In future studies, we aim to knock down or overexpress Naa10p/PGC‐1α/Pparγ2 in L‐arginine‐ or caerulein‐induced AP mouse models and assess mitochondrial function (e.g., oxygen consumption rate, mtDNA copy number), inflammatory markers (e.g., IL‐6, myeloperoxidase), and histopathological damage. Here, PPARGC1A is linked to alkaline phosphatase measurement.