AREGU Mar. 45/3
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چکیده
Bestle, Morten Heiberg, Niels Vidiendal Olsen, Poul Christensen, Benny Vittrup Jensen, and Peter Bie. Cardiovascular, endocrine, and renal effects of urodilatin in normal humans. Am. J. Physiol. 276 (Regulatory Integrative Comp. Physiol. 45): R684–R695, 1999.—Effects of urodilatin (5, 10, 20, and 40 ng·kg21 ·min21) infused over 2 h on separate study days were studied in eight normal subjects with use of a randomized, double-blind protocol. All doses decreased renal plasma flow (hippurate clearance, 13–37%) and increased fractional Li1 clearance (7–22%) and urinary Na1 excretion (by 30, 76, 136, and 99% at 5, 10, 20, and 40 ng·kg21 ·min21, respectively). Glomerular filtration rate did not increase significantly with any dose. The two lowest doses decreased cardiac output (7 and 16%) and stroke volume (10 and 20%) without changing mean arterial blood pressure and heart rate. The two highest doses elicited larger decreases in stroke volume (17 and 21%) but also decreased blood pressure (6 and 14%) and increased heart rate (15 and 38%), such that cardiac output remained unchanged. Hematocrit and plasma protein concentration increased with the three highest doses. The renin-angiotensin-aldosterone system was inhibited by the three lowest doses but activated by the hypotensive dose of 40 ng·kg21 ·min21. Plasma vasopressin increased by factors of up to 5 during infusion of the three highest doses. Atrial natriuretic peptide immunoreactivity (including urodilatin) and plasma cGMP increased dose dependently. The urinary excretion rate of albumin was elevated up to 15-fold (37 6 17 μg/min). Use of a newly developed assay revealed that baseline urinary urodilatin excretion rate was low (,10 pg/min) and that fractional excretion of urodilatin remained below 0.1%. The results indicate that even moderately natriuretic doses of urodilatin exert protracted effects on systemic hemodynamic, endocrine, and renal functions, including decreases in cardiac output and renal blood flow, without changes in arterial pressure or glomerular filtration rate, and that filtered urodilatin is almost completely removed by the renal tubules.
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AREGU Mar. 45/3
M. J. P. LENCZOWSKI,1 R.-M. BLUTHÉ,2 J. ROTH,3 G. S. REES,4 D. A. RUSHFORTH,5 A.-M. VAN DAM,1 F. J. H. TILDERS,1 R. DANTZER,2 N. J. ROTHWELL,5 AND G. N. LUHESHI5 1Department of Pharmacology, Faculty of Medicine, Research Institute Neurosciences Vrije Universiteit, Graduate School Neurosciences Amsterdam, 1081 BT Amsterdam, The Netherlands; 2Institut François Magendie, Institut National de la Re...
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Boulton, M., M. Flessner, D. Armstrong, R. Mohamed, J. Hay, and M. Johnston. Contribution of extracranial lymphatics and arachnoid villi to the clearance of a CSF tracer in the rat. Am. J. Physiol. 276 (Regulatory Integrative Comp. Physiol. 45): R818–R823, 1999.—The objective of this study was to determine the relative roles of arachnoid villi and cervical lymphatics in the clearance of a cereb...
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Khan, Janine Y., Rosario A. Rajakumar, Robert A. McKnight, Uday P. Devaskar, and Sherin U. Devaskar. Developmental regulation of genes mediating murine brain glucose uptake. Am. J. Physiol. 276 (Regulatory Integrative Comp. Physiol. 45): R892–R900, 1999.—We examined the molecular mechanisms that mediate the developmental increase in murine whole brain 2-deoxyglucose uptake. Northern and Western...
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McDonald, Roger B., Tana M. Hoban-Higgins, Rodney C. Ruhe, Charles A. Fuller, and Barbara A. Horwitz. Alterations in endogenous circadian rhythm of core temperature in senescent Fischer 344 rats. Am. J. Physiol. 276 (Regulatory Integrative Comp. Physiol. 45): R824–R830, 1999.—We assessed whether alterations in endogenous circadian rhythm of core temperature (CRT) in aging rats are associated wi...
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Rogausch, Heinz, Adriana Del Rey, Jörg Oertel, and Hugo O. Besedovsky. Norepinephrine stimulates lymphoid cell mobilization from the perfused rat spleen via b-adrenergic receptors. Am. J. Physiol. 276 (Regulatory Integrative Comp. Physiol. 45): R724–R730, 1999.—The possibility that norepinephrine (NE) influences lymphoid cell outflow independently of its vasoconstrictor action was investigated ...
متن کاملAREGU Mar. 45/3
Fanestil, Darrell D., Duke A. Vaughn, Ronald H. Hyde, and Patricia Blakely. Genetic control of renal thiazide receptor response to dietary NaCl and hypertension. Am. J. Physiol. 276 (Regulatory Integrative Comp. Physiol. 45): R901–R904, 1999.—Excess NaCl increases blood pressure in some strains of animals but not others. An 8% NaCl diet did not change renal thiazide receptor (TZR) density in tw...
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