Inhibition of tetrahydrobiopterin synthesis reduces in vivo nitric oxide production in experimental endotoxic shock

被引:41
作者
Bune, AJ
Brand, MP
Heales, SJR
Shergill, JK
Cammack, R
Cook, HT
机构
[1] UNIV LONDON IMPERIAL COLL SCI & TECHNOL, SCH MED, DEPT HISTOPATHOL, LONDON W2 1PG, ENGLAND
[2] UNIV LONDON, NEUROL INST, DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
[3] UNIV LONDON, UNIV LONDON KINGS COLL, DIV LIFE SCI, CTR STUDY MET BIOL & MED, LONDON W8 7AH, ENGLAND
关键词
D O I
10.1006/bbrc.1996.0348
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
Nitric oxide synthesis requires the cofactor tetrahydrobiopterin. We have examined the effect on nitric oxide synthesis in experimental endotoxic shock of 2,4-diamino-6-hydroxypyrimidine (DAHP), an inhibitor of GTP cyclohydrolase I, the first and rate limiting enzyme for tetrahydrobiopterin synthesis. Rats given lipopolysaccharide (LPS, 10 mg/kg) showed a large rise in plasma nitrate at 4 and 8 hours which was significantly reduced by DAHP (1 g/kg) given at the same time as LPS. There was a 40-50% reduction in the haem-NO signal detected in kidney by electron paramagnetic resonance spectroscopy. LPS produced hypotension at 3 hours and 6 hours and this was ameliorated at 6 hours in rats given DAHP. DAHP abolished the rise in kidney tetrahydrobiopterin levels seen 4 hours after LPS but no effect was seen on induction of inducible nitric oxide synthase (iNOS) as assessed by immunohistochemistry and reverse transcriptase PCR. consistent with the effect of DAHP being by reduction of tetrahydrobiopterin levels. The results show that inhibition of tetrahydrobiopterin synthesis is an effective strategy to reduce nitric oxide synthesis by iNOS in vivo. (C) 1996 Academic Press, Inc.
引用
收藏
页码:13 / 19
页数:7
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