Literature DB >> 8801538

Leptin enters the brain by a saturable system independent of insulin.

W A Banks1, A J Kastin, W Huang, J B Jaspan, L M Maness.   

Abstract

Leptin, or OB protein, is produced by fat cells and may regulate body weight by acting on the brain. To reach the brain, circulating leptin must cross the blood-brain barrier (BBB). Intravenously injected radioiodinated leptin (125I-leptin) had an influx constant (Ki) into brain of (5.87)10(-4) ml/g-min, a rate 20 times greater than that of labeled albumin. Unlabeled leptin inhibited the influx of 125I-leptin in a dose-dependent manner whereas unlabeled tyrosine and insulin, which have saturable transport systems, were without effect. HPLC and acid precipitation showed that the radioactivity in brain and serum represented intact 125I-leptin. About 75% of the extravascular 125I-leptin in brain completely crossed the BBB to reach brain parenchyma. Autoradiography detected uptake at the choroid plexus, arcuate nuclei of the hypothalamus, and the median eminence. Saturable transport did not occur out of the brain. The results show that leptin is transported intact from blood to brain by a saturable system.

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Year:  1996        PMID: 8801538     DOI: 10.1016/0196-9781(96)00025-3

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  257 in total

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Review 3.  Electrophysiological analysis of circuits controlling energy homeostasis.

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6.  Permeability of the blood-brain barrier to a rhenacarborane.

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Journal:  J Pharmacol Exp Ther       Date:  2009-01-29       Impact factor: 4.030

7.  Ghrelin signaling contributes to fasting-induced attenuation of hindbrain neural activation and hypophagic responses to systemic cholecystokinin in rats.

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8.  Modulation of AgRP-neuronal function by SOCS3 as an initiating event in diet-induced hypothalamic leptin resistance.

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9.  Maternal high-fat diet results in cognitive impairment and hippocampal gene expression changes in rat offspring.

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10.  Systemic leptin dose-dependently increases STAT3 phosphorylation within hypothalamic and hindbrain nuclei.

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