This proposal examines the hypothesis that right sided events affecting venous return, particularly the development of vascular waterfalls, are the major determinants of respiration's influence on the cardiovascular system during spontaneous and positive pressure ventilation.
The specific aims seek to systematically develop a critical body of knowledge to explain how ventilatory produced stresses affect venous return under normal and pathologic states by combining a new method for measuring blood flow in veins with measures of vascular and surface pressures in the thorax and abdomen in intact and isolated liver preparations in the dog and pig. Computer modelling will be used to test hypotheses prospectively against experimental results. The dominant role of abdominal rather than thoracic pressures in determining venous return moves the focus of respiration's influence from the thorax to the abdomen. By developing the concept of abdominal vascular zone conditions (AVZC) similar to those describes in the lung, much of the confusion in the literature on the effects of changes in thoracic or abdominal pressures on cardiac output can be resolved. The concept of AVZC, locally within organs, regionally within the abdomen, and generally at the boundaries of the abdominal compartment is the unifying theme of this proposal. The same stress may produce an increase in venous return in one AVZC, but a decrease in another AVZC. Ventilatory stresses placed on the abdominal vascular compartments could contribute to circulatory and hepatic failure with ventricular dysfunction or sepsis to be modelled by endotoxin infusion. Understanding how ventilatory stresses produce substantial changes in venous return is directly related to understanding venous return from the same beds during CPR when externally applied stresses to the thorax and abdomen will alter the AVZC. Testing the usefulness of the AVZC to account for total and regional venous return over a wide spectrum of clinically relevant states should provide valuable information to physiologists and clinicians.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL039138-05
Application #
3355753
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1987-08-01
Project End
1995-03-31
Budget Start
1992-04-01
Budget End
1993-03-31
Support Year
5
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Mebazaa, A; Wetzel, R C; Dodd-o, J M et al. (1998) Potential paracrine role of the pericardium in the regulation of cardiac function. Cardiovasc Res 40:332-42
Yamamoto, S; Burman, H P; O'Donnell, C P et al. (1997) Endothelin causes portal and pulmonary hypertension in porcine endotoxemic shock. Am J Physiol 272:H1239-49
Shah, A M; Mebazaa, A; Yang, Z K et al. (1997) Inhibition of myocardial crossbridge cycling by hypoxic endothelial cells: a potential mechanism for matching oxygen supply and demand? Circ Res 80:688-98
Pannen, B H; Bauer, M; Noldge-Schomburg, G F et al. (1997) Regulation of hepatic blood flow during resuscitation from hemorrhagic shock: role of NO and endothelins. Am J Physiol 272:H2736-45
Pannen, B H; Bauer, M; Zhang, J X et al. (1996) Endotoxin pretreatment enhances portal venous contractile response to endothelin-1. Am J Physiol 270:H7-15
Revelly, J P; Ayuse, T; Brienza, N et al. (1996) Endotoxic shock alters distribution of blood flow within the intestinal wall. Crit Care Med 24:1345-51
Pannen, B H; Bauer, M; Zhang, J X et al. (1996) A time-dependent balance between endothelins and nitric oxide regulating portal resistance after endotoxin. Am J Physiol 271:H1953-61
Revelly, J P; Ayuse, T; Brienza, N et al. (1995) Dysregulation of the veno-arterial response in the superior mesenteric artery during endotoxic shock. Crit Care Med 23:1519-27
Brienza, N; Revelly, J P; Ayuse, T et al. (1995) Effects of PEEP on liver arterial and venous blood flows. Am J Respir Crit Care Med 152:504-10
Pannen, B H; Maeda, K; Ayuse, T et al. (1995) Hepatic heat shock and acute-phase gene expression are induced simultaneously after celiotomy in the anesthetized pig. Anesthesiology 83:850-9

Showing the most recent 10 out of 26 publications