Sex differences in the effects of acute stress on cerebral glucose metabolism: A microPET study

Brain Res. 2019 Nov 1:1722:146355. doi: 10.1016/j.brainres.2019.146355. Epub 2019 Jul 26.

Abstract

Stress has been considered as a risk factor for the development and aggravation of several diseases. The hypothalamic-pituitary-adrenal axis (HPA) is one of the main actors for the stress response and homeostasis maintenance. Positron emission tomography (PET) has been used to evaluate neuronal activity and to study brain regions that may be related to the HPA axis response. Since neuroimaging is an important tool in detecting neuroendocrine-related changes, we used fluorodeoxyglucose-18 (18F-FDG) and positron emission microtomography (microPET) to evaluate sexual differences in the glucose brain metabolism after 10, 30 and 40 min of acute stress in Balb/c mice. We also investigated the effects of restraint stress in blood, liver and adrenal gland 18F-FDG biodistribution using a gamma counter. A decreased glucose uptake in the whole brain in both females and males was found. Additionally, there were time and sex-dependent alterations in the 18F-FDG uptake after restraint stress in specific brain regions, indicating that males could be more vulnerable to the short-term effects of acute stress. According to the gamma counter biodistribution, only females showed a significant decreased glucose uptake in the blood, liver and right adrenal after restraint stress. In addition, in comparisons between the sexes, males showed a decreased glucose uptake in the whole brain and in several brain regions compared to females. In conclusion, exposure to acute restraint stress resulted in significant decreased glucose metabolism in the brain, with particular effects in different regions and organs in a sex-specific manner.

Keywords: (18)F-FDG; Gender differences; Restraint stress; Stress; microPET.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • Female
  • Fluorodeoxyglucose F18
  • Glucose / metabolism*
  • Male
  • Mice, Inbred BALB C
  • Positron-Emission Tomography
  • Restraint, Physical
  • Sex Characteristics*
  • Stress, Psychological / metabolism*

Substances

  • Fluorodeoxyglucose F18
  • Glucose