Key result
Removal of adventitia significantly reduced contractile responses to KCl and norepinephrine and enhanced acetylcholine-induced relaxation in rat arterial rings.
Why the study?
Does removal of adventitia alter vascular smooth muscle contraction and relaxation in rat arteries?
Does removal of adventitia alter vascular smooth muscle contraction and relaxation in rat arteries?
The adventitia plays a functional role in the contractile capacity and endothelium-modulated responses of large arteries.
Answers are grounded in this paper and cite their sources.
Adventitial removal alters rat arterial reactivity; leaves open relevance to human vascular disease.
The aim of the present study was to determine whether the adventitia of large arteries modulates vascular function. We developed a method to obtain functional vascular rings devoid of adventitia. Carotid and iliac arteries from 3-mo-old Sprague-Dawley rats were denuded from adventitia after treatment with collagenase followed by gentle peeling. Adventitia removal and integrity of the media was demonstrated by optical and confocal microscopy. Arterial rings with or without adventitia and with or without endothelium were mounted in an organ bath for isometric tension recording. Responses to 75 mM KCl or norepinephrine (0.1 nM-1 microM) were significantly reduced in segments without adventitia. Acetylcholine-induced relaxation (0.1 microM-0.1 mM) was enhanced in arteries without adventitia, whereas sodium nitroprusside-induced responses were not modified. These results demonstrate that the combination of stripping with a previous collagenase treatment allows us to obtain functional rings devoid of adventitia and that this layer plays a role in contractile capacity and in endothelium-modulated responses.
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González et al. (2001) studied this question. Removal of adventitia vs. Arterial rings with adventitia was evaluated on Vascular smooth muscle contraction and relaxation. Removal of adventitia significantly reduced contractile responses to KCl and norepinephrine and enhanced acetylcholine-induced relaxation in rat arterial rings.
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