Antihypertensive therapy and cardiovascular reactivity during isometric stress

J Hum Hypertens. 1988 Dec;2(4):247-51.

Abstract

The cardiovascular reactivity to isometric stress test before and after antihypertensive therapy was evaluated by invasive haemodynamic techniques in 23 patients with mild to moderate essential hypertension. A beta-blocking agent (atenolol 50 to 100 mg daily) was given to 11 patients; 12 patients received calcium entry blockers (diltiazem 240 to 360 mg daily or verapamil 240 to 480 mg per day). The pressor response to isometric stress before therapy consisted of an increase in systolic, diastolic, and mean arterial pressure (all P less than 0.01) that was similar in both treatment groups. The rise in arterial pressure was mainly due to an increase in cardiac output (P less than 0.01), as total peripheral resistance did not change significantly. After treatment with the beta-blocker, the increase in total peripheral resistance during isometric stress was exaggerated (P less than 0.01), and, conversely, the increase in cardiac output was attenuated (P less than 0.01). In contrast, treatment with calcium entry blockers preserved the haemodynamic reactivity pattern of the untreated state: arterial pressure increased during isometric stress through an increase in cardiac output, while total peripheral resistance remained unchanged. Since the haemodynamic culprit of essential hypertension is an elevated peripheral resistance, a drug that numerically increases this culprit under conditions of resting and isometric stress becomes less attractive than one that lowers peripheral resistance and preserves the physiologic response pattern.

MeSH terms

  • Adult
  • Antihypertensive Agents / therapeutic use*
  • Cardiovascular System / drug effects*
  • Cardiovascular System / physiopathology
  • Female
  • Hemodynamics
  • Humans
  • Hypertension / drug therapy
  • Hypertension / physiopathology
  • Isometric Contraction*
  • Male
  • Middle Aged
  • Muscle Contraction*

Substances

  • Antihypertensive Agents