Effect of the flavonoid galangin on urinary bladder rat contractility in-vitro

被引:15
作者
Capasso, R
Tavares, IA
机构
[1] Univ Naples Federico 2, Dept Expt Pharmacol, I-80131 Naples, Italy
[2] Kings Coll London, Rayne Inst, GKT Sch Med, Acad Dept Surg, London SE5 9NU, England
关键词
D O I
10.1211/002235702320266334
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Galangin is a flavanol with several biological activities. We have evaluated the effect of galangin on the contractile response elicited by electrical field stimulation (EFS) in the rat isolated urinary bladder. Galangin (10(-8)-10(-4)m) produced a concentration-de pendent inhibition of the EFS contractile response without modifying the contractions produced by exogenous acetylcholine (10(-6) m). Blockade of adrenergic and cholinergic nerves with a combination of atropine (10(-6) M), phentolamine (10(-6) m) and propranolol (10(-6) m) or blockade of tachykinin NK1, and NK2 receptors with SR140333 (10(-7) m) and SR48968 (10(-6) m) did not modify the inhibitory effect of galangin. However, verapamil (10(-7) m) significantly reduced the inhibitory effect of galangin. It is concluded that the galangin inhibits EFS-induced contractions of the rat urinary bladder by acting on L-type calcium channels on presynaptic nerves.
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页码:1147 / 1150
页数:4
相关论文
共 31 条
[1]   Protective effect of a bioflavonoid proanthocyanidin-BP1 in glycerol-induced acute renal failure in the rat: Renal stereological study [J].
Avramovic, V ;
Vlahovic, P ;
Mihailovic, D ;
Stefanovic, V .
RENAL FAILURE, 1999, 21 (06) :627-634
[2]  
BUENING MK, 1981, CANCER RES, V41, P67
[3]   ATROPINE RESISTANT EXCITATION OF URINARY-BLADDER - POSSIBILITY OF TRANSMISSION VIA NERVES RELEASING A PURINE NUCLEOTIDE [J].
BURNSTOCK, G ;
SMYTHE, A ;
DUMSDAY, B .
BRITISH JOURNAL OF PHARMACOLOGY, 1972, 44 (03) :451-+
[4]   INHIBITORY EFFECTS OF PHENOLIC-COMPOUNDS ON CCL4-INDUCED MICROSOMAL LIPID-PEROXIDATION [J].
CHOLBI, MR ;
PAYA, M ;
ALCARAZ, MJ .
EXPERIENTIA, 1991, 47 (02) :195-199
[5]   The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor [J].
Ciolino, HP ;
Yeh, GC .
BRITISH JOURNAL OF CANCER, 1999, 79 (9-10) :1340-1346
[6]   Flavonoids: Old and new aspects of a class of natural therapeutic drugs [J].
Di Carlo, G ;
Mascolo, N ;
Izzo, AA ;
Capasso, F .
LIFE SCIENCES, 1999, 65 (04) :337-353
[7]   Effect of treatment with calcium antagonists in vitro and in vivo on the contractile response of isolated rat and human detrusor muscle [J].
Elliott, RA ;
Norman, RI ;
Parker, SG ;
Whitaker, RP ;
Castleden, CM .
CLINICAL SCIENCE, 1996, 91 (04) :467-474
[8]  
GABOR M, 1991, ACTA PHYSIOL HUNG, V77, P197
[9]   High intake of specific carotenoids and flavonoids does not reduce the risk of bladder cancer [J].
Garcia, R ;
Gonzalez, CA ;
Agudo, A ;
Riboli, E .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1999, 35 (02) :212-214
[10]   A PHARMACOLOGICAL STUDY OF NK1-TACHYKININ AND NK2-TACHYKININ RECEPTOR CHARACTERISTICS IN THE RAT ISOLATED URINARY-BLADDER [J].
HALL, JM ;
FLOWERS, JM ;
MORTON, IKM .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 107 (03) :777-784