The contribution of adrenoceptor subtype(s) in the renal vasculature of diabetic spontaneously hypertensive rats

被引:44
作者
Armenia, A
Munavvar, AS
Abdullah, NA
Helmi, A
Johns, EJ
机构
[1] Natl Univ Ireland Univ Coll Cork, Dept Physiol, Cork, Ireland
[2] Univ Sci Malaysia, Sch Pharmaceut Sci, George Town 11800, Malaysia
[3] Univ Malaya, Fac Med, Dept Pharmacol, Kuala Lumpur 50603, Malaysia
关键词
spontaneously hypertensive rats; streptozotocin induced diabetes; renal vasoconstriction; alpha-adrenoceptor subtypes;
D O I
10.1038/sj.bjp.0705842
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
1 Diabetes and hypertension are both associated with an increased risk of renal disease and are associated with neuropathies, which can cause defective autonomic control of major organs including the kidney. This study aimed to examine the alpha(1)-adrenoceptor subtype(s) involved in mediating adrenergically induced renal vasoconstriction in a rat model of diabetes and hypertension. 2 Male spontaneously hypertensive rats (SHR), 220-280 g, were anaesthetized with sodium pentobarbitone 7-day poststreptozotocin (55 mg kg(-1) i.p.) treatment. The reductions in renal blood flow (RBF) induced by increasing frequencies of electrical renal nerve stimulation (RNS), close intrarenal bolus doses of noradrenaline (NA), phenylephrine ( PE) or methoxamine were determined before and after administration of nitrendipine (Nit), 5-methylurapidil (5-MeU), chloroethylclonidine (CEC) and BMY 7378. 3 In the nondiabetic SHR group, mean arterial pressure (MAP) was 146+/-6 mmHg, RBF was 28.0+/-1.4 ml min(-1) kg(-1) and blood glucose was 112.3+/-4.7 mg dl(-1), and in the diabetic SHR Group, MAP was 144+/-3 mmHg, RBF 26.9+/-1.3 ml(-1) min kg(-1) and blood glucose 316.2+/-10.5 mg dl(-1). Nit, 5-MeU and BMY 7378 blunted all the adrenergically induced renal vasoconstrictor responses in SHR and diabetic SHR by 25-35% (all P<0.05), but in diabetic rats the responses induced by RNS and NA treated with 5-MeU were not changed. By contrast, during the administration of CEC, vasoconstrictor responses to all agonists were enhanced by 20-25% (all P<0.05) in both the SHR and diabetic SHR. 4 These findings suggest that alpha(1A) and alpha(1D)-adrenoceptor subtypes contribute in mediating the adrenergically induced constriction of the renal vasculature in both the SHR and diabetic SHR. There was also an indication of a greater contribution of presynaptic adrenoceptors, that is, alpha(1B)-, and/or alpha(2)-subtypes. British Journal of Pharmacology (2004).
引用
收藏
页码:719 / 726
页数:8
相关论文
共 57 条
[1]
Vascular responsiveness in isolated perfused kidneys of diabetic hypertensive rats [J].
Beenen, OHM ;
Mathy, MJ ;
Pfaffendorf, M ;
vanZwieten, PA .
JOURNAL OF HYPERTENSION, 1996, 14 (09) :1125-1130
[2]
FUNCTIONAL EVIDENCE EQUATING THE PHARMACOLOGICALLY-DEFINED ALPHA(1A)-ADRENOCEPTOR AND CLONED ALPHA(1C)-ADRENOCEPTOR - STUDIES IN THE ISOLATED-PERFUSED KIDNEY OF RAT [J].
BLUE, DR ;
BONHAUS, DW ;
FORD, APDW ;
PFISTER, JR ;
SHARIF, NA ;
SHIEH, IA ;
VIMONT, RL ;
WILLIAMS, TJ ;
CLARKE, DE .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 115 (02) :283-294
[3]
EVIDENCE FOR A NORADRENERGIC INNERVATION TO ALPHA-1A-ADRENOCEPTORS IN RAT-KIDNEY [J].
BLUE, DR ;
VIMONT, RL ;
CLARKE, DE .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 107 (02) :414-417
[4]
BOER R, 1989, EUR J PHARMACOL, V297, P241
[5]
BYLUND DB, 1994, PHARMACOL REV, V46, P121
[6]
CAUVIN C, 1984, J PHARMACOL EXP THER, V230, P413
[7]
VASCULAR ALPHA-1-ADRENOCEPTORS IN RAT-KIDNEY - AGONIST AND ANTAGONIST [PRAZOSIN, IDAZOXAN, WB-4101, (+)-NIGULDIPINE] CHARACTERIZATION [J].
CLARKE, DE ;
VIMONT, RL ;
BLUE, DR .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 183 (03) :733-733
[8]
SIGNALING AND REGULATION OF THE ALPHA(1B)-ADRENERGIC RECEPTOR [J].
COTECCHIA, S ;
LATTION, AL ;
DIVIANI, D ;
CAVALLI, A .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1995, 23 (01) :121-125
[9]
DEMEY JGR, 1997, J AUTON PHARMACOL, V7, P211
[10]
Neural control of renal function [J].
DiBona, GF ;
Kopp, UC .
PHYSIOLOGICAL REVIEWS, 1997, 77 (01) :75-197