Effects of Hydrazines on the Metabolism of Certain Amines and Amino Acids

Item

Title
Effects of Hydrazines on the Metabolism of Certain Amines and Amino Acids
Date
1964
Index Abstract
Not Available
Photo Quality
Not Needed
Report Number
AMRL TR 64-113
Corporate Author
Oregon State University
Laboratory
Biomedical Laboratory
Extent
46
Identifier
AD0610570
Access Rights
CFSTI
Distribution Classification
1
Contract
AF 33(657)-11757
DoD Project
6302
DoD Task
630202
DTIC Record Exists
No
Distribution Change Authority Correspondence
None
Distribution Conflict
No
Abstract
Certain effects of simple hydrazines via i.p. administration upon the metabolism of amines and amino acids by rats were examined. Unsymmetrical dimethylhydrazine (UDMH), monomethylhydrazine (MMH) and hydrazine strongly inhibited oxidation of putrescine-1, 4-C14 (1, 4-diamino butane) and methylamine-C14 to C14O2 by intact rats. MMH caused a virtually complete inhibition of monoamine oxidase activity in vivo, but inhibition by UDMH and hydrazine was limited. In vivo and in vitro diamine oxidase activity was heavily suppressed by all three hydrazines. The inhibition duration of methylamine oxidase by UDMH and hydrazine was found to last several days. Inhibition of putrescine oxidation was reversed within 3 days, indicating a possible difference between the enzyme systems which metabolize methylamine and putrescine. The metabolism of varied oral and intraperitoneal doses of L-glutamic acid-1-C14 by rats was inhibited by hydrazine, but not by UDMH or MMH. Oxidation of large oral doses of L-alanine-1-C14 to respiratory C14O2 was slightly inhibited by UDMH, MMH and blocked to a greater extent by hydrazine. Similar results were found in the metabolism of low levels of gamma -aminobutyric acid-1-C14 (GABA-1-C14) except that hydrazine intoxication caused an almost complete inhibition of GABA-1-C14 conversion to C14O2.
Report Availability
Full text available
Date Issued
1964-12
Provenance
RAF Centre of Aviation Medicine
Type
report
Format
1 online resource
Creator
Reed, D. J.
Dost, F. N.
Wang, C. H.