Evidence for the formation of a novel nitrosothiol from the gaseous mediators nitric oxide and hydrogen sulphide

被引:332
作者
Whiteman, M [1 ]
Li, L
Kostetski, I
Chu, SH
Siau, JL
Bhatia, M
Moore, PK
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Cardiovasc Biol Res Grp, Singapore 117597, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Cardiovasc Biol Res Grp, Singapore 117597, Singapore
[3] Natl Univ Singapore, Fac Engn, Div Bioengn, Singapore 119260, Singapore
基金
英国医学研究理事会;
关键词
reactive oxygen species; hydrogen sulphide; nitric oxide; peroxynitrite; cysthionine-beta-synthase; cystathionine-gamma-synthase;
D O I
10.1016/j.bbrc.2006.02.154
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
The gaseous mediators hydrogen sulphide (H2S) and nitric oxide ((NO)-N-.) are synthesised in the body from L-cysteine and L-arginine, respectively. In the cardiovascular system, (NO)-N-. is an important regulator of vascular tone and its over- or under-production has been linked to a variety of diseases. The physiological significance of H2S is not yet clear but, like (NO)-N-., it exhibits vasodilator activity and may play a part in septic and haemorrhagic shock, hypertension, regulation of cardiac contractility, and in inflammation. To date. there have been no reports of a chemical interaction between H2S and (NO)-N-.. Here we show that incubation of the HAS donor, sodium hydrosulphide, with a range of (NO)-N-. donors and (NO)-N-. gas in vitro leads to the formation of a nitrosothiol molecule as determined by a combination of techniques; electron paramagnetic resonance, amperometry, and measurement of nitrite. We further show that this nitrosothiol did not induce cGMP accumulation in cultured RAW264.7 cells unless (NO)-N-. was released with Cu2+. Finally, using liver homogenates froth LPS treated rats we present evidence for the endogenous formation of this nitrosothiol. These findings provide the first evidence for the formation of a novel nitrosothiol generated by reaction between H2S and (NO)-N-.. We propose that generation of this nitrosothiol in the body may regulate the physiological effects of both (NO)-N-. and H2S. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:303 / 310
页数:8
相关论文
共 40 条
[1]  
Abe K, 1996, J NEUROSCI, V16, P1066
[2]  
Angulo J, 2000, J PHARMACOL EXP THER, V295, P586
[3]  
[Anonymous], 2006, J PHYSIOL-LONDON, DOI DOI 10.1113/jphysiol.2006.116632
[4]  
BECKMAN JS, 1994, METHOD ENZYMOL, V233, P229
[5]   Hydrogen sulfide as a vasodilator [J].
Bhatia, M .
IUBMB LIFE, 2005, 57 (09) :603-606
[6]   Role of hydrogen sulfide in acute pancreatitis and associated lung injury [J].
Bhatia, M ;
Wong, FL ;
Fu, D ;
Lau, HY ;
Moochhala, SM ;
Moore, PK .
FASEB JOURNAL, 2005, 19 (01) :623-+
[7]   Hydrogen sulphide is a mediator of carrageenan-induced hindpaw oedema in the rat [J].
Bhatia, M ;
Sidhapuriwala, J ;
Moochhala, SM ;
Moore, PK .
BRITISH JOURNAL OF PHARMACOLOGY, 2005, 145 (02) :141-144
[8]   HYPERHOMOCYSTEINEMIA - AN INDEPENDENT RISK FACTOR FOR VASCULAR-DISEASE [J].
CLARKE, R ;
DALY, L ;
ROBINSON, K ;
NAUGHTEN, E ;
CAHALANE, S ;
FOWLER, B ;
GRAHAM, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (17) :1149-1155
[9]   Endothelial dysfunction in a murine model of mild hyperhomocyst(e)inemia [J].
Eberhardt, RT ;
Forgione, MA ;
Cap, A ;
Leopold, JA ;
Rudd, MA ;
Trolliet, M ;
Heydrick, S ;
Stark, R ;
Klings, ES ;
Moldovan, NI ;
Yaghoubi, M ;
Goldschmidt-Clermont, PJ ;
Farber, HW ;
Cohen, R ;
Loscalzo, J .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (04) :483-491
[10]  
GEORGE MJ, 1995, J INVEST MED, V43, P451