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Sex-dependent metabolic remodeling of kidneys revealed by arteriovenous metabolomics
Preprint   Open access

Sex-dependent metabolic remodeling of kidneys revealed by arteriovenous metabolomics

Miranda E. Kelly, Lauren A. Hoffner, Cuauhtemoc B. Ramirez, Alexis L. Anica, Joohwan Kim, Gregory Tong, Yeojin Kim, Wonsuk Choi, Kihong Jang, Yasmine H. Alam, …
bioRxiv
Cold Spring Harbor Laboratory, 1.1
09/02/2024
DOI: 10.1101/2024.09.02.610869
PMID: 39282331
url
https://doi.org/10.1101/2024.09.02.610869View
Preprint (Author's original) This preprint has not been evaluated by subject experts through peer review. Preprints may undergo extensive changes and/or become peer-reviewed journal articles. Open Access

Abstract

Sex is a fundamental biological variable important in biomedical research, drug development, clinical trials, and prevention approaches. Among many organs, kidneys are known to exhibit remarkable structural, histological, and pathological differences between sexes. However, whether and how kidneys display distinct metabolic activities between sexes is poorly understood. By developing kidney-specific arteriovenous (AV) metabolomics combined with transcriptomics, we report striking sex differences in both basal metabolic activities and adaptive metabolic remodeling of kidneys after a fat-enriched ketogenic diet (KD), a regimen known to mitigate kidney diseases and improve immunotherapy for renal cancer. At the basal state, female kidneys show highly accumulated aldosterone and various acylcarnitines. In response to the KD, aldosterone levels remain high selectively in females but the sex difference in acylcarnitines disappears. AV data revealed that, under KD, female kidneys avidly take up circulating fatty acids and release 3-hydroxybutyrate (3-HB) whereas male kidneys barely absorb fatty acids but consistently take up 3-HB. Although both male and female kidneys take up gluconeogenic substrates such as glycerol, glutamine and lactate, only female kidneys exhibit net glucose release. Kidney transcriptomics data incompletely predict these sex differences, suggesting post-transcriptional/translational regulation mechanisms. This study provides foundational insights into the sex-dependent and diet-elicited metabolic flexibility of the kidneys in vivo, serving as a unique resource for understanding variable disease prevalence and drug responses between male and female kidneys.
 Biochemistry

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