Effect of Hypoxia on Monoamine Synthesis in Brains of Developing Rats

Neonatology ◽  
1977 ◽  
Vol 31 (1-2) ◽  
pp. 122-126 ◽  
Author(s):  
T. Hedner ◽  
P. Lundborg ◽  
J. Engel
Keyword(s):  
Monoamine Synthesis

Effects of 5-HT1AReceptor Agonists on Patterns of Rat Motor Activity in Relation to Effects on Forebrain Monoamine Synthesis

1993 ◽  
Vol 72 (6) ◽  
pp. 398-406 ◽  
Author(s):  
Sven Ahlenius ◽  
Viveka Hillegaart ◽  
Peter Salmi ◽  
Agneta Wijkström
Keyword(s):  
Motor Activity ◽  
Monoamine Synthesis

The effects of himantane and cycloprolylglycine on the enzymatic linkage of monoamine synthesis in the rat brain

2012 ◽  
Vol 6 (4) ◽  
pp. 272-277 ◽  
Author(s):  
V. B. Narkevich ◽  
I. P. Ovchinnikova ◽  
P. M. Klodt ◽  
V. S. Kudrin
Keyword(s):  
Rat Brain ◽  
Monoamine Synthesis

INFLUENCE OF DRUGS ON MONOAMINE SYNTHESIS IN RAT F0REBRAIN AFTER AX0T0MY

Abstracts ◽  
1977 ◽  
pp. 546
Author(s):  
Wolfgang Kehr ◽  
Wolfgang Speckenbach ◽  
Renate Zimmermann
Keyword(s):  
Monoamine Synthesis

Methamphetamine-Induced Depression of Monoamine Synthesis in the Rat: Development of Tolerance

1985 ◽  
Vol 44 (3) ◽  
pp. 852-855 ◽  
Author(s):  
Christopher J. Schmidt ◽  
Patricia K. Somalia ◽  
Glen R. Hanson ◽  
Michael A. Peat ◽  
James W. Gibb
Keyword(s):  
Monoamine Synthesis ◽  
Rat Development ◽  
Development Of Tolerance

Pediatric Neurotransmitter Disorders

2017 ◽  
Author(s):  
Phillip L. Pearl ◽  
William P. Welch
Keyword(s):  
Elevated Serum ◽  
Serum Levels ◽  
Acid Decarboxylase ◽  
Succinic Semialdehyde ◽  
Monoamine Synthesis ◽  
Succinic Semialdehyde Dehydrogenase ◽  
Amino Acid Decarboxylase ◽  
Semialdehyde Dehydrogenase ◽  
Glycine Encephalopathy ◽  
Heterozygous Form

The pediatric neurotransmitter disorders represent an enlarging group of neurological syndromes characterized by inherited abnormalities of neurotransmitter synthesis, metabolism, and transport. Disorders involving monoamine synthesis include guanosine triphosphate cyclohydrolase deficiency (Segawa disease or classical Dopa-responsive dystonia as the heterozygous form), aromatic amino acid decarboxylase deficiency, tyrosine hydrolase deficiency, sepiapterin reductase deficiency, and disorders of tetrahydrobiopterin synthesis. These disorders can be classified according to whether they feature elevated serum levels of phenylalanine. Disorders of γ-amino butyric acid (GABA) metabolism include succinic semialdehyde dehydrogenase deficiency and GABA-transaminase deficiency. Glycine encephalopathy is typically manifested by refractory neonatal seizures due to a defect in the glycine degradative pathway. Pyridoxine-responsive seizures have now been associated with deficiency of α-aminoadipic semialdehyde dehydrogenase as well as a variants requiring therapy with pyridoxal-5-phosphate and folinic acid.

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