Nitric oxide is generated on the skin surface by reduction of sweat nitrate

被引:135
作者
Weller, R
Pattullo, S
Smith, L
Golden, M
Ormerod, A
Benjamin, N
机构
[1] UNIV ABERDEEN,SCH MED,DEPT MED & THERAPEUT,ABERDEEN AB9 2ZD,SCOTLAND
[2] ABERDEEN ROYAL HOSP,DEPT DERMATOL,ABERDEEN,SCOTLAND
关键词
infection; L-arginine analog;
D O I
10.1111/1523-1747.ep12363167
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Nitric oxide (NO) is known to be synthesized by mammalian cells from L-arginine by a group of NO synthase enzymes. We now show that NO is generated from human skin and propose a different mechanism of production. Whereas enzymatic NO synthesis is inhibited by monomethyl L-arginine, this arginine analog, when infused into the brachial artery at concentrations sufficient to inhibit endothelial NO synthase activity, has Little effect on hand skin NO production, Hand skin NO production is increased by topical acidification of the skin surface and greatly increased by the addition of nitrite solutions, We propose that NO generation from skin derives from sweat nitrite (the concentration of which was found to average 3.4 mu M in six subjects) due to chemical reduction consequent to the acidic nature of sweat. Sweat contains nitrate in appreciable amounts, and skin commensal bacteria can synthesize nitrate reductase enzyme. Patients on long-term tetracycline antibiotics showed significantly reduced skin NO synthesis, although topical antiseptic and antibiotics had little effect on NO generation in the short-term, We propose that NO generation from skin is dependent on bacterial nitrate reduction to nitrite and subsequent reduction by acidification. We speculate that this has a physiologic role in the inhibition of infection by pathogenic fungi and other susceptible microorganisms and may affect cutaneous T-cell function, keratinocyte differentiation, and skin blood flow.
引用
收藏
页码:327 / 331
页数:5
相关论文
共 42 条
[1]  
ADAMS LB, 1991, J IMMUNOL, V147, P1642
[2]   STOMACH NO SYNTHESIS [J].
BENJAMIN, N ;
ODRISCOLL, F ;
DOUGALL, H ;
DUNCAN, C ;
SMITH, L ;
GOLDEN, M ;
MCKENZIE, H .
NATURE, 1994, 368 (6471) :502-502
[3]   LOCAL INHIBITION OF CONVERTING ENZYME AND VASCULAR-RESPONSES TO ANGIOTENSIN AND BRADYKININ IN THE HUMAN FOREARM [J].
BENJAMIN, N ;
COCKCROFT, JR ;
COLLIER, JG ;
DOLLERY, CT ;
RITTER, JM ;
WEBB, DJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1989, 412 :543-555
[4]  
BLANCO FJ, 1995, AM J PATHOL, V146, P75
[5]   A MODIFIED ANAEROBIC METHOD OF SWEAT COLLECTION [J].
BOYSEN, TC ;
YANAGAWA, S ;
SATO, F ;
SATO, K .
JOURNAL OF APPLIED PHYSIOLOGY, 1984, 56 (05) :1302-1307
[6]  
BRAUN C, 1991, J BIOL CHEM, V266, P22785
[7]   INTERLEUKIN-4 AND INTERLEUKIN-10 INHIBIT NITRIC OXIDE-DEPENDENT MACROPHAGE KILLING OF CANDIDA-ALBICANS [J].
CENCI, E ;
ROMANI, L ;
MENCACCI, A ;
SPACCAPELO, R ;
SCHIAFFELLA, E ;
PUCCETTI, P ;
BISTONI, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (05) :1034-1038
[8]   RELEASE BY ULTRAVIOLET-B (UVB) RADIATION OF NITRIC-OXIDE (NO) FROM HUMAN KERATINOCYTES - A POTENTIAL ROLE FOR NITRIC-OXIDE IN ERYTHEMA PRODUCTION [J].
DELICONSTANTINOS, G ;
VILLIOTOU, V ;
STRAVRIDES, JC .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (06) :1257-1265
[9]   INVOLVEMENT OF NITRIC-OXIDE IN THE REFLEX RELAXATION OF THE STOMACH TO ACCOMMODATE FOOD OR FLUID [J].
DESAI, KM ;
SESSA, WC ;
VANE, JR .
NATURE, 1991, 351 (6326) :477-479
[10]   DISTRIBUTION OF CONSTITUTIVE NITRIC-OXIDE SYNTHASE IMMUNOREACTIVITY AND NADPH-DIAPHORASE ACTIVITY IN MURINE TELOGEN AND ANAGEN SKIN [J].
DIPPEL, E ;
MAYER, B ;
SCHONFELDER, G ;
CZARNETZKI, BM ;
PAUS, R .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1994, 103 (01) :112-115