Adenosine has been proposed to contribute to the pathophysiology of schizop
renia and as a target for therapeutic intervention. In the lack of direct a
denosine agonists, allopurinol may indirectly elevate adenosine levels by i
nhibiting degradation of purines. We report two cases of poorly responsive
schizophrenic patients who improved considerably with add-on allopurinol 30
0 mg / day. Their clear clinical improvement warrant further investigation
of allopurinol, as well as other purinergic strategies, for the treatment o
f schizophrenia. (C) 2001 Lippincott Williams & Wilkins.