Amitriptyline: A controlled trial in chronic depressive states

1962 ◽  
Vol 108 (457) ◽  
pp. 859-861 ◽  
Author(s):  
Andrew Skarbek ◽  
Daphne Smedberg

Amitriptyline hydrochloride is 5–(3 dimethylaminopropylidine)–dibenzo (a,d) (1,4) cycloheptadiene hydrochloride. Structurally it is not related to the hydrazines and is not a monoamine oxidase inhibitor. It bears some resemblance to the phenothiazines and its chemical structure is related to imipramine, in which the central seven numbered ring is azepine, nitrogen replacing the partially unsaturated carbon of the amitriptyline cycloheptadiene ring (Dorfman, 1960; Vernier, 1961).

1965 ◽  
Vol 111 (480) ◽  
pp. 1095-1100 ◽  
Author(s):  
J. C. Barker ◽  
I. A. Jan ◽  
M. David Enoch

Mebanazine (‘Actomol’) introduced in 1960 for the treatment of depression is a monoamine-oxidase inhibitor hydrazine derivative having the following structural formula:


1972 ◽  
Vol 50 (9) ◽  
pp. 923-926 ◽  
Author(s):  
John G. Sinclair

Previous reports indicate that meperidine but not morphine produces a marked hyperpyrexia and death in monoamine oxidase inhibitor (MAOI) pretreated rabbits. Since this interaction may be predictive of a serious clinical drug–drug interaction, several other narcotic or structurally related agents were similarly tested in this study. Ethoheptazine citrate (10 mg/kg i.v.), whose chemical structure closely resembles that of meperidine, was found to produce extreme hyperpyrexia and death in rabbits pretreated with an MAOI, phenelzine sulfate (30 mg/kg i.p.), 42 and 18 h prior to temperature recording. This interaction appears to be due to an exaggerated 5-hydroxytryptamine effect. Of the other drugs tested, methadone was found to be inconsistent in its actions whereas anileridine alphaprodine, piminodine, dextropropoxyphene, levorphanol, levallorphan, codeine, and nalorphine were shown to be inactive.


1960 ◽  
Vol 106 (445) ◽  
pp. 1533-1538 ◽  
Author(s):  
R. Middlefell ◽  
I. Frost ◽  
G. P. Egan ◽  
H. Eaton

Phenelzine, β-phenylethylhydrazine, of structural formula, is regarded as a potent, rapidly acting, long-lasting monoamine oxidase (M.A.O.) inhibitor. The administration of such compounds protects 5-hydroxytryptamine (serotonin) which is destroyed by M.A.O. 5-hydroxytryptamine is believed to act in the brain as a chemical mediator, the function of which is to control the pulsating action of oligodendroglial cells which supply the other brain tissues with nutrient. It has been suggested that a relative 5-hydroxytryptamine deficiency is the fundamental biochemical disorder of severe depressive states and that M.A.O. inhibitors such as phenelzine tend to promote restoration to more normal concentration and activity.


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 ◽  
...  

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