Assessment of transcapillary glucose exchange in human skeletal muscle and adipose tissue
1 Department of Biophysics, Institute of Biomedical Engineering, Graz University of Technology; and Departments of 2 Biochemical Analysis and Mass Spectrometry and 3 Internal Medicine, Diabetes and Metabolism, Karl Franzens University Graz, A-8010 Graz, Austria Submitted 9 August 2002 ; accepted in...
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Veröffentlicht in: | American journal of physiology: endocrinology and metabolism 2003-08, Vol.285 (2), p.E241-E251 |
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Zusammenfassung: | 1 Department of Biophysics, Institute of
Biomedical Engineering, Graz University of Technology; and Departments of
2 Biochemical Analysis and Mass Spectrometry and
3 Internal Medicine, Diabetes and Metabolism, Karl
Franzens University Graz, A-8010 Graz, Austria
Submitted 9 August 2002
; accepted in final form 5 April 2003
We studied the kinetics of glucose exchange between plasma and interstitial
fluid (ISF) in human skeletal muscle and adipose tissue under fasting
conditions. Five normal human subjects received an intravenous
[6,6- 2 H 2 ]glucose infusion in a prime-continuous fashion.
During the tracer infusion, the open-flow microperfusion technique was
employed to frequently sample ISF from quadriceps muscle and subcutaneous
adipose tissue. The tracer glucose kinetics observed in muscle and adipose
tissue ISF were found to be well described by a capillary-tissue exchange
model. As a measure of transcapillary glucose exchange efficiency, the 95%
equilibrium time was calculated from the identified model parameters. This
time constant was similar for skeletal muscle and adipose tissue (28.6
± 3.2 vs. 26.8 ± 3.6 min; P = 0.60). Furthermore, we
found that the (total) interstitial glucose concentration was significantly
lower ( P < 0.01) in muscle (3.32 ± 0.46 mmol/l) and adipose
tissue (3.51 ± 0.17 mmol/l) compared with arterialized plasma levels
(5.56 ± 0.13 mmol/l). Thus the observed gradients and dynamic
relationships between plasma and ISF glucose in muscle and adipose tissue
provide evidence that transcapillary exchange of glucose is limited in these
two tissues under fasting conditions.
open-flow microperfusion; interstitial fluid; capillary-tissue exchange model
Address for reprint requests and other correspondence: W. Regittnig, Dept. of
Biophysics, Institute of Biomedical Engineering, Graz Univ. of Technology,
Krenngasse 37, A-8010 Graz, Austria (E-mail:
werner.regittnig{at}healthgate.at ). |
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ISSN: | 0193-1849 1522-1555 |
DOI: | 10.1152/ajpendo.00351.2002 |