &#x00B1; 3.65%, 16.92% &#x00B1; 5.16%, and 30.09% &#x00B1; 6.13% (<italic>p</italic> &#x3c; 0.01), respectively.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Effect of ALO on I<sub>to</sub> in atrial myocytes (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements). <bold>(A)</bold> Effect of ALO on the original current for the single stimulus diagram of I<sub>to</sub>. <bold>(B)</bold> The effects of different concentrations of ALO on I<sub>to</sub>. &#x2a;<italic>p</italic> &#x3c; 0.05, &#x2a;&#x2a;<italic>p</italic> &#x3c; 0.01 <italic>versus</italic> the control.</p>
</caption>
<graphic xlink:href="fphar-15-1372973-g001.tif"/>
</fig>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Peak current density measured at 70&#xa0;mV for various concentrations of ALO.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Group (concentration)</th>
<th align="left">Current density (pA/pF)</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Control</td>
<td align="left">85.80 &#xb1; 3.59</td>
</tr>
<tr>
<td align="left">1&#xa0;&#xb5;M ALO</td>
<td align="left">80.64 &#xb1; 3.65</td>
</tr>
<tr>
<td align="left">3&#xa0;&#xb5;M ALO</td>
<td align="left">68.38 &#xb1; 4.12&#x2a;&#x2a;</td>
</tr>
<tr>
<td align="left">10&#xa0;&#xb5;M ALO</td>
<td align="left">45.75 &#xb1; 5.32&#x2a;&#x2a;</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s3-2">
<title>3.2 Effect of ALO on the I-V curve of I<sub>to</sub> channels</title>
<p>To investigate the impact of ALO on I<sub>to</sub> across various voltage conditions, we maintained the potential at &#x2212;80&#xa0;mV in the voltage clamp mode. We applied a square wave ranging from &#x2212;50&#x2013;70&#xa0;mV in 10&#xa0;mV increments for 500&#xa0;ms at 0.5&#xa0;Hz to elicit I<sub>to</sub> response before and after ALO administration. As presented in <xref ref-type="fig" rid="F2">Figures 2A</xref>, <xref ref-type="fig" rid="F3">3</xref> and 10&#xa0;&#x3bc;M ALO treatments reduced the current compared to the control group. <xref ref-type="fig" rid="F2">Figure 2B</xref> indicates that 3 and 10&#xa0;&#x3bc;M ALO treatments significantly shifted the I-V curve down without changes in the curve shape. Specifically, the curve moved toward the positive direction of the current axis, with the current density exhibiting a significant increase at different membrane potentials (particularly at 70&#xa0;mV).</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>I-V curve recordings of I<sub>to</sub> (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements). <bold>(A)</bold> I-V traces recorded before and after the administration of ALO. <bold>(B)</bold> Effects of ALO on I<sub>to</sub> current density under different voltages. Values are presented as mean &#xb1; SD. &#x2a;<italic>p</italic> &#x3c; 0.05, &#x2a;&#x2a;<italic>p</italic> &#x3c; 0.01 vs. the control.</p>
</caption>
<graphic xlink:href="fphar-15-1372973-g002.tif"/>
</fig>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Effects of ALO on the activation gated-kinetic characteristics of I<sub>to</sub> (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements). Values are presented as mean &#xb1; SDs (<italic>n</italic> &#x3d; 6). &#x2a;<italic>p</italic> &#x3c; 0.05, &#x2a;&#x2a;<italic>p</italic> &#x3c; 0.01 vs. the control.</p>
</caption>
<graphic xlink:href="fphar-15-1372973-g003.tif"/>
</fig>
</sec>
<sec id="s3-3">
<title>3.3 Effect of ALO on I<sub>to</sub> activation curves</title>
<p>To investigate the relationship between the inhibitory effect of ALO on I<sub>to</sub> and the activation state of voltage-gated potassium channels, we fitted the activation curve based on the relevant data from the I-V curves. This allowed us to assess the impact of ALO on activation kinetics curves. As presented in <xref ref-type="fig" rid="F3">Figure 3</xref>, various concentrations of ALO induced a shift in the activation curve of I<sub>to</sub> in a positive direction. Particularly, the administration of 3 and 10&#xa0;&#x3bc;M ALO in an increase in the V<sub>1/2-ac</sub> value from 12.58 &#xb1; 1.70&#xa0;mV (pre-administration) to 19.48 &#xb1; 1.74 and 37.55 &#xb1; 1.67&#xa0;mV (data from double determinations in n &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements; <italic>p</italic> &#x3c; 0.01 vs. control), respectively. Furthermore, the slope (&#x3ba;) values were 16.73 &#xb1; 1.76 (pre-administration), 18.79 &#xb1; 1.88 (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements; <italic>p</italic> &#x3e; 0.05 vs. control), and 30.17 &#xb1; 1.72 (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of n &#x3d; 6 measurements; <italic>p</italic> &#x3c; 0.01 vs. control). Consequently, ALO slowed the activation of I<sub>to</sub>, thus blocking the opening of the potassium channel.</p>
</sec>
<sec id="s3-4">
<title>3.4 Effect of ALO on I<sub>to</sub> inactivation curves</title>
<p>To test the relationship between ALO and the inactivation state in the gating dynamics characteristics, the stimulus protocols were as follows: the condition pulse was gradually depolarized from &#x2212;120 mV to 30&#xa0;mV in 10&#xa0;mV increments for 1,000&#xa0;ms at a holding potential of &#x2212;80&#xa0;mV, and a test pulse was set to 70&#xa0;mV for 300&#xa0;ms. The currents before and after ALO administration were induced by the double-pulse stimulation (<xref ref-type="fig" rid="F4">Figure 4A</xref>). The steady-state inactivation curve was fitted using the Boltzmann equation <inline-formula id="inf1">
<mml:math id="m1">
<mml:mrow>
<mml:mfenced open="(" close=")" separators="|">
<mml:mrow>
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<mml:mi>max</mml:mi>
</mml:msub>
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<mml:mrow>
<mml:mi mathvariant="normal">V</mml:mi>
<mml:mo>&#x2212;</mml:mo>
<mml:msub>
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<mml:mrow>
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<mml:mo>/</mml:mo>
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</mml:mrow>
</mml:mfenced>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:mfenced>
</mml:mrow>
</mml:mrow>
<mml:mtext>&#x2009;</mml:mtext>
<mml:mo>;</mml:mo>
<mml:mtext>&#x2009;Eq</mml:mtext>
<mml:mo>.</mml:mo>
<mml:mtext>&#x2009;</mml:mtext>
<mml:mn>1</mml:mn>
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</mml:mrow>
</mml:math>
</inline-formula>, where V<sub>1/2</sub> indicates the potential corresponding to the half-maximal inactivation point and &#x3ba; represents the slope factor. As presented in <xref ref-type="fig" rid="F4">Figure 4B</xref>, 10&#xa0;&#x3bc;M ALO significantly shifted the inactivation curve of I<sub>to</sub> to the left in the direction of hyperpolarization, whereas 3&#xa0;&#x3bc;M ALO resulted in no obvious changes compared to the control group. The V<sub>1/2-in</sub> values before and after the administration of ALO were changed from &#x2212;46.62 &#xb1; 1.94&#xa0;mV (pre-administration) to &#x2212;48.74 &#xb1; 1.09&#xa0;mV (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of n &#x3d; 6 measurements; <italic>p</italic> &#x3e; 0.05 vs. control) and &#x2212;65.56 &#xb1; 1.02&#xa0;mV (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements; <italic>p</italic> &#x3c; 0.01 vs. control), respectively. Moreover, the &#x3ba; values were 15.86 &#xb1; 0.87 (pre-administration), 15.90 &#xb1; 1.07 (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements; <italic>p</italic> &#x3e; 0.05 vs. control), and 29.83 &#xb1; 1.97 (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements; <italic>p</italic> &#x3c; 0.01 vs. control), respectively. These results reveal that the steady-state inactivation process was only affected by 10&#xa0;&#x3bc;M ALO.</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>Effects of ALO before and after administration on the inactivation curve (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements). <bold>(A)</bold> Original traces of I<sub>to</sub> recorded in the presence or absence of ALO. <bold>(B)</bold> Steady-state inactivation dynamic characteristics for control and after 3 and 10&#xa0;&#x3bc;M ALO treatments. Data are provided as the mean &#xb1; SDs (<italic>n</italic> &#x3d; 6). &#x2a;<italic>p</italic> &#x3c; 0.05, &#x2a;<italic>p</italic> &#x3c; 0.01 vs. the control.</p>
</caption>
<graphic xlink:href="fphar-15-1372973-g004.tif"/>
</fig>
</sec>
<sec id="s3-5">
<title>3.5 Effects of ALO on the recovery curve after inactivation of I<sub>to</sub>
</title>
<p>The steady-state recovery curves after inactivation were acquired <italic>via</italic> the double pulse voltage protocol as follows: Initially, a holding potential of &#x2212;80&#xa0;mV was maintained, followed by a depolarization to 70&#xa0;mV stimulus for 200&#xa0;ms. Subsequently, repolarization to 70&#xa0;mV for 200&#xa0;ms was conducted, and the interval time between two pulses was gradually increased by 50&#xa0;ms for a total of 20 pulses. The original current of the curve before and after ALO administration was documented (<xref ref-type="fig" rid="F5">Figure 5A</xref>), and it is provided in <xref ref-type="fig" rid="F5">Figure 5B</xref>. The steady-state recovery curves after inactivation of I<sub>to</sub> were fitted by the one-phase association equation described as <inline-formula id="inf2">
<mml:math id="m2">
<mml:mrow>
<mml:mi mathvariant="normal">I</mml:mi>
<mml:mo>/</mml:mo>
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<mml:mo>/</mml:mo>
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</mml:math>
</inline-formula>, where t represents the time interval between two pulses and &#x3c4; is the time constant of reactivation after inactivation. Thereafter, the &#x3c4; value was changed from 43.51 &#xb1; 3.06&#xa0;ms under control conditions to 56.73 &#xb1; 3.03&#xa0;ms in response to 3&#xa0;&#x3bc;M ALO (n &#x3d; 6; <italic>p</italic> &#x3c; 0.05 vs. control) and 65.93 &#xb1; 3.55&#xa0;ms in response to 10&#xa0;&#x3bc;M ALO (<italic>n</italic> &#x3d; 6; <italic>p</italic> &#x3c; 0.01 vs. control). The results indicated that 3 and 10&#xa0;&#x3bc;M ALO significantly inhibited I<sub>to</sub> by affecting the recovery kinetic characteristics after inactivation and prolonging the recovery time after inactivation.</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>Effects of ALO on the I<sub>to</sub> recovery curve after inactivation in atrial myocytes (data from double determinations in <italic>n</italic> &#x3d; 3 rats, representing a total of <italic>n</italic> &#x3d; 6 measurements). <bold>(A)</bold> Original traces in control and in response to 3 or 10&#xa0;&#x3bc;M ALO. <bold>(B)</bold> Kinetic characteristics of the recovery curve after inactivation were analyzed in both control conditions and in response to ALO (3 or 10&#xa0;&#x3bc;M). Values are presented as mean &#xb1; SD. &#x2a;<italic>p</italic> &#x3c; 0.05, &#x2a;&#x2a;<italic>p</italic> &#x3c; 0.01 vs. the control.</p>
</caption>
<graphic xlink:href="fphar-15-1372973-g005.tif"/>
</fig>
</sec>
<sec id="s3-6">
<title>3.6 Effect of ALO on the ECG of rats with AF</title>
<p>The representative ECGs in rats are presented in <xref ref-type="fig" rid="F6">Figure 6</xref>. The control group exhibited a normal ECG. Varying RR intervals, the appearance of f waves, and the disappearance of p waves are considered indicators of AF onset, while the disappearance of f waves and the appearance of p waves are considered indicators of AF termination. AF models were successfully established in other groups. The induction rate of AF in model group is greater than 80%. Compared to the model group, pretreatment with amiodarone and ALO prolonged the induction time of AF and reduced the duration of AF in the animal models, as shown in <xref ref-type="table" rid="T2">Table 2</xref>.</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption>
<p>Representative ECG recordings, from a normal rat <bold>(A)</bold>, and of an AF rat <bold>(B)</bold>.</p>
</caption>
<graphic xlink:href="fphar-15-1372973-g006.tif"/>
</fig>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Induction and duration time of AF among rats in each group.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Group</th>
<th align="left">Induction time of AF/s</th>
<th align="left">Duration of AF/s</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">control</td>
<td align="left">-</td>
<td align="left">-</td>
</tr>
<tr>
<td align="left">model</td>
<td align="left">4.64 &#xb1; 1.25</td>
<td align="left">7.64 &#xb1; 1.05</td>
</tr>
<tr>
<td align="left">amiodarone</td>
<td align="left">8.65 &#xb1; 1.13&#x2a;</td>
<td align="left">3.25 &#xb1; 1.02&#x2a;</td>
</tr>
<tr>
<td align="left">ALO</td>
<td align="left">6.75 &#xb1; 1.32&#x2a;</td>
<td align="left">5.73 &#xb1; 0.87&#x2a;</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>&#x2a;<italic>p</italic> &#x3c; 0.05 vs. the model.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3-7">
<title>3.7 Docking results</title>
<p>XP docking results should be interpreted based on the XP Gscore. Typically, a value below &#x2212;6 is considered indicative of stable binding performance between the ligand and the protein. MM-GBSA analysis results should be referred to as MM-GBSA dG Bind, and when this value is below &#x2212;30&#xa0;kcal/mol, it suggests low binding free energy and indicates a stable binding between the ligand and the protein. The docking score of ALO with KCND2 is &#x2212;3.990, and the MM-GBSA dG Bind result is &#x2212;30.68&#xa0;kcal/mol, thus indicating stable binding. In contrast, the docking scores of ALO with KCND3 and KCNIP4 are &#x2212;2.106 and &#x2212;5.339, with MM-GBSA dG Bind results of &#x2212;10.67 and &#x2212;7.2&#xa0;kcal/mol, respectively. The higher binding free energy suggests fewer stable interactions of ALO with these two proteins. Additionally, the docking score of amiodarone with KCND2 is &#x2212;1.75, and the MM-GBSA result is &#x2212;35.26&#xa0;kcal/mol. Despite the low binding free energy, the high docking score suggests a low likelihood of binding between amiodarone and KCND2, but the stability after binding may still be substantial. The docking scores of amiodarone with KCND3 and KCNIP4 are &#x2212;5.363 and &#x2212;3.004, respectively, with MM-GBSA results of &#x2212;23.67 and &#x2212;27.66&#xa0;kcal/mol. Both the binding free energy and docking scores are relatively low, thus indicating a stable binding of amiodarone with these two proteins. The results of the molecular docking assessments are presented in <xref ref-type="table" rid="T3">Table 3</xref> and <xref ref-type="fig" rid="F7">Figure 7</xref>.</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Molecular docking results.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Compound</th>
<th align="center">Target</th>
<th align="center">XP Gscore</th>
<th align="center">MM-GBSA dG Bind(kcal/mol)</th>
<th align="center">Hydrophobic interaction</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">ALO</td>
<td rowspan="2" align="center">KCND2</td>
<td align="center">&#x2212;3.990</td>
<td align="center">&#x2212;30.68</td>
<td align="center">ILE128, PRO126, ILE125, LEU124</td>
</tr>
<tr>
<td align="center">Amiodarone</td>
<td align="center">&#x2212;1.750</td>
<td align="center">&#x2212;35.26</td>
<td align="center">LEU124&#x3001;ILE125&#x3001;PRO126&#x3001;ILE128&#x3001;PRO63</td>
</tr>
<tr>
<td align="center">ALO</td>
<td rowspan="2" align="center">KCND3</td>
<td align="center">&#x2212;2.106</td>
<td align="center">&#x2212;10.67</td>
<td align="center">TYR105, PRO106, CYS132</td>
</tr>
<tr>
<td align="center">Amiodarone</td>
<td align="center">&#x2212;5.363</td>
<td align="center">&#x2212;23.67</td>
<td align="center">TYR108&#x3001;TYR132</td>
</tr>
<tr>
<td align="center">ALO</td>
<td rowspan="2" align="center">KCNIP4</td>
<td align="center">&#x2212;5.339</td>
<td align="center">&#x2212;7.20</td>
<td align="center">PHE115, TYR112, PHE108, PHE94, LEU40</td>
</tr>
<tr>
<td align="center">Amiodarone</td>
<td align="center">&#x2212;3.004</td>
<td align="center">&#x2212;27.66</td>
<td align="center">LEU41&#x3001;LEU153&#x3001;MET38</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>Molecular docking between ALO and the three proteins (KCND2, KCND3, and KCNIP4) based on crystal structures: <bold>(A)</bold>. The ligand forms a salt bridge with the residue ASP64; <bold>(B)</bold>. The ligand forms a &#x3c0;-cation bond with the residue HIE104; <bold>(C)</bold>. KCNIP4. Molecular docking between amiodarone and the three proteins (KCND2, KCND3, and KCNIP4) based on crystal structures: <bold>(D)</bold>. The ligand forms a &#x3c0;-&#x3c0; bond with the residue TYR62; <bold>(E)</bold>. The ligand forms two &#x3c0;-&#x3c0; bonds with the residue HIE104 and a halogen bond with the residue ARG92; <bold>(F)</bold>. The ligand forms a &#x3c0;-cation bond with the residue ARG154 and a hydrogen bond with a salt bridge with the GLU86 residue.</p>
</caption>
<graphic xlink:href="fphar-15-1372973-g007.tif"/>
</fig>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>4 Discussion</title>
<p>AF often leads to high disability and mortality rates, as well as complications such as stroke and heart failure, imposing significant economic burdens on society (<xref ref-type="bibr" rid="B23">Varr&#xf3; et al., 2021</xref>). It is currently a serious cardiovascular disease that seriously endangers public health. Kv channels, crucial for cardiac electrical activity, primarily influence the repolarization process of AP and contribute significantly to excitation-contraction coupling and arrhythmias (<xref ref-type="bibr" rid="B31">Zhang et al., 2006</xref>; <xref ref-type="bibr" rid="B1">Amin et al., 2010</xref>). Inhibiting I<sub>to</sub> can prolong APD, reduce ventricular prematureness, halt phase 2 re-entry, and ultimately prevent the occurrence of ventricular tachycardia and fibrillation (<xref ref-type="bibr" rid="B17">Marquez et al., 2007</xref>). Moreover, alterations in the current amplitude and dynamic properties of I<sub>to</sub> indirectly influence the activation and inactivation of other ion channels, consequently impacting the AP shape, APD, and ERP. Therefore, I<sub>to</sub> is an important current that controls the AP in myocardial cells. Repolarization is governed by a delicate balance of various inward and outward transmembrane ionic currents, along with electrogenic pump mechanisms. Repolarization reserve plays a crucial role in elucidating the pathogenesis of arrhythmias stemming from repolarization abnormalities and drug-induced proarrhythmic adverse effects (<xref ref-type="bibr" rid="B22">Varr&#xf3; and Baczk&#xf3;, 2011</xref>; <xref ref-type="bibr" rid="B24">Vir&#xe1;g et al., 2011</xref>). Understanding the impact of I<sub>to</sub> inhibition on patients with impaired repolarization reserve is essential for elucidating the mechanisms underlying arrhythmias and guiding potential therapeutic interventions. In a study, inhibiting I<sub>to</sub> in cases of impaired repolarization reserve may lead to excessive prolongation of repolarization, resulting in the formation of early afterdepolarizations, thereby increasing the risk of arrhythmias (<xref ref-type="bibr" rid="B22">Varr&#xf3; and Baczk&#xf3;, 2011</xref>). An increase in I<sub>to</sub> is the mechanism that causes Brugada syndrome and early repolarization syndrome. Excessive inhibition or an increase in I<sub>to</sub> may induce abnormal changes in the channel, ultimately resulting in cardiovascular disease. In our experiment, we utilized 3 and 10&#xa0;&#x3bc;M ALO, without employing higher concentrations. In our current study, 10&#xa0;&#xb5;M of ALO inhibited I<sub>to</sub>, suggesting its ability to block transient outward potassium channels. However, as the concentration increased to 30 and 100&#xa0;&#x3bc;M, we noted an increasing trend in I<sub>to</sub> (pA/pF). This result may stem from the complex mechanisms of action of ALO on ion channels. At higher doses, ALO may interact with other cellular components or pathways that counteract its effects on I<sub>to</sub>, or it may produce other effects on cellular electrophysiology. This change may be attributed to the concentration-dependent effects of ALO, where its selectivity or affinity for ion channels may vary at different concentrations. Additionally, another possibility is that at higher concentrations, ALO may saturate its target binding sites, leading to a plateau effect on I<sub>to</sub> inhibition. The combined effects of these factors may result in the observed increasing trend in I<sub>to</sub> at concentrations of 30 and 100&#xa0;&#xb5;M. Further research is needed to elucidate the detailed molecular mechanisms.</p>
<p>Our data indicate that 3 and 10&#xa0;&#x3bc;M ALO treatments inhibited the current density of I<sub>to</sub>. The gated kinetics analyses revealed that ALO decreased the I<sub>to</sub> current density, possibly by decelerating the steady-state activation process of the channel and shifting the half-activation voltage to a positive value. This indicates a reduction in the opening of the channel under the same depolarization voltage stimulation. Additionally, ALO accelerated the inactivation of I<sub>to</sub>, shifted the inactivation curve to the left, and extended the recovery time after steady-state inactivation. This caused the recovery curve to move to the right, and this slowed down the recovery process from the inactive state. Hence, the antiarrhythmic mechanism of ALO might be elucidated by its inhibition of I<sub>to</sub> in a concentration-dependent manner, which impacts the processes of steady-state activation, inactivation, and recovery after inactivation.</p>
<p>Acetylcholine exposure increases the opening of the acetylcholine-sensitive potassium channel (IK-Ach) in the atrium, leading to a notable enhancement in the potassium outflow current intensity. This results in the shortening of atrial repolarization time and action potential duration (APD), subsequently shortening the effective inactivity period, and contributing to fold formation, and further promoting AF (<xref ref-type="bibr" rid="B18">Moss et al., 2018</xref>). Moreover, acetylcholine can diminish sinoatrial node autoregulation by activating M receptors, resulting in a relative increase in atrial potential pacing point autoregulation, thereby contributing to folding and AF formation. Calcium chloride increases inward Ca<sup>2&#x2b;</sup> flow during the phase 2 plateau, thus leading to shortened ERP and APD and facilitating easier maintenance of AF (<xref ref-type="bibr" rid="B11">Li et al., 2018</xref>; <xref ref-type="bibr" rid="B5">Fan et al., 2023</xref>). The administration of ALO prolonged the induction time of AF and shortened the duration of AF in rats. The results for the <italic>in vivo</italic> ECG parameters revealed that ALO may prevent acetylcholine-induced AF in rats. The principle of clinical drug administration is to administer the drug as sparingly as possible to achieve therapeutic effects, ensuring optimal dosage, maximizing its protective effects, and minimizing side effects. The blood concentration of a drug serves as a measure of its concentration in the body and is directly linked to the efficacy and toxicity of the drug. A LC-MS/MS method was effectively developed and validated to quantitatively measure ALO in rat plasma with speed and sensitivity, demonstrating its suitability for investigating ALO pharmacokinetics. The method unveiled a relatively high oral bioavailability of 44.87% following both oral and intravenous administrations (<xref ref-type="bibr" rid="B7">Huang et al., 2021</xref>).</p>
<p>Although the mechanism of AF induced by calcium chloride and acetylcholine is clearly understood, additional arrhythmias and abnormal electrocardiographic phenomena have been observed in AF animal models. Further studies are required to determine if calcium chloride and acetylcholine play a role in these processes (<xref ref-type="bibr" rid="B2">Bayer et al., 2019</xref>). In addition to atria, calcium chloride and acetylcholine can act on the ventricular muscle, particularly calcium chloride (<xref ref-type="bibr" rid="B19">Murray et al., 2022</xref>). The transient atrioventricular block after administration that lasts &#x3c;1&#xa0;min is associated with an atrioventricular conduction disturbance caused by acetylcholine that disappears naturally after acetylcholine is hemodiluted and metabolized. Overloaded intracellular calcium leads to myocardial cell damage resulting in conduction disturbances in the ventricular myocardium, delayed post-depolarization leading to increased autoregulation at ectopic rhythm points, and increased Ca<sup>2&#x2b;</sup> inward flow that leads to shortened ERP and APD and forms the basis for all types of ventricular tachycardia (<xref ref-type="bibr" rid="B27">Wleklinski et al., 2020</xref>). Myocardial conduction disturbances results in heterogeneous myocardial repolarization and increased dispersion of myocardial repolarization across the wall, which may be associated with QRS-T-wave electrical alternations. Polymorphic ventricular premature beats can occur due to increased autoregulation and shortened effective inactivity at ectopic rhythm points. When ventricular premature beats occur late, the atria cannot be excited by retrograde transmission, but can be excited by the sinoatrial node. As a result, normal P waves may be observed earlier in the ventricle.</p>
<p>Kv4.2 (encoded by <italic>KCND2</italic>) is a predominant transient outward potassium channel. In the molecular docking stimulation, ALO binds to the surface of the active pocket of the <italic>KCND2</italic> protein, forming hydrophobic interactions with residues ILE128, PRO126, ILE125, and LEU124 of the Kcnd2 protein. Additionally, this ligand formed a salt bridge with residue ASP64. ALO binds to the active pocket surfaces of both KCND3 and KCNIP4 proteins, but the interactions are relatively unstable. The results of molecular docking experiments revealed that ALO could stably bind to the KCND2 protein. These results provide a rational explanation for how ALO affects cardiomyocyte I<sub>to</sub> gating kinetics.</p>
<p>However, it is important to acknowledge the limitations of our study. Cardiac potassium channels are classified into transient outward, delayed rectifier outward, and inward rectifier currents. Our investigation primarily focused on the inhibitory effects of ALO on I<sub>to</sub> in rat ventricular myocytes and did not explore its potential effects on other potassium ion channels or cardiac electrophysiological parameters. Future comprehensive studies, including both basic research and clinical trials, are needed to provide more robust evidence.</p>
<p>In conclusion, ALO regulates I<sub>to</sub> by reducing the current densities of I<sub>to</sub> and affecting the channel gating kinetic characteristics to stabilize the cardiac repolarization process and reduce the risk of arrhythmias.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s5">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec id="s6">
<title>Ethics statement</title>
<p>The animal study was approved by the Institutional Animal Care and Ethics Committee of Medicine School of Yangzhou University. The study was conducted in accordance with the local legislation and institutional requirements.</p>
</sec>
<sec id="s7">
<title>Author contributions</title>
<p>X-ND: Funding acquisition, Investigation, Software, Validation, Visualization, Writing&#x2013;review and editing. M-TL: Conceptualization, Data curation, Investigation, Writing&#x2013;original draft.</p>
</sec>
<sec sec-type="funding-information" id="s8">
<title>Funding</title>
<p>The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.</p>
</sec>
<ack>
<p>We thank the Center of Pharmaceutical Technology of Tsinghua University for the support of Schrodinger software and molecular docking. We would like to thank Editage (<ext-link ext-link-type="uri" xlink:href="http://www.editage.cn">www.editage.cn</ext-link>) for English language editing.</p>
</ack>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s10">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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