Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/68663
metadata.dc.identifier.doi: https://doi.org/10.56042/ijbb.v63i10.21526
Title: Oldenlandia umbellata as a promising agent for obesity management: Enzyme inhibition and antiadipogenic effects
Authors: Manoharan, Athista
Pandurangan, Prakash
Nellore, Jayshree
Nachiyar Chandrasekaran, Valli
Sunkar, Swetha
Keywords: 3T3-L1 Preadipocytes;Adipogenesis;Diospyros ebenum,;Enzymes,;Oldenlandia umbellata
Issue Date: Oct-2026
Publisher: NIScPR-CSIR, India
Abstract: Obesity is a major global health challenge associated with metabolic disorders and the need for effective interventions, particularly from natural sources. This study evaluated the metabolic enzyme inhibitory and anti-adipogenic potential of Diospyros ebenum and Oldenlandia umbellata ethanolic extracts using in vitro assays and a 3T3-L1 preadipocyte model. Both extracts exhibited inhibitory activity against α-amylase, α-glucosidase, and pancreatic lipase, with O. umbellata showing comparatively stronger inhibition particularly against α-glucosidase, and pancreatic lipase. Cytotoxicity assessment indicated no substantial cytotoxicity of the extracts toward Vero cells at concentrations ≤100 μg/mL under the tested conditions. Treatment of 3T3-L1 adipocytes with O. umbellata extract significantly reduced intracellular lipid accumulation and triglyceride levels. Gene-expression analysis showed reduced PPARγ and FAS expression and increased adiponectin expression compared with differentiated controls, whereas SREBP-1c was not significantly altered and leptin showed modest increase. In silico ADME and toxicity analyses indicated favorable predicted pharmacokinetic and drug-likeness characteristics for several putatively identified phytoconstituents. Overall, the findings support the potential of O. umbellata as a source of bioactive compounds with enzyme inhibitory and anti-adipogenic activities. Further studies are required to identify the active constituents, elucidate the underlying molecular mechanisms, and validate these effects in appropriate in vivo models.
Page(s): 1213-1231
ISSN: 0975-0959 (Online) ; 0301-1208 (Print)
Appears in Collections:IJBB Vol.63(10) [October 2026]

Files in This Item:
File Description SizeFormat 
IJBB Vol.63(10) 1213-1231.pdf7.63 MBAdobe PDFView/Open
IJBB Vol.63(10) 1213-1231 Suppl.pdf141.94 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.