Contribution of extrinsic factors and intrinsic vascular alterations to reduced arteriolar reactivity with high-salt diet and hypertension

Citation
Jc. Frisbee et al., Contribution of extrinsic factors and intrinsic vascular alterations to reduced arteriolar reactivity with high-salt diet and hypertension, MICROCIRCUL, 7(4), 2000, pp. 281-289
Citations number
29
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
MICROCIRCULATION
ISSN journal
10739688 → ACNP
Volume
7
Issue
4
Year of publication
2000
Pages
281 - 289
Database
ISI
SICI code
1073-9688(200008)7:4<281:COEFAI>2.0.ZU;2-I
Abstract
Objective: To determine whether relaxation of skeletal muscle arterioles of rats on high-salt diet or with reduced renal mass hypertension (RRM-HT) re presents intrinsic alterations to microvessels alone, or whether extravascu lar influences also contribute to reduced dilator responses. Methods: Normotensive (NT) Sprague-Dawley rats were fed low-salt (LS) or hi gh-salt (HS) diets, and RRM-HT rats were fed HT diet for 4-6 weeks. In situ and isolated cremaster muscle first-order arterioles (1A) were examined us ing television microscopy, and a video micrometer was used to measure diame ter changes in response to acetylcholine (ACH), cholera toxin (CT), and sod ium nitroprusside (SNP). Results: Compared to normotensive low-salt (NT-LS) rats, responses of 1A to the agonists were reduced in normotensive high-salt (NT-H) and RRM-HT rats . Arteriolar reactivity to the agonists in NT-LS rats and in NT-HS rats was not different between in situ and in vitro environments. However, in RRM-H T rats, the reactivity of 1A to each agonist was greater in isolated arteri oles than in in situ arterioles. Conclusions: These results suggest that the impaired response of skeletal m uscle arterioles to vasodilator stimuli in normotensive rats on high-salt d iet primarily reflects alterations to microvessels alone, while reduced dil ator responses in RRM-HT rats represent a combination of extravascular infl uences and intrinsic alterations to arterioles themselves.