Metabolism, Distribution, and Disappearance of Infected β-Phenylethylamine in the Rat

1975 ◽  
Vol 53 (1) ◽  
pp. 42-50 ◽  
Author(s):  
P. H. Wu ◽  
Alan A. Boulton

In the absence of a monoamine oxidase inhibitor, the bulk of intravenously injected radioactively labelled β-phenylethylamine was oxidized to phenylacetic acid. In the presence of pargyline, most of the label in tissues remained as unchanged phenylethylamine; small amounts of labelled phenylethanolamine, tyramine and octopamine were also identified. After intravenous injection of [14C]phenylalanine, only very small amounts of [14C]phenylethylamine could be located in urine and faeces. β-Phenylethylamine became concentrated in all tissues, including brain, following intravenous introduction both in the presence and absence of pargyline. Its clearance from these tissues and from brain regions was very fast.

1974 ◽  
Vol 52 (5) ◽  
pp. 374-381 ◽  
Author(s):  
P. H. Wu ◽  
Alan A. Boulton

The major cerebral metabolic products of intraventricularly injected p-tyramine were octopamine and p-hydroxyphenylacetaldehyde. Only tiny amounts of p-hydroxyphenylacetic acid and p-hydroxyphenylethanol were found and these were located in the cerebral cortex (i.e. 'rest'). In brain regions isolated in the absence of pargyline the principal metabolite was p-hydroxyphenylacetaldehyde recovered in an acidic–neutral fraction; in the presence of pargyline, however, the majority of the label was associated with the amines tyramine and octopamine. In the caudate nucleus octopamine was essentially absent both in the presence and absence of pargyline.The loss of octopamine from all regions in the presence of pargyline was approximately exponential (i.e. first order) whereas in the absence of the monoamine oxidase inhibitor the loss was more complicated than first order. In most cases the loss of p-tyramine was greater than first order. Approximate half-lives based on these clearance values indicated a rapid turnover for p-tyramine and octopamine in all regions both in the presence and absence of pargyline.


1989 ◽  
Vol 4 (3) ◽  
pp. 175-181
Author(s):  
J.F. Lipinski ◽  
R.C. Alexander

SummaryThe authors have reviewed 13 published studies on methionine administration, usually in combination with a monoamine oxidase inhibitor (MAOI), to chronically psychotic patients, using modern (DSM-III) diagnostic criteria. Four of these studies contained sufficient descriptive data to allow reappraisal of the effects. The results of the review suggest that a proportion of the patients experienced the induction of a manic episode/antidepressant effects rather than the reported worsening of schizophrenia while treated with a methionine-MAOI combination. It is suggested that these observations are consistent with recent findings that S-adenosyl-L-methionine (SAMe) has antidepressant and mania-inducing effects.


1995 ◽  
Vol 22 (s1) ◽  
pp. S86-S87 ◽  
Author(s):  
N. Hamaue ◽  
T. Endo ◽  
M. Hirafuji ◽  
N. Yamazaki ◽  
H. Togashi ◽  
...  

2010 ◽  
Vol 3 (4) ◽  
pp. 213-215
Author(s):  
Junji Takeshita ◽  
Deborah Goebert ◽  
John Huh ◽  
Brett Lu ◽  
Diane Thompson ◽  
...  

2000 ◽  
Vol 52 (4) ◽  
pp. 451-459 ◽  
Author(s):  
B. D. SLOLEY ◽  
L. J. URICHUK ◽  
P. MORLEY ◽  
J. DURKIN ◽  
J. J. SHAN ◽  
...  

Author(s):  
Amedeo S. Marrazzi ◽  
E. Ross Hart ◽  
Jose M. Rodriguez ◽  
Melvyn I. Gluckman ◽  
Zola P. Horovitz ◽  
...  

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