Circadian Disruption across Lifespan Impairs Glucose Homeostasis and Insulin Sensitivity in Adult Mice

Bibliographic Details
Title: Circadian Disruption across Lifespan Impairs Glucose Homeostasis and Insulin Sensitivity in Adult Mice
Authors: Tracy K. Her, Jin Li, Hao Lin, Dong Liu, Kate M. Root, Jean F. Regal, Emilyn U. Alejandro, Ruifeng Cao
Source: Metabolites, Vol 14, Iss 2, p 126 (2024)
Publisher Information: MDPI AG, 2024.
Publication Year: 2024
Collection: LCC:Microbiology
Subject Terms: circadian disruption, glucose, insulin, obesity, mice, Microbiology, QR1-502
More Details: Circadian rhythm disruption is associated with impaired glucose homeostasis and type 2 diabetes. For example, night shift work is associated with an increased risk of gestational diabetes. However, the effects of chronic circadian disruption since early life on adult metabolic health trajectory remain unknown. Here, using the “Short Day” (SD) mouse model, in which an 8 h/8 h light/dark (LD) cycle was used to disrupt mouse circadian rhythms across the lifespan, we investigated glucose homeostasis in adult mice. Adult SD mice were fully entrained into the 8 h/8 h LD cycle, and control mice were entrained into the 12 h/12 h LD cycle. Under a normal chow diet, female and male SD mice displayed a normal body weight trajectory. However, female but not male SD mice under a normal chow diet displayed glucose intolerance and insulin resistance, which are associated with impaired insulin signaling/AKT in the skeletal muscle and liver. Under high-fat diet (HFD) challenges, male but not female SD mice demonstrated increased body weight gain compared to controls. Both male and female SD mice developed glucose intolerance under HFD. Taken together, these results demonstrate that environmental disruption of circadian rhythms contributes to obesity in a sexually dimorphic manner but increases the risk of glucose intolerance and insulin resistance in both males and females.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2218-1989
Relation: https://www.mdpi.com/2218-1989/14/2/126; https://doaj.org/toc/2218-1989
DOI: 10.3390/metabo14020126
Access URL: https://doaj.org/article/207548a9a9a24260887e01b423551431
Accession Number: edsdoj.207548a9a9a24260887e01b423551431
Database: Directory of Open Access Journals
More Details
ISSN:22181989
DOI:10.3390/metabo14020126
Published in:Metabolites
Language:English