This study investigates the interaction of alkaloids of Withania somnifera with Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), an enzyme implicated in the pathology of various neurodegenerative diseases. Initially, the Withania somnifera phytochemicals were optimised then molecular dockings were performed. The molecular docking results identified key interactions between these alkaloids and active sites of the enzyme. Several alkaloids from Withania somnifera exhibited better binding affinities to GAPDH such as Withanolides G, I, and K with binding affinity of -10.1, -10, and - 10 kcal/mol. The binding orientations and stability of these withanolide derivatives complexes GAPDH were investigated through comprehensive molecular dynamics simulations over 100 nanoseconds. The molecular dynamics simulations revealed stable interactions over the simulation period, suggesting a strong binding propensity. Furthermore, we determined the free energy binding profiles with GAPDH using BAR method, whichresulted in improved free energybinding forWithanolide-G and I.The results envisage that withanolides showed excellent bindings and stable interaction with the GAPDH, making them an effective therapeutic agent. The current study providesan excellent platform for developing new therapeutic agents derived from Withania somniferaagainst neurodegenerative diseasesassociated with GAPDH malfunction. These novel results open novel avenues for future research in drug discovery, particularly in developing novel treatments for Alzheimer's, Parkinson's, and other neurodegenerative diseases where GAPDH dysfunction plays crucial roles.Furthermore, experimental validation is required to validate the results of the current study.
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http://dx.doi.org/10.1186/s13568-025-01826-4 | DOI Listing |
Cureus
February 2025
Department of Pharmacology, Krishna Institute of Medical Sciences, Krishna Vishwa Vidyapeeth (Deemed to be University), Karad, IND.
Background: The rising prevalence of type II diabetes mellitus (T2DM) has increased the risk of hepatic dysfunction, necessitating effective therapeutic interventions. Natural products, particularly (BA) and (WS), are known for their hepatoprotective properties.
Objectives: This study investigates the hepatoprotective effects of BA, WS, and their polyherbal combination in streptozotocin-nicotinamide-induced T2DM in Wistar rats.
J Alzheimers Dis Rep
December 2024
Regeneration and Stem Cell Biology Lab, Centre for Molecular and Nanomedical Sciences, International Research Centre, Sathyabama Institute of Science and Technology, Chennai, India.
Background: Alzheimer's disease (AD) is a progressive neurodegenerative disorder, which subdues over 55 million people and finding a cure, still remains disenchanting. Indian medicinal herbs notably, , , , and are traditionally utilized for their memory-enhancing properties.
Objective: We computationally investigated the therapeutic potential of four nootropic herbs by uncovering the molecular mechanisms underlying their treatment for AD.
Drug Metab Dispos
February 2025
Department of Drug Discovery and Development, Harrison College of Pharmacy, Auburn University, Auburn, Alabama. Electronic address:
It is important to understand the potential of botanical-drug interactions to ensure the safe use of botanical dietary supplements (BDS). Cytochrome P450 (P450) is one of the most abundant phase 1 drug-metabolizing enzymes and is accountable for a great deal of pharmacokinetic botanical-drug interactions. This problem is particularly acute for older adults who often consume BDS with multiple prescription medicines.
View Article and Find Full Text PDFInt J Biomater
February 2025
Department of Chemistry, Wollega University, P.O. Box 395, Nekemte, Oromia, Ethiopia.
In recent years, green synthesis methods for producing nanomaterials have gained significant interest due to their environmentally friendly nature and wide-ranging applications. The present study addresses a novel green synthesis of graphene quantum dots (GQDs) using leaves of The size, morphology, and stability of the green-synthesized GQDs were characterized using TEM, UV-Visible spectroscopy, Fluorescence spectrophotometer, XRD, and DLS. The bio-functional properties of the GQDs were investigated, with a focus on their antidiabetic and antioxidant capabilities.
View Article and Find Full Text PDFPharmaceuticals (Basel)
February 2025
Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah 27272, United Arab Emirates.
: Doxorubicin (DOX) is a very powerful chemotherapy drug. However, its severe toxicity and potential for resistance development limit its application. L.
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