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Time-restricted feeding reduces cardiovascular disease risk in obese mice

  • ,
  • Carmen De Miguel
    ,
  • Jodi R. Paul
    ,
  • Dingguo Zhang
    ,
  • Jackson Colson
    ,
  • John Miller Allan
*Corresponding author for this work
  • University of Alabama at Birmingham
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Disrupted feeding and fasting cycles as well as chronic high-fat diet–induced (HFD-induced) obesity are associated with cardiovascular disease risk factors. We designed studies that determined whether 2 weeks of time-restricted feeding (TRF) intervention in mice fed a chronic HFD would reduce cardiovascular disease risk factors. Mice were fed a normal diet (ND; 10% fat) ad libitum or HFD (45% fat) for 18 weeks ad libitum to establish diet-induced obesity. ND or HFD mice were continued on ad libitum diet or subjected to TRF (limiting food availability to 12 hours only during the dark phase) during the final 2 weeks of the feeding protocol. TRF improved whole-body metabolic diurnal rhythms without a change in body weight. HFD mice showed reduced blood pressure dipping compared with ND, which was restored by TRF. Further, TRF reduced aortic wall thickness, decreased aortic stiffness, as well as increased kidney tubular brush border integrity, decreased renal medullary fibrosis, and reduced renal medullary T cell inflammation in HFD mice. These findings indicate that TRF may be an effective intervention for improving vascular and kidney health in a model of established diet-induced obesity.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

e160257 e160257

Journal (Volume, Issue Number)

JCI insight (Volume 10, Issue 4)

Publication milestones

  • Published - 02/24/2025

Publication status

Published - 02/24/2025

ISSN

2379-3708

Publication IDs

  • Scopus: 85219002742
  • PubMed: 39812779

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Scopus
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Fractional count
1
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0.06
Fractional count
16
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0.94
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1
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1

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12
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Funding Details

The authors gratefully acknowledge Martin Young for his thoughtful discussions in designing these studies. The authors thank Xiaofen Liu for her outstanding histology expertise. The authors acknowledge the UAB Nutrition Obesity Research Center (NORC) for conducting QMR measurements in the Small Animal Phenotyping Core funded through the UAB NORC (NIH P30DK056336). The authors also acknowledge the UAB Mouse Comprehensive Cardiovascular Core for performing PWV measurements. The authors thank the UAB O’Brien Center Core (NIH P30 DK 079337) for plasma creatinine measurements. This work was supported by grants from UAB AMC21 Multi-Investigator Grant (to SMB, KLG, DMP, and JSP), American Heart Association Grant postdoctoral fellowship 18POST34070051 (to PP), NIH postdoctoral fellowship 1F32HL146179 (to PP), American Heart Association Grant predoctoral fellowship 18PRE33990345 (to DZ), NIH predoctoral fellowship F31 DK111067 (to RS), NIH predoctoral fellowship F31 HL149235 (to LSD), NIH R25DK112731 (to JSP) in support of JMA, NIH K01HL145324 (to CDM), NIH R21AA026906 (to SMB), NIH R01NS082413 (to KLG), and NIH R01DK134562 (to DMP and JSP).
FundersFunding numbers
NORC
-
UAB
-
Grant postdoctoral fellowship
-
Grant predoctoral fellowship
-
Nutrition Obesity Research Center, University of Alabama at Birmingham
-
UAB O’Brien Center Core
P30 DK 079337
AHA
R25DK112731, R01NS082413, 1F32HL146179, K01HL145324, 18POST34070051, 18PRE33990345, R21AA026906, F31 DK111067, F31 HL149235, R01DK134562
NIH
P30DK056336