Abstract
In 22 patients with major affective disorders, phenyl-ethylamine (PE) excretion tended to be higher and more variable in 12 females (25 ± 39 μg/d) than in 10 males (8 ± 1 μg/day). In a subgroup of 15 patients studied intensively as part of a treatment trial with the MA0-inhibitors, clorgyline and pargyline, pretreatment PE excretion was not consistently associated with differences in severity of depression, anxiety, activation or hypomania, although almost all correlations with psychopathology were in the negative direction, including several [self-rated dysphoria (r=-.55), anger (r=-.49), functional deficit (r=-.59)] which were statistically significant. Excretion of m-tyramine (m-TA) also exhibited generally negative associations with psychopathology, including self-rated depression (r=-.52) and anxiety (r=-.59), while hypomania was positively correlated (r=.72). Significant cross-correlations among PE, m-TA, and p-TA were not present at baseline, but MAO-inhibitor treatment led to intercorrelated increases in these trace amines, as well as phenylethanolamine, o-TA and platelet MAO activity changes. Increased PE excretion was associated with significantly decreased self-rated depression and anxiety during MAO-inhibitor treatment. Some baseline cardiovascular measures were negatively correlated with PE excretion, including systolic blood pressure, pulse and plasma norepinephrine concentrations, while baseline p-TA excretion was significantly correlated with pulse increases and systolic and diastolic blood pressure reductions produced by standing. These associations suggest that further study of behavioral connections with PE and m-TA excretion and of cardiovascular interactions with p-TA and PE might be of interest. Our data could be considered consistent with an amended hypothesis relating phenylethylamine to a cluster of depression-related symptoms including dysphoria and anger, but not depressed mood alone.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Baldessarini R. J. & Fischer J. E. (1978) Trace amines and alternative neurotransmitters in the central nervous system. Biochem. Pharmcol. 27, 621–626.
Bonham Carter S. M., Reveley M. A., Sandler M., Dewhurst S. J., Little B. C., Hayworth J. & Priest R. G. (1980) Decreased urinary output of conjugated tyramine is associated with lifetime vulnerability to depressive illness. Psychiatry Res. 3, 13–21.
Fischer B. & Heller B. (1972) Phenethylamine as a neurohumoral agent in brain. Behav. Neuropsychiat. 4, 8–11.
Fischer E., Spatz H., Saavedra J. M., Reggiani H., Miro A. H. & Heller B. (1972) Urinary elimination of phenethylamine. Biol. Psychiatry 5, 139–147.
Jeste D. V., Doongaji D. R., Panjwani D., Datta M., Potkin, S. G., Karoum F., Thatte S., Sheth A. S., Apte J. S. & Wyatt R. J. (1980) Cross-cultural study of a biochemical abnormality in paranoid schizophrenia. Psychiatry Res. 3, 341–352.
Jones R. S. G. (1982) Tryptamine: A neuromodulator or neurotransmitter in mammalian brain? Prog. Neurobiol. 19, 117–139.
Karoum F., Nasrallah H., Potkin S., Chuang L., Moyer-Schwing J., Phillips I. & Wyatt R. J. (1979) Mass fragmentography of phenylethylamine, m- and p-tyramine and related amines in plasma, cerebrospinal fluid, urine and brain. J. Neurochem. 33, 201–212.
Karoum F., Speciale S. G. Jr., Chuang L.-W. & Wyatt R. J. (1982a) Selective effects of phenylethylamine on central catecholamines: A comparative study with amphetamine. J. Pharmacol. Ther. 223, 432–439.
Karoum F., Linniola M., Potter W. Z., Chuang L.-W., goodwin, F. K. & Wyatt R. J. (1982b) Fluctuating high urinary phenylethylamine excretion rates in some bipolar affective disorder patients. Psychiatry Res. 6, 215–222.
Lake C. R., Pickar D., Ziegler M. G., Lipper S., Slater S. & Murphy D. L. (1982) High plasma norepinephrine levels in patients with major affective disorder. Am. J. Psychiatry 139, 1315–1318.
Lipper S., Murphy D. L., Slater S. & Buchsbaum M. S. (1979) Comparative behavioral effects of clorgyline and pargy- line in man: A preliminary evaluation. Psychopharmacology 62, 123–128.
Mosnaim A. D. & Wolf M. E. (1978) Noncatecholic Phenylethylamines - Part 1 - Phenylethylamine: Biological Mechanisms and Clinical Aspects, Marcel Dekker, Inc., New York.
Mosnaim A. D. & Wolf M. E. (1980) Noncatecholic Phenylethylamines - Part 2 - Phenylethanolamine, Tyramines, and Octopamine. Marcel Dekker, Inc., New York.
Murphy D. L. (1972) Amine precursors, amines and false neurotransmitters in depressed patients. Am. J. Psychiatry 129, 141–148.
Murphy D. L., Lipper S., Pickar D., Jimerson D., Cohen R. M., Garrick N. A., Alterman I. S. & Campbell I. C. (1981) Selective inhibition of monoamine oxidase type A: Clinical antidepressant effects and metabolic changes in man, in Monoamine Oxidase Inhibitors. The State of the Art ( Youdim M.B.H. & Paykel E.S., eds.) pp. 189–205. John Wiley & Sons, New York.
Murphy D. L., Cohen R. M., Siever L. J., Roy B., Karoum F., Wyatt R. J., Garrick N. A. & Linnoila M. (1983) Clinical and laboratory studies with selective monoamine-oxidase- inhibiting drugs: Implications for hypothesized neurotransmitter changes associated with depression and antidepressant drug effects, in Monoamine Oxidase and Its Selective Inhibitors: New Concepts in Therapy and Research ( Beckmann H. & Riederer P., eds.) pp. 287–303. Basel, Karger.
Paulos M. A. & Tessel R. E. (1982) Excretion of β-phenethylamine is elevated in humans after profound stress. Science 215, 1127–1129.
Potkin A. G., Karoum F., Chuang L.-W., Cannon-Spoor H. E., Phillips I. & Wyatt R. J. (1979) Phenylethylamine in paranoid chronic schizophrenia. Science 206, 470–471.
Roy B. F., Murphy D. L., Lipper S., Siever L. J., Alterman I. S. Jimerson D., Lake C. R. & Cohen R. M. (submitted) Cardiovascular effects of the selective monoamine oxidase- inhibiting antidepressant clorgyline: Correlations with clinical responses and changes in catecholamine metabolism.
Sabelli H. C. & Mosnaim A. D. (1974) Phenylethylamine hypothesis of affective behavior. Am. J. Psychiatry 131, 695–699.
Sabelli H. C., B0ris0n R. L., Diamond B. I., Havdala H. S. & Narasimhachar N. (1978) β-Phenylethylamine and brain function. Biochem. Pharmacol. 27, 1729–1730.
Sandler M., Ruthven C. R., Goodwin R. L. & Coppen A. (1979a) Decreased cerebrospinal fluid concentration of free phenylacetic acid in depressive illness. Clin. Chem. Acta 93, 169–171.
Sandler M., Ruthven C. R. J., Goodwin B. L. & Reynolds G. P. (1979b) Deficient production of tyramine and octopamine in cases of depression. Nature 278, 357–358.
Spatz H. & Spatz N. (1978) Urinary and brain phenylethyl- amine levels under normal and pathological conditions, in Noncatecholic Phenylethylamines - Part 1 - Phenylethyl- amine: Biological Mechanisms and Clinical Aspects ( Mosnaim A.D. & Wolf M.E., eds.) pp. 447–474. Marcel Dekker, New York.
Van Kammen D. P. & Murphy D. L. (1975) Attenuation of the euphoriant and activating effects of d- and 1-amphetamine by lithium carbonate treatment. Psychopharmacologia 44, 215–224.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1984 The Humana Press Inc.
About this chapter
Cite this chapter
Murphy, D.L., Karoum, F., Alterman, I., Lipper, S., Wyatt, R.J. (1984). Phenylethylamine, Tyramine and Other Trace Amines in Patients with Affective Disorders: Associations with Clinical State and Antidepressant Drug Treatment. In: Boulton, A.A., Baker, G.B., Dewhurst, W.G., Sandler, M. (eds) Neurobiology of the Trace Amines. Humana Press. https://doi.org/10.1007/978-1-4612-5312-9_43
Download citation
DOI: https://doi.org/10.1007/978-1-4612-5312-9_43
Publisher Name: Humana Press
Print ISBN: 978-1-4612-9781-9
Online ISBN: 978-1-4612-5312-9
eBook Packages: Springer Book Archive