Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis

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Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis. / Henriksen, Jens Henrik Sahl; Lassen, N A; Parving, H H; Winkler, K.

In: Scandinavian Journal of Clinical & Laboratory Investigation, Vol. 40, No. 6, 1980, p. 503-13.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Henriksen, JHS, Lassen, NA, Parving, HH & Winkler, K 1980, 'Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis', Scandinavian Journal of Clinical & Laboratory Investigation, vol. 40, no. 6, pp. 503-13.

APA

Henriksen, J. H. S., Lassen, N. A., Parving, H. H., & Winkler, K. (1980). Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis. Scandinavian Journal of Clinical & Laboratory Investigation, 40(6), 503-13.

Vancouver

Henriksen JHS, Lassen NA, Parving HH, Winkler K. Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis. Scandinavian Journal of Clinical & Laboratory Investigation. 1980;40(6):503-13.

Author

Henriksen, Jens Henrik Sahl ; Lassen, N A ; Parving, H H ; Winkler, K. / Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis. In: Scandinavian Journal of Clinical & Laboratory Investigation. 1980 ; Vol. 40, No. 6. pp. 503-13.

Bibtex

@article{2cade3f04e0911df928f000ea68e967b,
title = "Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis",
abstract = "Fractional peritoneal reabsorption rates (FPRR) were determined from the plasma activity after simultaneous intraperitoneal injection of 131I-labelled serum albumin (a) and 125I-labelled immunoglobulin G-IgG (g) in eight patients with cirrhosis (+ ascites 6, -ascites 2) and in one patient with carcinomatous ascites. Trans-vascular escape rates of albumin (TERa) and IgG (TERg) were determined in the cirrhotic patients from the disappearance of simultaneously intravenously injected 131I-labelled serum albumin and 124I-labelled IgG. Peritoneal space to plasma appearance times ranged 0.1-3.3 h, and the appearance times of albumin and IgG were almost identical. In patients with cirrhosis FPRRa and FPRRg were on average 1.27 and 1.21% of intraperitoneal protein masses returning to plasma per hour, respectively. Mean FPRRg/FPRRa ratio was 0.95 and this value was not significantly different from unity, but significantly higher (P < 0.001) than the ratio between the free diffusion coefficients of IgG and albumin (0.06). The calculated ascitic fluid flow rate was on average 61 ml/h. TERa and TERg were on average 9.6 and 8.6% of intravascular protein masses per hour, mean TERg/TERa ratio was 0.95. Peritoneal space to plasma protein flux averaged 0.4% of the intravascular protein mass per hour. The results point to filtration (convective flux) as the main transport mechanism responsible for protein passage into the peritoneal cavity as well as for the protein passage (lymphatic drainage) back into the plasma. Pressure measurements during catheterization confirmed pressure differences essential for convective flux.",
author = "Henriksen, {Jens Henrik Sahl} and Lassen, {N A} and Parving, {H H} and K Winkler",
note = "Keywords: Adult; Aged; Albumins; Ascitic Fluid; Biological Transport; Female; Filtration; Humans; Immunoglobulin G; Liver Cirrhosis; Male; Middle Aged; Peritoneal Cavity; Proteins; Serum Albumin, Radio-Iodinated",
year = "1980",
language = "English",
volume = "40",
pages = "503--13",
journal = "Scandinavian Journal of Clinical & Laboratory Investigation",
issn = "0036-5513",
publisher = "Taylor & Francis",
number = "6",

}

RIS

TY - JOUR

T1 - Filtration as the main transport mechanism of protein exchange between plasma and the peritoneal cavity in hepatic cirrhosis

AU - Henriksen, Jens Henrik Sahl

AU - Lassen, N A

AU - Parving, H H

AU - Winkler, K

N1 - Keywords: Adult; Aged; Albumins; Ascitic Fluid; Biological Transport; Female; Filtration; Humans; Immunoglobulin G; Liver Cirrhosis; Male; Middle Aged; Peritoneal Cavity; Proteins; Serum Albumin, Radio-Iodinated

PY - 1980

Y1 - 1980

N2 - Fractional peritoneal reabsorption rates (FPRR) were determined from the plasma activity after simultaneous intraperitoneal injection of 131I-labelled serum albumin (a) and 125I-labelled immunoglobulin G-IgG (g) in eight patients with cirrhosis (+ ascites 6, -ascites 2) and in one patient with carcinomatous ascites. Trans-vascular escape rates of albumin (TERa) and IgG (TERg) were determined in the cirrhotic patients from the disappearance of simultaneously intravenously injected 131I-labelled serum albumin and 124I-labelled IgG. Peritoneal space to plasma appearance times ranged 0.1-3.3 h, and the appearance times of albumin and IgG were almost identical. In patients with cirrhosis FPRRa and FPRRg were on average 1.27 and 1.21% of intraperitoneal protein masses returning to plasma per hour, respectively. Mean FPRRg/FPRRa ratio was 0.95 and this value was not significantly different from unity, but significantly higher (P < 0.001) than the ratio between the free diffusion coefficients of IgG and albumin (0.06). The calculated ascitic fluid flow rate was on average 61 ml/h. TERa and TERg were on average 9.6 and 8.6% of intravascular protein masses per hour, mean TERg/TERa ratio was 0.95. Peritoneal space to plasma protein flux averaged 0.4% of the intravascular protein mass per hour. The results point to filtration (convective flux) as the main transport mechanism responsible for protein passage into the peritoneal cavity as well as for the protein passage (lymphatic drainage) back into the plasma. Pressure measurements during catheterization confirmed pressure differences essential for convective flux.

AB - Fractional peritoneal reabsorption rates (FPRR) were determined from the plasma activity after simultaneous intraperitoneal injection of 131I-labelled serum albumin (a) and 125I-labelled immunoglobulin G-IgG (g) in eight patients with cirrhosis (+ ascites 6, -ascites 2) and in one patient with carcinomatous ascites. Trans-vascular escape rates of albumin (TERa) and IgG (TERg) were determined in the cirrhotic patients from the disappearance of simultaneously intravenously injected 131I-labelled serum albumin and 124I-labelled IgG. Peritoneal space to plasma appearance times ranged 0.1-3.3 h, and the appearance times of albumin and IgG were almost identical. In patients with cirrhosis FPRRa and FPRRg were on average 1.27 and 1.21% of intraperitoneal protein masses returning to plasma per hour, respectively. Mean FPRRg/FPRRa ratio was 0.95 and this value was not significantly different from unity, but significantly higher (P < 0.001) than the ratio between the free diffusion coefficients of IgG and albumin (0.06). The calculated ascitic fluid flow rate was on average 61 ml/h. TERa and TERg were on average 9.6 and 8.6% of intravascular protein masses per hour, mean TERg/TERa ratio was 0.95. Peritoneal space to plasma protein flux averaged 0.4% of the intravascular protein mass per hour. The results point to filtration (convective flux) as the main transport mechanism responsible for protein passage into the peritoneal cavity as well as for the protein passage (lymphatic drainage) back into the plasma. Pressure measurements during catheterization confirmed pressure differences essential for convective flux.

M3 - Journal article

C2 - 7444354

VL - 40

SP - 503

EP - 513

JO - Scandinavian Journal of Clinical & Laboratory Investigation

JF - Scandinavian Journal of Clinical & Laboratory Investigation

SN - 0036-5513

IS - 6

ER -

ID: 19398361