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Prostacyclin and thromboxane A2 production in nitric oxide-deficient hypertension in vivo.: Effects of high calcium diet and angiotensin receptor blockade
被引:5
作者:
Alanko, J
Jolma, P
Kööbi, P
Riutta, A
Kaillovalkama, J
Tolvanen, JP
Pörsti, K
机构:
[1] Tampere Univ Hosp, Dept Internal Med, FIN-33521 Tampere, Finland
[2] Dept Pharmacol Sci, FIN-33014 Tampere, Finland
[3] Tampere Univ Hosp, Dept Anaesthesia, FIN-33521 Tampere, Finland
[4] Tampere Univ Hosp, Dept Intens Care, FIN-33521 Tampere, Finland
[5] Univ Helsinki, Cent Hosp, Div Nephrol, Dept Med, FIN-00029 HUS, Finland
来源:
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS
|
2003年
/
69卷
/
05期
关键词:
D O I:
10.1016/S0952-3278(03)00148-0
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The effects of chronic nitric oxide deficiency on prostacyclin and thromboxane A(2) production in vivo are unknown. Therefore, we treated rats with N-G-nitro-L-arginine methyl ester (L-NAME), and used losartan and high calcium diet as antihypertensive treatments. Forty eight Wistar rats were divided into six groups: control; losartan (20 mg kg(-1) day(-1)); high calcium diet (dietary calcium elevated from 1.1% to 3%); L-NAME (20 mg kg(-1) day(-1)); losartan + L-NAME and high calcium diet + L-NAME. Prostacyclin and thromboxane A(2) production were measured after eight weeks as urinary 2,3-dinor-6-keto-PGF(1alpha) and 11-dehydro-TXB2, respectively. Both the high calcium diet and losartan reduced blood pressure in L-NAME hypertension. Chronic nitric oxide deficiency did not modulate prostacyclin production but it nearly doubled thromboxane A(2) production in vivo. This effect was not influenced by lowering of blood pressure by blockade of angiotensin II type 1 receptors. Independent of the level of blood pressure and blockade of nitric oxide synthesis the high calcium diet decreased prostacyclin production by one third and increased thromboxane A(2) production almost two-fold in vivo. (C) 2003 Elsevier Ltd. All rights reserved.
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页码:345 / 350
页数:6
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