Human amylin proteotoxicity impairs protein biosynthesis, and alters major cellular signaling pathways in the heart, brain and liver of humanized diabetic rat model in vivo.


Journal Article

INTRODUCTION: Chronic hypersecretion of the 37 amino acid amylin is common in type 2 diabetics (T2D). Recent studies implicate human amylin aggregates cause proteotoxicity (cell death induced by misfolded proteins) in both the brain and the heart. OBJECTIVES: Identify systemic mechanisms/markers by which human amylin associated with cardiac and brain defects might be identified. METHODS: We investigated the metabolic consequences of amyloidogenic and cytotoxic amylin oligomers in heart, brain, liver, and plasma using non-targeted metabolomics analysis in a rat model expressing pancreatic human amylin (HIP model). RESULTS: Four metabolites were significantly different in 3 or more of the the four compartments (heart, brain, liver, and plasma) in HIP rats. When compared to a T2D rat model, HIP hearts uniquely had significant DECREASES in five amino acids (lysine, alanine, tyrosine, phenylalanine, serine), with phenylalanine decreased across all four tissues investigated, including plasma. In contrast, significantly INCREASED circulating phenylalanine is reported in diabetics in multiple recent studies. CONCLUSION: DECREASED phenylalanine may serve as a unique marker of cardiac and brain dysfunction due to hyperamylinemia that can be differentiated from alterations in T2D in the plasma. While the deficiency in phenylalanine was seen across tissues including plasma and could be monitored, reduced tyrosine was seen only in the brain. The 50% reduction in phenylalanine and tyrosine in HIP brains is significant given their role in supporting brain chemistry as a precursor for catecholamines (dopamine, norepinephrine, epinephrine), which may contribute to the increased morbidity and mortality in diabetics at a multi-system level beyond the effects on glucose metabolism.

Full Text

Duke Authors

Cited Authors

  • Ilaiwy, A; Liu, M; Parry, TL; Bain, JR; Newgard, CB; Schisler, JC; Muehlbauer, MJ; Despa, F; Willis, MS

Published Date

  • May 2016

Published In

Volume / Issue

  • 12 / 5

PubMed ID

  • 28775675

Pubmed Central ID

  • 28775675

International Standard Serial Number (ISSN)

  • 1573-3882

Digital Object Identifier (DOI)

  • 10.1007/s11306-016-1022-9


  • eng

Conference Location

  • United States