AI Article Synopsis

  • Most animal studies often focus on males, missing important differences in diseases like depression and type 2 diabetes between sexes.
  • Research using diurnal fat sand rats revealed that males displayed more depression-like behavior and poorer glucose tolerance than females when exposed to short photoperiods.
  • Results indicate that circadian disruption affects health differently in males and females, suggesting a need for more studies on females to improve sex-specific health treatments.

Article Abstract

Most animal model studies on physiological functions and pathologies are conducted in males. However, diseases such as depression, type 2 diabetes (T2DM) and cardiovascular disease, all show different prevalence and characteristics in females and males. Moreover, most mammal studies are conducted in nocturnal mice and rats, while modelling diurnal humans. We therefore used male and female fat sand rats (), which are diurnal in the wild, as an animal model for T2DM, to explore the effects of mild circadian disruption on behavior, glucose tolerance, cholesterol and heart weight. We found significant differences between the sexes: on average, in response to short photoperiods (SP) acclimation, males showed higher levels of depression-like behavior, lower glucose tolerance, and increased plasma cholesterol levels compared with females, with no effect on heart/body weight ratio. Females, however did show an increase in heart/body weight ratio in response to SP acclimation. We also found that regardless of sex, arrhythmic animals showed higher blood glucose levels, cholesterol levels, heart/body weight ratio, and depressive-like behavior compared with rhythmic animals. Hence, we suggest that the expression of the Circadian Syndrome could be different between males and females. Additional work with females is required to clearly delineate the specific effects in both sexes, and promote sex-based health care, prevention measures and therapies.

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Source
http://dx.doi.org/10.1080/07420528.2021.1989448DOI Listing

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