Rumex acetosella Inhibits Platelet Function via Impaired MAPK and Phosphoinositide 3-Kinase Signaling

Chin J Integr Med. 2022 Sep;28(9):802-808. doi: 10.1007/s11655-021-2873-0. Epub 2021 Sep 21.

Abstract

Objective: To examine the antiplatelet and antithrombotic activity of Rumex acetosella extract.

Methods: Standard light aggregometry was used for platelet aggregation, intracellular calcium mobilization assessed using Fura-2/AM, granule secretion (ATP release) by luminometer, and fibrinogen binding to integrin αIIbβ3 detected using flow cytometry. Western blotting is carried out to determine the phosphorylation of mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase (PI3K)/Akt signaling.

Results: Rumex acetosella displayed the ability to inhibit platelet aggregation, calcium mobilization, granule secretion, and fibrinogen binding to integrin αIIbβ3. Rumex acetosella has also down-regulated MAPK and PI3K/Akt phosphorylation (all P<0.01).

Conclusion: Rumex acetosella extract exhibits antiplatelet activity via modulating GPVI signaling, and it may protect against the development of platelet-related cardiovascular diseases.

Keywords: Rumex acetosella L; antiplatelet; ethnomedicine; integrin α IIb β 3; mitogen-activated protein kinase.

MeSH terms

  • Blood Platelets / metabolism
  • Calcium / metabolism
  • Fibrinogen / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • Phosphatidylinositol 3-Kinase / metabolism
  • Phosphatidylinositol 3-Kinase / pharmacology
  • Phosphatidylinositol 3-Kinases* / metabolism
  • Phosphorylation
  • Plant Extracts / pharmacology
  • Platelet Aggregation
  • Platelet Aggregation Inhibitors / pharmacology
  • Platelet Glycoprotein GPIIb-IIIa Complex / metabolism
  • Platelet Glycoprotein GPIIb-IIIa Complex / pharmacology
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rumex* / metabolism

Substances

  • Plant Extracts
  • Platelet Aggregation Inhibitors
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Fibrinogen
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases
  • Calcium