Laminectomy animals served as surgical controls. Mice in SCT groups experienced similar percent body mass (BM) losses at 7 days postinjury. Soleus muscle mass (MM) and MMto-BM ratio were lower at 7 days postinjury in SCT vs. laminectomy mice, with no differences observed between strains. However, soleus muscles from MT Ϫ/Ϫ trans mice showed reduced maximal specific tension compared with MT Ϫ/Ϫ lami animals. Mean cross-sectional area (m 2 ) of type I and type IIa fibers decreased similarly in SCT groups compared with laminectomy controls, and no difference in fiber distribution was observed. Lipid peroxidation (4-hydroxynoneal) was greater in MT Ϫ/Ϫ trans vs. MT Ϫ/Ϫ lami mice, but protein oxidation (protein carbonyls) was not altered by MT deficiency or SCT. Expression of key antioxidant proteins (catalase, manganese, and copper-zinc superoxide dismutase) was similar between the groups. In summary, MT deficiency did not impact soleus MM loss, but resulted in contractile dysfunction and increased lipid peroxidation following acute SCT. These findings suggest a role of MT in mediating protective adaptations in skeletal muscle following disuse mediated by spinal cord injury. muscle atrophy; oxidative stress; spinal cord transection; antioxidant; stress protein METALLOTHIONEIN (MT) IS A small molecular weight metal binding protein expressed as four isoforms in humans, mice, and other mammals (reviewed in Ref. 18). Metallothionein-1 (MT-1) and metallothionein-2 (MT-2) proteins are ubiquitously expressed and are inducible isoforms of MT. Conversely, metallothionein-3 (MT-3) and metallothionein-4 (MT-4) display more limited expression and are found primarily in the brain and skin, respectively. MT appears to be involved in numerous cellular processes that include free radical scavenging, intracellular zinc transport and storage, metal detoxification, and zinc exchange with metalloproteins (reviewed in Ref.