EFFECTS OF CALCIUM-CHANNEL ANTAGONISTS AND PERTUSSIS TOXIN ON NORADRENALINE-INDUCED CONTRACTIONS IN PULMONARY-ARTERY FROM PULMONARY HYPERTENSIVE RATS

被引:6
作者
TABRIZCHI, R
MACNICOL, BJ
LIN, BP
机构
[1] Department of Pharmacology and Therapeutics, Faculty of Medicine The University of British Columbia, Vancouver
基金
英国医学研究理事会;
关键词
PULMONARY HYPERTENSION; MONOCROTALINE; CALCIUM CHANNEL ANTAGONISTS; PULMONARY ARTERY;
D O I
10.1016/0024-3205(95)00056-C
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The influence of calcium channel antagonists, felodipine and cadmium, as well as pertussis toxin on noradrenaline-induced contractions in pulmonary artery rings from rats with pulmonary hypertension induced by monocrotaline (MCT) were examined. MCT-treated rats had pulmonary hypertension, right ventricular hypertrophy and lung oedema, as compared to corresponding vehicle-treated rats. The MCT-treated animals did not have polycythemia as compared to vehicle-treated rats. Pre-treatment of pulmonary artery rings from MCT-treated rats with felodipine and cadmium significantly reduced the maximum response without altering the EC(50) or the Hill coefficient of concentration-response curve to noradrenaline. In pulmonary artery rings from vehicle-treated rats, felodipine significantly increased the EC(50) and reduced the maximum response and the Hill coefficient of the concentration-response curve to noradrenaline. In contrast, cadmium did not alter these parameters in pulmonary artery rings from vehicle-treated rats. Pertussis toxin did not affect noradrenaline-induced contractions in pulmonary artery rings from vehicle- or MCT-treated rats. Felodipine, cadmium and pertussis toxin were ineffective in inhibiting noradrenaline-induced contractions in aortic rings from either vehicle- or MCT-treated rats. Our results can be interpreted to indicate that alteration to voltage operated, felodipine-sensitive, calcium channels as well as, cadmium-sensitive sites contribute to the changes observed in the functional behavior of pulmonary blood vessels from pulmonary hypertensive rats.
引用
收藏
页码:1173 / 1185
页数:13
相关论文
共 27 条
[1]  
ALTIERE RJ, 1986, J PHARMACOL EXP THER, V236, P390
[2]  
CAMERINI F, 1980, BRIT HEART J, V44, P352
[3]   CHANGES IN PULMONARY STRUCTURE AND FUNCTION INDUCED BY MONOCROTALINE INTOXICATION [J].
GHODSI, F ;
WILL, JA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1981, 240 (02) :H149-H155
[4]   VASCULAR HYPERRESPONSIVENESS IN PERFUSED LUNGS FROM MONOCROTALINE-TREATED RATS [J].
GILLESPIE, MN ;
OLSON, JW ;
REINSEL, CN ;
OCONNOR, WN ;
ALTIERE, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (01) :H109-H114
[5]   ALPHA-ADRENOCEPTOR SUBTYPES IN DOG SAPHENOUS-VEIN THAT MEDIATE CONTRACTION AND INOSITOL PHOSPHATE PRODUCTION [J].
HICKS, PE ;
BARRAS, M ;
HERMAN, G ;
MAUDUIT, P ;
ARMSTRONG, JM ;
ROSSIGNOL, B .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 102 (01) :151-161
[6]  
HILLIKER KS, 1985, AM REV RESPIR DIS, V131, P46
[7]   THE INHIBITION OF ALPHA-ADRENOCEPTOR-MEDIATED CONTRACTIONS OF RABBIT PULMONARY-ARTERY BY CA-2+-WITHDRAWAL, PERTUSSIS TOXIN AND N-ETHYLMALEIMIDE IS DEPENDENT ON AGONIST INTRINSIC EFFICACY [J].
LIEBAU, S ;
HOHLFELD, J ;
FORSTERMANN, U .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1989, 339 (05) :496-502
[8]   CALCIUM CURRENTS IN THE A7R5 SMOOTH MUSCLE-DERIVED CELL-LINE [J].
MARKS, TN ;
DUBYAK, GR ;
JONES, SW .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1990, 417 (04) :433-439
[9]   DEVELOPMENT OF CROTALARIA PULMONARY-HYPERTENSION - HEMODYNAMIC AND STRUCTURAL STUDY [J].
MEYRICK, B ;
GAMBLE, W ;
REID, L .
AMERICAN JOURNAL OF PHYSIOLOGY, 1980, 239 (05) :H692-H702
[10]   CHARACTERIZATION IN RAT AORTA OF THE BINDING-SITES RESPONSIBLE FOR BLOCKADE OF NORADRENALINE-EVOKED CALCIUM ENTRY BY NISOLDIPINE [J].
MOREL, N ;
GODFRAIND, T .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 102 (02) :467-477