Evidence map›Paper›PMID 18559657›Full record

ArticleDiabetes2008

Brain apolipoprotein E: an important regulator of food intake in rats.

Ling Shen, Patrick Tso, Stephen C Woods, Deborah J Clegg, Kyna L Barber, Katherine Carey, Min Liu

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Sex and Exposure to Postnatal Chlorpyrifos Influence the Epigenetics of Feeding-Related Genes in a TransgenicInternational journal of environmental research and public health · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Obesity and sex interact in the regulation of Alzheimer's disease.Neuroscience and biobehavioral reviews · 2016
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Apolipoprotein E does not cross the blood-cerebrospinal fluid barrier, as revealed by an improved technique for sampling CSF from mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2012
    Article
  20. 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

7 authors at 1 institution in 1 country.

Ling ShenCincinnati Obesity Research Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Patrick Tso
Stephen C Woods
Deborah J Clegg
Kyna L Barber
Katherine Carey
Min Liu
University of Cincinnati Medical Center · US

Funding

High Fat Diet-Induced ObesityP01DK056863 · NIDDK · UNIVERSITY OF CINCINNATI · PI TSCHOP, MATTHIAS H · 2001 to 2010
$12.0M
MOLECULAR MECHANISMS OF CHOLESTEROL ABSORPTIONP01DK054504 · NIDDK · UNIVERSITY OF CINCINNATI · PI HUI, DAVID Y · 1999 to 2003
$4.0M
INSULIN AND CNS CONTROL OF BODY WEIGHT AND FOOD INTAKER01DK017844 · NIDDK · UNIVERSITY OF WASHINGTON · PI WOODS, STEPHEN C · 1986 to 2013
$3.8M
MODULATION OF INTESTINAL OBESITY SIGNALSR01DK056910 · NIDDK · UNIVERSITY OF CINCINNATI · PI TSO, PATRICK · 2000 to 2004
$1.7M
Regulation of Food Intake and Body Weight by Brain Apo ER01DK070992 · NIDDK · UNIVERSITY OF CINCINNATI · PI LIU, MIN · 2007 to 2011
$1.4M
Brain Apolipoprotein AIV, Food Intake and ObesityR01DK063907 · NIDDK · UNIVERSITY OF CINCINNATI · PI LIU, MIN · 2003 to 2007
$1.3M
TRANSGENIC MOUSE MODEL FOR STUDY OF VIRAL HEPATITIS CZ01DK054504 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LIANG, T. JAKE · 1997 to 2008
$1.0M
INSULIN AND CNS CONTROL OF BODY WEIGHT AND FOOD INTAKER37DK017844 · NIDDK · UNIVERSITY OF WASHINGTON · PI WOODS, STEPHEN C · 1993 to 2000
$382k
Intramural NIH HHS Z01 DK054504NIDDK NIH HHS DK17844NIDDK NIH HHS DK54504NIDDK NIH HHS DK56863NIDDK NIH HHS DK56910NIDDK NIH HHS DK63907NIDDK NIH HHS DK70992NIDDK NIH HHS P01 DK054504NIDDK NIH HHS P01 DK056863NIDDK NIH HHS R01 DK017844NIDDK NIH HHS R01 DK056910NIDDK NIH HHS R01 DK063907NIDDK NIH HHS R01 DK070992NIDDK NIH HHS R37 DK017844
6 · The paper itself

Abstract

objectiveThe worldwide prevalence of obesity is increasing at an alarming rate, along with the associated increased rates of type 2 diabetes, heart disease, and some cancers. While efforts to address environmental factors responsible for the recent epidemic must continue, investigation into the anorectic functions of potential molecules we present here, such as apolipoprotein (apo)E, offers exciting possibilities for future development of successful anti-obesity therapies. RESEARCH DESIGN AND

methodsChanges in feeding behavior after intracerebroventricular injection of apoE, the regulation of hypothalamic apoE gene expression by energy status, and the interaction of hypothalamic apoE with other neuropeptides were studied.

resultsIntracerebroventricular apoE significantly decreased food intake without causing malaise, whereas intracerebroventricular infusion of apoE antiserum stimulated feeding, implying that endogenous apoE tonically inhibits food intake. Consistent with this, apoE was present in the hypothalamus, a brain site intimately involved in the integration of signals for energy homeostasis. Fasted rats exhibited significantly decreased apoE gene expression in the hypothalamus, and refeeding of these rats for 4 h evoked a significant increase of hypothalamic apoE mRNA levels. Both genetically obese (ob/ob) mice and rats with high-fat diet-induced obesity had significantly reduced hypothalamic apoE mRNA levels compared with their lean control counterparts, suggesting that decreased apoE may contribute to hyperphagia in these obese animals. Additionally, apoE-stimulated hypothalamic proopiomelanocortin gene expression and SHU9119, a melanocortin 3/4 receptor antagonist, attenuated the inhibitory function of apoE on feeding.

conclusionsThese data demonstrate that apoE suppresses food intake via a mechanism enhancing melanocortin signaling in the hypothalamus.

Indexed as

AnimalsAntibodiesApolipoproteins EBlotting, WesternBody WeightBrainDietary FatsEatingFastingHypothalamusImmunohistochemistryInjections, IntraventricularLithium ChlorideMaleMelanocyte-Stimulating HormonesMiceAntibodiesApolipoproteins EDietary FatsLithium ChlorideMelanocyte-Stimulating HormonesNeuropeptidesRNA, MessengerSHU 9119

Identifiers

PMID18559657
PMCPMC2494691
OpenAlexW2098813173

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.