J
Jonathan D. Schertzer
Researcher at McMaster University
Publications - 153
Citations - 10035
Jonathan D. Schertzer is an academic researcher from McMaster University. The author has contributed to research in topics: Insulin resistance & Skeletal muscle. The author has an hindex of 47, co-authored 132 publications receiving 7887 citations. Previous affiliations of Jonathan D. Schertzer include Hospital for Sick Children & University of Guelph.
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Journal ArticleDOI
Age-Associated Microbial Dysbiosis Promotes Intestinal Permeability, Systemic Inflammation, and Macrophage Dysfunction.
Netusha Thevaranjan,Alicja Puchta,Christian Schulz,Avee Naidoo,Jake C. Szamosi,Chris P. Verschoor,Dessi Loukov,Louis P. Schenck,Jennifer Jury,Kevin P. Foley,Jonathan D. Schertzer,Maggie Larché,Donald J. Davidson,Elena F. Verdu,Michael G. Surette,Dawn M. E. Bowdish +15 more
TL;DR: It is found that, when maintained under germ-free conditions, mice do not display an age-related increase in circulating pro-inflammatory cytokine levels, suggesting that aging-associated microbiota promote inflammation and that reversing these age- related microbiota changes represents a potential strategy for reducing age-associated inflammation and the accompanying morbidity.
Journal ArticleDOI
Single phosphorylation sites in Acc1 and Acc2 regulate lipid homeostasis and the insulin-sensitizing effects of metformin
Morgan D. Fullerton,Sandra Galic,Katarina Marcinko,Sarah Sikkema,Thomas Pulinilkunnil,Zhi-Ping Chen,Hayley M. O'Neill,Rebecca J. Ford,Rengasamy Palanivel,Matthew L. O'Brien,Matthew L. O'Brien,D. Grahame Hardie,S. Lance Macaulay,Jonathan D. Schertzer,Jason R.B. Dyck,Bryce J. W. van Denderen,Bruce E. Kemp,Bruce E. Kemp,Gregory R. Steinberg,Gregory R. Steinberg +19 more
TL;DR: It is established that inhibitory phosphorylation of Acc by Ampk is essential for the control of lipid metabolism and, in the setting of obesity, for metformin-induced improvements in insulin action.
Journal ArticleDOI
The ancient drug salicylate directly activates AMP-activated protein kinase
Simon A. Hawley,Morgan D. Fullerton,Fiona A. Ross,Jonathan D. Schertzer,Cyrille Chevtzoff,Katherine J. Walker,Mark Peggie,Darya Zibrova,Kevin A. Green,Kirsty J. Mustard,Bruce E. Kemp,Kei Sakamoto,Gregory R. Steinberg,Gregory R. Steinberg,D. Grahame Hardie +14 more
TL;DR: The results suggest that AMPK activation could explain some beneficial effects of salsalate and aspirin in humans, and a possible molecular mechanism of action for a metabolite of aspirin is described.
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Inhibiting peripheral serotonin synthesis reduces obesity and metabolic dysfunction by promoting brown adipose tissue thermogenesis
Justin D. Crane,Rengasamy Palanivel,Emilio P. Mottillo,Adam L. Bujak,Huaqing Wang,Rebecca J. Ford,Andrew Collins,Regje M. E. Blümer,Morgan D. Fullerton,Julian M. Yabut,Janice J. Kim,Jean-Eric Ghia,Shereen M. Hamza,Katherine M. Morrison,Jonathan D. Schertzer,Jason R.B. Dyck,Waliul I. Khan,Gregory R. Steinberg +17 more
TL;DR: It is found that Tph1-deficient mice fed a high-fat diet (HFD) are protected from obesity, insulin resistance and nonalcoholic fatty liver disease (NAFLD) while exhibiting greater energy expenditure by BAT.
Journal ArticleDOI
Amp-activated protein kinase regulates glut4 transcription by phosphorylating histone deacetylase 5
Sean L. McGee,Sean L. McGee,Bryce J. W. van Denderen,Kirsten F. Howlett,Janelle P. Mollica,Jonathan D. Schertzer,Bruce E. Kemp,Mark Hargreaves +7 more
TL;DR: It is reported that AMP-activated protein kinase (AMPK) regulates GLUT4 transcription through the histone deacetylase (HDAC)5 transcriptional repressor through the signal transduction pathway linking cellular energy charge to gene transcription directed at restoring cellular and whole-body energy balance.