Hypertension, Vol 21, 1020-1023, Copyright © 1993 by American Heart Association
HA Pershadsingh, J Szollosi, S Benson, WC Hyun, BG Feuerstein and TW Kurtz
Ciglitazone is the prototype of the thiazolidinedione class of compounds
currently being developed for the treatment of insulin resistance and
non-insulin-dependent diabetes. The effects of thiazolidinediones on blood
pressure and cell calcium metabolism are not well defined. In the obese
Zucker rat, a widely studied model of insulin resistance associated with
mild hypertension, we investigated the effects of ciglitazone on plasma
insulin levels and mean arterial pressure. We also evaluated the effects of
ciglitazone on the changes in cytosolic calcium induced by platelet-derived
growth factor in A172 human glioblastoma cells and rat A10 vascular smooth
muscle cells. Oral administration of ciglitazone, approximately 45 mg/kg
per day for 4 weeks, induced significant reductions in plasma insulin
levels (p < 0.001) and blood pressure (p < 0.05). Ciglitazone was
also found to significantly attenuate the capacity of platelet-derived
growth factor BB homodimer to induce sustained increases in intracellular
free calcium. These findings suggest that thiazolidinediones may offer a
novel pharmacological approach to the treatment of hypertension, and raise
the possibility that these compounds may affect blood pressure not only by
affecting insulin metabolism but also by modifying the cell calcium
response to pressor agents, growth factors, or both.
ARTICLES
Effects of ciglitazone on blood pressure and intracellular calcium metabolism
Department of Family Practice, Kern Medical Center, Bakersfield, Calif.
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