COMPARATIVE EVALUATION OF THE ANTI-EXUDATIVE ACTIVITY OF BETTA-ESCINAND «ESCUZAN® PREPARATIONS IN EXPERIMENTAL PROLONGED COMPRESSION SYNDROME (SDS, CRASH SYNDROME) IN LABORATORY RATS.
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Keywords

Aesculus hippocastanum L.
Betta-Escin
herbal medicine

How to Cite

Makhmaraimov, S., Allayeva, M., & Achilov, D. (2024). COMPARATIVE EVALUATION OF THE ANTI-EXUDATIVE ACTIVITY OF BETTA-ESCINAND «ESCUZAN® PREPARATIONS IN EXPERIMENTAL PROLONGED COMPRESSION SYNDROME (SDS, CRASH SYNDROME) IN LABORATORY RATS. JOURNAL OF EDUCATION AND SCIENTIFIC MEDICINE, 1(6), 101-105. Retrieved from https://mail.journals.tma.uz/index.php/jesm/article/view/964

Abstract

Background. The study highlights the anti-inflammatory and anti-exudative effects of preparations derived from Aesculus hippocastanum L., specifically Escuzan® and Betta-Escin, in treating vascular inflammation in the lower extremities and preventing atherosclerosis. These properties make them promising agents for managing conditions involving vascular damage and inflammation.

Materials. The preparations evaluated were Escuzan® and Betta-Escin. The anti-inflammatory efficacy of these agents was studied in a long-term compression syndrome (DFS) model. The proliferative phase of inflammation was assessed using the Cotton pellet method, with granulation tissue weight in the control group set at 50.4 g ± 0.5 mg (100%) as a baseline.

Results. Betta-Escin demonstrated significant anti-exudative activity, reducing exudation by 32.1%, 38.4%, and 42.1% at doses of 10, 30, and 50 mg/kg, respectively. Comparatively, Escuzan® reduced exudation by 30.2%. In the proliferative phase of inflammation, Betta-Escin reduced inflammatory cell proliferation by 22.3%, 27.2%, and 31.2%, whereas Escuzan® achieved a reduction of 20.8%. Betta-Escin exhibited statistically superior efficacy (P<0.05) in reducing both exudation and inflammatory cell proliferation compared to Escuzan®.

Conclusion. Betta-Escin showed greater efficacy than Escuzan® in reducing exudation and inflammatory cell proliferation in an experimental DFS model. These findings suggest that Betta-Escin is a more effective therapeutic option for managing vascular inflammation and promoting recovery in conditions such as long-term compression syndrome.

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