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Molecular insights to in vitro biocompatibility of endodontic Pulpotec with macrophages determined by oxidative stress and apoptosis

Authors :
Mohanty, Ankita
Patro, Swadheena
Jha, Ealisha
Patel, Paritosh
Nandi, Aditya
Sinha, Adrija
Naser, Shaikh Sheeran
Das, Antarikshya
Panda, Pritam Kumar
Rout, Prabhat Kumar
Mishra, Richa
Kaushik, Nagendra Kumar
Singh, Deobrat
Suar, Mrutyunjay
Verma, Suresh K.
Mohanty, Ankita
Patro, Swadheena
Jha, Ealisha
Patel, Paritosh
Nandi, Aditya
Sinha, Adrija
Naser, Shaikh Sheeran
Das, Antarikshya
Panda, Pritam Kumar
Rout, Prabhat Kumar
Mishra, Richa
Kaushik, Nagendra Kumar
Singh, Deobrat
Suar, Mrutyunjay
Verma, Suresh K.
Publication Year :
2024

Abstract

Pulp therapy has been emerged as a one of the efficient therapies in the field of endodontics. Among different types of new endodontic materials, pulpotec has been materialized as a recognized material for vital pulp therapy. However, its efficacy has been challenged due to lack of information about its cellular biocompatibility. This study evaluates the mechanistic biocompatibility of pulpotec cement with macrophage cells (RAW 264.7) at cellular and molecular level. The biocompatibility was evaluated using experimental and computational techniques like MTT assay, oxidative stress analysis and apoptosis analysis through flow cytometry and fluorescent microscopy. The results showed concentration-dependent cytotoxicity of pulpotec cement extract to RAW 264.7 cells with an LC 50 of X/10 -X/20. The computational analysis depicted the molecular interaction of pulpotec cement extract components with metabolic proteins like Sod1 and p53. The study revealed the effects of Pulpotec cement's extract, showing a concentration-dependent induction of oxidative stress and apoptosis. These effects were due to influential structural and functional abnormalities in the Sod1 and p53 proteins, caused by their molecular interaction with internalized components of Pulpotec cement. The study provided a detailed view on the utility of Pulpotec in endodontic applications, highlighting its biomedical aspects.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1457291072
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.biopha.2024.116921