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Diabetes Care, Vol 21, Issue 9 1481-1488, Copyright © 1998 by American Diabetes Association
Microdialysis of glucose in subcutaneous adipose tissue up to 3 weeks in healthy volunteers
KJ Wientjes, P Vonk, Y Vonk-van Klei, AJ Schoonen and NW Kossen
Department of Pharmaceutical Technology and Biopharmacy, University Center of Pharmacy, University of Groningen, The Netherlands.
OBJECTIVE: To measure possible changes in dialysate glucose concentrations
over time, to validate the diffusional model for glucose transport from
tissue to the probe, and to evaluate the actual glucose concentration in
adipose tissue. RESEARCH DESIGN AND METHODS: Glucose concentrations in the
subcutaneous adipose tissue of five healthy subjects (age 25 +/- 2.7 years,
BMI 23.2 +/- 2.3 kg/m2 [mean +/- SD]) were measured by the microdialysis
technique and compared with blood glucose. We applied microdialysis probes
with hollow fibers of various membrane length (10-35 mm), used eight
perfusion flow rates (0.5-20 microl/min), and perfused four glucose
solutions (0.0, 2.8, 8.3, 11.1 mmol/l). RESULTS: After implantation, a
substantial decrease in glucose recovery to the lowest value of 26 +/- 10%
of the final plateau value was noted during the first few hours (n = 4).
Recovery increased and stabilized after 5-9 days at 84.0 +/- 7.4% of
capillary blood glucose when a flow rate of 0.5 microl/min was applied.
According to the zero net-flux method, the glucose concentration in
equilibrium, Cequi, with the surrounding tissue can be obtained. This
concentration also decreases; however, 1 h after recovery, Cequi increases
again over 1 or 2 days to a stable value that is not significantly
different from the measured capillary blood glucose (P < 0.05). Using
various perfusion flow rates and probes (membrane length 10-35 mm), it is
shown that diffusion is the rate-limiting process for glucose transport
through tissue. CONCLUSIONS: Insertion of the microdialysis probes causes
damage to the adipose cells and the vascular bed around the probe. Glucose
recovery decreases because of a lower blood supply. In 5-9 days, glucose
recovery increases; apparently, this time is needed to repair the
microstructure of tissue around the probe. After stabilization of the
recovery, no loss of probe permeability, which is due to biocompatibility
problems, was seen. The change during the 2 days in equilibrium
concentration is probably caused by an inflammation reaction that consumes
glucose around the probe. The individual increase in recovery during the
1st days after probe insertion until a stable plateau value is reached
(flow rate >0 microl/min) is complicated for short-term clinical glucose
measurements in adipose tissue. After stabilization, the mean equilibrium
concentration of all subjects was equal to the mean capillary blood glucose
concentration. Therefore, we conclude that capillary blood glucose
concentration probably is the driving force for diffusion through the
capillary wall into the probe and is not some interstitial concentration.

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Copyright © 1998 by the American Diabetes Association.
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