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They also found that HMGB1 knockdown inhibited the high glucose-induced toll-like receptor 4 (TLR4)/NF-B signaling pathway and promoted the expression of Nrf2 and its downstream targets, such as HO-1, NQO1, glutamate-cysteine ligase catalytic subunit (GCLC) and modifier subunit of glutamate cysteine ligase (GCLM)[86]

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