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Abstract Title:

Naringin protects against HIV-1 protease inhibitors-induced pancreaticβ-cell dysfunction and apoptosis.

Abstract Source:

Mol Cell Endocrinol. 2016 12 5 ;437:1-10. Epub 2016 Aug 2. PMID: 27496642

Abstract Author(s):

Sanelisiwe Nzuza, Duduzile E Ndwandwe, Peter M O Owira

Article Affiliation:

Sanelisiwe Nzuza

Abstract:

INTRODUCTION: The protective effects of grapefruit-derived naringin against HIV-1 Protease Inhibitors (PIs)-associated oxidative damage to pancreaticβ-cells and apoptosis were investigated in RIN-5F cells in culture.

METHODS: Cells in culture medium were challenged with 11-25 mM glucose with or without nelfinavir (1-10 μM), saquinavir (1-10 μM) and atazanavir (5-20 μM), respectively for 24 h to determine insulin secretion. The cells were further treated with nelfinavir (10 μM), saquinavir (10 μM), atazanavir (20 μM) with and without naringin or glibenclamide (10 μM) for 24 h to determine insulin secretion, lipid peroxidation, Superoxide Dismutase (SOD) activity, glutathione (GSH) levels, ATP production and caspase-3 and-9 activities, respectively.

RESULTS: Glucose-dependent insulin secretion was significantly reduced by PIs in a concentration-dependent manner. Treatment with either naringin or glibenclamide significantly reduced lipid peroxidation, Superoxide Dismutase (SOD) activities and also increased glutathione (GSH) and ATP levels in the cells that were treated with PIs. Furthermore, naringin or glibenclamide significantly reduced caspase-3 and caspase-9 activities in cells that were treated with PIs.

CONCLUSIONS: PIs impairβ-cell functions by increasing oxidative stress and apoptosis. Treatment with naringin protected RIN-5F cells from PI-induced oxidative damage and apoptosis. Our results therefore suggest that nutritional supplements with naringin could prevent pancreatic β-cell dysfunction and the attendant metabolic complications caused by PIs in patients on antiretroviral therapy.

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Sayer Ji
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