Effect of prolonged incubation with copper on endothelium-dependent relaxation in rat isolated aorta

被引:19
作者
Chiarugi, A
Pitari, GM
Costa, R
Ferrante, M
Villari, L
Amico-Roxas, M
Godfraind, T
Bianchi, A
Salomone, S
机构
[1] Univ Catania, Dipartimento Farmacol Sperimentale & Clin, Fac Med & Chirurg, I-95125 Catania, Italy
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Stroke & Neurovasc Regulat Lab,Dept Neurosci, Charlestown, MA 02129 USA
[3] Univ Catania, Fac Med & Chirurg, Ist Igiene & Med Preventiva, I-95124 Catania, Italy
[4] Univ Catania, Fac Med & Chirurg, Ist Anat & Istol Patol, I-95125 Catania, Italy
[5] Catholic Univ Louvain, Pharmacol Lab, B-1200 Brussels, Belgium
关键词
copper; endothelium; nitric oxide; superoxide; eNOS; PECAM-1; tiron;
D O I
10.1038/sj.bjp.0704816
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 We investigated the effects of prolonged exposure to copper (Cu2+) on vascular functioning of isolated rat aorta. 2 Aortic rings were exposed to CuSO4 (3-24 h) in Dulbecco's modified Eagle medium with or without 10% foetal bovine serum (FBS) and then challenged with vasoconstrictors or vasodilators in the absence Of Cu2+. 3 Exposure to 2 pm Cu2+ in the absence of FBS did not modify the response to phenylephrine (PE) or acetylcholine (ACh) in aortic rings incubated for 24 h. Identical exposure in the presence of FBS increased the contractile response to 1 muM PE by 30% (P<0.05) and impaired the relaxant response to 3 muM ACh or 1 muM A23187 (ACh, from 65.7 +/- 7.1 to 6.2 +/- 1.1%, n = 8; A23187, from 74.6 +/- 8.2 to 12.0 +/- 0.8%, n = 6; P<0.01 for both). Cu2+ exposure did not affect the relaxant response to NO-donors. 4 Impairment of vasorelaxation appeared 3 h after incubation with 2 muM Cu2+ and required 12 h ;to attain a steady state. Vasorelaxation to ACh was partially restored by 1 mm tiron (intracellular scavenger of superoxide ions; maximum relaxation 34.2 +/- 6.4%, n = 10, P<0.01 VS Cu2+ alone), whereas catalase, superoxide dismutase or cycloheximide were ineffective. 5 Twenty-four hour-exposure to 2 muM Cu2+ did not affect endothelium integrity or eNOS expression, and increased the Cu content in arterial rings from 6.8 +/- 1.1 to 18.9 +/- 2.9 ng mg(-1) wet weight, n = 8; P<0.01. 6 Our results show that, in the presence of FBS, prolonged exposure to submicromolar concentrations Of Cu2+ impaired endothelium-dependent vasorelaxation in aortic rings, probably through an intracellular generation of superoxide ions.
引用
收藏
页码:1185 / 1193
页数:9
相关论文
共 44 条
[1]   HEMOLYTIC AND MICROBICIDAL ACTIONS OF DIETHYLDITHIOCARBAMIC ACID [J].
AGAR, NS ;
MAHONEY, JR ;
EATON, JW .
BIOCHEMICAL PHARMACOLOGY, 1991, 41 (6-7) :985-993
[2]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[3]   Inhibition of endothelial nitric-oxide synthase by ceruloplasmin [J].
Bianchini, A ;
Musci, G ;
Calabrese, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (29) :20265-20270
[4]   Fast cytochrome bo from Escherichia coli binds two molecules of nitric oxide at CuB [J].
Butler, CS ;
Seward, HE ;
Greenwood, C ;
Thomson, AJ .
BIOCHEMISTRY, 1997, 36 (51) :16259-16266
[5]  
CAMPBELL CH, 1981, BIOCHIM BIOPHYS ACTA, V678, P27
[6]   Ceruloplasmin impairs endothelium-dependent relaxation of rabbit aorta [J].
Cappelli-Bigazzi, M ;
Ambrosi, G ;
Musci, G ;
Battaglia, C ;
Di Patti, MCB ;
Golino, P ;
Ragni, M ;
Chiariello, M ;
Calabrese, L .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (06) :H2843-H2849
[7]   Nitric oxide ejects electrons from the binuclear centre of cytochrome c oxidase by reacting with oxidised copper: a general mechanism for the interaction of copper proteins with nitric oxide? [J].
Cooper, CE ;
Torres, J ;
Sharpe, MA ;
Wilson, MT .
FEBS LETTERS, 1997, 414 (02) :281-284
[8]   Nitric oxide and cytochrome oxidase: substrate, inhibitor or effector? [J].
Cooper, CE .
TRENDS IN BIOCHEMICAL SCIENCES, 2002, 27 (01) :33-39
[9]  
Cox DA, 1996, J PHARMACOL EXP THER, V276, P1095
[10]   The copper chaperone for superoxide dismutase [J].
Culotta, VC ;
Klomp, LWJ ;
Strain, J ;
Casareno, RLB ;
Krems, B ;
Gitlin, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (38) :23469-23472