Evidence map›Paper›PMID 28694154›Full record

ArticlePhysiology & behavior2018

Short photoperiod reverses obesity in Siberian hamsters via sympathetically induced lipolysis and Browning in adipose tissue.

Vitaly Ryu, Eleen Zarebidaki, H Elliott Albers, Bingzhong Xue, Timothy J Bartness

Open access · greenAbstract read
In one paragraph

Article in Physiology & behavior, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Vitaly RyuDepartment of Biology, Center for Obesity Reversal, Neuroscience Institute, Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA 30302-4010, USA. Electronic address: vryu@gsu.edu.
Eleen ZarebidakiDepartment of Biology, Center for Obesity Reversal, Neuroscience Institute, Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA 30302-4010, USA.
H Elliott AlbersDepartment of Biology, Center for Obesity Reversal, Neuroscience Institute, Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA 30302-4010, USA.
Bingzhong XueDepartment of Biology, Center for Obesity Reversal, Neuroscience Institute, Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA 30302-4010, USA.
Timothy J BartnessDepartment of Biology, Center for Obesity Reversal, Neuroscience Institute, Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA 30302-4010, USA.
Georgia State University · US

Funding

PHOTOPERIODIC CONTROL OF OBESITYR01DK035254 · NIDDK · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI XUE, BINGZHONG · 1988 to 2015
$3.3M
Photoperiodic Control of ObesityR37DK035254 · NIDDK · GEORGIA STATE UNIVERSITY · PI BARTNESS, TIMOTHY JON · 2009 to 2014
$2.9M
NIDDK NIH HHS R01 DK035254NIDDK NIH HHS R37 DK035254
6 · The paper itself

Abstract

Changes in photoperiod length are transduced into neuroendocrine signals by melatonin (MEL) secreted by the pineal gland triggering seasonally adaptive responses in many animal species. Siberian hamsters, transferred from a long-day 'summer-like' photoperiod (LD) to a short-day 'winter-like' photoperiod (SD), exhibit a naturally-occurring reversal in obesity. Photoperiod-induced changes in adiposity are mediated by the duration of MEL secretion and can be mimicked by exogenously administered MEL into animals housed in LD. Evidence suggests that MEL increases the sympathetic nervous system (SNS) drive to white adipose tissue (WAT). Here, we investigated whether MEL-driven seasonally adaptive losses in body fat are associated with WAT lipolysis and browning. Hamsters were subcutaneously administered vehicle (LD+VEH) or 0.4mg/kg MEL (LD+MEL) daily for 10weeks while animals housed in SD served as a positive control. MEL and SD exposure significantly decreased the retroperitoneal (RWAT), inguinal (IWAT), epididymal (EWAT) WAT, food intake and caused testicular regression compared with the LD+VEH group. MEL/SD induced lipolysis in the IWAT and EWAT, browning of the RWAT, IWAT, and EWAT, and increased UCP1 expression in the IBAT. Additionally, MEL/SD significantly increased the number of shared MEL receptor 1a and dopamine beta-hydroxylase-immunoreactive neurons in discrete brain sites, notably the paraventricular hypothalamic nucleus, dorsomedial hypothalamic nucleus, arcuate nucleus, locus coeruleus and dorsal motor nucleus of vagus. Collectively, these findings support our hypothesis that SD-exposed Siberian hamsters undergo adaptive decreases in body adiposity due to SNS-stimulated lipid mobilization and generalized WAT browning.

Indexed as

PhodopusPhotoperiodAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsBody WeightBrainColonCricetinaeDopamine beta-HydroxylaseEatingLipolysisMaleMelatoninNeuronsReceptor, Melatonin, MT1Dopamine beta-HydroxylaseMelatoninReceptor, Melatonin, MT1Uncoupling Protein 1BeigeingDopamine beta-hydroxylaseMelatoninSiberian hamstersSympathetic nervous systemWhite adipose tissue

Identifiers

PMID28694154
PMCPMC5988232
OpenAlexW2730267088

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.