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Role of apoptosis induced by Helicobacter pylori infection in the development of duodenal ulcer

Research-use statement For laboratory research use only

After pharmacological intervention in 96-well cell culture plates for 24, 48 or 72 h, the culture medium was removed and replaced with 0.1 mg MTT reagent (Beyotime, ST1537) per well dissociated in 100 L basal DMEM (Procell, PM150210)

Thus a reduction in a protective antioxidant such as UA may result in increased oxidative stress and subsequent damage

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