Author

Matvey Goldberg

VA Puget Sound Health Care SystemORCID 0009-0004-0757-5656Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 1 Pharmacology & Toxicology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:rat· 2 Research Focus:host-pathogen & immune response· 1 Research Focus:metabolism & bioenergetics· 1 Organism:mouse· 1

Frequent Co-Authors

James Ernest BlevinsiD· 3 shared Christian Ludwig RothiD· 2 shared Clinton T. ElfersiD· 2 shared Edison W. TsuiiD· 2 shared Emily F. AshlawiD· 2 shared Jared D. Slattery· 2 shared June R. Rambousek· 2 shared Kylie S. Chichura· 2 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersPhysiology

James Ernest BlevinsORCID

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3 papers

Recent·Most cited

The Chimeric Peptide (GEP44) Reduces Body Weight and Both Energy Intake, and Energy Expenditure in Diet-Induced Obese Rats

Matvey Goldberg, James Ernest Blevins, Tami Wolden‐Hanson, Clinton Elfers, Kylie S. Chichura, Emily F. Ashlaw, Laura J. den Hartigh, Christian Ludwig Roth, Robert P. Doyle

International Journal of Molecular Sciences · Mar 26, 2025Peer-reviewedPhysiology

Effects of systemic oxytocin and beta-3 receptor agonist (CL 316243) treatment on body weight and adiposity in male diet-induced obese rats

Jared D. Slattery, June R. Rambousek, Edison W. Tsui, Mackenzie K. Honeycutt, Matvey Goldberg, James Lawrence Graham, Tomasz Wietecha, Tami Wolden‐Hanson, Amber L. Williams, Kevin D. O’Brien, Peter Joseph Havel, James Ernest Blevins

This study investigates the combined effects of systemic oxytocin and beta-3 receptor agonist on weight loss in diet-induced obese rats, finding additive effects on body weight and adiposity reduction.

Frontiers in Endocrinology · Mar 4, 2025Peer-reviewedNeuroscience

The Novel Chimeric Multi-Agonist Peptide (GEP44) Reduces Energy Intake and Body Weight in Male and Female Diet-Induced Obese Mice in a Glucagon-Like Peptide-1 Receptor-Dependent Manner

James Ernest Blevins, Mackenzie K. Honeycutt, Jared D. Slattery, Matvey Goldberg, June R. Rambousek, Edison W. Tsui, Andrew Dale Dodson, Kyra A. Shelton, Therese S. Salemeh, Clinton T. Elfers, Kylie S. Chichura, Emily F. Ashlaw, Sakeneh Zraika, Robert P. Doyle, Christian Ludwig Roth

This study shows that the chimeric peptide GEP44 reduces body weight and energy intake in diet-induced obese mice, primarily through GLP-1R signaling, with some GLP-1R-independent effects in males.

Frontiers in Endocrinology · Jul 22, 2024Peer-reviewedPharmacology & Toxicology