Liproxstatin‐1 alleviates ferroptosis in sevoflurane anesthesia‐induced cognitive deficits of aged mice: The role oxidative stress

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Main Authors: Shunyuan Li, Yingle Chen, Yingmei Wang, Xianmei Zhong, Xiaoquan Yu, Zhenming Kang, Yangyi Li
Format: Artículo Open Access
Published: Wiley 2024
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author Shunyuan Li
Yingle Chen
Yingmei Wang
Xianmei Zhong
Xiaoquan Yu
Zhenming Kang
Yangyi Li
author_facet Shunyuan Li
Yingle Chen
Yingmei Wang
Xianmei Zhong
Xiaoquan Yu
Zhenming Kang
Yangyi Li
Shunyuan Li
Yingle Chen
Yingmei Wang
Xianmei Zhong
Xiaoquan Yu
Zhenming Kang
Yangyi Li
collection Wiley Open Access
contents Liproxstatin‐1 alleviates ferroptosis in sevoflurane anesthesia‐induced cognitive deficits of aged mice: The role oxidative stress Shunyuan Li Yingle Chen Yingmei Wang Xianmei Zhong Xiaoquan Yu Zhenming Kang Yangyi Li Synapse AbstractIn this study, we aimed to validate the hypothesis that the interplay between sevoflurane, oxidative stress and ferroptosis is crucial for the pathogenesis of sevoflurane‐induced cognitive impairment in aged individuals. The mice with sevoflurane‐induced cognitive impairment were used to explore the effects of sevoflurane on oxidative stress, iron homeostasis, and cognitive function in aged mice. Iron content and oxidative stress markers were analyzed in hippocampal tissue homogenates using specific assays. Additionally, the levels of iron death‐related markers (Fth1 and Gpx4) were assessed by real‐time PCR and Western blotting. Morris Water Maze and novel object recognition (NOR) tests were conducted to evaluate cognitive function. Sevoflurane exposure in aged mice resulted in a significant increase in iron overloading in the hippocampus, followed by a subsequent stabilization. Oxidative stress levels were elevated in the hippocampal tissue of sevoflurane‐exposed mice, and a significant correlation was observed between iron death and oxidative stress. Liproxstatin‐1, a ferroptosis inhibitor, effectively ameliorated the decline in memory and learning abilities induced by sevoflurane anesthesia. Liproxstatin‐1 treatment reduced iron overload and oxidative stress in the hippocampal tissue of aged mice. The expression of Fth1 and Gpx4, iron death‐related markers, was downregulated following Liproxstatin‐1 intervention. Our findings suggest that sevoflurane anesthesia disrupts iron homeostasis, leading to increased oxidative stress and cognitive impairment in aged mice. These results highlight the potential of targeting iron‐mediated processes to mitigate sevoflurane‐induced cognitive impairment in the aging population. 10.1002/syn.22286 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/syn.22286
format Artículo Open Access
id wiley_oa_10_1002_syn_22286
institution Wiley Open Access
license_str_mv http://onlinelibrary.wiley.com/termsAndConditions#vor
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle Liproxstatin‐1 alleviates ferroptosis in sevoflurane anesthesia‐induced cognitive deficits of aged mice: The role oxidative stress
Shunyuan Li
Yingle Chen
Yingmei Wang
Xianmei Zhong
Xiaoquan Yu
Zhenming Kang
Yangyi Li
Synapse
Liproxstatin‐1 alleviates ferroptosis in sevoflurane anesthesia‐induced cognitive deficits of aged mice: The role oxidative stress Shunyuan Li Yingle Chen Yingmei Wang Xianmei Zhong Xiaoquan Yu Zhenming Kang Yangyi Li Synapse AbstractIn this study, we aimed to validate the hypothesis that the interplay between sevoflurane, oxidative stress and ferroptosis is crucial for the pathogenesis of sevoflurane‐induced cognitive impairment in aged individuals. The mice with sevoflurane‐induced cognitive impairment were used to explore the effects of sevoflurane on oxidative stress, iron homeostasis, and cognitive function in aged mice. Iron content and oxidative stress markers were analyzed in hippocampal tissue homogenates using specific assays. Additionally, the levels of iron death‐related markers (Fth1 and Gpx4) were assessed by real‐time PCR and Western blotting. Morris Water Maze and novel object recognition (NOR) tests were conducted to evaluate cognitive function. Sevoflurane exposure in aged mice resulted in a significant increase in iron overloading in the hippocampus, followed by a subsequent stabilization. Oxidative stress levels were elevated in the hippocampal tissue of sevoflurane‐exposed mice, and a significant correlation was observed between iron death and oxidative stress. Liproxstatin‐1, a ferroptosis inhibitor, effectively ameliorated the decline in memory and learning abilities induced by sevoflurane anesthesia. Liproxstatin‐1 treatment reduced iron overload and oxidative stress in the hippocampal tissue of aged mice. The expression of Fth1 and Gpx4, iron death‐related markers, was downregulated following Liproxstatin‐1 intervention. Our findings suggest that sevoflurane anesthesia disrupts iron homeostasis, leading to increased oxidative stress and cognitive impairment in aged mice. These results highlight the potential of targeting iron‐mediated processes to mitigate sevoflurane‐induced cognitive impairment in the aging population. 10.1002/syn.22286 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Liproxstatin‐1 alleviates ferroptosis in sevoflurane anesthesia‐induced cognitive deficits of aged mice: The role oxidative stress
topic Synapse
url https://onlinelibrary.wiley.com/doi/10.1002/syn.22286