Choline supplementation attenuates experimental sepsis-associated acute kidney injury

Author:

Hasson Denise C.1,Watanabe-Chailland Miki2,Romick-Rosendale Lindsey2,Koterba Adeleine1,Miner Dashiell S.1,Lahni Patrick1ORCID,Ma Qing3,Goldstein Stuart L.34,Devarajan Prasad34ORCID,Standage Stephen W.14ORCID

Affiliation:

1. Division of Critical Care Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

2. Division of Pathology and Laboratory Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

3. Division of Nephrology and Hypertension, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

4. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio

Abstract

Altered choline metabolism plays a role in both human and murine sepsis-associated acute kidney injury (SA-AKI), and choline administration in experimental SA-AKI improved renal function. These findings indicate that 1) mouse models can help interrogate clinically relevant mechanisms and 2) choline supplementation may ameliorate human SA-AKI. Future research will investigate clinically the impact of choline supplementation on human renal function in sepsis and, using model systems, how choline mediates its effects.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

HHS | NIH | National Institute of General Medical Sciences

Publisher

American Physiological Society

Subject

Physiology

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