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Systemic hemodynamics and renal function in hemorrhaged dogs resuscitated with cross-linked hemoglobin

Authors :
J. A. Haas
Juan C. Romero
John M. Stulak
Luis A. Juncos
Source :
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 278:R28-R33
Publication Year :
2000
Publisher :
American Physiological Society, 2000.

Abstract

Cross-linked hemoglobin (XL-Hb) infused into dogs increases mean arterial pressure (MAP) but decreases blood flow to the renal (RBF), mesenteric (MBF), and iliac (IBF) circulations. These actions differ markedly from dextran infusion (which increases RBF, MBF, and IBF without altering MAP) and may be due to scavenging of nitric oxide by XL-Hb. However, because the hormonal milieu regulating regional circulation is altered during hemorrhage (when XL-Hb may be used), we studied whether systemic hemodynamics, RBF, MBF, IBF, and renal excretory function in hemorrhaged dogs was altered when resuscitated with XL-Hb compared with dextran ( n = 6 each). Hemorrhage decreased MAP by 25% due to a 75% decline in cardiac output. RBF, MBF, and IBF all fell by 33, 64, and 72%, respectively ( P < 0.05 each). There was also a fall in glomerular filtration rate (GFR), urinary flow, and sodium excretion ( P < 0.05 each). After resuscitation, MAP, cardiac output, RBF, MBF, IBF, and GFR all recovered to basal values with either XL-Hb or dextran. Urinary flow and sodium excretion increased to above basal levels with dextran (both by 3.5-fold; P < 0.05) or XL-Hb (by 7.5- and 10-fold, respectively; P < 0.05). We conclude that resuscitation with XL-Hb after hemorrhage not only increases MAP, but also restores RBF, MBF, IBF, GFR, and urinary sodium and volume excretion analogously to dextran. The results contrast with those in normal dogs and suggest that nitric oxide inhibition does not impair hemodynamic and renal function recovery during hemorrhage.

Details

ISSN :
15221490 and 03636119
Volume :
278
Database :
OpenAIRE
Journal :
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
Accession number :
edsair.doi.dedup.....6957ec7190a163902505c207541fcf57
Full Text :
https://doi.org/10.1152/ajpregu.2000.278.1.r28