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In TrxRs, electrons from NADPH are used to reduce an active site disulfide in oxidized Trx (Trx-disulfide), yielding NADP + and a reduced Trx-dithiol [30, 36, 39]

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oxylipins) are able to directly influence microglia, by modulating their phagocytic capacity, motility and their capacity to produce inflammatory factors [23, 187]

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