Evidence map›Paper›PMID 30585393›Full record

ArticleAging cell2019

Hypothalamic gene transfer of BDNF promotes healthy aging in mice.

Travis McMurphy, Wei Huang, Xianglan Liu, Jason J Siu, Nicholas J Queen, Run Xiao, Lei Cao

Abstract read
In one paragraph

Article in Aging cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. The Hypothalamic Epigenetic Landscape in Dietary Obesity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  12. Article
  13. Adult Neurogenesis, Learning and Memory.Advances in neurobiology · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Hypothalamic AAV-BDNF gene therapy improves metabolic function and behavior in theMolecular therapy. Methods & clinical development · 2022
    Article
  19. Article
  20. Hypothalamic control of energy expenditure and thermogenesis.Experimental & molecular medicine · 2022
    Review
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.

Travis McMurphyDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, Ohio.
Wei HuangDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, Ohio.
Xianglan LiuDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, Ohio.
Jason J SiuDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, Ohio.
Nicholas J QueenDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, Ohio.
Run XiaoDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, Ohio.
Lei CaoDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, Ohio.ORCID 0000-0003-0322-4985

Funding

Cancer Prevention and Treatment by Activation of a Brain-Adipocyte AxisR01CA166590 · NCI · OHIO STATE UNIVERSITY · PI CAO, LEI · 2013 to 2022
$3.4M
The role of hypothalamic-sympathoneural-adipocyte axis in healthy agingR01AG041250 · NIA · OHIO STATE UNIVERSITY · PI CAO, LEI · 2013 to 2017
$1.6M
Identifying brain mediators distinguishing eustress and distress impact on cancerR01CA163640 · NCI · OHIO STATE UNIVERSITY · PI CAO, LEI · 2013 to 2017
$1.2M
The role of hypothalamic-sympathoneural-adipocyte axis in healthy agingR56AG041250 · NIA · OHIO STATE UNIVERSITY · PI CAO, LEI · 2019 to 2019
$390k
Modulating cancer progression by adipogenic human adenovirus type 36R21CA178227 · NCI · OHIO STATE UNIVERSITY · PI CAO, LEI · 2013 to 2014
$375k
NCI NIH HHS R01 CA163640NCI NIH HHS R01 CA166590NCI NIH HHS R21 CA178227NIA NIH HHS R01 AG041250NIA NIH HHS R56 AG041250
6 · The paper itself

Abstract

The aging process and age-related diseases all involve perturbed energy adaption and impaired ability to cope with adversity. Brain-derived neurotrophic factor (BDNF) in the hypothalamus plays important role in regulation of energy balance. Our previous studies show that recombinant adeno-associated virus (AAV)-mediated hypothalamic BDNF gene transfer alleviates obesity, diabetes, and metabolic syndromes in both diet-induced and genetic models. Here we examined the efficacy and safety of a built-in autoregulatory system to control transgene BDNF expression mimicking the body's natural feedback systems in middle-aged mice. Twelve-month-old mice were treated with either autoregulatory BDNF vector or yellow fluorescence protein (YFP) control, maintained on normal diet, and monitored for 28 weeks. BDNF gene transfer prevented the development of aging-associated metabolic declines characterized by: preventing aging-associated weight gain, reducing adiposity, reversing the decline of brown fat activity, increasing adiponectin while reducing leptin and insulin in circulation, improving glucose tolerance, increasing energy expenditure, alleviating hepatic steatosis, and suppressing inflammatory genes in the hypothalamus and adipose tissues. Moreover, BDNF treatment reduced anxiety-like and depression-like behaviors. These safety and efficacy data provide evidence that hypothalamic BDNF is a target for promoting healthy aging.

Indexed as

Healthy AgingAnimalsBrain-Derived Neurotrophic FactorFemaleHypothalamusMiceMice, Inbred C57BLBdnf protein, mouseBrain-Derived Neurotrophic Factoradipose tissueagingBDNFgene transferhypothalamussteatosis

Identifiers

PMID30585393
PMCPMC6413658

What OpenQuestion holds

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Registered trials

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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.