Arterial myogenic properties of the spontaneously hypertensive rat

When subject to a transmural pressure gradient resistance arteries develop a spontaneous, intrinsically initiated contraction which varies according to the pressure stimulus and occurs in the absence of vasoconstrictor agonists. Such pressure-dependent active changes in vascular tone are indicative...

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Bibliographic Details
Published in:Experimental physiology 2002-09, Vol.87 (5), p.527-534
Main Authors: Hughes, Jennifer M., Bund, Stuart J.
Format: Article
Language:English
Subjects:
Animals
Arteries - physiology
Hypertension - physiopathology
Mini Review
Muscle, Smooth, Vascular - physiology
Rats
Rats, Inbred SHR - physiology
Vascular Resistance - physiology
Vasoconstriction - physiology
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Summary:When subject to a transmural pressure gradient resistance arteries develop a spontaneous, intrinsically initiated contraction which varies according to the pressure stimulus and occurs in the absence of vasoconstrictor agonists. Such pressure-dependent active changes in vascular tone are indicative of the vascular myogenic response and contribute to autoregulation and the setting of total peripheral resistance and hence blood pressure regulation. The myogenic behaviour of blood vessels provides the background tone upon which other vasomotor influences act. Hypertension is associated with a raised vascular resistance and in this article the evidence for increased myogenic activity contributing to the raised vascular resistance is reviewed. Although there are some cases that provide evidence for exaggerated myogenic responsiveness in resistance arteries taken from hypertensive animals it is not possible to conclude that enhanced myogenic contractile responses within normal pressure ranges contribute to the raised total peripheral resistance. However, the myogenic tone of the resistance arteries of the various vascular beds is subject to differing modulatory influences in hypertensive animals and their normotensive controls which may contribute to the aetiology of hypertension. Experimental Physiology (2002) 87.5, 527-534.
ISSN:0958-0670
1469-445X
DOI:10.1113/eph8702399