Amla (Emblica officinalis Gaertn.) extract inhibits lipopolysaccharide-induced procoagulant and pro-inflammatory factors in cultured vascular endothelial cells

TP Rao, T Okamoto, N Akita, T Hayashi… - British journal of …, 2013 - cambridge.org
TP Rao, T Okamoto, N Akita, T Hayashi, N Kato-Yasuda, K Suzuki
British journal of nutrition, 2013cambridge.org
Amla (Emblica officinalis Gaertn.) has been used for many centuries in traditional Indian
Ayurvedic formulations for the prevention and treatment of many inflammatory diseases. The
present study evaluated the anti-inflammatory and anticoagulant properties of amla fruit
extract. The amla fruit extract potentially and significantly reduced lipopolysaccharide (LPS)-
induced tissue factor expression and von Willebrand factor release in human umbilical vein
endothelial cells (HUVEC) in vitro at clinically relevant concentrations (1–100 μg/ml). In a …
Amla (Emblica officinalis Gaertn.) has been used for many centuries in traditional Indian Ayurvedic formulations for the prevention and treatment of many inflammatory diseases. The present study evaluated the anti-inflammatory and anticoagulant properties of amla fruit extract. The amla fruit extract potentially and significantly reduced lipopolysaccharide (LPS)-induced tissue factor expression and von Willebrand factor release in human umbilical vein endothelial cells (HUVEC) in vitro at clinically relevant concentrations (1–100 μg/ml). In a leucocyte adhesion model of inflammation, it also significantly decreased LPS-induced adhesion of human monocytic cells (THP-1) to the HUVEC, as well as reduced the expression of endothelial-leucocyte adhesion molecule-1 (E-selectin) in the target cells. In addition, the in vivo anti-inflammatory effects were evaluated in a LPS-induced endotoxaemia rat model. Oral administration of the amla fruit extract (50 mg/kg body weight) significantly decreased the concentrations of pro-inflammatory cytokines, TNF-α and IL-6 in serum. These results suggest that amla fruit extract may be an effective anticoagulant and anti-inflammatory agent.
Cambridge University Press