Superoxide dismutases (SODs) are metalloenzymes that detoxify superoxi
de radicals, and occur in cytosolic (Cu,Zn-SOD) and mitochondrial (Mn-
SOD) forms in multiple tissues, including brain. A neuroprotective eff
ect against oxide stressor exposures may be provided by SOD, although
excessive enzyme activity can produce cell injury by formation of hydr
oxyl radical from hydrogen peroxide. We measured Cu,Zn-SOD and Mn-SOD
activities in peripheral lymphocytes of 43 newly diagnosed idiopathic
Parkinson's disease (PD) cases and 62 age- and sex-matched controls fr
ee of neurodegenerative disorders. Significant excesses of both SOD fo
rms were found among PD cases compared with controls; however, the exc
esses were found exclusively among FD patients treated with the monoam
ine oxidase inhibitor selegiline (L-deprenyl). Enzyme-linked immunosor
bent assays (ELISAs) confirmed that the activity excesses were due to
increased protein rather than more highly reactive enzymes in lymphocy
tes of PD cases. Our findings clearly indicate the importance of seleg
iline on measured Cu,Zn-SOD and Mn-SOD activity in peripheral lymphocy
tes. Characterizing a possible therapeutic value of SOD will require l
ongitudinal assessments of SOD in relation to PD progerssion.