Results 141 to 150 of about 67,094 (276)
Experimental Physiology, EarlyView.Abstract Prolonged glucocorticoid exposure induces skeletal muscle atrophy through suppression of protein synthesis and activation of catabolic signalling pathways. Although exercise attenuates glucocorticoid‐induced muscle loss, whether exercise‐induced increases in body temperature contribute remains unclear.
Berkay Ozerklig +6 more
wiley +1 more source
Effects of Corticosterone in Drinking Water [PDF]
, 2019 Every day we experience some type of stress. High levels of stress are a common contributor to health problems. In our lab we have previously found that exposure to 10 days of unpredictable stress reduced motivation for a sucrose reward (Bond, Anderson ...
Corey, Samantha A.
core +1 more source
Post-stress corticosterone levels.
, 2013 After 31 days of the predator exposure/psychosocial stress regimen, plasma corticosterone levels were higher in the PTSD group. Corticosterone was measured in plasma collected at the time of sacrifice and frozen prior to testing.
Leslie D. McLaughlin (468615) +5 more
core +1 more source
The Journal of Physiology, EarlyView.Abstract figure legend Suboptimal maternal nutrition alters placental and developing blood–brain barrier (BBB) protective function and is associated with increased fetal brain vulnerability. In the placenta, nutritional adversity may reduce the exchange surface area and promote meta‐inflammation, compromising barrier efficiency in a model‐ and context ...
Kristin L. Connor +4 more
wiley +1 more source
The Journal of Physiology, EarlyView.Abstract figure legend A mouse model of exogenous glucocorticoid (GC) treatment was used to determine (1) if corticosterone induced the same metabolic dysregulation as cortisol, and (2) whether these differences were mediated by the corticosterone‐specific transmembrane exporter Abcc1.
Mhairi A. Paul +9 more
wiley +1 more source
Aldosterone and corticosterone levels.
, 2014 Plasma aldosterone (A) and corticosterone (B) concentrations. Aldosterone content (C) and corticosterone content (D) of LV tissue. Number of mice per group is indicated in bar graph. Values are the mean±SEM.
Kimi Koide (541515) +7 more
core +1 more source
The Journal of Physiology, EarlyView.Abstract figure legend Temporal scaling physiology differs significantly between mice and humans. Mice have higher metabolism, heart and respiratory rate, as well as faster blood flow rates, brain activity and physiological dynamics over time. These differences influence the temporal resolution needed in preclinical imaging of mouse models to ...
Sara Gargiulo, Matteo Gramanzini
wiley +1 more source
The Journal of Physiology, EarlyView.Abstract figure legend Maternal protein restriction (MPR) induced persistent renal histopathological alterations accompanied by elevated serum creatinine levels. Nephron‐segment proteomic analysis revealed region‐specific molecular dysregulation affecting Bowman's capsule (PARK7, oxidative stress sensor; MSN, cytoskeletal organization), the proximal ...
Marina Pereira Pires +15 more
wiley +1 more source
Animal Genetics, Volume 57, Issue 5, October 2026.ABSTRACT Environmental stressors in commercial poultry systems can negatively affect bird welfare, although individuals vary considerably in their responses. Neuroplasticity within the hippocampus, measured through the density of doublecortin‐positive (DCX+) neurons, provides a potential biomarker of stress experience in laying hens.
Lindsay Neuert +8 more
wiley +1 more source
On the importance of including both sexes in animal studies – insights from home‐cage monitoring
Biological Reviews, Volume 101, Issue 5, Page 2408-2426, October 2026.ABSTRACT A review of behavioural studies using home‐cage monitoring (HCM) systems revealed that over 61% of studies used only male subjects, with only 24% including both sexes, despite evidence of substantial behavioural differences between male and female animals. This bias could influence the outcomes of biomedical research.
Maša Čater +12 more
wiley +1 more source