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January 1, 1988Circulation Research158 citationsOpen Access

Mechanics of cerebral arterioles in hypertensive rats.

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GBGary L. BaumbachABB (United States)PDPhilip B. DobrinNorthwestern UniversityMHM. N. HartGeorgia State University

Key Points

  • The study aims to analyze the mechanical properties of cerebral arterioles under chronic hypertension and assess if their stiffness is altered.
  • Developed a method to measure vascular mechanics of cerebral arterioles in vivo.

Structured PICO

Does chronic hypertension alter the stiffness and mechanics of cerebral arterioles in a rat model?

P
Population
3-4-month-old age-matched, anesthetized stroke-prone spontaneously hypertensive rats (SHRSP) and Wistar Kyoto rats (WKY)
I
Intervention
Deactivation of smooth muscle with ethylenediaminetetraacetic acid (EDTA) and step-wise reductions in pressure
C
Comparator
Wistar Kyoto rats (WKY) as normotensive controls
O
Outcome
Circumferential stress and strain of pial arterioles, pial arteriolar pressure, inner diameter, and wall thicknesssurrogate

In a rat model, chronic hypertension increases pial arteriolar pressure and decreases diameter, but structural properties like wall thickness and passive diameter remain similar to normotensive controls.

Abstract

Chronic hypertension is associated with hypertrophy of cerebral blood vessels. Previous studies of the mechanical properties of cerebral vessels in chronic hypertension have examined large cerebral arteries. The goals of this study were first to develop a method to examine vascular mechanics of cerebral arterioles in vivo and second to determine whether the stiffness of cerebral arterioles is altered in the presence of chronic hypertension. We calculated circumferential stress and strain of pial arterioles in age-matched, anesthetized stroke-prone spontaneously hypertensive rats (SHRSP) and in Wistar Kyoto rats (WKY) from measurements of pial arteriolar pressure, inner diameter, and wall thickness. Pial arteriolar pressure was measured with a servonull system. Smooth muscle of pial arterioles was deactivated with ethylenediaminetetraacetic acid (EDTA), and pressure-diameter relations were examined during step-wise reductions in pressure. Prior to deactivation of smooth muscle in 3-4-month-old rats, pial arteriolar pressure was greater in SHRSP than in WKY (110 +/- 4 versus 75 +/- 2 mm Hg mean +/- SE; p less than 0.05). Pial arteriolar diameter, which was measured at prevailing levels of pial arteriolar pressure, was less in SHRSP than in WKY (52 +/- 5 versus 63 +/- 3 microns; p less than 0.05). Following deactivation of smooth muscle, diameter of pial arterioles at 70 mm Hg of pial arteriolar pressure was similar in the two groups: 104 +/- 6 microns in SHRSP and 109 +/- 3 microns in WKY (p greater than 0.05). Wall thickness was 4.5 +/- 0.2 microns in SHRSP and 4.1 +/- 0.1 microns in WKY (p greater than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

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Cite This Study

Baumbach et al. (1988) studied this question.

synapsesocial.com/papers/6a2024db40c8e71b0ba1b7f9https://doi.org/10.1161/01.res.62.1.56
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Compressibility of the Arterial Wall1968 · 467 citations
  2. 2Morphometric study on cerebral vessels in spontaneously hypertensive rats.1980 · 114 citations
  3. 3Biochemical and mechanical properties of resistance arteries from normotensive and hypertensive rats.1983 · 102 citations
  4. 4Lower limit of cerebral blood flow autoregulation in experimental renovascular hypertension in the baboon.1976 · 165 citations
  5. 5Adaptive changes in “reactivity” and wall/lumen ratio in cat blood vessels exposed to prolonged transmural pressure difference1968 · 53 citations