PENGARUH RESVERATROL TERHADAP JALUR PERMEABILITAS BARU SEBAGAI TARGET KERJA ANTIMALARIA

Fahmy Ahsanul Haq; Faizal Hermanto; Afifah Bambang Sutjiatmo; Mutiara Hadi Lutfi

doi:10.36805/jbf.v4i4.1157

Fahmy Ahsanul Haq Fakultas Farmasi, Universitas Jenderal Achmad Yani, Cimahi, Jawa Barat, Indonesia
Faizal Hermanto Fakultas Farmasi, Universitas Jenderal Achmad Yani, Cimahi, Jawa Barat, Indonesia
Afifah Bambang Sutjiatmo Fakultas Farmasi, Universitas Jenderal Achmad Yani, Cimahi, Jawa Barat, Indonesia
Mutiara Hadi Lutfi Fakultas Farmasi, Universitas Jenderal Achmad Yani, Cimahi, Jawa Barat, Indonesia

DOI: https://doi.org/10.36805/jbf.v4i4.1157

Keywords: New Permeability Pathway, Resveratrol, Hemolysis Inhibition, Malaria, Plasmodium berghei

Abstract

Plasmodium is a parasite that causes malaria, which is transmitted to humans through the bite of female Anopheles mosquitoes. Plasmodium that infects red blood cells will cause the formation of new permeability pathway (NPP) in the red blood cell membrane. This change makes the red blood cell membrane more permeable, allowing various nutrients the parasite needs to enter the red blood cells. Resveratrol is a polyphenol compound that is reported to have antimalarial activity by inhibiting the growth of Plasmodium berghei. This study aims to activate the activity of resveratrol in inhibiting NPP. The study began with the preparation of blood suspensions that showed infection and non-infection, then test preparations were added and induced using sorbitol, and then hemolysis was measured using a UV-visible spectrophotometer. The test group consisted of normal groups, control and various concentrations of resveratrol, namely 1.25, 2.5, 5, 10 and 20 μM. The observation parameters in this study were the percentage of hemolysis inhibition. Based on the study’s results, the percentage of hemolysis inhibition increased with increasing resveratrol concentration. The IC50 value of the NPP inhibition activity test of resveratrol was 1.025 μM. This study concludes that resveratrol can inhibit NPP in erythrocytes infected with Plasmodium berghei.

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