Key result
Calcium channel blocker therapy enables insulin to reduce angiotensin II-induced intracellular calcium rise by ~29%.
Why the study?
Does treatment with calcium channel blockers improve platelet sensitivity to insulin in patients with essential hypertension and non-insulin-dependent diabetes?
Does treatment with calcium channel blockers improve platelet sensitivity to insulin in patients with essential hypertension and non-insulin-dependent diabetes?
Treatment with calcium channel blockers in diabetic hypertensive patients reduces hyperinsulinemia and restores platelet sensitivity to the inhibitory effects of insulin.
Answers are grounded in this paper and cite their sources.
May restore platelet insulin sensitivity in diabetic hypertension; hypothesis-generating, needs randomized confirmation before practice change.
Insulin influences platelet function by reducing platelet responsiveness to vasoactive agonists. In hypertension these insulin-related inhibitory effects are blunted. The aim of this study was to determine whether platelet sensitivity to insulin is affected after 12 weeks of antihypertensive treatment with calcium channel blockers. Eleven patients with essential hypertension and non-insulin-dependent diabetes were treated with either isradipine or diltiazem. Platelet free calcium concentration was measured spectrofluorometrically in nonstimulated and in angiotensin II (1 nmol/L)-stimulated platelets that had been pre-exposed to insulin (70 microU/mL). Platelets were studied before therapy and after 12 weeks of treatment. Systolic blood pressure and mean arterial pressure decreased significantly during treatment. Both calcium channel blockers equally decreased fasting serum insulin levels (from 138 +/- 2.7 pmol/L before therapy to 106 +/- 9.9 pmol/L after therapy). Results with both calcium channel antagonists were similar and have been pooled. In the pretreatment phase, insulin pre-incubation had no effect on angiotensin II-stimulated intracellular free calcium and responses to angiotensin II were similar in the absence (265 +/- 10.5 nmol/L) and presence of insulin (233 +/- 12.1 nmol/L). After treatment with calcium channel blockers, insulin significantly (P < .001) reduced angiotensin II-induced rise of intracellular free calcium from 214 +/- 7.7 nmol/L (absence of insulin) to 153 +/- 9.3 nmol/L (presence of insulin). Whether these effects are due specifically to calcium channel blockers or whether they are the result of lowering of blood pressure remains unclear. Serum insulin levels were positively correlated with angiotensin II-stimulated increase in intracellular free calcium in platelets pre-exposed to insulin, (r = 0.46; P < .05) suggesting that with increasing levels of insulin resistance, the inhibitory effects of insulin are reduced. This study shows that treatment of non-insulin-dependent diabetic hypertensive patients with these calcium channel blockers reduces hyperinsulinemia and increases sensitivity of platelets to the inhibitory effect of insulin on angiotensin II-stimulated calcium responses.
No takes yet. Share an insight, caveat, or question.
Touyz et al. (1995) studied Essential hypertension and non-insulin-dependent diabetes (n=11). Calcium channel blockers (isradipine or diltiazem) vs. Pretreatment phase / Absence of insulin was evaluated on Angiotensin II-induced rise of intracellular free calcium in platelets (p=<.001). After 12 weeks of calcium channel blocker therapy, insulin significantly reduced the angiotensin II-induced rise of intracellular free calcium from 214 nmol/L to 153 nmol/L (P < .001).
Synapse has enriched 10 related papers. Consider them for comparative context: