scholarly journals Cerebral extraction of N-13 ammonia: its dependence on cerebral blood flow and capillary permeability, surface area product. [Dogs; monkeys]

1979 ◽  
Author(s):  
M.E. Phelps ◽  
S.C. Huang ◽  
D.E. Kuhl ◽  
E.J. Hoffman ◽  
C. Slin
1986 ◽  
Vol 6 (3) ◽  
pp. 338-341 ◽  
Author(s):  
Nicholas V. Todd ◽  
Piero Picozzi ◽  
H. Alan Crockard

CBF obtained by the hydrogen clearance technique and cerebral blood volume (CBV) calculated from the [14C]dextran space were measured in three groups of rats subjected to temporary four-vessel occlusion to produce 15 min of ischaemia, followed by 60 min of reperfusion. In the control animals, mean CBF was 93 ± 6 ml 100 g−1 min−1, which fell to 5.5 ± 0.5 ml 100 g−1 min−1 during ischaemia. There was a marked early postischaemic hyperaemia (262 ± 18 ml 100g−1 min−1), but 1 h after the onset of ischaemia, there was a significant hypoperfusion (51 ± 3 ml 100 g−1 min−1). Mean cortical dextran space was 1.58 ± 0.09 ml 100 g−1 prior to ischaemia. Early in reperfusion there was a significant increase in CBV (1.85 ± 0.24 ml 100 g−1) with a decrease during the period of hypoperfusion (1.33 ± 0.03 ml 100 g−1). Therefore, following a period of temporary ischaemia, there are commensurate changes in CBF and CBV, and alterations in the permeability–surface area product at this time may be due to variations in surface area and not necessarily permeability.


1997 ◽  
Vol 80 (5) ◽  
pp. 645-654 ◽  
Author(s):  
Carl A. Goresky ◽  
André Simard ◽  
Andreas J. Schwab

1997 ◽  
Vol 272 (1) ◽  
pp. R163-R171
Author(s):  
K. Mori ◽  
M. Maeda

Local maximal velocities of transport (Tmax) and the half-maximum transport constants (KT) for glucose transport across the blood-brain barrier have been determined in local regions of the brain in normal conscious rats. [14C]iodoantipyrine and [3H]methylglucose were infused together intravenously for 2 min in rats with plasma glucose concentrations maintained at different levels, and the time courses of the tracer levels in arterial blood were measured. Local 14C and 3H concentrations were then measured in tissue samples dissected from the frozen brains. By comparing the transport-limited uptake of [3H]methylglucose with the blood flow-limited uptake of [14C]iodoantipyrine, the value of m, a factor between 0 and 10 that accounts for diffusion and/or transport limitations, was derived, and from the equation, m = 1 - PS/F (where PS is capillary permeability-surface area product and F is cerebral blood flow), the permeability-capillary surface area for methylglucose was calculated (S. S. Kety. Pharmacol. Rev. 3: 1-41, 1951). Values for Tmax and KT for glucose were calculated by application of Michaelis-Menten kinetic relationships adapted for the competition for transport between glucose and methylglucose. Tmax was determined in three representative gray structures and one white structure of the brain: Tmax was 5.3 +/- 0.3 (SD) mumol.g-1.min-1 in the gray structures and 4.3 mumol.g-1.min-1 in the white structure. KT was 3.6 +/- 0.4 (SD) mM in the gray structures and 5.9 mM in the white structure. This approach allows the simultaneous determination of local values of Tmax and KT for glucose and the rates of blood flow in various regions of the brain in conscious animals.


1982 ◽  
Vol 242 (5) ◽  
pp. G435-G441 ◽  
Author(s):  
A. P. Shepherd

Increasing evidence indicates that capillary recruitment plays a significant role in regulating the oxygenation of intestinal tissue. Measurements of permeability-surface area product (PS) and capillary filtration coefficients (Kf) in isolated perfused gut loops indicate that changes in capillary density modulate oxygen extraction in a variety of experimental circumstances. Moreover, the intestinal microvasculature seems capable of independently regulating resistance and capillary exchange. Although "precapillary sphincters" have been identified in the intestine, the capillary density changes have not yet been confirmed by intravital microscopy, as they have been in skeletal muscle. Nevertheless, these changes in capillary density have quantitatively significant effects on oxygen extraction. For example, sympathetic stimulation depresses oxygen uptake in gut loops perfused at constant blood flow, presumably by reducing capillary density to such an extent that oxygen extraction becomes diffusion limited. The microvascular elements that control intestinal capillary density (presumably precapillary sphincters) are apparently under the control of neurogenic, myogenic, and local metabolic mechanisms, but the interaction among these mechanisms is poorly understood. In addition, the PS and Kf data, although well documented, could result from a redistribution of blood flow or an alteration in capillary permeability rather than a change in capillary density. Thus, the physiological mechanisms regulating capillary permeability and the intramural distribution of intestinal blood flow will have to be better understood before the role of capillary recruitment in regulating intestinal oxygenation will be firmly established.


1959 ◽  
Vol 197 (6) ◽  
pp. 1205-1210 ◽  
Author(s):  
Eugene M. Renkin

A method is described for studying transcapillary diffusion of K42 in isolated perfused muscles of dogs. Blood flow and arteriovenous K42 differences are measured and blood-tissue clearance calculated by the Fick principle. A theoretical relation between blood flow and blood-tissue clearance is developed for a uniform circulation characterized by a constant permeability—surface area product (PS). The experimental observations conform reasonably closely to prediction. However, systematic variation in measured PS product with changes in blood flow and vascular resistance indicate that the capillary circulation is not uniform.


1997 ◽  
Vol 273 (3) ◽  
pp. H1239-H1245 ◽  
Author(s):  
J. Dupuis ◽  
C. A. Goresky ◽  
C. P. Rose ◽  
D. J. Stewart ◽  
P. Cernacek ◽  
...  

Myocardial metabolism of endothelin-1 (ET-1) and its effect on coronary microcirculatory exchanges were obtained in anesthetized dogs by combining the indicator-dilution technique with immunoreactive ET-1 measurements. The myocardium extracted 17.7 +/- 4.6% of tracer ET-1 (n = 12). Simultaneously measured ET-1 levels in the aorta (0.97 +/- 0.46 pg/ml) and coronary sinus (0.96 +/- 0.53 pg/ml) were not different, supporting a production of ET-1 by the heart that balances the amount extracted. Intracoronary infusion of ET-1 (5 ng.kg-1.min-1) increased coronary sinus ET-1 levels approximately 50-fold, decreased coronary blood flow per unit of interstitial space by approximately 30% (P = 0.006), and increased myocardial microcirculatory transit times (n = 6). Permeability to albumin was unaffected by ET-1, whereas the permeability-surface area product for sucrose decreased following derecruitment of myocardial capillaries. We conclude that there is a normal myocardial metabolic balance of ET-1 and that the heart marginally contributes to circulating ET-1. Pharmacological doses of ET-1 may adversely affect myocardial metabolism by reducing blood flow and the permeability-surface area product for small circulating substances.


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