SUBSTANCE-P-INDUCED RELAXATION AND HYPERPOLARIZATION IN HUMAN CEREBRAL-ARTERIES

被引:63
作者
PETERSSON, J
ZYGMUNT, PM
BRANDT, L
HOGESTATT, ED
机构
[1] UNIV LUND HOSP,DEPT CLIN PHARMACOL,S-22185 LUND,SWEDEN
[2] MALMO GEN HOSP,DEPT NEUROL,S-21401 MALMO,SWEDEN
[3] UNIV LUND HOSP,DEPT NEUROSURG,S-22185 LUND,SWEDEN
关键词
CEREBRAL ARTERIES; HYPERPOLARIZATION; NITRIC OXIDE; RELAXATION; SUBSTANCE P; VASCULAR ENDOTHELIUM;
D O I
10.1111/j.1476-5381.1995.tb15893.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Vascular effects of substance P were studied in human isolated pial arteries removed from 14 patients undergoing cerebral cortical resection. 2 Substance P induced a concentration-dependent relaxation in the presence of indomethacin. No relaxation was seen in arteries where the endothelium had been removed. 3 N-omega-nitro-L-arginine (L-NOARG, 0.3 mM) abolished the relaxation in arteries from six patients. The relaxation was only partially inhibited in the remaining eight patients, the reduction of the maximum relaxation being less than 50% in each patient. 4 The L-NOARG-resistant relaxation was abolished when the external K+ concentration was raised above 30 mM. 5 Substance P caused a smooth muscle hyperpolarization (in the presence of L-NOARG and indomethacin), but only when the artery showed an L-NOARG-resistant relaxation. 6 The results indicate that nitric oxide is an important mediator of endothelium-dependent relaxation in human cerebral arteries. Furthermore, another endothelium-dependent pathway, causing hyperpolarization and vasodilatation, was identified in arteries from more than half the population of patients.
引用
收藏
页码:889 / 894
页数:6
相关论文
共 40 条
[1]   VARYING EXTRACELLULAR [K+] - A FUNCTIONAL-APPROACH TO SEPARATING EDHF-RELATED AND EDNO-RELATED MECHANISMS IN PERFUSED RAT MESENTERIC ARTERIAL BED [J].
ADEAGBO, ASO ;
TRIGGLE, CR .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1993, 21 (03) :423-429
[2]   THE ENDOTHELIUM-DEPENDENT RELAXATION OF HUMAN MIDDLE CEREBRAL-ARTERY - EFFECTS OF ACTIVATED NEUTROPHILS [J].
AKOPOV, SE ;
GRIGORIAN, MR ;
GABRIELIAN, ES .
EXPERIENTIA, 1992, 48 (01) :34-36
[3]   ENDOTHELIUM-DERIVED RELAXING FACTOR [J].
ANGUS, JA ;
COCKS, TM .
PHARMACOLOGY & THERAPEUTICS, 1989, 41 (1-2) :303-352
[4]   INDIVIDUAL VARIATIONS IN RESPONSE OF HUMAN CEREBRAL ARTERIOLES TO VASOACTIVE SUBSTANCES, HUMAN-PLASMA, AND CSF FROM PATIENTS WITH ANEURYSMAL SAH [J].
BRANDT, L ;
LJUNGGREN, B ;
ANDERSSON, KE ;
HINDFELT, B .
JOURNAL OF NEUROSURGERY, 1981, 55 (03) :431-437
[5]   ENDOTHELIUM-DEPENDENT DILATION OF FELINE CEREBRAL-ARTERIES - ROLE OF MEMBRANE-POTENTIAL AND CYCLIC-NUCLEOTIDES [J].
BRAYDEN, JE ;
WELLMAN, GC .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1989, 9 (03) :256-263
[6]   MEMBRANE HYPERPOLARIZATION IS A MECHANISM OF ENDOTHELIUM-DEPENDENT CEREBRAL VASODILATION [J].
BRAYDEN, JE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (03) :H668-H673
[7]   THE ROLE OF NITRIC-OXIDE IN MEDIATING ENDOTHELIUM DEPENDENT RELAXATIONS IN THE HUMAN EPICARDIAL CORONARY-ARTERY [J].
CHESTER, AH ;
ONEIL, GS ;
TADJKARIMI, S ;
PALMER, RMJ ;
MONCADA, S ;
YACOUB, MH .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 1990, 29 (03) :305-309
[8]   DIFFERENT INFLUENCE OF ENDOTHELIUM IN THE MECHANICAL RESPONSES OF HUMAN AND CAT ISOLATED CEREBRAL-ARTERIES TO SEVERAL AGENTS [J].
CONDE, MV ;
MARCO, EJ ;
FRAILE, ML ;
BENITO, JM ;
MORENO, MJ ;
SANZ, ML ;
DEPABLO, ALL .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1991, 43 (04) :255-261
[9]  
COWAN CL, 1993, J PHARMACOL EXP THER, V266, P1482
[10]   ENDOTHELIUM-INDEPENDENT CONTRACTIONS OF HUMAN CEREBRAL-ARTERIES IN RESPONSE TO VASOPRESSIN [J].
DEAGUILERA, EM ;
VILA, JM ;
IRURZUN, A ;
MARTINEZ, MC ;
CUESTA, MAM ;
LLUCH, S .
STROKE, 1990, 21 (12) :1689-1693