2-aminoaethanesulfonic acid compounds possess protective property in reperfusion-induced heart jnjury

Авторы

  • Nikolay A. Kurganov Ogarev Mordovia State University
  • Ekaterina V. Blinova Ogarev Mordovia State University ORCID logo https://orcid.org/0000-0003-0050-0251
  • Elena V. Semeleva Ogarev Mordovia State University
  • Irina A. Gromova Ogarev Mordovia State University
  • Dmirty S. Blinov All-Union Research Center for Safety of Biologically Active Substances ORCID logo https://orcid.org/0000-0002-8385-4356
  • Andrei V. Novikov Ogarev Mordovia State University
  • Julija N. Mashkova Ogarev Mordovia State University
  • Olga V. Vasilkina Ogarev Mordovia State University

DOI:

https://doi.org/10.3897/rrpharmacology.4.27435

Аннотация

The study aim was to explore pharmacological effects of 2-aminoaethansulfonic acid compounds in reperfusion-induced heart injury.

Materials and methods. The study was performed on rats and dogs of both sexes, isolated rats’ hearts. Two compounds of 2-aminoethanesulfonic acid, magnesium-containing (LBK-527) and phenylacetamide-containing (LKhT-317) were investigated. Antiarrhythmic effects of the compounds were studied in coronary artery reperfusion 7, 30 and 120 min after acute myocardial ischemia modeling. The ability of the substances to limit the volume of reperfusion injury was investigated by differential indicator method. The influence of substances on the intensity of free radical processes in the myocardium, as well as the metabolic profile of coronary venous blood during reperfusion, was studied. Hemodynamic effects of the substances were studied during in vivo experiments, as well as on an isolated heart.

Results and discussion. The compounds effectively prevent cardiac arrhythmias generation caused by myocardial reperfusion after 7, 30 and 120 minutes of ischemia. Prophylactic intravenous administration of LHT-317 and LBK-527 at higher therapeutic doses limit the size of rats’ heart necrosis zone after occlusion-reperfusion syndrome develops, prevent reperfusion-induced excessive activation of free-radical processes in rat myocardium, activate the antiradical activity of the heart tissues, and optimize [O2] and [CO2] in coronary venous sinus blood of dogs. Cardioprotective effect of the compounds manifests in preserving myocardium contractile function, maintaing BP and stabilizing heart chronotropic function.

Conclusions. The study analysis shows that 2-aminoethanesulfonic acid compounds have cardioprotective effect in reperfusion syndrome.

Ключевые слова:

ischemic and reperfusion heart injury, 2-aminoaethanesulfonic acid compounds, arrhythmia, hemodynamics, lipid oxidation, metabolic profile, isolated heart

Вклад авторов

Nikolay A. Kurganov, Ogarev Mordovia State University

Postgraduate Student, Department of Intermediate Level Surgery.

Ekaterina V. Blinova, Ogarev Mordovia State University

Doctor of Medical Sciences, Professor, Department of Intermediate Level Surgery.

Elena V. Semeleva, Ogarev Mordovia State University

PhD in Medicine, Associate Professor, Department of Outpatient and Inpatient Therapy with a course in Public Health and Healthcare Organization.

Irina A. Gromova, Ogarev Mordovia State University

Postgraduate Student, Department of Genetics. I.A. Gromova conducted experiments in isolated rats’ hearts.

Dmirty S. Blinov, All-Union Research Center for Safety of Biologically Active Substances

Doctor of Medical Sciences, Senior Researcher, Laboratory of Pharmacology.
Scopus

Andrei V. Novikov, Ogarev Mordovia State University

Postgraduate Student, Department of Intermediate Level Surgery.

Julija N. Mashkova, Ogarev Mordovia State University

PhD in Medicine, Associate Professor, Department of Pharmacology.

Olga V. Vasilkina, Ogarev Mordovia State University

PhD in Medicine, Assistant, Department of Hospital Surgery.

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Опубликован

19.06.2018

Как цитировать

Kurganov NA, Blinova EV, Semeleva EV, Gromova IA, Blinov DS, Novikov AV, Mashkova JN, Vasilkina OV (2018) 2-aminoaethanesulfonic acid compounds possess protective property in reperfusion-induced heart jnjury. Research Results in Pharmacology 4(2): 19–26. https://doi.org/10.3897/rrpharmacology.4.27435

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