Variable responses of regional renal oxygenation and perfusion to vasoactive agents in awake sheep

被引:37
作者
Calzavacca, Paolo [1 ,2 ]
Evans, Roger G. [3 ,4 ]
Bailey, Michael [5 ]
Bellomo, Rinaldo [6 ,7 ]
May, Clive N. [1 ]
机构
[1] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic 3052, Australia
[2] AO Melegnano, Dept Anaesthesia & Intens Care, Cernusco Sul Naviglio, Italy
[3] Monash Univ, Biomed Discovery Inst, Cardiovasc Dis Program, Melbourne, Vic 3004, Australia
[4] Monash Univ, Dept Physiol, Melbourne, Vic 3168, Australia
[5] Monash Univ, Australian & New Zealand Intens Care Res Ctr, Melbourne, Vic 3004, Australia
[6] Austin Hlth, Dept Intens Care, Heidelberg, Vic, Australia
[7] Austin Hlth, Dept Med, Heidelberg, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
intrarenal oxygenation; intrarenal perfusion; renal blood flow; hypoxia angiotensin II; vasopressin; norepinephrine; captopril; MEDULLARY TISSUE OXYGENATION; KIDNEY OXYGENATION; VOLUME EXPANSION; SEPTIC SHOCK; BLOOD-FLOW; VASOPRESSIN;
D O I
10.1152/ajpregu.00228.2015
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Vasoactive agents are used in critical care to optimize circulatory function, but their effects on renal tissue oxygenation in the absence of anesthesia remain largely unknown. Therefore, we assessed the effects of multiple vasoactive agents on regional kidney oxygenation in awake sheep. Sheep were surgically instrumented with pulmonary and renal artery flow probes, and combination fiber-optic probes, in the renal cortex and medulla, comprising a fluorescence optode to measure tissue PO2 and a laser-Doppler probe to assess tissue perfusion. Carotid arterial and renal venous cannulas enabled measurement of arterial pressure and total renal oxygen delivery and consumption. Norepinephrine (0.1 or 0.8 mu g.kg(-1).min(-1)) dose-dependently reduced cortical and medullary laser Doppler flux (LDF) and PO2 without significantly altering renal blood flow (RBF), or renal oxygen delivery or consumption. Angiotensin II (9.8 +/- 2.1 mu g/h) reduced RBF by 21%, renal oxygen delivery by 28%, oxygen consumption by 18%, and medullary PO2 by 38%, but did not significantly alter cortical PO2 or cortical or medullary LDF. Arginine vasopressin (3.3 +/- 0.5 mu g/h) caused similar decreases in RBF and renal oxygen delivery, but did not significantly alter renal oxygen consumption or cortical or medullary LDF or PO2. Captopril had no observable effects on cortical or medullary LDF or PO2, at a dose that increased renal oxygen delivery by 24%, but did not significantly alter renal oxygen consumption. We conclude that vasoactive agents have diverse effects on regional kidney oxygenation in awake sheep that are not predictable from their effects on LDF, RBF, or total renal oxygen delivery and consumption.
引用
收藏
页码:R1226 / R1233
页数:8
相关论文
共 26 条
[1]   Low-dose vasopressin increases glomerular filtration rate, but impairs renal oxygenation in post-cardiac surgery patients [J].
Bragadottir, G. ;
Redfors, B. ;
Nygren, A. ;
Sellgren, J. ;
Ricksten, S. -E. .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 2009, 53 (08) :1052-1059
[2]  
Calzavacca P, CRIT CARE M IN PRESS
[3]   Long-term measurement of renal cortical and medullary tissue oxygenation and perfusion in unanesthetized sheep [J].
Calzavacca, Paolo ;
Evans, Roger G. ;
Bailey, Michael ;
Lankadeva, Yugeesh R. ;
Bellomo, Rinaldo ;
May, Clive N. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2015, 308 (10) :R832-R839
[4]  
Dellinger RP, 2013, INTENS CARE MED, V41, P580, DOI [DOI 10.1097/CCM.0B013E31827E83AF, DOI 10.1007/s00134-012-2769-8]
[5]   Mechanisms underlying the differential control of blood flow in the renal medulla and cortex [J].
Evans, RG ;
Eppel, GA ;
Anderson, WP ;
Denton, KM .
JOURNAL OF HYPERTENSION, 2004, 22 (08) :1439-1451
[6]   Mechanisms mediating pressure natriuresis: What we know and what we need to find out [J].
Evans, RG ;
Majid, DSA ;
Eppel, GA .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2005, 32 (5-6) :400-409
[7]   Intrarenal oxygenation: unique challenges and the biophysical basis of homeostasis [J].
Evans, Roger G. ;
Gardiner, Bruce S. ;
Smith, David W. ;
O'Connor, Paul M. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2008, 295 (05) :F1259-F1270
[8]   METHODS FOR STUDYING THE PHYSIOLOGY OF KIDNEY OXYGENATION [J].
Evans, Roger G. ;
Gardiner, Bruce S. ;
Smith, David W. ;
O'Connor, Paul M. .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2008, 35 (12) :1405-1412
[9]   Basal renal O2 consumption and the efficiency of O2 utilization for Na+ reabsorption [J].
Evans, Roger G. ;
Harrop, Gerard K. ;
Ngo, Jennifer P. ;
Ow, Connie P. C. ;
O'Connor, Paul M. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2014, 306 (05) :F551-F560
[10]   Haemodynamic influences on kidney oxygenation: Clinical implications of integrative physiology [J].
Evans, Roger G. ;
Ince, Can ;
Joles, Jaap A. ;
Smith, David W. ;
May, Clive N. ;
O'Connor, Paul M. ;
Gardiner, Bruce S. .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2013, 40 (02) :106-122