Abstract

Current investigations were carried out for the validation of in-vitro anti-inflammatory and anti-arthritic property of leaves of Skimmia anquetilia using red blood cells membrane stabilization and protein denaturation methods respectively. Defatted ethylacetate extracts at different concentration levels (50, 100, 200 and 400 mg/ml) were used in these studies. Dose dependent inhibition of protein denaturation was found 92.41% at 400 mg/ml of extracts and 96.21 % at 100 mg/ml of acetyl salicylic acid as standard in antiarthritic study. Similarly, in membrane stabilization methods, maximum effect found 90.70 % at 400 mg/ml of extracts and 94.88 % at 100 mg/ml of diclofenac sodium as standard for anti-inflammatory evaluation. The results concluded that, ethyl acetate extract of S. anquetilia leaves has shown significant (*aP<0.05) anti-inflammatory and anti-arthritic effects.

Highlights

  • Inflammation is a self defense mechanism of the body to protect against reaction to infection, irritation or allegens or any other harmful irritation

  • Human red blood cell (HRBC) or erythrocyte membrane is analogous to the lysosomal membrane and its stabilization implies that the extract may as well stabilize lysosomal membranes

  • Human red blood cell membrane stabilization method reflects the effect of drugs on cellular membrane i.e. red blood cell

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Summary

INTRODUCTION

Inflammation is a self defense mechanism of the body to protect against reaction to infection, irritation or allegens or any other harmful irritation. It is a part of the host defense mechanisms. Stabilization of human red blood cell membrane by hypotonicity induced membrane lysis can be taken as an in-vitro measure of anti-inflammatory activity of the untapped drugs or plant extracts. Skimmia anquetilia is an aromatic gregarious shrub belonging to family Rutaceae. It is mostly found in Western part of Himalayas and Kashmir in India. The present investigations are scientifically validated in vitro anti- inflammatory effects using human red blood cell membrane stabilization and anti-arthritic activity by protein denaturation assay methods

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