Abstract Peripheral nerve defect repair remains a clinical challenge. Nerve guidance conduits (NGCs) are potential alternatives to autografts, but their performance can be compromised by the oxidative and inflammatory microenvironment after injury. Here, we fabricated MnO 2 -loaded hydrogel NGCs at concentrations of 10, 50, and 100 μg ml −1 and evaluated them in a rat model of a 10-mm sciatic nerve defect. Among the three concentrations, the MnO 2 @NMgel-10 (10 μg ml −1 ) group yielded a higher sciatic functional index, denser and more orderly regenerated nerve tissue, and less gastrocnemius muscle atrophy than the hydrogel-only and higher-dose conduit groups. Early tissue analysis showed that the MnO 2 @NMgel-10 group exhibited increased infiltration of CD86 + CD206 + cells, upregulated expression of IL-10, and significantly downregulated expression of IL-1 β , TNF- α , and 4-HNE. Furthermore, the MnO 2 @NMgel-10 group showed satisfactory biosafety and biocompatibility. These findings reveal a non-monotonic concentration response and preliminarily confirm the feasibility of low-dose MnO 2 -functionalized hydrogel NGCs for repairing peripheral nerve defects, providing new insights into the application of MnO 2 as a supplementary material for NGC fabrication.