Evidence map›Paper›PMID 23080264›Full record

ArticleSynapse (New York, N.Y.)2013

Targeting presynaptic norepinephrine transporter in brown adipose tissue: a novel imaging approach and potential treatment for diabetes and obesity.

M Reza Mirbolooki, Cristian C Constantinescu, Min-Liang Pan, Jogeshwar Mukherjee

Abstract read
In one paragraph

Article in Synapse (New York, N.Y.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Comparisons of α2-Adrenergic Agents, Medetomidine and Xylazine, with Pentobarbital for Anesthesia: Important Pitfalls in Diabetic and Nondiabetic Rats.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. PreclinicalFrontiers in pharmacology · 2016
    Review
  9. Article
  10. Article
  11. Atomoxetine prevents dexamethasone-induced skeletal muscle atrophy in mice.The Journal of pharmacology and experimental therapeutics · 2014
    Article
  12. Article
  13. Article
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

4 authors at 1 institution in 1 country.

M Reza MirbolookiPreclinical Imaging, Department of Radiological Sciences, University of California Irvine, Irvine, California 92697-5000, USA. rezam@uci.edu
Cristian C Constantinescu
Min-Liang Pan
Jogeshwar Mukherjee
University of California, Irvine · US

Funding

PET Imaging Agent for Diabetes MellitusRC1DK087352 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI MUKHERJEE, JOGESHWAR · 2009 to 2010
$985k
Small Animal PET (microPET)S10RR019269 · NCRR · UNIVERSITY OF CALIFORNIA-IRVINE · PI MUKHERJEE, JOGESHWAR · 2007 to 2007
$500k
Small Animal MicroCTS10RR024546 · NCRR · UNIVERSITY OF CALIFORNIA-IRVINE · PI MUKHERJEE, JOGESHWAR · 2009 to 2009
$431k
Imaging Adrenergic Stimulation of Brown Adipose TissueR21DK092917 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI MUKHERJEE, JOGESHWAR · 2011 to 2012
$421k
NCRR NIH HHS S10 RR019269NCRR NIH HHS S10 RR024546NIDDK NIH HHS R21 DK092917NIDDK NIH HHS R21DK092917NIDDK NIH HHS RC1 DK087352NIDDK NIH HHS RC1DK087352
6 · The paper itself

Abstract

Brown adipose tissue (BAT) plays a significant role in metabolism. In this study, we report the use of atomoxetine (a clinically applicable norepinephrine reuptake inhibitor) for (18)F-FDG PET imaging of BAT and its effects on heat production and blood glucose concentration. Fasted-male Sprague-Dawley rats were administered with intravenous (18)F-FDG. The same rats were treated with atomoxetine (0.1 mg/kg, i.v.) 30 min before (18)F-FDG administration. To confirm the β-adrenergic effects, propranolol (β-adrenergic inhibitor) 5 mg/kg was given intraperitoneally 30 min prior to atomoxetine administration. The effect of atomoxetine on BAT metabolism was assessed in fasted and non-fasted rats and on BAT temperature and blood glucose in fasted rats. In (18)F-FDG PET/CT images, interscapular BAT (IBAT) and other areas of BAT were clearly visualized. When rats were fasted, atomoxetine (0.1 mg/kg) increased the (18)F-FDG uptake of IBAT by factor of 24 within 30 min. Propranolol reduced the average (18)F-FDG uptake of IBAT significantly. Autoradiography of IBAT and white adipose tissue confirmed the data obtained by PET. When rats were not fasted, atomoxetine-induced increase of (18)F-FDG uptake in IBAT was delayed and occurred in 120 min. For comparison, direct stimulation of β(3)-adrenreceptors in non-fasted rats with CL-316, 243 occurred within 30 min. Atomoxetine-induced IBAT activation was associated with higher IBAT temperature and lower blood glucose. This was mediated by inhibition of norepinephrine reuptake transporters in IBAT leading to increased norepinephrine concentration in the synapse. Increased synaptic norepinephrine activates β(3)-adrenreceptors resulting in BAT hypermetabolism that is visible and quantifiable by (18)F-FDG PET/CT.

Indexed as

Adipose Tissue, BrownAdrenergic beta-AntagonistsAdrenergic Uptake InhibitorsAnimalsAtomoxetine HydrochlorideBlood GlucoseDiabetes Mellitus, Type 2Fluorodeoxyglucose F18MaleNorepinephrine Plasma Membrane Transport ProteinsObesityPropranololPropylaminesRadionuclide ImagingRatsRats, Sprague-DawleyAdrenergic beta-AntagonistsAdrenergic Uptake InhibitorsAtomoxetine HydrochlorideBlood GlucoseFluorodeoxyglucose F18Norepinephrine Plasma Membrane Transport ProteinsPropranololPropylamines

Identifiers

PMID23080264
PMCPMC3808851
OpenAlexW2140804756

What OpenQuestion holds

Textmetadata
LicenceTDM
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.