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Journal ArticleDOI

Impaired transport of leptin across the blood-brain barrier in obesity.

William A. Banks, +2 more
- 01 Nov 1999 - 
- Vol. 20, Iss: 11, pp 1341-1345
TLDR
It is shown that the transport rate of leptin across the blood-brain barrier is reduced about 2/3 in 12-month-old obese CD-1 mice, suggesting a new model for obesity in which a defect in the BBB transport of leptin into the CNS underlies the insensitivity to leptin and leads to obesity.
About
This article is published in Peptides.The article was published on 1999-11-01. It has received 325 citations till now. The article focuses on the topics: Leptin & Thermogenesis.

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Citations
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Journal ArticleDOI

Adipose Tissue as an Endocrine Organ

TL;DR: The discovery of leptin in the mid-1990s has focused attention on the role of proteins secreted by adipose tissue, which is also involved in the regulation of neuroendocrine and immune function and the metabolic and cardiovascular complications associated with obesity.
Journal ArticleDOI

Leptin regulation of neuroendocrine systems.

TL;DR: It is shown that leptin's effects on energy balance and the neuroendocrine axis are mediated by projections to other hypothalamic nuclei, e.g., paraventricular, lateral, and perifornical areas, as well as other sites in the brainstem, spinal cord, and cortical and subcortical regions.
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Region-Specific Leptin Resistance within the Hypothalamus of Diet-Induced Obese Mice

TL;DR: The study suggests that the ARC is selectively leptin resistant in DIO mice and that this may be caused by elevated suppressor of cytokine signaling 3 in this hypothalamic nucleus.
Journal ArticleDOI

From blood–brain barrier to blood–brain interface: new opportunities for CNS drug delivery

TL;DR: Some of the most important areas that have recently redefined the BBB are reviewed and how they can be applied to the development of CNS therapeutics are discussed.
Journal ArticleDOI

Extent and Direction of Ghrelin Transport Across the Blood-Brain Barrier Is Determined by Its Unique Primary Structure

TL;DR: It is shown that ghrelin transport across the blood-brain barrier is a complex, highly regulated bidirectional process, defining a new role for the unique post-translational octanoylation.
References
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Journal ArticleDOI

Positional cloning of the mouse obese gene and its human homologue

TL;DR: The ob gene product may function as part of a signalling pathway from adipose tissue that acts to regulate the size of the body fat depot.
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Serum Immunoreactive-Leptin Concentrations in Normal-Weight and Obese Humans

TL;DR: Serum leptin concentrations are correlated with the percentage of body fat, suggesting that most obese persons are insensitive to endogenous leptin production.
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Graphical Evaluation of Blood-to-Brain Transfer Constants from Multiple-Time Uptake Data:

TL;DR: A theoretical model of blood–brain exchange is developed and a procedure is derived that can be used for graphing multiple-time tissue uptake data and determining whether a unidirectional transfer process was dominant during part or all of the experimental period.
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Leptin enters the brain by a saturable system independent of insulin.

TL;DR: Results show that leptin is transported intact from blood to brain by a saturable system and inhibited the influx of 125I-leptin in a dose-dependent manner whereas unlabeled tyrosine and insulin, which have saturable transport systems, were without effect.
Journal ArticleDOI

Decreased cerebrospinal-fluid/serum leptin ratio in obesity: a possible mechanism for leptin resistance

TL;DR: The data suggest that leptin enters the brain by a saturable transport system, lower in obese individuals, and may provide a mechanism for leptin resistance.
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