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Szabo provided cysteamine as a dopamine antagonist and its close similarity with the parkinsongenic neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) (that also induced duodenal ulcers)[129,130] in support of the theory holding schizophrenia, Parkinson’s disease, and ulcer disease as dopamine system failures, and dopamine antagonists (ulcerogenic potential)/dopamine agonists (therapy) in peptic ulcer therapy[131]