Abstract
Diets high in calories can be used to model metabolic diseases, including obesity and its associated comorbidities, in animals. Drosophila melanogaster fed high-sugar diets (HSDs) exhibit complications of human obesity including hyperglycemia, hyperlipidemia, insulin resistance, cardiomyopathy, increased susceptibility to infection, and reduced longevity. We hypothesize that lipid storage in the high-sugar-fed fly's fat body (FB) reaches a maximum capacity, resulting in the accumulation of toxic lipids in other tissues or lipotoxicity. We took two approaches to characterize tissue-specific lipotoxicity. Ultra-HPLC-MS/MS and MALDI-MS imaging enabled spatial and temporal localization of lipid species in the FB, heart, and hemolymph. Substituent chain length was diet dependent, with fewer odd chain esterified FAs on HSDs in all sample types. By contrast, dietary effects on double bond content differed among organs, consistent with a model where some substituent pools are shared and others are spatially restricted. Both di- and triglycerides increased on HSDs in all sample types, similar to observations in obese humans. Interestingly, there were dramatic effects of sugar feeding on lipid ethers, which have not been previously associated with lipotoxicity. Taken together, we have identified candidate endocrine mechanisms and molecular targets that may be involved in metabolic disease and lipotoxicity.
Highlights
Diets high in calories can be used to model metabolic diseases, including obesity and its associated comorbidities, in animals
We used traditional UHPLC-MS/MS to compare the effects of control diet and high-sugar diet (HSD) in individual tissues
A slight overlap in 95% confidence interval ellipses is observed between control and HS fat body (FB), hemolymph, and hearts, indicating that a portion of the dietdependent metabolome differed in each sample type
Summary
Diets high in calories can be used to model metabolic diseases, including obesity and its associated comorbidities, in animals. Dietary effects on double bond content differed among organs, consistent with a model where some substituent pools are shared and others are spatially restricted. Both di- and triglycerides increased on HSDs in all sample types, similar to observations in obese humans. Tissue-specific analysis of lipid species in Drosophila during overnutrition by UHPLC-MS/MS and MALDI-MSI. Lipidomics, using LC-mass spectrometric methods has previously identified an array of lipids in Drosophila whole animal [20, 21] and tissue-specific homogenates, including lysophospholipids (Lyso-PLs), ceramides, and phospholipids (PLs) as well as other nonlipid metabolites [22]. Considering the small size of Drosophila and the extensive genetic tools available, the development of specific quantitative MSI methods could enable increased efficiency
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