AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATE

Objective: To assess the potential of a new approach to altering the heart rate by expression inhibition of the SCN5A gene, encoding a classical sodium channel, Nav1.5, with an antisense oligonucleotide derivative in the case study of the mouse. Material and methods: C57BL/6J male mice; oligonucleot...

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Main Authors: S. I. Oshevskii, Yu. I. Ragino, E. V. Kashtanova, Yu. V. Polonskaya, E. M. Stakhneva, V. P. Nikolin, N. A. Popova, N. A. Kolchanov, M. I. Voevoda
Format: Article
Language:Russian
Published: Siberian Branch of Russian Academy of Sciences, Research Institute of Internal and Preventive Medicine, branch of the Institute of Cytology and Genetics 2017-06-01
Series:Атеросклероз
Subjects:
Online Access:https://ateroskleroz.elpub.ru/jour/article/view/41/41
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author S. I. Oshevskii
Yu. I. Ragino
E. V. Kashtanova
Yu. V. Polonskaya
E. M. Stakhneva
V. P. Nikolin
N. A. Popova
N. A. Kolchanov
M. I. Voevoda
author_facet S. I. Oshevskii
Yu. I. Ragino
E. V. Kashtanova
Yu. V. Polonskaya
E. M. Stakhneva
V. P. Nikolin
N. A. Popova
N. A. Kolchanov
M. I. Voevoda
author_sort S. I. Oshevskii
collection DOAJ
description Objective: To assess the potential of a new approach to altering the heart rate by expression inhibition of the SCN5A gene, encoding a classical sodium channel, Nav1.5, with an antisense oligonucleotide derivative in the case study of the mouse. Material and methods: C57BL/6J male mice; oligonucleotide derivative with a length of 15 nucleotides protected from nucleases by the presence of internucleotide phosphorothioate bonds and LNA (locked nucleic acids) blocks at the 5ʹ and 3ʹ ends (ASO); standard injection of ASO in physiological saline solution into the mouse caudal vein; standard technique for determination of the heart rate and blood pressure in mice with a CODA Surgical Monitor (Kent Scientific, United States); and standard quantification of apoB apolipoprotein and lipoproteins HDL-C, LDL-C, total cholesterol, TG, and ALT in the blood serum. Results: ASO decreases the heart rate in mice by 12 % over 10 days and further uniformly accelerates the heart rate to almost initial level by day 16 as well as gently decreases the mean values of systolic and diastolic pressures with their subsequent increase and gradual redistribution of “excess” pressure in the control and experimental animal groups. The level of lipid metabolism in experimental animals is decreased. Conclusions: The new approach to alter the heart rate by inhibition of the SCN5A gene expression with an antisense oligonucleotide derivative is shown to be feasible. The impact is accompanied by minor changes in the systolic and diastolic pressures and a decrease in the level of lipid metabolism. The preparation is promising in terms of the influence on the heart rate taking into account the further insight into its effect at different concentrations and possible insignificant side effects.
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spelling doaj.art-7a694bcacb77474e9c1f62a2090332062023-01-03T09:14:59ZrusSiberian Branch of Russian Academy of Sciences, Research Institute of Internal and Preventive Medicine, branch of the Institute of Cytology and GeneticsАтеросклероз2078-256X2017-06-011321217AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATES. I. Oshevskii0Yu. I. Ragino1E. V. Kashtanova2Yu. V. Polonskaya3E. M. Stakhneva4V. P. Nikolin5N. A. Popova6N. A. Kolchanov7M. I. Voevoda8The Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences Russian FederationInstitute of Internal and Preventive Medicine Russian FederationInstitute of Internal and Preventive Medicine Russian FederationInstitute of Internal and Preventive Medicine Russian FederationInstitute of Internal and Preventive Medicine Russian FederationThe Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences Russian FederationThe Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences; National Reseach Novosibirsk State University Russian FederationThe Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences Russian FederationThe Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences; Institute of Internal and Preventive Medicine; National Reseach Novosibirsk State University Russian FederationObjective: To assess the potential of a new approach to altering the heart rate by expression inhibition of the SCN5A gene, encoding a classical sodium channel, Nav1.5, with an antisense oligonucleotide derivative in the case study of the mouse. Material and methods: C57BL/6J male mice; oligonucleotide derivative with a length of 15 nucleotides protected from nucleases by the presence of internucleotide phosphorothioate bonds and LNA (locked nucleic acids) blocks at the 5ʹ and 3ʹ ends (ASO); standard injection of ASO in physiological saline solution into the mouse caudal vein; standard technique for determination of the heart rate and blood pressure in mice with a CODA Surgical Monitor (Kent Scientific, United States); and standard quantification of apoB apolipoprotein and lipoproteins HDL-C, LDL-C, total cholesterol, TG, and ALT in the blood serum. Results: ASO decreases the heart rate in mice by 12 % over 10 days and further uniformly accelerates the heart rate to almost initial level by day 16 as well as gently decreases the mean values of systolic and diastolic pressures with their subsequent increase and gradual redistribution of “excess” pressure in the control and experimental animal groups. The level of lipid metabolism in experimental animals is decreased. Conclusions: The new approach to alter the heart rate by inhibition of the SCN5A gene expression with an antisense oligonucleotide derivative is shown to be feasible. The impact is accompanied by minor changes in the systolic and diastolic pressures and a decrease in the level of lipid metabolism. The preparation is promising in terms of the influence on the heart rate taking into account the further insight into its effect at different concentrations and possible insignificant side effects.https://ateroskleroz.elpub.ru/jour/article/view/41/41antisense oligonucleotide derivativescn5a genec57bl/6j miceheart rate
spellingShingle S. I. Oshevskii
Yu. I. Ragino
E. V. Kashtanova
Yu. V. Polonskaya
E. M. Stakhneva
V. P. Nikolin
N. A. Popova
N. A. Kolchanov
M. I. Voevoda
AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATE
Атеросклероз
antisense oligonucleotide derivative
scn5a gene
c57bl/6j mice
heart rate
title AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATE
title_full AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATE
title_fullStr AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATE
title_full_unstemmed AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATE
title_short AN ANTISENSE OLIGONUCLEOTIDE DERIVATIVE TO THE MRNA OF THE NAV1.5 SODIUM CHANNEL GENE (SCN5A) DECREASES THE HEART RATE
title_sort antisense oligonucleotide derivative to the mrna of the nav1 5 sodium channel gene scn5a decreases the heart rate
topic antisense oligonucleotide derivative
scn5a gene
c57bl/6j mice
heart rate
url https://ateroskleroz.elpub.ru/jour/article/view/41/41
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