4.4 Article

The fasting polypeptide FGF21 can enter brain from blood

Journal

PEPTIDES
Volume 28, Issue 12, Pages 2382-2386

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.peptides.2007.10.007

Keywords

FGF21; blood-brain barrier; metabolism

Funding

  1. NIDDK NIH HHS [R56 DK054880, DK54880, R01 DK054880] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS045751, R01 NS046528-05, NS46528, R01 NS045751-05, NS45751, R01 NS046528] Funding Source: Medline

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FGF21 recently has been proposed as a missing link in the biology of fasting, raising the question of whether it directly reaches the brain. We used multiple time-regression analysis to quantify the influx rate of this polypeptide across the blood-brain barrier (BBB), size-exclusion chromatography to examine degradation, capillary depletion to differentiate entry into brain parenchyma from retention in the microvasculature, and measurement of efflux rate to determine a possible confounding effect on measurement of entry. FGF21 was 94% intact in serum and 75% in brain 10 min after intravenous bolus delivery. its influx rate was 0.23 +/- 0.12 mu l/g-min, nearly four times faster than that of the vascular marker albumin. At 10 min, about 0.5% of the administered FGF21 was present in a gram of brain tissue. of this, 70% reached the parenchyma of the brain. Co-injection of excess FGF21 failed to inhibit the influx, showing a lack of saturation. Efflux, which occurred at the same rate as the bulk reabsorption of cerebrospinal fluid, also was not saturable. In summary, FGF21 shows significant, non-saturable, unidirectional influx across the BBB. (c) 2007 Elsevier Inc. All rights reserved.

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