Abstract

Pulmonary embolism (PE) is the third most common cardiovascular disease. It is still associated with high hospital mortality, as well as with the development of acute and chronic complications. Treatment and prevention of PE and its complications requires high-tech approaches aimed at improving the prognosis of patients. In this regard, experimental studies aimed at studying the pathogenesis, improving diagnostic methods and searching for new pharmacological substances for the prevention and treatment of PE are in demand from the point of view of clinical practice. Considering the current trends in preclinical research, experimental work on rodents — mice, rats, hamsters, as well as on medium-sized laboratory animals (rabbits) is becoming more and more common. The use of these animal species is ethically acceptable and economically viable. The choice of a specific type of animal and a method for modeling PE is primarily determined by the objectives of the study. This article provides an overview of the main approaches to modeling PE, as well as discusses the advantages and disadvantages of each method. Special attention is paid to the modeling of chronic thromboembolic pulmonary hypertension (CTEPH) as one of the most dangerous complications of PE. The work analyzed publications from 1978 to 2020, in which PE was simulated in rodents and medium laboratory animals.

Highlights

  • Лечение и профилактика Тромбоэмболия легочной артерии (ТЭЛА), а также ее осложнений требуют высокотехнологичных подходов, направленных на улучшение прогноза пациентов

  • It is still associated with high hospital mortality

  • its complications requires high-tech approaches aimed at improving the prognosis of patients

Read more

Summary

Introduction

Лечение и профилактика ТЭЛА, а также ее осложнений требуют высокотехнологичных подходов, направленных на улучшение прогноза пациентов. И соавторов [8] для моделирования ТЭЛА у мышей использовалось изолированное внутривенное введение коллагена в дозе 0,075 мкг/г. F. и соавторов [25] для моделирования ТЭЛА на мышах использовали три различных протромботических агента: АДФ в дозе 40 мг/100 г, коллаген в дозе 2,5 мг/100 г или арахидоновая кислота в дозе 9 мг/100 г массы животного.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call