Publications by authors named "S Bloomer"

Article Synopsis
  • Ferroptosis is a type of cell death that involves iron and the peroxidation of lipids, linked to liver damage due to the liver's role in iron metabolism.
  • This study investigated how ferroptosis mediators differ between male and female rats as they age, hypothesizing that females are more resistant due to better antioxidant defenses.
  • Results showed that female rats had higher non-haem iron levels and different ferroptosis-related protein expressions, indicating that they might actually be more susceptible to ferroptosis as they age, despite having stronger antioxidant defenses.
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Aging impairs overall physiological function, particularly the response to environmental stressors. Repeated heat stress elevates reactive oxygen species and macromolecular damage in the livers of aged animals, likely due to mitochondrial dysfunction. The goal of this investigation was to determine potential mechanisms for mitochondrial dysfunction after heat stress by evaluating key redox-sensitive and antioxidant proteins (Sirt-3, MnSOD, Trx-2, and Ref-1).

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The goal of the current study was to examine associations between hormonal contraceptive use and indicators of well-being including body image, eating behavior, sleep and energy level. Drawing on a health protection framework, we expected that individuals who use hormonal contraceptives would be more attuned to health and report more positive health attitudes and behaviors on these dimensions. Undergraduate college women ( = 270;  = 19.

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Although health and wellness behaviors are associated with positive body image, research is limited regarding the relationship between sleep and positive body image. We propose that negative affective states may link sleep and body image. Specifically, we examined whether better sleep may relate to positive body image through reductions in negative affective experiences.

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Liver macrophages serve important roles in iron homeostasis through phagocytosis of effete erythrocytes and the export of iron into the circulation. Conversely, intracellular iron can alter macrophage phenotype. Aging increases hepatic macrophage number and nonparenchymal iron, yet it is unknown whether age-related iron accumulation alters macrophage number or phenotype.

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