(Hypertension. 1995;25:748-751.)
© 1995 American Heart Association, Inc.
Articles |
From the Departamento de Farmacología y Terapéutica, Facultad de Medicina, Universidad Autónoma de Madrid (Spain).
Abstract The endothelium exerts a large influence on the
underlying vascular smooth muscle, not only by the release of both
contracting and relaxing factors but also by its ability to synthesize
a large number of molecules that influence vascular smooth muscle
growth. In addition to well-characterized growth promoters or growth
inhibitors, some endothelium-derived factors,
originally described as vasoactive compounds, seem to possess
growth-regulatory properties. The vasoconstrictor endothelin-1 elicited
a dose-dependent increase of cultured vascular smooth muscle cell DNA
synthesis with a maximal effect of 57±14% over basal levels, whereas
vasodilators such as prostacyclin, sodium nitroprusside, and
8-bromoguanosine 3':5'-cyclic monophosphate reduced DNA synthesis by
19±5%, 22±2%, and 31±3%, respectively. Medium conditioned by
cultured bovine aortic endothelial cells markedly stimulated both DNA
synthesis and proliferation of smooth muscle cells. When medium
was conditioned in the presence of the endothelin-converting enzyme
inhibitor phosphoramidon, the mitogenic effect was significantly
reduced, thus indicating a role for endothelin in the stimulation of
smooth muscle cell growth by endothelial cells. However, when both cell
types were maintained in a coculture system, a 13±2% decrease of DNA
synthesis was observed in smooth muscle cultures. The addition of the
nitric oxide synthase inhibitor
N
-nitro-L-arginine methyl
ester, the cyclooxygenase inhibitor indomethacin, or both during
the coculture period did not revert the antiproliferative effect
of endothelial cells in coculture, thereby indicating it is not
likely due to these unstable endothelium-derived
vasorelaxant molecules.
Key Words: endothelium vasoconstrictor agents vasodilator agents muscle, smooth, vascular growth
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