Mercury was largely sequestered within the midgut epithelia of Drosophila after oral administration.
Mercury stimulation induced excess production of reactive oxygen species in the midgut epithelia.
Mercury stimulation caused increased cell death.
Mercury stimulation triggered tissue regeneration through accelerated proliferation and differentiation of intestinal stem cells.
Vitamin E efficiently alleviated the HgCl2-induced tissue damages and improved the survival rate.
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