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Title

GC-MS and in silico analyses revealed the potential inhibitory activity of compounds isolated from Ciplukan herb (Physalis angulata L.) targeting GLUT-4 receptors.

Authors

Rakhmawati, Rita; Wahyudi, Setyanto Tri; Hartati Wahyuningsih, Mae Sri; Mustofa, Mustofa; Sadewa, Ahmad Hamim

Abstract

The escalating prevalence of diabetes mellitus (DM), a major global health threat and one of the top 10 causes of mortality, is a worrying trend. Prolonged hyperglycemia in people with diabetes triggers oxidative stress, leading to accelerated tissue damage, increased levels of free radicals, and the onset of complications. Our initial exploration of Physalis angulata L, using bioassay-guided isolation and C2C12 insulin resistance monitoring, revealed the compound’s ability to increase cellular glucose uptake. Consequently, there is an urgent need for further drug discovery efforts aimed at deciphering the mechanism of action of compounds targeting GLUT4 receptors in silico. The focus of this study was to predict the mechanism of action of compounds against the AS160 protein to facilitate GLUT4 translocation to the cell surface. Using GC-MS analysis and molecular docking via Autodock Vina, a mixture of blind and targeted docking approaches, isolated compounds were identified. Notably, this study marks the first identification, to the best of our knowledge, of campesterol and stigmasterol in P. angulata L herbs by GC-MS analysis. Through in silico simulations, campesterol and stigmasterol show promising potential in the treatment of type 2 diabetes by targeting the glucose transporter GLUT4 via facilitating GLUT4 translocation. Given their favorable pharmacokinetic properties, these phytoconstituents are potential hypoglycemic agents.

Subjects

GAS chromatography/Mass spectrometry (GC-MS); TYPE 2 diabetes; FREE radicals; PHYSALIS; DRUG discovery; PEOPLE with diabetes

Publication

Journal of Applied Pharmaceutical Science, 2024, Vol 14, Issue 8, p142

ISSN

2231-3354

Publication type

Academic Journal

DOI

10.7324/JAPS.2024.171953

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