Hypertension, Vol 13, 416-421, Copyright © 1989 by American Heart Association
K Sudhir, GL Jennings, MD Esler, PI Korner, PA Blombery, GW Lambert, B Scoggins and JA Whitworth
Oral hydrocortisone increases blood pressure and enhances pressor
responsiveness in normal human subjects. We studied the effects of 1 week
of oral hydrocortisone (200 mg/day) on blood pressure, cardiac output,
total peripheral resistance, forearm vascular resistance, and
norepinephrine spillover to plasma in eight healthy male volunteers.
Although diastolic blood pressure remained unchanged, systolic blood
pressure increased from 119 to 135 mm Hg (SED +/- 3.4, p less than 0.01),
associated with an increased cardiac output (5.85-7.73 l/min, SED +/- 0.46,
p less than 0.01). Total peripheral vascular resistance fell from 15.1 to
12.2 mm Hg/l/min (SED +/- 1.03, p less than 0.05). Resting forearm vascular
resistance remained unchanged, but the reflex response to the cold pressor
test was accentuated, the rise in resistance increasing from 10.5 mm
Hg/ml/100 ml/min (R units) before treatment to 32.6 R units after treatment
(SED +/- 6.4, p less than 0.025). The rise in forearm vascular resistance
accompanying intra- arterial norepinephrine (25, 50, and 100 ng/min) was
also significantly greater after hydrocortisone, increasing from an average
of 14.9 +/- 2.4 R units before treatment to 35.1 +/- 5.5 R units after
hydrocortisone (SED +/- 6.0, p less than 0.05). A shift to the left in the
dose-response relation and fall in threshold suggested increased
sensitivity to norepinephrine after treatment. Measurement of resting
norepinephrine spillover rate to plasma and norepinephrine uptake indicated
that overall resting sympathetic nervous system activity was not increased.
The rise in resting blood pressure with hydrocortisone is associated with
an increased cardiac output (presumably due to increased blood
volume).(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Hydrocortisone-induced hypertension in humans: pressor responsiveness and sympathetic function
Clinical Research Unit, Baker Medical Research Institute, Prahran, Victoria, Australia.
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