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Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study

BACKGROUND/AIM: Ankaferd hemostat (ABS; Ankaferd blood stopper, İstanbul, Turkey) is a prohemostatic agent affecting erythrocytes. The hemostatic action of ABS depends upon fibrinogen gamma chain, prothrombin, and red blood cells. The aim of this study was to assess the effects of ABS on erythrocyte...

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Autores principales: ÇİFTÇİLER, Rafiye, AKSU, Salih, DİKMENOĞLU FALKMARKEN, Neslihan, HAZNEDAROĞLU, Ibrahim Celalettin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350838/
https://www.ncbi.nlm.nih.gov/pubmed/30761848
http://dx.doi.org/10.3906/sag-1808-60
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author ÇİFTÇİLER, Rafiye
AKSU, Salih
DİKMENOĞLU FALKMARKEN, Neslihan
HAZNEDAROĞLU, Ibrahim Celalettin
author_facet ÇİFTÇİLER, Rafiye
AKSU, Salih
DİKMENOĞLU FALKMARKEN, Neslihan
HAZNEDAROĞLU, Ibrahim Celalettin
author_sort ÇİFTÇİLER, Rafiye
collection PubMed
description BACKGROUND/AIM: Ankaferd hemostat (ABS; Ankaferd blood stopper, İstanbul, Turkey) is a prohemostatic agent affecting erythrocytes. The hemostatic action of ABS depends upon fibrinogen gamma chain, prothrombin, and red blood cells. The aim of this study was to assess the effects of ABS on erythrocyte aggregation via hemorheological analyses. MATERIALS AND METHODS: To measure erythrocyte aggregation, blood samples were obtained from healthy, nonsmoker volunteers who had not taken any medication in the previous 10 days. One mL of blood was placed into the laser-assisted optical rotational cell analyzer (LORCA), into the chamber formed by the gap between two concentric glass cylinders. The solution prepared with ABS and saline was added to blood in incremental amounts of 10 µL, 20 µL, 30 µL, 40 µL, 50 µL, 60 µL, 70 µL, and 100 µL. Erythrocyte aggregation was determined by laser-assisted optical rotational cell analyzer at 37 °C. RESULTS: AMP was found to be 17.7 ± 2.1 au in the blood without ABS, whereas it was lower in the blood with ABS. AMP was 16.0 ± 3.3 in the ABS-added blood group. RBC aggregates did not form faster when cells contacted ABS. The t t½ value was 4.6 ± 2.6 in the ABS-added blood group and 1.9 ± 0.20 in the control group. Aggregation was faster in the control group (P = 0.03). AI, which is a combination of AMP and t½, was lowered in the ABS group (48.7 ± 12.3) compared to the control group (65.8 ± 1.6) (P = 0.02). It was notable that the γIsc max (sec-1) value of the control was higher (200 ± 106) than the ABS-added blood group (141 ± 51.0). CONCLUSION: ABS has antierythroid aggregation effect. ABS inhibits pathological aggregation of red blood cells. Antithrombotic clinical effects of ABS may be ascribed to the antierythroid aggregan actions of the drug.
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spelling pubmed-73508382020-07-13 Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study ÇİFTÇİLER, Rafiye AKSU, Salih DİKMENOĞLU FALKMARKEN, Neslihan HAZNEDAROĞLU, Ibrahim Celalettin Turk J Med Sci Article BACKGROUND/AIM: Ankaferd hemostat (ABS; Ankaferd blood stopper, İstanbul, Turkey) is a prohemostatic agent affecting erythrocytes. The hemostatic action of ABS depends upon fibrinogen gamma chain, prothrombin, and red blood cells. The aim of this study was to assess the effects of ABS on erythrocyte aggregation via hemorheological analyses. MATERIALS AND METHODS: To measure erythrocyte aggregation, blood samples were obtained from healthy, nonsmoker volunteers who had not taken any medication in the previous 10 days. One mL of blood was placed into the laser-assisted optical rotational cell analyzer (LORCA), into the chamber formed by the gap between two concentric glass cylinders. The solution prepared with ABS and saline was added to blood in incremental amounts of 10 µL, 20 µL, 30 µL, 40 µL, 50 µL, 60 µL, 70 µL, and 100 µL. Erythrocyte aggregation was determined by laser-assisted optical rotational cell analyzer at 37 °C. RESULTS: AMP was found to be 17.7 ± 2.1 au in the blood without ABS, whereas it was lower in the blood with ABS. AMP was 16.0 ± 3.3 in the ABS-added blood group. RBC aggregates did not form faster when cells contacted ABS. The t t½ value was 4.6 ± 2.6 in the ABS-added blood group and 1.9 ± 0.20 in the control group. Aggregation was faster in the control group (P = 0.03). AI, which is a combination of AMP and t½, was lowered in the ABS group (48.7 ± 12.3) compared to the control group (65.8 ± 1.6) (P = 0.02). It was notable that the γIsc max (sec-1) value of the control was higher (200 ± 106) than the ABS-added blood group (141 ± 51.0). CONCLUSION: ABS has antierythroid aggregation effect. ABS inhibits pathological aggregation of red blood cells. Antithrombotic clinical effects of ABS may be ascribed to the antierythroid aggregan actions of the drug. The Scientific and Technological Research Council of Turkey 2019-02-11 /pmc/articles/PMC7350838/ /pubmed/30761848 http://dx.doi.org/10.3906/sag-1808-60 Text en Copyright © 2019 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
ÇİFTÇİLER, Rafiye
AKSU, Salih
DİKMENOĞLU FALKMARKEN, Neslihan
HAZNEDAROĞLU, Ibrahim Celalettin
Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study
title Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study
title_full Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study
title_fullStr Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study
title_full_unstemmed Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study
title_short Effects of Ankaferd Hemostat on red blood cell aggregation: a hemorheological study
title_sort effects of ankaferd hemostat on red blood cell aggregation: a hemorheological study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350838/
https://www.ncbi.nlm.nih.gov/pubmed/30761848
http://dx.doi.org/10.3906/sag-1808-60
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