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    <subfield code="2">doi</subfield>
    <subfield code="a">10.3389/fphys.2023.1189464</subfield>
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    <subfield code="a">ART-2023-137382</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Celotto, Chiara</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">The frequency of atrial fibrillatory waves is modulated by the spatiotemporal pattern of acetylcholine release: a 3D computational study</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2023</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">In atrial fibrillation (AF), the ECG P-wave, which represents atrial depolarization, is replaced with chaotic and irregular fibrillation waves (f waves). The f-wave frequency, Ff, shows significant variations over time. Cardiorespiratory interactions regulated by the autonomic nervous system have been suggested to play a role in such variations. We conducted a simulation study to test whether the spatiotemporal release pattern of the parasympathetic neurotransmitter acetylcholine (ACh) modulates the frequency of atrial reentrant circuits. Understanding parasympathetic involvement in AF may guide more effective treatment approaches and could help to design autonomic markers alternative to heart rate variability (HRV), which is not available in AF patients. 2D tissue and 3D whole-atria models of human atrial electrophysiology in persistent AF were built. Different ACh release percentages (8% and 30%) and spatial ACh release patterns, including spatially random release and release from ganglionated plexi (GPs) and associated nerves, were considered. The temporal pattern of ACh release, ACh(t), was simulated following a sinusoidal waveform of frequency 0.125 Hz to represent the respiratory frequency. Different mean concentrations (ACh̄) and peak-to-peak ranges of ACh (ΔACh) were tested. We found that temporal variations in Ff, Ff(t), followed the simulated temporal ACh(t) pattern in all cases. The temporal mean of Ff(t), F̄f, depended on the fibrillatory pattern (number and location of rotors), the percentage of ACh release nodes and ACh̄. The magnitude of Ff(t) modulation, ΔFf, depended on the percentage of ACh release nodes and ΔACh. The spatial pattern of ACh release did not have an impact on F̄f and only a mild impact on ΔFf. The f-wave frequency, being indicative of vagal activity, has the potential to drive autonomic-based therapeutic actions and could replace HRV markers not quantifiable from AF patients.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/LMP141-21</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/LMP94_21</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/T39-23R</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/766082/EU/MultidisciplinarY training network for ATrial fibRillation monItoring, treAtment and progression/MY-ATRIA</subfield>
    <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 766082-MY-ATRIA</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/PID2019-104881RB-I00</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/PID2019-105674RB-I00</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/PID2022-140556OB-I00</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/EUR/MICINN/TED2021-130459B-I00</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">by</subfield>
    <subfield code="u">http://creativecommons.org/licenses/by/3.0/es/</subfield>
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    <subfield code="a">PHYSIOLOGY</subfield>
    <subfield code="b">24 / 85 = 0.282</subfield>
    <subfield code="c">2023</subfield>
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    <subfield code="a">Physiology (medical)</subfield>
    <subfield code="c">2023</subfield>
    <subfield code="d">Q2</subfield>
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    <subfield code="a">Physiology</subfield>
    <subfield code="c">2023</subfield>
    <subfield code="d">Q2</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sánchez, Carlos</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-4273-5403</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Abdollahpur, Mostafa</subfield>
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    <subfield code="a">Sandberg, Frida</subfield>
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    <subfield code="a">Rodriguez Matas, Jose F.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Laguna, Pablo</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3434-9254</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Pueyo, Esther</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1960-407X</subfield>
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    <subfield code="1">5007</subfield>
    <subfield code="2">520</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Informát.Ingenie.Sistms.</subfield>
    <subfield code="c">Área Ingen.Sistemas y Automát.</subfield>
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    <subfield code="1">5008</subfield>
    <subfield code="2">800</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Ingeniería Electrón.Com.</subfield>
    <subfield code="c">Área Teoría Señal y Comunicac.</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">14 (2023), [18 pp.]</subfield>
    <subfield code="p">Front. physiol.</subfield>
    <subfield code="t">Frontiers in physiology</subfield>
    <subfield code="x">1664-042X</subfield>
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    <subfield code="s">668505</subfield>
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    <subfield code="a">2024-11-22-12:08:27</subfield>
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