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Research Article Free access | 10.1172/JCI105754

Biochemical and pharmacologic effects of α-methyltyrosine in man

Karl Engelman, David Horwitz, Eric Jéquier, and Albert Sjoerdsma

Experimental Therapeutics Branch, National Heart Institute, Bethesda, Maryland

Find articles by Engelman, K. in: PubMed | Google Scholar

Experimental Therapeutics Branch, National Heart Institute, Bethesda, Maryland

Find articles by Horwitz, D. in: PubMed | Google Scholar

Experimental Therapeutics Branch, National Heart Institute, Bethesda, Maryland

Find articles by Jéquier, E. in: PubMed | Google Scholar

Experimental Therapeutics Branch, National Heart Institute, Bethesda, Maryland

Find articles by Sjoerdsma, A. in: PubMed | Google Scholar

Published March 1, 1968 - More info

Published in Volume 47, Issue 3 on March 1, 1968
J Clin Invest. 1968;47(3):577–594. https://doi.org/10.1172/JCI105754.
© 1968 The American Society for Clinical Investigation
Published March 1, 1968 - Version history
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Abstract

Alpha methyltyrosine (α-MPT) was administered to 52 patients from 4 days to 10 months; 22 patients were cases of pheochromocytoma and 20 had essential hypertension. Inhibition of catecholamine synthesis in the range of 50-80% was achieved with divided daily drug dosage of from 1.0 to 4.0 g. Striking clinical benefit was noted in patients with pheochromocytoma in whom the drug was used in preparation for surgery and during chronic medical management. The drug appeared to have limited usefulness when used in essential hypertension, unless added to existing therapy with conventional agents. No beneficial effects were noted in thyrotoxicosis, glaucoma, and Raynaud's phenomenon. Untoward effects in order of decreasing incidence were: sedation (with insomnia on withdrawal), anxiety, tremor, diarrhea, and galactorrhea. Drug crystalluria, which has been observed in animals and is currently restrictive of clinical trials, was not observed in these studies. Evidence is presented that the minor conversion of α-MPT to methyldopa probably does not contribute significantly to the central and peripheral effects of the drug.

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