Role of smooth muscle cell membrane potential in neointima formation in arteries of spontaneously hypertensive rats

Based on observations that vascular smooth muscle cells (VSMC) from spontaneously hypertensive rats (SHR) have altered resting potentials as well as abnormal cell proliferation rates, neointima formation after controlled balloon injury was compared in arteries from SHR and Wistar Kyoto rats (WKY). S...

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Bibliographic Details
Published in:Pathophysiology (Amsterdam) Vol. 7; no. 4; pp. 245 - 250
Main Authors: Dalle Lucca, Jurandir J., Borges, Antonio C.R., Ponchirolli, Renato, Melo, Simone A.C.S., Ihara, Silvia S.M., Lindsey, Charles J., Paiva, Therezinha B.
Format: Journal Article
Language:English
Published: Netherlands Elsevier Ireland Ltd 01-03-2001
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Summary:Based on observations that vascular smooth muscle cells (VSMC) from spontaneously hypertensive rats (SHR) have altered resting potentials as well as abnormal cell proliferation rates, neointima formation after controlled balloon injury was compared in arteries from SHR and Wistar Kyoto rats (WKY). SHR aortic VSMC showed hyperpolarized resting membrane potentials (−93±8 mV) when compared to those from WKY (−61±6 mV). Histomorphometric analysis of cross sections from aortic segments submitted to balloon injury showed reduced neointima formation in SHR (neointima/media ratio: 0.04±0.03) as compared to WKY (0.2±0.1). On the other hand, in injured carotid arteries, neointima formation was more extensive in SHR (neointima/media ratio 5.0±0.9) than in WKY (0.8±0.7), leading in most cases to luminal occlusion. Measurements of VSMC resting potential showed that carotid artery cells from SHR were depolarized with respect to those from WKY (−46±4 vs. −69±5 mV, respectively). The results demonstrate an inverse relationship between VSMC membrane polarization and neointima formation in SHR arteries, suggesting that genetic modifications in SHR determine a dysfunctional cellular physiology that may influence cell proliferation subsequent to injury.
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ISSN:0928-4680
1873-149X
DOI:10.1016/S0928-4680(00)00055-9