Altered Vascular Resistance Properties and Acute Pressure-Natriuresis Mechanism in Neonatal and Weaning Spontaneously Hypertensive Rats

被引:15
作者
Komolova, Marina [1 ]
Friberg, Peter [2 ]
Adams, Michael A. [1 ]
机构
[1] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K71 3N6, Canada
[2] Univ Goteborg, Sahlgrenska Univ Hosp, Dept Clin Physiol, Gothenburg, Sweden
基金
加拿大健康研究院;
关键词
vascular resistance properties; renal hemodynamics; hydrostatic pressure; arterial pressure; pressure-natriuresis; SHR; WKY; INTERSTITIAL HYDROSTATIC-PRESSURE; RENAL MEDULLARY CIRCULATION; ARTERIAL-PRESSURE; MESENTERIC-ARTERIES; SODIUM; REACTIVITY; HYPERTROPHY; HEMODYNAMICS; KIDNEYS; VESSELS;
D O I
10.1161/HYPERTENSIONAHA.111.178194
中图分类号
R6 [外科学];
学科分类号
100210 [外科学];
摘要
Although it has been extensively scrutinized, the factor(s) involved in the initiation and development of hypertension in spontaneously hypertensive rats (SHRs) remains unresolved. The objective of the present study was to determine whether, early in development, the causal mechanism(s) for the development of hypertension in young SHRs involves an integration of 2 processes, specifically an upregulation of structurally based vascular resistance properties and a rightward shift in the hemodynamic component of pressure-natriuresis. Mean arterial pressure was determined in conscious 4-week old SHRs and Wistar-Kyoto rats via previously implanted aortic catheters. Structurally based hindlimb vascular resistance properties were assessed in 2- and 4-week old SHRs and Wistar-Kyoto rats. Renal interstitial hydrostatic pressure was measured after short-term manipulations of renal arterial pressure (RAP) in 4-week old, anesthetized rats, Although mean arterial pressure in conscious SHRs (113 +/- 5 mmHg) and Wistar-Kyoto rats (110 +/- 6 mmHg) was not significantly different at 4 weeks of age, SHRs at 2 and 4 weeks of age already had increases in structurally based vascular resistance properties of approximate to 30% above age- and weight-matched Wistar-Kyoto rats, Furthermore, the acute RAP-renal interstitial hydrostatic pressure relationship was found to be linear in both strains, and the temporal coupling of the stimulus to response was rapid; that is, renal interstitial hydrostatic pressure responses to changes in RAP were <2 s. Although the slope of the RAP-renal interstitial hydrostatic pressure relationship was not significantly different between strains, the relationship was significantly shifted (18%) to higher RAPs in SHRs. These results suggest that alterations in both vascular structure and renal function in young SHRs occur before elevations in mean arterial pressure. (Hypertension. 2012;59:979-984.) circle Online Data Supplement
引用
收藏
页码:979 / +
页数:13
相关论文
共 46 条
[1]
DIFFERENTIAL DEVELOPMENT OF VASCULAR AND CARDIAC-HYPERTROPHY IN GENETIC-HYPERTENSION - RELATION TO SYMPATHETIC FUNCTION [J].
ADAMS, MA ;
BOBIK, A ;
KORNER, PI .
HYPERTENSION, 1989, 14 (02) :191-202
[2]
ELECTROLYTE AND WATER-BALANCE IN YOUNG SPONTANEOUSLY HYPERTENSIVE RATS [J].
BEIERWALTES, WH ;
ARENDSHORST, WJ ;
KLEMMER, PJ .
HYPERTENSION, 1982, 4 (06) :908-915
[3]
ALTERATIONS IN RENAL VASCULAR-RESISTANCE AND REACTIVITY IN SPONTANEOUS HYPERTENSION OF RATS [J].
BERECEK, KH ;
SCHWERTSCHLAG, U ;
GROSS, F .
AMERICAN JOURNAL OF PHYSIOLOGY, 1980, 238 (03) :H287-H293
[4]
Long-term circulatory consequences of perinatal iron deficiency in male Wistar rats [J].
Bourque, Stephane L. ;
Komolova, Marina ;
Nakatsu, Kanji ;
Adams, Michael A. .
HYPERTENSION, 2008, 51 (01) :154-159
[5]
BRUNO L, 1979, JAP HEART J S1, V20, P90
[6]
Renal hemodynamics during development of hypertension in young spontaneously hypertensive rats [J].
Christiansen, REF ;
Roald, AB ;
Tenstad, O ;
Iversen, BM .
KIDNEY & BLOOD PRESSURE RESEARCH, 2002, 25 (05) :322-328
[7]
COWLEY AW, 1992, J HYPERTENS, V10, pS187
[9]
ARTERIAL HYPERTROPHY IN THE FETAL AND NEONATAL SPONTANEOUSLY HYPERTENSIVE RAT [J].
ECCLESTONJOYNER, CA ;
GRAY, SD .
HYPERTENSION, 1988, 12 (05) :513-518
[10]
Mechanisms mediating pressure natriuresis: What we know and what we need to find out [J].
Evans, RG ;
Majid, DSA ;
Eppel, GA .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2005, 32 (5-6) :400-409