Why the study?
Dilevalol is a novel antihypertensive drug with combined nonselective beta blockade and selective beta 2-agonist activity, requiring evaluation of its clinical pharmacology and therapeutic use in hypertension.
Answers are grounded in this paper and cite their sources.
Dilevalol is a novel antihypertensive drug that combines nonselective beta blockade with selective beta 2-receptor agonist activity. Its antihypertensive effect is mediated through arterial vasodilation and a decrease in systemic vascular resistance. At rest, dilevalol has little effect on heart rate or cardiac output. The drug is rapidly and completely absorbed but undergoes significant first-pass hepatic extraction. Its elimination half-life of approximately 12 hours allows for once-daily administration. In controlled clinical trials, dilevalol was at least as effective as angiotensin-converting enzyme inhibitors and comparable to beta blockers in antihypertensive efficacy. Preliminary data indicate that dilevalol reverses left ventricular hypertrophy in some patients. It does not adversely affect renal function and may have a favorable effect on plasma lipids, especially high-density lipoprotein cholesterol. The agent is usually well tolerated and may prove to be a useful addition to our antihypertensive drugs.
No takes yet. Share an insight, caveat, or question.
Lalonde et al. (1990) studied Uterine contractility. Phenylephrine vs. Vehicle control (DMSO) or baseline was evaluated on Spontaneous and oxytocin-induced uterine contractions (EC50 1.1 µM (spontaneous); EC50 0.3 µM (oxytocin-induced), p=<0.01).
Synapse has enriched 10 related papers. Consider them for comparative context: