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Protective effects of madecassoside, a triterpenoid from Centella asiatica, against oxidative stress in INS-1E cells.
Tan, Swee Ching; Rajendran, Ramkumar; Bhattamisra, Subrat Kumar; Krishnappa, Purushotham; Davamani, Fabian; Chitra, Ebenezer; Ambu, Stephen; Furman, Brian; Candasamy, Mayuren.
Afiliación
  • Tan SC; School of Postgraduate Studies, International Medical University, Kuala Lumpur, Malaysia.
  • Rajendran R; Faculty of Medicine, University of Adelaide, Adelaide, Australia.
  • Bhattamisra SK; Department of Life Sciences, School of Pharmacy, International Medical University, Kuala Lumpur, Malaysia.
  • Krishnappa P; Department of Life Sciences, School of Pharmacy, International Medical University, Kuala Lumpur, Malaysia.
  • Davamani F; School of Pharmacy, GITAM (Deemed to be University), Visakhapatnam, India.
  • Chitra E; Department of Pathology, School of Medicine, International Medical University, Kuala Lumpur, Malaysia.
  • Ambu S; Division of Applied Biomedical Sciences and Biotechnology, School of Health Sciences, International Medical University, Kuala Lumpur, Malaysia.
  • Furman B; Division of Applied Biomedical Sciences and Biotechnology, School of Health Sciences, International Medical University, Kuala Lumpur, Malaysia.
  • Candasamy M; School of Postgraduate Studies, International Medical University, Kuala Lumpur, Malaysia.
Nat Prod Res ; : 1-8, 2024 Feb 10.
Article en En | MEDLINE | ID: mdl-38340357
ABSTRACT
Progressive decline in ß cell function and reduction in the ß cell mass is important in type 2 diabetes. Here, we tested the hypothesis that madecassoside's previously demonstrated in vivo protective effects on the ß cell in experimental diabetes were exerted directly. We investigated the effects of madecassoside in protecting a ß cell line (INS-1E) against a variety of agents. INS-1E cells were treated with madecassoside in the presence of high glucose (HG), a cytokine mixture, hydrogen peroxide (H2O2), or streptozotocin (STZ). HG, the cytokine mixture, H2O2 and STZ each produced a significant decrease in cell viability; this was significantly reversed by madecassoside. Pre-treatment with madecassoside reduced the number of apoptotic cells induced by HG, the cytokine mixture, H2O2, and STZ, and concentration-dependently reduced ROS production. Madecassoside also significantly enhanced glucose-induced insulin secretion. The results suggest that madecassoside's in vivo effects are exerted directly on the ß cell.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article País de afiliación: Malasia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article País de afiliación: Malasia