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Salt-induced hypertension in Dahl salt-resistant and salt-sensitive rats with NOSII inhibition
被引:43
|作者:
Rudd, MA
[1
]
Trolliet, M
[1
]
Hope, S
[1
]
Scribner, AW
[1
]
Daumerie, G
[1
]
Toolan, G
[1
]
Cloutier, T
[1
]
Loscalzo, J
[1
]
机构:
[1] Boston Univ, Sch Med, Whitaker Cardiovasc Inst, Evans Dept Med, Boston, MA 02118 USA
来源:
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
|
1999年
/
277卷
/
02期
关键词:
salt-sensitive hypertension;
Dahl rats;
N-G-nitro-L-arginine methyl ester;
2-amino-5,6-dihydro-6-methyl-4H-1,3-thiazine;
N-[3-(aminomethyl)benzyl]acetamidine hydrochloride;
D O I:
10.1152/ajpheart.1999.277.2.H732
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Although recent evidence suggests that reduced nitric oxide (NO) production maybe involved in salt-induced hypertension, the specific NO synthase (NOS) responsible for the conveyance of salt sensitivity remains unknown. To determine the role of inducible NOS (NOS II) in salt-induced hypertension, we treated Dahl salt-resistant (DR) rats with the selective NOS II inhibitor 2-amino-5,6-dihydro-6-methyl-4H-1,3-thiazine (AMT) for 12 days. Tail-cuff systolic blood pressures rose 29 +/- 6 and 42 +/- 8 mmHg in DR rats given 150 and 300 nmol AMT/h, respectively (P < 0.01, 2-way ANOVA) after 7 days of 8% NaCl diet. We observed similar results with two other potent selective NOS II inhibitors, S-ethylisourea (EIT) and N-[3-(aminomethyl)benzyl]acetamidine hydrochloride (1400W). Additionally, AMT effects were independent of alterations in endothelial function as assessed by diameter change of mesenteric arterioles in response to methacholine using videomicroscopy. We, therefore, conclude from those data that NOS II is important in salt-induced hypertension.
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页码:H732 / H739
页数:8
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