Effect of quercetin on plasma extravasation in rat CNS and dura mater by ACE and NEP inhibition

被引:16
作者
Cyrino, LAR [1 ]
Cardoso, RCF [1 ]
Hackl, LPN [1 ]
Nicolau, M [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Physiol, CCB, BR-88040900 Florianopolis, SC, Brazil
关键词
quercetin; substance P; plasma protein extravasation; dura mater; neutral endopeptidase; angiotensin-converting enzyme;
D O I
10.1002/ptr.987
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The effects of quercetin on substance P-induced plasma protein extravasation (PE) in the rat dura mater, cerebellum, olfactory bulb and cortex and also its modulation by endopeptidases, angiotensin-converting enzyme (ACE) and neutral endopeptidase (NEP) were studied. PE was assessed by photometric measurement of extravasated Evans blue. Substance P (SP) and NEP or ACE inhibitors increased the PE in dura mater. Pretreatment with captopril or phosphoramidon potentiated PE induced by SP in the dura mater and cerebellum, respectively. Quercetin increased the PE in the dura mater, cerebellum and cortex. Further results suggested that the PE induced by SP in the dura mater was enhanced by pretreatment with quercetin, similar to that observed with selective peptidase inhibitors. Quercetin-stimulated extravasation in all tissues was abolished by NK-1 receptor blockade. These results suggest that quercetin increases PE in the dura mater and CNS tissues by inhibiting NEP and/or ACE, showing that the effect induced in the dura mater, cerebellum and cortex occurs through endogenous SP accumulation. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:545 / 549
页数:5
相关论文
共 30 条
[1]  
Bertrand C, 1996, TRENDS PHARMACOL SCI, V17, P255, DOI 10.1016/0165-6147(96)10027-4
[2]   The neurobiology of pain [J].
Besson, JM .
LANCET, 1999, 353 (9164) :1610-1615
[3]   Translocation of the neutrophil kinin moiety and changes in the regulation of kinin receptors in inflammation [J].
Bhoola, KD .
IMMUNOPHARMACOLOGY, 1996, 33 (1-3) :247-256
[4]   DIRECT OBSERVATION OF SUBSTANCE-P-INDUCED INTERNALIZATION OF NEUROKININ-1 (NK1) RECEPTORS AT SITES OF INFLAMMATION [J].
BOWDEN, JJ ;
GARLAND, AM ;
BALUK, P ;
LEFEVRE, P ;
GRADY, EF ;
VIGNA, SR ;
BUNNETT, NW ;
MCDONALD, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8964-8968
[5]   DIFFERENTIAL-EFFECTS OF PHOSPHORAMIDON AND CAPTOPRIL ON NK1 RECEPTOR-MEDIATED PLASMA EXTRAVASATION IN THE RAT TRACHEA [J].
BROKAW, JJ ;
WHITE, GW .
AGENTS AND ACTIONS, 1994, 42 (1-2) :34-39
[6]   Release of substance P, calcitonin gene-related peptide and prostaglandin E2 from rat dura mater encephali following electrical and chemical stimulation in vitro [J].
Ebersberger, A ;
Averbeck, B ;
Messlinger, K ;
Reeh, PW .
NEUROSCIENCE, 1999, 89 (03) :901-907
[7]  
El-Bacha RS, 1999, CELL MOL BIOL, V45, P15
[8]   Acute ACE inhibition causes plasma extravasation in mice that is mediated by bradykinin and substance P [J].
Emanueli, C ;
Grady, EF ;
Madeddu, P ;
Figini, M ;
Bunnett, NW ;
Parisi, D ;
Regoli, D ;
Geppetti, P .
HYPERTENSION, 1998, 31 (06) :1299-1304
[9]   Substance P and bradykinin stimulate plasma extravasation in the mouse gastrointestinal tract and pancreas [J].
Figini, M ;
Emanueli, C ;
Grady, EF ;
Kirkwood, K ;
Payan, DG ;
Ansel, J ;
Gerard, C ;
Geppetti, P ;
Bunnett, N .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 272 (04) :G785-G793
[10]   Review of the biology of quercetin and related bioflavonoids [J].
Formica, JV ;
Regelson, W .
FOOD AND CHEMICAL TOXICOLOGY, 1995, 33 (12) :1061-1080