Multiple-indicator dilution experiments with labeled lactate were performed
in the livers of anesthetized dogs. A mixture of Cr-51-labeled erythrocyte
s, [H-3]sucrose, and L-[1-C-14]lactate or a mixture of 51Cr-labeled erythro
cytes, [C-14]sucrose, and L-[2-H-3]lactate was injected into the portal vei
n, and samples were obtained from the hepatic vein. Data were evaluated usi
ng a model comprising flow along sinusoids, exchange of lactate between pla
sma and erythrocytes and between plasma and hepatocytes, and, in the case o
f L- [1-C-14]lactate, metabolism to H[C-14]O-3(-) within hepatocytes. The c
oefficient for lactate efflux from erythrocytes was 0.62 +/- 0.24 s(-1), an
d those for influx into and efflux from hepatocytes were 0.44 +/- 0.13 and
0.14 +/- 0.07 s(-1), respectively. The influx permeability-surface area pro
duct of the hepatocyte membrane for lactate (PinS, in ml . s(-1) . g(-1)) v
aried with total flow rate (F, in mi s(-1) . g(-1)) according to PinS = (3.
1 +/- 0.5)F + (0.021 +/- 0.014). Lactate in plasma, erythrocytes, and hepat
ocytes was close to equilibrium, whereas lactate metabolism was rate limiti
ng.