BRAIN DISORDERS INDUCED BY PHARMACOLOGICAL BLOCKADE OF PENTOSE PHOSPHATE PATHWAY

被引:95
作者
HERKEN, H
LANGE, K
KOLBE, H
机构
[1] Pharmakologisches Institut der Freien Universität Berlin, Thielallee 69 /73
关键词
D O I
10.1016/0006-291X(69)90654-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
6-ANADP synthesized by the endoplasmic glycohydrolase in the brain cells of rats after application of 6-AN is an inhibitor of NADP-dependent dehydrogenases. Under conditions in vivo, 6-phosphogluconate dehydrogenase seems to be the most sensitive enzyme. In the brain, a high accumulation of 6-phosphogluconate and, to a smaller extent, of glucose 6-phosphate was found. The determination of the ratio glucose 6-phosphate: fructose 6-phosphate in the brains of animals pre-treated with 6-AN showed that the accumulation of 6-phosphogluconate also seems to inhibit the PGI in vivo. After application of 14C D-glucose the specific activity of the RNA from cell nuclei of the brain is considerably decreased in animals pretreated with 6-AN. This is supposed to be caused by the inhibition of the oxidative and the non-oxidative part of the pentose phosphate cycle. © 1969.
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页码:93 / &
相关论文
共 26 条
[1]  
BASS R, 1967, THESIS FU BERLIN
[2]  
BRUNNEMANN A, 1964, N-S ARCH EX PATH PH, V246, P493
[3]   UNTERSUCHUNGEN ZUM MECHANISMUS ZENTRALNERVOSER FUNKTIONSSTORUNGEN DURCH 6-AMINONICOTINAMID [J].
COPER, H ;
HADASS, H ;
LISON, H .
NAUNYN-SCHMIEDEBERGS ARCHIV FUR PHARMAKOLOGIE, 1966, 255 (01) :97-&
[4]   EINFLUSS VON NADP-ANALOGEN AUF DIE REAKTIONSGESCHWINDIGKEIT EINIGER NADP-BEDURFTIGER OXYDOREDUKTASEN [J].
COPER, H ;
NEUBERT, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1964, 89 (01) :23-&
[5]   SCHADIGUNG DES ZENTRALNERVENSYSTEMS DURCH ANTIABOLITEN DES NIKOTINSAUREAMIDS - EIN BEITRAG ZUR MOLEKULARPATHOLOGIE DER PYRIDINNUKLEOTIDE [J].
COPER, H ;
HERKEN, H .
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1963, 88 (42) :2025-+
[6]  
DIETRICH LS, 1958, J BIOL CHEM, V233, P964
[7]   THE INHIBITION OF PHOSPHOGLUCOSE ISOMERASE BY D-ERYTHROSE 4-PHOSPHATE [J].
GRAZI, E ;
DEFLORA, A ;
PONTREMOLI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1960, 2 (02) :121-125
[8]  
HERKEN H, 1968, 3 P PHARM M, V4, P3
[9]  
HORECKER BL, 1968, CARBOHYD METABOL, V1, P139
[10]  
JOHNSON WJ, 1956, FED PROC, V15, P284