Evidence map›Paper›PMID 20826762›Full record

ArticleAmerican journal of physiology. Cell physiology2010

Functional expression of SGLTs in rat brain.

Amy S Yu, Bruce A Hirayama, Gerald Timbol, Jie Liu, Ernest Basarah, Vladimir Kepe, Nagichettiar Satyamurthy, Sung-Cheng Huang, Ernest M Wright, Jorge R Barrio

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 117 citations in OpenAlex.

  1. Review
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  14. Review
  15. Fluorinated carbohydrates forChemical Society reviews · 2023
    Review
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  20. Brain Metabolic Alterations in Alzheimer's Disease.International journal of molecular sciences · 2022
    Review

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Amy S YuDepartment of Molecular and Medical Pharmacology, David Geffen School of Medicine, Universityof California Los Angeles, California 90095-1751, USA.
Bruce A Hirayama
Gerald Timbol
Jie Liu
Ernest Basarah
Vladimir Kepe
Nagichettiar Satyamurthy
Sung-Cheng Huang
Ernest M Wright
Jorge R Barrio
University of California, Los Angeles · US

Funding

VISUALIZING BRAIN A-BETA, TAU /SEROTONIN RECEPTOR DENSITP01AG025831 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SMALL, GARY WILLIAM · 2005 to 2010
$7.0M
Role of SGLTs in Glucose Homeostasis and Tissue MetabolismR01DK077133 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WRIGHT, ERNEST M · 2008 to 2011
$1.3M
NIA NIH HHS P01 AG025831NIA NIH HHS P01-AG-025831NIDDK NIH HHS R01 DK077133NIDDK NIH HHS R01-DK077133
6 · The paper itself

Abstract

This work provides evidence of previously unrecognized uptake of glucose via sodium-coupled glucose transporters (SGLTs) in specific regions of the brain. The current understanding of functional glucose utilization in brain is largely based on studies using positron emission tomography (PET) with the glucose tracer 2-deoxy-2-[F-18]fluoro-D-glucose (2-FDG). However, 2-FDG is only a good substrate for facilitated-glucose transporters (GLUTs), not for SGLTs. Thus, glucose accumulation measured by 2-FDG omits the role of SGLTs. We designed and synthesized two high-affinity tracers: one, α-methyl-4-[F-18]fluoro-4-deoxy-D-glucopyranoside (Me-4FDG), is a highly specific SGLT substrate and not transported by GLUTs; the other one, 4-[F-18]fluoro-4-deoxy-D-glucose (4-FDG), is transported by both SGLTs and GLUTs and will pass through the blood brain barrier (BBB). In vitro Me-4FDG autoradiography was used to map the distribution of uptake by functional SGLTs in brain slices with a comparable result from in vitro 4-FDG autoradiography. Immunohistochemical assays showed that uptake was consistent with the distribution of SGLT protein. Ex vivo 4-FDG autoradiography showed that SGLTs in these areas are functionally active in the normal in vivo brain. The results establish that SGLTs are a normal part of the physiology of specific areas of the brain, including hippocampus, amygdala, hypothalamus, and cerebral cortices. 4-FDG PET imaging also established that this BBB-permeable SGLT tracer now offers a functional imaging approach in humans to assess regulation of SGLT activity in health and disease.

Indexed as

AnimalsBlood-Brain BarrierBrainDeoxyglucoseFemaleGlucoseGlucosidesGlutamate Plasma Membrane Transport ProteinsPositron-Emission TomographyRatsRats, Sprague-DawleySodium-Glucose Transport Proteins4-fluoro-4-deoxyglucoseDeoxyglucoseGlucoseGlucosidesGlutamate Plasma Membrane Transport Proteinsmethyl-4-fluoro-4-deoxyglucoseSodium-Glucose Transport Proteins

Identifiers

PMID20826762
PMCPMC3006325
OpenAlexW2084966416

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.