Evidence map›Paper›PMID 28431320›Full record

ArticleThe Journal of nutritional biochemistry2017

Trehalose supplementation reduces hepatic endoplasmic reticulum stress and inflammatory signaling in old mice.

Michael J Pagliassotti, Andrea L Estrada, William M Hudson, Yuren Wei, Dong Wang, Douglas R Seals, Melanie L Zigler, Thomas J LaRocca

Abstract read
In one paragraph

Article in The Journal of nutritional biochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 56 citations in OpenAlex.

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  15. Review
  16. Hepatoprotective Effect of Trehalose: Insight into Its Mechanisms of Action.Advances in experimental medicine and biology · 2021
    Article
  17. Article
  18. Article
  19. Using trehalose to prevent and treat metabolic function: effectiveness and mechanisms.Current opinion in clinical nutrition and metabolic care · 2019
    Review
  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

8 authors at 2 institutions in 1 country.

Michael J PagliassottiDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523-1571, USA. Electronic address: michael.pagliassotti@colostate.edu.
Andrea L EstradaDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523-1571, USA.
William M HudsonDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523-1571, USA.
Yuren WeiDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523-1571, USA.
Dong WangDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523-1571, USA.
Douglas R SealsDepartment of Integrative Physiology, University of Colorado, Boulder, CO 80309, USA.
Melanie L ZiglerDepartment of Integrative Physiology, University of Colorado, Boulder, CO 80309, USA.
Thomas J LaRoccaDepartment of Integrative Physiology, University of Colorado, Boulder, CO 80309, USA.
Colorado State University · USUniversity of Colorado Boulder · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI BRYAN C BERGMAN · 1995 to 2026
$32.6M
SODIUM RESTRICTION &ARTERIAL COMPLIANCE IN OLDER HUMANSR01AG013038 · NIA · UNIVERSITY OF COLORADO AT BOULDER · PI SEALS, DOUGLAS R · 1996 to 2018
$4.0M
Human Aging, Exercise &FMD: Translational PhysiologyR37AG013038 · NIA · UNIVERSITY OF COLORADO AT BOULDER · PI SEALS, DOUGLAS R · 2004 to 2013
$3.0M
Obesity and Hepatic SteatosisR01DK072017 · NIDDK · COLORADO STATE UNIVERSITY-FORT COLLINS · PI PAGLIASSOTTI, MICHAEL J · 2005 to 2014
$2.2M
Obesity and Hepatic SteatosisR56DK072017 · NIDDK · COLORADO STATE UNIVERSITY · PI PAGLIASSOTTI, MICHAEL J · 2010 to 2010
$249k
Role of Autophagy in Vascular Endothelial Dysfunction with AgingF31AG039210 · NIA · UNIVERSITY OF COLORADO · PI LAROCCA, THOMAS · 2011 to 2012
$65k
NIA NIH HHS F31 AG039210NIA NIH HHS R01 AG013038NIA NIH HHS R37 AG013038NIDDK NIH HHS P30 DK048520NIDDK NIH HHS R01 DK072017NIDDK NIH HHS R56 DK072017
6 · The paper itself

Abstract

The accumulation of damaged proteins can perturb cellular homeostasis and provoke aging and cellular damage. Quality control systems, such as the unfolded protein response (UPR), inflammatory signaling and protein degradation, mitigate the residence time of damaged proteins. In the present study, we have examined the UPR and inflammatory signaling in the liver of young (~6 months) and old (~28 months) mice (n=8/group), and the ability of trehalose, a compound linked to increased protein stability and autophagy, to counteract age-induced effects on these systems. When used, trehalose was provided for 4 weeks in the drinking water immediately prior to sacrifice (n=7/group). Livers from old mice were characterized by activation of the UPR, increased inflammatory signaling and indices of liver injury. Trehalose treatment reduced the activation of the UPR and inflammatory signaling, and reduced liver injury. Reductions in proteins involved in autophagy and proteasome activity observed in old mice were restored following trehalose treatment. The autophagy marker, LC3B-II, was increased in old mice treated with trehalose. Metabolomics analyses demonstrated that reductions in hexosamine biosynthetic pathway metabolites and nicotinamide in old mice were restored following trehalose treatment. Trehalose appears to be an effective intervention to reduce age-associated liver injury and mitigate the need for activation of quality control systems that respond to disruption of proteostasis.

Indexed as

AgingAMP-Activated Protein Kinase KinasesAnimalsAutophagyBiomarkersBlood GlucoseDietary SupplementsEndoplasmic Reticulum StressInflammationLiverMaleMice, Inbred C57BLNiacinamideProtein KinasesTrehaloseTriglyceridesAMP-Activated Protein Kinase KinasesBiomarkersBlood GlucoseNiacinamideProtein KinasesTrehaloseTriglyceridesAgingHexosamine biosynthetic pathwayInflammationLiverProteostasisUnfolded protein response

Identifiers

PMID28431320
PMCPMC5492939
OpenAlexW2605281852

What OpenQuestion holds

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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.