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Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice

Changes in intracellular calcium levels in the sinus node modulate cardiac pacemaking (the calcium clock). Trimeric intracellular cation (TRIC) channels are counterion channels on the surface of the sarcoplasmic reticulum and compensate for calcium release from ryanodine receptors, which play a majo...

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Autores principales: Murakami, Manabu, Toyama, Yuichi, Yonekura, Manabu, Ohba, Takayoshi, Matsuzaki, Yasushi, Sawamura, Daisuke, Murakami, Agnieszka M., Nishi, Miyuki, Itagaki, Shirou, Tomita, Hirofumi, Takeshima, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751866/
https://www.ncbi.nlm.nih.gov/pubmed/33347504
http://dx.doi.org/10.1371/journal.pone.0244254
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author Murakami, Manabu
Toyama, Yuichi
Yonekura, Manabu
Ohba, Takayoshi
Matsuzaki, Yasushi
Sawamura, Daisuke
Murakami, Agnieszka M.
Nishi, Miyuki
Itagaki, Shirou
Tomita, Hirofumi
Takeshima, Hiroshi
author_facet Murakami, Manabu
Toyama, Yuichi
Yonekura, Manabu
Ohba, Takayoshi
Matsuzaki, Yasushi
Sawamura, Daisuke
Murakami, Agnieszka M.
Nishi, Miyuki
Itagaki, Shirou
Tomita, Hirofumi
Takeshima, Hiroshi
author_sort Murakami, Manabu
collection PubMed
description Changes in intracellular calcium levels in the sinus node modulate cardiac pacemaking (the calcium clock). Trimeric intracellular cation (TRIC) channels are counterion channels on the surface of the sarcoplasmic reticulum and compensate for calcium release from ryanodine receptors, which play a major role in calcium-induced calcium release (CICR) and the calcium clock. TRIC channels are expected to affect the calcium clock in the sinus node. However, their physiological importance in cardiac rhythm formation remains unclear. We evaluated the importance of TRIC channels on cardiac pacemaking using TRIC-A-null (TRIC-A(–/–)) as well as TRIC-B(+/–)mice. Although systolic blood pressure (SBP) was not significantly different between wild-type (WT), TRIC-B(+/–), and TRIC-A(–/–)mice, heart rate (HR) was significantly lower in TRIC-A(–/–)mice than other lines. Interestingly, HR and SBP showed a positive correlation in WT and TRIC-B(+/–)mice, while no such correlation was observed in TRIC-A(–/–)mice, suggesting modification of the blood pressure regulatory system in these mice. Isoproterenol (0.3 mg/kg) increased the HR in WT mice (98.8 ± 15.1 bpm), whereas a decreased response in HR was observed in TRIC-A(–/–)mice (23.8 ± 5.8 bpm), suggesting decreased sympathetic responses in TRIC-A(–/–)mice. Electrocardiography revealed unstable R-R intervals in TRIC-A(–/–)mice. Furthermore, TRIC-A(–/–)mice sometimes showed sinus pauses, suggesting a significant role of TRIC-A channels in cardiac pacemaking. In isolated atrium contraction or action potential recording, TRIC-A(–/–)mice showed decreased response to a β-adrenergic sympathetic nerve agonist (isoproterenol, 100 nM), indicating decreased sympathetic responses. In summary, TRIC-A(–/–)mice showed decreased cardiac pacemaking in the sinus node and attenuated responses to β-adrenergic stimulation, indicating the involvement of TRIC-A channels in cardiac rhythm formation and decreased sympathetic responses.
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spelling pubmed-77518662021-01-05 Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice Murakami, Manabu Toyama, Yuichi Yonekura, Manabu Ohba, Takayoshi Matsuzaki, Yasushi Sawamura, Daisuke Murakami, Agnieszka M. Nishi, Miyuki Itagaki, Shirou Tomita, Hirofumi Takeshima, Hiroshi PLoS One Research Article Changes in intracellular calcium levels in the sinus node modulate cardiac pacemaking (the calcium clock). Trimeric intracellular cation (TRIC) channels are counterion channels on the surface of the sarcoplasmic reticulum and compensate for calcium release from ryanodine receptors, which play a major role in calcium-induced calcium release (CICR) and the calcium clock. TRIC channels are expected to affect the calcium clock in the sinus node. However, their physiological importance in cardiac rhythm formation remains unclear. We evaluated the importance of TRIC channels on cardiac pacemaking using TRIC-A-null (TRIC-A(–/–)) as well as TRIC-B(+/–)mice. Although systolic blood pressure (SBP) was not significantly different between wild-type (WT), TRIC-B(+/–), and TRIC-A(–/–)mice, heart rate (HR) was significantly lower in TRIC-A(–/–)mice than other lines. Interestingly, HR and SBP showed a positive correlation in WT and TRIC-B(+/–)mice, while no such correlation was observed in TRIC-A(–/–)mice, suggesting modification of the blood pressure regulatory system in these mice. Isoproterenol (0.3 mg/kg) increased the HR in WT mice (98.8 ± 15.1 bpm), whereas a decreased response in HR was observed in TRIC-A(–/–)mice (23.8 ± 5.8 bpm), suggesting decreased sympathetic responses in TRIC-A(–/–)mice. Electrocardiography revealed unstable R-R intervals in TRIC-A(–/–)mice. Furthermore, TRIC-A(–/–)mice sometimes showed sinus pauses, suggesting a significant role of TRIC-A channels in cardiac pacemaking. In isolated atrium contraction or action potential recording, TRIC-A(–/–)mice showed decreased response to a β-adrenergic sympathetic nerve agonist (isoproterenol, 100 nM), indicating decreased sympathetic responses. In summary, TRIC-A(–/–)mice showed decreased cardiac pacemaking in the sinus node and attenuated responses to β-adrenergic stimulation, indicating the involvement of TRIC-A channels in cardiac rhythm formation and decreased sympathetic responses. Public Library of Science 2020-12-21 /pmc/articles/PMC7751866/ /pubmed/33347504 http://dx.doi.org/10.1371/journal.pone.0244254 Text en © 2020 Murakami et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Murakami, Manabu
Toyama, Yuichi
Yonekura, Manabu
Ohba, Takayoshi
Matsuzaki, Yasushi
Sawamura, Daisuke
Murakami, Agnieszka M.
Nishi, Miyuki
Itagaki, Shirou
Tomita, Hirofumi
Takeshima, Hiroshi
Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice
title Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice
title_full Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice
title_fullStr Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice
title_full_unstemmed Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice
title_short Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice
title_sort decreased cardiac pacemaking and attenuated β-adrenergic response in tric-a knockout mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751866/
https://www.ncbi.nlm.nih.gov/pubmed/33347504
http://dx.doi.org/10.1371/journal.pone.0244254
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