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In the STZ-induced diabetic mouse model, oral administration of betaine reduced the levels of reactive oxygen species (ROS) and malondialdehyde (MDA) in the testicular tissue and increased the activities of superoxide dismutase (SOD), catalase (CAT), and glutathione (GSH), thereby inhibiting the p38 mitogen-activated protein kinase (p38 MAPK) signaling pathway and protecting against blood-testis barrier dysfunction (68) (Figure 4D)
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