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Comorbid impairments of emotional and cognitive functions induced by different sleep deprivation durations

Sleep deprivation (SD) is a major risk factor for neuropsychiatric disorders and is known to induce comorbid emotional and cognitive impairments; however, the temporal dynamics and underlying mechanistic pathways remain poorly defined. Here, we estab...

Body Mind StateJune 28, 20261 min read
Comorbid impairments of emotional and cognitive functions induced by different sleep deprivation durations

Key Findings

Sleep deprivation (SD) is a major risk factor for neuropsychiatric disorders and is known to induce comorbid emotional and cognitive impairments; however, the temporal dynamics and underlying mechanistic pathways remain poorly defined. Here, we established a standardized rotating rod-based SD model using male ICR mice (4-6 weeks old) to systematically investigate the effects of different SD durations. (1, 2, 3, or 7 days) on emotional and cognitive functions and the potential involvement of ferroptosis-related mechanisms. Emotional and cognitive functions were evaluated using a battery of behavioral tests. Hippocampal morphology was assessed by hematoxylin-eosin staining, while hippocampal ferrous iron content, systemic oxidative stress markers including total antioxidant capacity, glutathione, and malondialdehyde, together with ferroptosis-related protein expression were quantified. Our study demonstrated that 1-day SD induced anxiety-like behaviors and a stress-induced hyperactive state, accompanied by mild cognitive deficits. In contrast, prolonged SD (3- and 7-day SD) progressively promoted depressive-like behaviors accompanied by worsening cognitive deficits. Histological analysis revealed duration-dependent neuronal loss and structural damage in the hippocampal CA1 and CA3 regions. Biochemical analyses revealed duration-dependent alterations in hippocampal Fe2+ levels, with marked lipid peroxidation dysregulation emerging after 7-day SD. Western blotting analysis indicated that 7-day SD markedly disrupted hippocampal ferroptosis-related SIRT1/SLC7A11/GPX4 signaling pathways. In conclusion, SD induce duration-dependent comorbid emotional and cognitive dysfunction, accompanied by hippocampal injury and ferroptosis-related alterations. These findings provide preliminary evidence for a potential link between SD-induced neurobehavioral impairments and ferroptosis-related changes, warranting further mechanistic investigation.

Why This Matters for Body-Mind Practice

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Source

Original Publication
Journal of affective disorders
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