Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro

Background: Blackthorn flower (Prunus spinosa L.) is a traditional herbal remedy recommended for treating cardiovascular diseases (CVDs).Aim: This in vitro study investigates the effects of flavonol and A-type procyanidin-rich blackthorn flower extracts on the hemostatic system, including the blood...

Full description

Bibliographic Details
Main Authors: Anna Marchelak, Joanna Kolodziejczyk-Czepas, Michał B. Ponczek, Oleksandra Liudvytska, Magdalena Markowicz-Piasecka, Beata Bielska, Katarzyna Miłowska, Monika A. Olszewska
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-11-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2023.1307373/full
_version_ 1797450856206958592
author Anna Marchelak
Joanna Kolodziejczyk-Czepas
Michał B. Ponczek
Oleksandra Liudvytska
Magdalena Markowicz-Piasecka
Beata Bielska
Katarzyna Miłowska
Monika A. Olszewska
author_facet Anna Marchelak
Joanna Kolodziejczyk-Czepas
Michał B. Ponczek
Oleksandra Liudvytska
Magdalena Markowicz-Piasecka
Beata Bielska
Katarzyna Miłowska
Monika A. Olszewska
author_sort Anna Marchelak
collection DOAJ
description Background: Blackthorn flower (Prunus spinosa L.) is a traditional herbal remedy recommended for treating cardiovascular diseases (CVDs).Aim: This in vitro study investigates the effects of flavonol and A-type procyanidin-rich blackthorn flower extracts on the hemostatic system, including the blood plasma coagulation cascade and platelet aggregation.Methods: Six distinct extracts, characterized through various techniques, including LC-MS/MS, were assessed at in vivo-relevant levels (1–50 μg/mL) for their antithrombotic activity. The thrombin, prothrombin, and activated partial thromboplastin times were measured. Additionally, the thrombin enzymatic activity was tested using the chromogenic substrate S-2238 and fibrinogen as the physiological substrate of the enzyme. To gain insights into the mechanism of action, the interactions between the primary extracts’ constituents, their potential metabolites, and thrombin were examined in silico. The computational analyses were complemented by in vitro experiments and circular dichroism spectroscopy. The platelet aggregation in human platelet-rich plasma was assessed after ADP or collagen stimulation. Furthermore, the extracts’ biocompatibility was tested on human peripheral blood mononuclear cells (PBMCs) and red blood cells (RBCs).Results: The extracts slightly prolonged the prothrombin and thrombin times and effectively inhibited the thrombin’s enzymatic activity, reducing its amidolytic and proteolytic functions at 50 μg/mL by 91.2% and 74.8%, respectively. In silico molecular docking demonstrated a strong binding affinity of the examined polyphenols and their metabolites to thrombin. Most analytes bound exclusively within the enzyme active site; however, afzelin, kaempferitrin, and procyanidin A2 revealed the affinity to additional binding sites, including exosite I. The structure-activity relationship of flavonols as thrombin inhibitors was studied in vitro. Circular dichroism spectroscopy confirmed that the interactions between thrombin and the compounds (even at 1 μg/mL) induce alterations within the α-helices’ secondary structure, resulting in noticeable changes in the enzyme’s CD spectrum. On the other hand, the extracts did not influence platelet aggregation. Eventually, their cellular biocompatibility with PBMCs and RBCs was confirmed.Conclusion: The extracts directly inhibit thrombin, a critical serine protease in hemostasis and a prime anticoagulant drug target, and do not exhibit antiplatelet effects. This study enhances the knowledge of the biological activity of blackthorn flowers and supports their traditional use in CVDs.
first_indexed 2024-03-09T14:45:36Z
format Article
id doaj.art-a5dd95064c574b5c9f7558e8cfe3b47d
institution Directory Open Access Journal
issn 1663-9812
language English
last_indexed 2024-03-09T14:45:36Z
publishDate 2023-11-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Pharmacology
spelling doaj.art-a5dd95064c574b5c9f7558e8cfe3b47d2023-11-27T06:55:10ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122023-11-011410.3389/fphar.2023.13073731307373Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitroAnna Marchelak0Joanna Kolodziejczyk-Czepas1Michał B. Ponczek2Oleksandra Liudvytska3Magdalena Markowicz-Piasecka4Beata Bielska5Katarzyna Miłowska6Monika A. Olszewska7Department of General Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, PolandDepartment of General Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, PolandDepartment of General Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, PolandDepartment of General Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, PolandDepartment of Applied Pharmacy, Faculty of Pharmacy, Medical University of Lodz, Lodz, PolandDepartment of General Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, PolandDepartment of General Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, PolandDepartment of General Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, PolandBackground: Blackthorn flower (Prunus spinosa L.) is a traditional herbal remedy recommended for treating cardiovascular diseases (CVDs).Aim: This in vitro study investigates the effects of flavonol and A-type procyanidin-rich blackthorn flower extracts on the hemostatic system, including the blood plasma coagulation cascade and platelet aggregation.Methods: Six distinct extracts, characterized through various techniques, including LC-MS/MS, were assessed at in vivo-relevant levels (1–50 μg/mL) for their antithrombotic activity. The thrombin, prothrombin, and activated partial thromboplastin times were measured. Additionally, the thrombin enzymatic activity was tested using the chromogenic substrate S-2238 and fibrinogen as the physiological substrate of the enzyme. To gain insights into the mechanism of action, the interactions between the primary extracts’ constituents, their potential metabolites, and thrombin were examined in silico. The computational analyses were complemented by in vitro experiments and circular dichroism spectroscopy. The platelet aggregation in human platelet-rich plasma was assessed after ADP or collagen stimulation. Furthermore, the extracts’ biocompatibility was tested on human peripheral blood mononuclear cells (PBMCs) and red blood cells (RBCs).Results: The extracts slightly prolonged the prothrombin and thrombin times and effectively inhibited the thrombin’s enzymatic activity, reducing its amidolytic and proteolytic functions at 50 μg/mL by 91.2% and 74.8%, respectively. In silico molecular docking demonstrated a strong binding affinity of the examined polyphenols and their metabolites to thrombin. Most analytes bound exclusively within the enzyme active site; however, afzelin, kaempferitrin, and procyanidin A2 revealed the affinity to additional binding sites, including exosite I. The structure-activity relationship of flavonols as thrombin inhibitors was studied in vitro. Circular dichroism spectroscopy confirmed that the interactions between thrombin and the compounds (even at 1 μg/mL) induce alterations within the α-helices’ secondary structure, resulting in noticeable changes in the enzyme’s CD spectrum. On the other hand, the extracts did not influence platelet aggregation. Eventually, their cellular biocompatibility with PBMCs and RBCs was confirmed.Conclusion: The extracts directly inhibit thrombin, a critical serine protease in hemostasis and a prime anticoagulant drug target, and do not exhibit antiplatelet effects. This study enhances the knowledge of the biological activity of blackthorn flowers and supports their traditional use in CVDs.https://www.frontiersin.org/articles/10.3389/fphar.2023.1307373/fullPrunus spinosablackthorn flowerspolyphenolshemostasisthrombinanticoagulant
spellingShingle Anna Marchelak
Joanna Kolodziejczyk-Czepas
Michał B. Ponczek
Oleksandra Liudvytska
Magdalena Markowicz-Piasecka
Beata Bielska
Katarzyna Miłowska
Monika A. Olszewska
Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro
Frontiers in Pharmacology
Prunus spinosa
blackthorn flowers
polyphenols
hemostasis
thrombin
anticoagulant
title Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro
title_full Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro
title_fullStr Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro
title_full_unstemmed Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro
title_short Flavonol and A-type procyanidin-rich extracts of Prunus spinosa L. flower exhibit anticoagulant activity through direct thrombin inhibition, but do not affect platelet aggregation in vitro
title_sort flavonol and a type procyanidin rich extracts of prunus spinosa l flower exhibit anticoagulant activity through direct thrombin inhibition but do not affect platelet aggregation in vitro
topic Prunus spinosa
blackthorn flowers
polyphenols
hemostasis
thrombin
anticoagulant
url https://www.frontiersin.org/articles/10.3389/fphar.2023.1307373/full
work_keys_str_mv AT annamarchelak flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro
AT joannakolodziejczykczepas flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro
AT michałbponczek flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro
AT oleksandraliudvytska flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro
AT magdalenamarkowiczpiasecka flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro
AT beatabielska flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro
AT katarzynamiłowska flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro
AT monikaaolszewska flavonolandatypeprocyanidinrichextractsofprunusspinosalflowerexhibitanticoagulantactivitythroughdirectthrombininhibitionbutdonotaffectplateletaggregationinvitro