Abstract

Ankaferd hemostat (ABS; Ankaferd Blood Stopper®, İstanbul, Turkey) is a hemostatic agent having an impact on red blood cell–fibrinogen interactions. The hemostatic effect of ABS depends upon the quick promotion of a protein network, particularly fibrinogen gamma, in relation to the erythrocyte aggregation. The entire physiological process involves ABS-induced formation of the protein network by vital erythrocyte aggregation. Vital erythrocyte aggregation occurs with the spectrine, ankyrin, and actin proteins on the membrane of the red blood cells. ABS notably affects cell metabolism and cell cycle mechanisms. Meanwhile, ABS has antiproliferative effects on cancer cells. The aim of this review is to assess molecular basis of ABS as a hemostatic drug. The literature search on ABS was performed in PubMed, Web of Science (SCI expanded), and Scopus with particular focus on the studies of molecular basis of ABS, in vivo research, case series, and controlled randomized clinical studies. Current perspective for the utilization of ABS is to provide hemostasis with accelerating wound healing. Future controlled trials are needed to elucidate the pleiotropic clinical effects of ABS such as antineoplastic, antiinflammatory, antiinfective, antifungal, and antioxidative effects.

Highlights

  • Ankaferd hemostat (ABS; Ankaferd Blood Stopper®, İstanbul, Turkey) had been traditionally practiced in Anatolia as a hemostatic agent for centuries

  • Vital erythrocyte aggregation is established with spectrin, ankyrin, and actin proteins on the membranes of red blood cells

  • The results showed that ABS-derived ironinfluenced transcriptions of iron-regulated marker genes, including divalent metal transporter (Dmt1), transferrin receptor (TfR), ankyrin repeat domain 37 (Ankrd37), and hepcidin (Hamp)

Read more

Summary

Introduction

Ankaferd hemostat (ABS; Ankaferd Blood Stopper®, İstanbul, Turkey) had been traditionally practiced in Anatolia as a hemostatic agent for centuries. It is a hemostatic agent having an impact on the red blood cell–fibrinogen interactions [1]. ABS shows its hemostatic effect via affecting the physiology of red blood cells [1]. ABS has been introduced as a new topical hemostatic agent when conventional methods for the management of clinical bleeding are not effective [4,5,6]. ABS is effective in patients with primary or secondary hemostatic dysfunction as well as in patients with normal hemostatic parameters and bleeding [7,8]. The aim of this review is to assess essential molecular basis of ABS as a hemostatic drug

Objectives
Methods
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