INHIBITION OF DELTA-AMINOLEVULINIC-ACID SYNTHETASE AND DELTA-AMINOLEVULINIC-ACID DEHYDRASE BY L-2-AMINO-4-METHOXY-TRANS-3-BUTENOIC ACID IN THE RAT

被引:8
作者
DASHMAN, T
KAMM, JJ
机构
[1] Department of Biochemistry, Drug Metabolism Hoffmann-La Roche Inc., Nutley
关键词
D O I
10.1016/0024-3205(79)90129-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The rate limiting enzyme of heme biosynthesis, δ-aminolevulinic acid synthetase (ALA synthetase), and the second enzyme in the heme biosynthetic pathway, δ-aminolevulinic acid dehydrase (ALA dehydrase), were inhibited by the olefinic amino acid L-2-amino-4-methoxy - trans-3-butenoic acid (AMTB). Administration of AMTB (20 mg/kg; i.p.) to rats inhibited ALA synthetase and ALA dehydrase in control animals and in animals with markedly elevated activity of ALA synthetase which resulted from the administration of 3,5-dicarbethoxy-1,4-dimethyl-collidine (DDC, 200 mg/kg, i.p.) or allylisopropylacetamide (200 mg/kg, s.c.). AMTB also blocked the synthesis of rat hepatic porphyrins and inhibited the increase in the urinary excretion of δ-aminolevulinic acid and porphobilinogen following DDC (150 mg/kg, p.o.) administration. Preincubation of AMTB with liver mitochondria or a soluble fraction of liver decreased the activity of mitochondrial ALA synthetase and soluble ALA dehydrase, respectively. © 1979.
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页码:185 / 192
页数:8
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