Evidence map›Paper›PMID 23698719›Full record

ArticleEndocrinology2013

Integrated effects of leptin in the forebrain and hindbrain of male rats.

Bhavna N Desai, Ruth B S Harris

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Loss of leptin receptor-expressing cells in the hindbrain decreases forebrain leptin sensitivity.American journal of physiology. Endocrinology and metabolism · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Leptin in the hindbrain facilitates phosphorylation of STAT3 in the hypothalamus.American journal of physiology. Endocrinology and metabolism · 2015
    Article
  10. 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

2 authors at 2 institutions in 1 country.

Bhavna N DesaiDepartment of Physiology, Georgia Regents University, Augusta, GA 30912, USA. bdesai@gru.edu
Ruth B S Harris
Augusta University · USGeorgia Regents Medical Center · US

Funding

LEPTIN AND PERIPHERAL GLUCOSE METABOLISMR01DK053903 · NIDDK · UNIVERSITY OF GEORGIA (UGA) · PI HARRIS, RUTH B · 1999 to 2018
$4.6M
NIDDK NIH HHS DK 053903NIDDK NIH HHS R01 DK053903
6 · The paper itself

Abstract

Leptin receptors (ObRs) in the forebrain and hindbrain have been independently recognized as important mediators of leptin responses. It is unclear how leptin activity in these areas is integrated. We tested whether both forebrain and hindbrain ObRs have to be activated simultaneously to change energy balance and to maintain metabolic homeostasis. Previous studies used acute leptin injections in either the third ventricle (1-5 μg) or the fourth ventricle (3-10 μg); here we used 12-day infusions of low doses of leptin in one or both ventricles (0.1 μg/24 h in third, 0.6 μg/24 h in fourth). Male Sprague Dawley rats were fitted with third and fourth ventricle cannulas, and saline or leptin was infused from Alzet pumps for 6 or 12 days. Rats that received leptin into only the third or the fourth ventricle were not different from controls that received saline in both ventricles. By contrast, rats with low-dose leptin infusions into both the third and fourth ventricle showed a dramatic 60% reduction in food intake that was reversed on day 6, a 20% weight loss that stabilized on day 6, and a 50% decrease in body fat at day 12 despite the correction of food intake. They displayed normal activity and maintained energy expenditure despite weight loss, indicating inappropriately high thermogenesis that coincided with increased signal transducer and activator of transcription 3 (STAT3) phosphorylation in the brainstem. Altogether, these findings show that with low doses of leptin, chronic activation of both hypothalamic and brainstem ObRs is required to reduce body fat.

Indexed as

AnimalsBlotting, WesternDose-Response Relationship, DrugEatingEnergy MetabolismFourth VentricleInfusion PumpsIon ChannelsLeptinMaleMitochondrial ProteinsPhosphorylationProsencephalonRatsRats, Sprague-DawleyReceptors, LeptinIon ChannelsLeptinMitochondrial ProteinsReceptors, LeptinStat3 protein, ratSTAT3 Transcription FactorUncoupling Protein 1

Identifiers

PMID23698719
PMCPMC3713221
OpenAlexW2160657115

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.