A sexy approach to pacemaking: differences in function and molecular make up of the sinoatrial node; Histology and Histopathology; Vol. 34, iss. 11

ग्रंथसूची विवरण
Parent link:Histology and Histopathology
Vol. 34, iss. 11.— 2019.— [P. 1255-1268]
निगमित लेखक: Национальный исследовательский Томский политехнический университет Инженерная школа неразрушающего контроля и безопасности Отделение контроля и диагностики
अन्य लेखक: Doris U. Ursula, Kharche S. R. Sanjay, Petkova M. Maria, Borbas B. Balint, Logantha S. J. R. Sunil Jit, Fedorenko O. Yu. Olga Yurievna, Maczewski M. Michal, Mackiewicz U. Urszula, Zhang Yu., Chahal A. Anwar, D’Souza A. Alicia, Atkinson A. Andrew, Dobrzynski H. Halina, Joseph Ya. Yanni
सारांश:Title screen
Functional properties of the sinoatrial node (SAN) are known to differ between sexes. Women have higher resting and intrinsic heart rates. Sex determines the risk of developing certain arrhythmias such as sick sinus syndrome, which occur more often in women. We believe that a major contributor to these differences is in gender specific ion channel expression. Methods. qPCR was used to compare ion channel gene expression in the SAN and right atrium (RA) between male and female rats. Histology, immunohistochemistry and signal intensity analysis were used to locate the SAN and determine abundance of ion channels. The effect of nifedipine on extracellular potential recording was used to determine differences in beating rate between sexes. Results. mRNAs for Cav1.3, Kir3.1, and Nkx2-5, as well as expression of the L-Type Ca2+ channel protein, were higher in the female SAN. Females had significantly higher intrinsic heart rates and the effect of nifedipine on isolated SAN preparations was significantly greater in male SAN. Computer modelling using a SAN cell model demonstrated a higher propensity of pacemaker-related arrhythmias in females. Conclusion. This study has identified key differences in the expression of Cav1.3, Kir3.1 and Nkx2-5 at mRNA and/or protein levels between male and female SAN. Cav1.3 plays an important role in the pacemaker function of the SAN, therefore the higher intrinsic heart rate of the female SAN could be caused by the higher expression of Cav1.3. The differences identified in this study advance our understanding of sex differences in cardiac electrophysiology and arrhythmias.
भाषा:अंग्रेज़ी
प्रकाशित: 2019
विषय:
ऑनलाइन पहुंच:http://dx.doi.org/10.14670/HH-18-115
स्वरूप: इलेक्ट्रोनिक पुस्तक अध्याय
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=661081

MARC

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200 1 |a A sexy approach to pacemaking: differences in function and molecular make up of the sinoatrial node  |f U. Doris [et al.] 
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300 |a Title screen 
330 |a Functional properties of the sinoatrial node (SAN) are known to differ between sexes. Women have higher resting and intrinsic heart rates. Sex determines the risk of developing certain arrhythmias such as sick sinus syndrome, which occur more often in women. We believe that a major contributor to these differences is in gender specific ion channel expression. Methods. qPCR was used to compare ion channel gene expression in the SAN and right atrium (RA) between male and female rats. Histology, immunohistochemistry and signal intensity analysis were used to locate the SAN and determine abundance of ion channels. The effect of nifedipine on extracellular potential recording was used to determine differences in beating rate between sexes. Results. mRNAs for Cav1.3, Kir3.1, and Nkx2-5, as well as expression of the L-Type Ca2+ channel protein, were higher in the female SAN. Females had significantly higher intrinsic heart rates and the effect of nifedipine on isolated SAN preparations was significantly greater in male SAN. Computer modelling using a SAN cell model demonstrated a higher propensity of pacemaker-related arrhythmias in females. Conclusion. This study has identified key differences in the expression of Cav1.3, Kir3.1 and Nkx2-5 at mRNA and/or protein levels between male and female SAN. Cav1.3 plays an important role in the pacemaker function of the SAN, therefore the higher intrinsic heart rate of the female SAN could be caused by the higher expression of Cav1.3. The differences identified in this study advance our understanding of sex differences in cardiac electrophysiology and arrhythmias. 
461 |t Histology and Histopathology 
463 |t Vol. 34, iss. 11  |v [P. 1255-1268]  |d 2019 
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