Korean J Physiol Pharmacol.
1998 Oct;2(5):555-563.
Natriuresis induced by intracerebroventricular diazepam in rabbits
- Affiliations
-
- 1Departments of Pharmacology, Chonnam University Dental, Korea.
- 2Departments of Pharmacology, Medical Schools, Kwanaiu 501-190, Korea.
Abstract
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The renal function is under regulatory influence of central nervous
system (CNS), in which various neurotransmitter and neuromodulator
systems take part. However, a possible role of central
GABA-benzodiazepine system on the central regulation of renal function
has not been explored. This study was undertaken to delineate the renal
effects of diazepam. Diazepam, a benzodiazepine agonist, administered
into a lateral ventricle (icv) of the rabbit brain in doses ranging
from 10 to 100 microgram/kg, elicited dose-related diuresis and natriuresis
along with improved renal hemodynamics. However, when given
intravenously, 100 mug/kg diazepam did not produce any significant
changes in all parameters of renal function and systemic blood
pressure. Diazepam, 100 mug/kg icv, transiently decreased the renal
nerve activity (RNA), which recovered after 3 min. The plasma level of
atrial natriuretic peptide (ANP) increased 7-fold, the peak coinciding
with the natriuresis and diuresis. Muscimol, a GABAergic agonist, 1.0
mug/kg given icv, elicited marked antidiuresis and antinatriuresis,
accompanied by decreases in systemic blood pressure and renal
hemodynamics. When icv 0.3 microgram/kg muscimol was given 3 min prior to 30
mug/kg of diazepam icv, urinary flow and Na excretion rates did not
change significantly, while systemic hypotension was produced. These
results
indicate that icv diazepam may bring about natriuresis and
diuresis by influencing the central regulation of renal function, and
that the renal effects are related to the increased plasma ANP levels,
not to the decreased renal nerve activity, and suggest that the effects
may not be mediated by the activation of central GABAergic system.