Evaluation of the microdialysis technique in the dog fat pad

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Standard

Evaluation of the microdialysis technique in the dog fat pad. / Stallknecht, B; Madsen, J; Galbo, H; Bülow, J.

I: American Journal of Physiology: Endocrinology and Metabolism, Bind 276, Nr. 3 Pt 1, 1999, s. E588-95.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Stallknecht, B, Madsen, J, Galbo, H & Bülow, J 1999, 'Evaluation of the microdialysis technique in the dog fat pad', American Journal of Physiology: Endocrinology and Metabolism, bind 276, nr. 3 Pt 1, s. E588-95.

APA

Stallknecht, B., Madsen, J., Galbo, H., & Bülow, J. (1999). Evaluation of the microdialysis technique in the dog fat pad. American Journal of Physiology: Endocrinology and Metabolism, 276(3 Pt 1), E588-95.

Vancouver

Stallknecht B, Madsen J, Galbo H, Bülow J. Evaluation of the microdialysis technique in the dog fat pad. American Journal of Physiology: Endocrinology and Metabolism. 1999;276(3 Pt 1):E588-95.

Author

Stallknecht, B ; Madsen, J ; Galbo, H ; Bülow, J. / Evaluation of the microdialysis technique in the dog fat pad. I: American Journal of Physiology: Endocrinology and Metabolism. 1999 ; Bind 276, Nr. 3 Pt 1. s. E588-95.

Bibtex

@article{0da669e074c911dbbee902004c4f4f50,
title = "Evaluation of the microdialysis technique in the dog fat pad",
abstract = "In the present study the microdialysis technique was evaluated in an isolated autoperfused dog fat pad. Concentrations of glucose, lactate, and glycerol were measured in interstitial fluid by microdialysis and simultaneously in arterial and adipose venous plasma. Adipose tissue blood flow was measured by both 133Xe washout and timed weighing of venous blood. Metabolite concentrations in adipose venous plasma calculated from interstitial and arterial metabolite concentrations and 133Xe washout were positively correlated with measured venous concentrations (glucose: r = 0.95, lactate: r = 0.92, glycerol: r = 0.81). Calculated and measured venous plasma concentrations did not differ for either glucose or lactate, but for glycerol, calculated concentration was on average 76% of measured concentration. Metabolite exchanges (Fick's principle) calculated from interstitial metabolite concentrations were positively correlated with measured exchanges only for lactate (r = 0.69). In conclusion, metabolite concentrations in adipose venous plasma can be calculated from microdialysis measurements with greater accuracy for glucose and lactate than for glycerol. The precision, however, is too low to allow calculation of metabolite exchange when arteriovenous metabolite differences are low.",
author = "B Stallknecht and J Madsen and H Galbo and J B{\"u}low",
note = "Keywords: Adipose Tissue; Animals; Blood Glucose; Dogs; Evaluation Studies as Topic; Extracellular Space; Female; Glucose; Glycerol; Lactic Acid; Microdialysis; Osmolar Concentration; Veins",
year = "1999",
language = "English",
volume = "276",
pages = "E588--95",
journal = "American Journal of Physiology - Endocrinology and Metabolism",
issn = "0193-1849",
publisher = "American Physiological Society",
number = "3 Pt 1",

}

RIS

TY - JOUR

T1 - Evaluation of the microdialysis technique in the dog fat pad

AU - Stallknecht, B

AU - Madsen, J

AU - Galbo, H

AU - Bülow, J

N1 - Keywords: Adipose Tissue; Animals; Blood Glucose; Dogs; Evaluation Studies as Topic; Extracellular Space; Female; Glucose; Glycerol; Lactic Acid; Microdialysis; Osmolar Concentration; Veins

PY - 1999

Y1 - 1999

N2 - In the present study the microdialysis technique was evaluated in an isolated autoperfused dog fat pad. Concentrations of glucose, lactate, and glycerol were measured in interstitial fluid by microdialysis and simultaneously in arterial and adipose venous plasma. Adipose tissue blood flow was measured by both 133Xe washout and timed weighing of venous blood. Metabolite concentrations in adipose venous plasma calculated from interstitial and arterial metabolite concentrations and 133Xe washout were positively correlated with measured venous concentrations (glucose: r = 0.95, lactate: r = 0.92, glycerol: r = 0.81). Calculated and measured venous plasma concentrations did not differ for either glucose or lactate, but for glycerol, calculated concentration was on average 76% of measured concentration. Metabolite exchanges (Fick's principle) calculated from interstitial metabolite concentrations were positively correlated with measured exchanges only for lactate (r = 0.69). In conclusion, metabolite concentrations in adipose venous plasma can be calculated from microdialysis measurements with greater accuracy for glucose and lactate than for glycerol. The precision, however, is too low to allow calculation of metabolite exchange when arteriovenous metabolite differences are low.

AB - In the present study the microdialysis technique was evaluated in an isolated autoperfused dog fat pad. Concentrations of glucose, lactate, and glycerol were measured in interstitial fluid by microdialysis and simultaneously in arterial and adipose venous plasma. Adipose tissue blood flow was measured by both 133Xe washout and timed weighing of venous blood. Metabolite concentrations in adipose venous plasma calculated from interstitial and arterial metabolite concentrations and 133Xe washout were positively correlated with measured venous concentrations (glucose: r = 0.95, lactate: r = 0.92, glycerol: r = 0.81). Calculated and measured venous plasma concentrations did not differ for either glucose or lactate, but for glycerol, calculated concentration was on average 76% of measured concentration. Metabolite exchanges (Fick's principle) calculated from interstitial metabolite concentrations were positively correlated with measured exchanges only for lactate (r = 0.69). In conclusion, metabolite concentrations in adipose venous plasma can be calculated from microdialysis measurements with greater accuracy for glucose and lactate than for glycerol. The precision, however, is too low to allow calculation of metabolite exchange when arteriovenous metabolite differences are low.

M3 - Journal article

C2 - 10070028

VL - 276

SP - E588-95

JO - American Journal of Physiology - Endocrinology and Metabolism

JF - American Journal of Physiology - Endocrinology and Metabolism

SN - 0193-1849

IS - 3 Pt 1

ER -

ID: 193147