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The reason for the exceptional longevity of the naked mole rat () remains a mystery to researchers. We assumed that evolutionarily, acquired the ability to quickly stabilize the functioning of mitochondria and endoplasmic reticulum (ER) to adjust metabolism to external challenges. To test this, a comparison of the hepatic mitochondria and ER of and C57BL/6 mice was done. Electron microscopy showed that 2-months-old mice have more developed rough ER (RER) than smooth ER (SER), occupying ~17 and 2.5% of the hepatocytic area correspondingly, and these values do not change with age. On the other hand, in 1-week-old , RER occupies only 13% constantly decreasing with age, while SER occupies 35% in a 1-week-old animal, constantly rising with age. The different localization of mitochondria in and mouse hepatocytes was confirmed by confocal and electron microscopy: while in mitochondria were mainly clustered around the nucleus and on the periphery of the cell, in mouse hepatocytes they were evenly distributed throughout the cell. We suggest that the noted structural and spatial features of ER and mitochondria in reflect adaptive rearrangements aimed at greater tolerance of the cellular system to challenges, primarily hypoxia and endogenous and exogenous toxins. Different mechanisms of adaptive changes including an activated hepatic detoxification system as a hormetic response, are discussed considering the specific metabolic features of the naked mole rat.
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http://dx.doi.org/10.3390/ijms23169067 | DOI Listing |
Cell Mol Neurobiol
August 2025
Department of Biology, University of Ottawa, 30 Marie Curie Pvt., Ottawa, ON, K1N 6N5, Canada.
Deleterious perturbations in reactive oxygen species (ROS) and calcium (Ca) handling are key initiators of cell death in hypoxia-intolerant mammalian brain. Elevated cellular Ca can also inhibit ROS scavengers, exacerbating the deleterious impact of hypoxia on redox homeostasis. Conversely, such perturbations are typically absent in the brain of hypoxia-tolerant animals, including naked mole-rats (NMRs; Heterocephalus glaber), in which a remarkable ability to scavenge ROS has been observed in cardiac and skeletal muscle.
View Article and Find Full Text PDFStructural changes involving new neurons can occur through stem cell-driven neurogenesis, and through incorporation of late-maturing "immature" neurons into networks, namely undifferentiated neuronal precursors frozen in a state of arrested maturation. The latter have been found in the cerebral cortex and are particularly abundant in large-brained mammals, covarying with the size of the brain and cortex. Similar cells have been described in the amygdala of some species, although their features and interspecies variation remain poorly understood.
View Article and Find Full Text PDFbioRxiv
August 2025
Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
Ribosomes are central to protein synthesis in all organisms. Among mammals, the ribosome functional core is highly conserved. Remarkably, two rodent species, the naked mole-rat (NMR) and tuco-tuco display fragmented 28S rRNA, coupled with high translational fidelity and long lifespan.
View Article and Find Full Text PDFEcol Evol Physiol
August 2025
AbstractHypoxia-tolerant naked mole rats (NMRs) depress metabolic rate >85% in severe hypoxia and switch from mixed lipids/carbohydrates to total carbohydrate-fueled metabolism. Previous experiments have studied resting animals, but how exercising NMRs balance hypoxic hypometabolism with thermogenic and activity-related demands is unknown. Therefore, we explored how interactions between hypoxia and intense exercise impact metabolic rate (oxygen consumption rate [V̇o]), aerobic scope, and fuel usage in normoxia or hypoxia (7% O) and at 22°C or 30°C.
View Article and Find Full Text PDFOncogene
August 2025
School of Life Science and Technology, Harbin Institute of Technology, Harbin, China.