Evidence map›Paper›PMID 25477422›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2015

Role of FAT/CD36 in fatty acid sensing, energy, and glucose homeostasis regulation in DIO and DR rats.

Christelle Le Foll, Ambrose A Dunn-Meynell, Barry E Levin

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Prohibitions in the meta-inflammatory response: a review.Frontiers in molecular biosciences · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. The CD36-PPARγ Pathway in Metabolic Disorders.International journal of molecular sciences · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Fatty acid-induced astrocyte ketone production and the control of food intake.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Review
  17. Review
  18. Role of VMH ketone bodies in adjusting caloric intake to increased dietary fat content in DIO and DR rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    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

3 authors at 3 institutions in 1 country.

Christelle Le FollDepartment of Neurology and Neurosciences, Rutgers New Jersey Medical School, Newark, New Jersey; and christelle.lefoll@gmail.com.
Ambrose A Dunn-MeynellNeurology Service, Veterans Affairs Medical Center, East Orange, New Jersey.
Barry E LevinDepartment of Neurology and Neurosciences, Rutgers New Jersey Medical School, Newark, New Jersey; and Neurology Service, Veterans Affairs Medical Center, East Orange, New Jersey.
Rutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · USVeterans Biomedical Research Institute · US

Funding

BRAIN GLUCOSENSING NEURONS IN HEALTH AND DIABETESR01DK053181 · NIDDK · VETERANS BIOMEDICAL RESEARCH INSTITUTE · PI LEVIN, BARRY E · 1998 to 2014
$5.6M
NIDDK NIH HHS DK-53181
6 · The paper itself

Abstract

Hypothalamic fatty acid (FA) sensing neurons alter their activity utilizing the FA translocator/receptor, FAT/CD36. Depletion of ventromedial hypothalamus (VMH) CD36 with adeno-associated viral vector expressing CD36 shRNA (AAV CD36 shRNA) leads to redistribution of adipose stores and insulin resistance in outbred rats. This study assessed the requirement of VMH CD36-mediated FA sensing for the regulation of energy and glucose homeostasis in postnatal day 5 (P5) and P21 selectively bred diet-induced obese (DIO) and diet-resistant (DR) rats using VMH AAV CD36 shRNA injections. P5 CD36 depletion altered VMH neuronal FA sensing predominantly in DIO rats. After 10 wk on a 45% fat diet, DIO rats injected with VMH AAV CD36 shRNA at P21 ate more and gained more weight than DIO AAV controls, while DR AAV CD36 shRNA-injected rats gained less weight than DR AAV controls. VMH CD36 depletion increased inguinal fat pad weights and leptin levels in DIO and DR rats. Although DR AAV CD36 shRNA-injected rats became as obese as DIO AAV controls, only DIO control and CD36 depleted rats became insulin-resistant on a 45% fat diet. VMH CD36 depletion stunted linear growth in DIO and DR rats. DIO rats injected with AAV CD36 shRNA at P5 had increased fat mass, mostly due to a 45% increase in subcutaneous fat. They were also insulin-resistant with an associated 71% increase of liver triglycerides. These results demonstrate that VMH CD36-mediated FA sensing is a critical factor in the regulation of energy and glucose homeostasis and fat deposition in DIO and DR rats.

Indexed as

Blood GlucoseAdipose TissueAnimal FeedAnimalsBody WeightCD36 AntigensDisease Models, AnimalEnergy IntakeFatty AcidsHomeostasisInsulinLeptinMaleObesityRatsBlood GlucoseCD36 AntigensFatty AcidsInsulinLeptinCD36fatty acidhypothalamusneuronal sensingobesity

Identifiers

PMID25477422
PMCPMC4313072
OpenAlexW1996580021

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.