Hypertension, Vol 8, 16-23, Copyright © 1986 by American Heart Association
A Bobik, G Jennings, G Jackman, C Oddie and P Korner
We examined the time course and extent to which central and peripheral
mechanisms contribute to the short-term effects of a 500-mg oral dose of
alpha-methyldopa on supine mean arterial pressure, cardiac output, and
total peripheral resistance, as well as its effects on total urinary
excretion of norepinephrine and its metabolites, in five subjects with
essential hypertension. Total peripheral resistance was reduced
significantly 1 hour after alpha-methyldopa administration and remained so
for the ensuing 7 hours of the study (p less than 0.05). A small but
significant reduction in mean arterial pressure occurred 7 hours after the
dose (p less than 0.05), while cardiac output did not change significantly.
Total 24-hour urinary norepinephrine and metabolite excretion was reduced
by 8.1 mumol (35% compared with placebo). The relative distribution of
urinary norepinephrine metabolites was unaffected by alpha-methyldopa, and
the catecholamine metabolites of alpha-methyldopa,
alpha-methylnorepinephrine and alpha- methylnormetanephrine did not account
for this reduction. Competitive inhibition of methyldopa transport across
the blood-brain barrier and into the central nervous system by large oral
doses of isoleucine antagonized most of the effect of alpha-methyldopa. The
effects on total peripheral resistance were completely abolished, and
small, insignificant changes during the 7-hour study were similar to those
observed after placebo. Changes in mean arterial pressure were not
significant; however, 24-hour total urinary norepinephrine and metabolite
excretion increased by 6.1 mumol to 22.7 mumol (24.7 mumol excreted after
placebo). Adding benserazide to the alpha/methyldopa- isoleucine dose
regimen in an attempt to inhibit any residual, presumably peripheral,
effects of alpha-methyldopa caused little, if any, further
antagonism.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Evidence for a predominantly central hypotensive effect of alpha- methyldopa in humans
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