1Department of Pharmacology, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India
2Department of Pharmacology, Manipal University College, Melaka, 75150, Malaysia
3Department of Cell and Molecular Biology, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India
4Division of Pharmacology, Department of Basic Medical Sciences, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India
5Division of Siddha, Centre for Integrative Medicine and Research, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India
6Department of Dermatology, Venereology and Leprosy, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India
7Department of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India
8Centre for Cardiovascular Pharmacology (CCP), Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India
*Corresponding Author E-mail: vasudha.devi@manipal.edu
Online Published on 30 April, 2025.
Psoriasis is one of the chronic inflammatory conditions with multifactorial aetiology. Even though there are different treatments available, there is no cure for psoriasis. A Siddha polyherbal formulation, Sivanar vembu kuzhi thailam (SVKT), is used to treat various skin diseases. In this study, methanolic extract of SVKT was analysed using gas chromatography–mass spectrometry (GC-MS) which showed the presence of 86 compounds. They were further subjected to molecular docking to find the effect of SVKT on inflammatory proteins, IL-17A and TNF-α, involved in the pathogenesis of psoriasis. Four shortlisted compounds from SVKT exhibited their inhibitory potential on IL-17A with binding energy varying between -8.2 to -6.6 kcal/mol and three compounds on TNF-α with binding energy varying between -7.8 to -5.6 kcal/mol. Pharmacokinetic properties (Absorption, Distribution, Metabolism, Excretion and Toxicity-ADMET) were also evaluated in silico which showed favourable features. 2-(hydroxymethyl)-6-octylsulfanyloxane-3,4,5-triol and α-Lactose among the shortlisted constituents, inhibited both proteins through exhibiting multiple interactions. Hence this study provides valuable insights into the inhibitory effect of phytochemicals present in SVKT on IL-17A and TNF-α which may pave way to the discovery of new drugs to treat psoriasis.
Sivanar vembu kuzhi thailam, GCMS, ADMET, Psoriasis, TNF-α, IL-17A