The recurring interplay of oxidative stress, inflammatory activation, and disrupted cellular signalling provides a unifying mechanistic framework linking renal, musculoskeletal, cutaneous, immunological, respiratory, gastrointestinal, and reproductive dysfunctions to those already described in cardiovascular, hepatic, and gonadal tissues ( Taken together, the current body of evidence suggests that supraphysiological androgen exposure disrupts endocrine regulation at multiple levelsfrom hypothalamic control to testicular cellular architecturethrough oxidative, mitochondrial, and epigenetic mechanisms ( To facilitate synthesis of the extensive narrative data presented in Sections 6 and 7, a summary table is provided below, integrating the major psychological and physical adverse effects associated with non-medical testosterone and anabolicandrogenic steroid use across organ systems ( Table 2 )

These modifications exert their influence by modulating the protein stability and altering the expression levels of specific mediators
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P237, P472, P509, P757, P1086 Casciaro* S
doi: 10.3748/wjg.v31.i10.100194 42 GuoRLiYSongQHuangRGeXNietoNet al