scholarly journals A mutation in the enzyme monoamine oxidase explains part of the Astyanax cavefish behavioural syndrome

2014 ◽  
Vol 5 (1) ◽  
Author(s):  
Yannick Elipot ◽  
Hélène Hinaux ◽  
Jacques Callebert ◽  
Jean-Marie Launay ◽  
Maryline Blin ◽  
...  
1961 ◽  
Vol 107 (447) ◽  
pp. 239-243 ◽  
Author(s):  
W. G. Dewhurst ◽  
C. M. B. Pare

The discovery that iproniazid benefits certain subjects with depression, linked with the demonstration that it inhibits the enzyme monoamine oxidase (MAO), led to the hypothesis that inhibition of MAO was the essential mechanism by which iproniazid caused relief of symptoms (Pletscher, 1959). Iproniazid, unfortunately, can produce serious toxic effects, particularly on the liver (Pare and Sandler, 1959), and this has limited its clinical application. For this reason a search has been made for MAO inhibitors with an effective anti-depressant action yet without the serious toxic effects of iproniazid. Among the newer compounds for which such claims have been made is N-isonicotinoyl (-N-N-benzylcarboxamidoethyl) hydrazine or Nialamide.


2019 ◽  
Vol 46 (2) ◽  
pp. 2285-2292 ◽  
Author(s):  
Izaviany da Silva Schmitz ◽  
Larissa Finger Schaffer ◽  
Alcindo Busanello ◽  
Catiuscia Molz de Freitas ◽  
Roselei Fachinetto ◽  
...  

2019 ◽  
Vol 55 (88) ◽  
pp. 13267-13270 ◽  
Author(s):  
Won Young Kim ◽  
Miae Won ◽  
Abbas Salimi ◽  
Amit Sharma ◽  
Jong Hyeon Lim ◽  
...  

Mitochondrial enzyme monoamine oxidase (MAO-A) is known to be overexpressed in prostate cancer (PCa) cells.


1992 ◽  
Vol 18 (3-4) ◽  
pp. 191-200 ◽  
Author(s):  
M. Strolin Benedetti ◽  
P. Dosiert ◽  
K.F. Tipton

1977 ◽  
Vol 11 (2) ◽  
pp. 195-198
Author(s):  
V. Ya. Grinshtein ◽  
A. A. Prikulis ◽  
B. A. Grinberga ◽  
Ya. Ya. Shusters ◽  
A. P. Skutelis

ChemCatChem ◽  
2012 ◽  
Vol 4 (9) ◽  
pp. 1259-1261 ◽  
Author(s):  
Ian Rowles ◽  
Kirk J. Malone ◽  
Laura L. Etchells ◽  
Simon C. Willies ◽  
Nicholas J. Turner

Nukleonika ◽  
2014 ◽  
Vol 59 (3) ◽  
pp. 91-95 ◽  
Author(s):  
Sylwia Dragulska ◽  
Marianna Kańska

Abstract The enzymatic deamination of 5-fl uorotryptamine and 5-hydroxytryptamine, 5-HT, catalysed by enzyme monoamine oxidase A (MAO-A, EC 1.4.3.4) was investigated using the kinetic (KIE) and solvent (SIE) isotope effects methods. The numerical values of deuterium isotope effects in the (1R) positions of 5-F-tryptamine were determined using non-competitive spectrophotomeric method. Isotopologue 5-F-[(1R)- -2H]-tryptamine, needed for kinetic studies was obtained by enzymatic decarboxylation of 5´-fl uoro-L-tryptophan, 5´-F-L-Trp, in fully deuteriated medium.


1961 ◽  
Vol 107 (448) ◽  
pp. 572-574
Author(s):  
J. G. Hegarty ◽  
A. R. Dabbs ◽  
R. T. St. Blaize-Molony

Nialamide is claimed to inhibit the activity of the enzyme monoamine oxidase which is known to be responsible for the breakdown by catalytic oxidation of various amines, e.g. serotonin and norepinephrine. It has been suggested that depression may be associated with inadequate levels of serotonin and/or norepinephrine and that the administration of a monoamine oxidase inhibitor should rationally help to relieve depression. No serious side-effects have been reported in the available literature except that agitated patients might become somewhat more agitated and overactive.


1973 ◽  
Vol 73 (3) ◽  
pp. 509-517 ◽  
Author(s):  
H. Parvez ◽  
S. Parvez

ABSTRACT The activity of the enzyme monoamine oxidase (MAO) in the brain, heart, liver and spleen of rats 10 weeks after adrenalectomy was determined. Another group of adrenalectomized rats received 5 mg of hydrocortisone daily for the period of 10 days and their MAO activity was compared with that of control adrenalectomized rats. There was a significant rise in MAO activity following adrenalectomy in the tissue homogenate, mitochondrial and supernatant fractions of all the organs studied. Hydrocortisone administration decreased MAO activity to the level of normal rats. These results suggest that corticoids serve as a rate limiting factor for the activity of the enzyme MAO. This hypothesis was further tested in normal rats by blocking the biosynthesis of glucocorticoids with Metopirone®. Four hours after a single injection of 75 mg Metopirone the cerebral, hepatic and cardiac MAO showed marked increases from control levels. These results suggest that adrenal cortical steroids present in the circulation of normal animals regulate the activity of the enzyme MAO in most organs.


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