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Vol. 282, Issue 2, 609-616, 1997
Department of Physiological Sciences, Federal University of
Espirito Santo, Brazil (A.-M.C.) and the
Department of Pharmacology and
Experimental Therapeutics (K.J.V., D.R.K.), Louisiana State University
Medical Center, New Orleans, Louisiana
This study examined the renal excretory responses produced by the
intravenous (i.v.) infusion of the alpha-2 agonist,
xylazine, in ketamine-anesthetized rats. In addition, the renal
responses produced by the intracerebroventricular (i.c.v.) injection of opioid agonists were also examined with use of this anesthetic paradigm. In male Sprague-Dawley rats, the i.v. infusion of isotonic saline (55 µl/min) containing ketamine alone (1.0 mg/kg/min) produced low levels of urine flow rate (6.3 ± 1.3 µl/min/gkw) and
urinary sodium excretion (0.28 ± 0.08 µeq/min/gkw). However,
after adding xylazine (50 µg/kg/min) to the ketamine infusate, these
renal excretory responses were significantly augmented. Steady-state levels of urine flow rate and urinary sodium excretion were attained approximately 120 min after starting the xylazine infusion and were
similar in magnitude to the levels of water and sodium excretion previously observed in untreated, conscious rats. In
ketamine/xylazine-anesthetized rats, the i.c.v. injection of the
mu opioid agonist, dermorphin (0.1 nmol/kg), or the
kappa opioid agonist, U-50488H (1 µg total), produced
profound and concurrent diuretic and antinatriuretic responses. The
pattern (direction and magnitude) of these opioid-induced renal
excretory responses was similar to those previously reported in
conscious rats. Together, these results indicate that the i.v. infusion
of xylazine enhances the renal excretion of water and sodium in
ketamine-anesthetized rats. Moreover, the renal responses produced by
i.c.v. administration of opioids are similar in
ketamine/xylazine-anesthetized and conscious rats. Thus, it appears
that the ketamine/xylazine infusion protocol may provide a valid and
useful approach to investigate various aspects of the central opioid
control of renal function in rats during experimental procedures that
require anesthesia.
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