4.8 Article

Ketosis Ameliorates Renal Cyst Growth in Polycystic Kidney Disease

期刊

CELL METABOLISM
卷 30, 期 6, 页码 1007-+

出版社

CELL PRESS
DOI: 10.1016/j.cmet.2019.09.012

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资金

  1. National Institutes of Health (NIH) [DK109563]
  2. Jarrett Postdoctoral Fellowship from the Jarrett Family Fund
  3. University of Missouri Gilbreath McLorn Endowment
  4. Office of Research and Development, Medical Research Service, Department of Veterans Affairs [1 I01 BX004232-01A2]
  5. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the NIH [DK056943, DK056956, DK056957, DK056961]
  6. NIDDK [DK106912, DK090728, DK074038]
  7. National Center for Research Resources (Emory University) [RR000039]
  8. National Center for Research Resources (Mayo College of Medicine) [RR00585]
  9. National Center for Research Resources (Kansas University Medical Center) [RR23940]
  10. National Center for Research Resources (University of Alabama at Birmingham) [RR000032]
  11. National Center for Advancing Translational Sciences (Emory) [RR025008, TR000454]
  12. National Center for Advancing Translational Sciences (Mayo College of Medicine) [RR024150, TR000135]
  13. National Center for Advancing Translational Sciences (Kansas University Medical Center) [RR033179, TR000001]
  14. National Center for Advancing Translational Sciences (University of Alabama at Birmingham) [RR025777, TR000165, TR001417]
  15. National Center for Advancing Translational Sciences (University of Pittsburgh School of Medicine) [RR024153, TR000005]
  16. [R01 DK113111]

向作者/读者索取更多资源

Mild reduction in food intake was recently shown to slow polycystic kidney disease (PKD) progression in mouse models, but whether the effect was due to solely reduced calories or some other aspect of the diet has been unclear. We now show that the benefit is due to the induction of ketosis. Time-restricted feeding, without caloric reduction, strongly inhibits mTOR signaling, proliferation, and fibrosis in the affected kidneys in a PKD rat model. A ketogenic diet had a similar effect and led to regression of renal cystic burden. Acute fasting in rat, mouse, and feline models of PKD results in rapid reduction of cyst volume, while oral administration of the ketone beta-hydroxybutyrate (BHB) in rats strongly inhibits PKD progression. These results suggest that cystic cells in PKD are metabolically inflexible, which could be exploited by dietary interventions or supplementation with BHB, representing a new therapeutic avenue to treat PKD.

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