Adiponectin deficiency is a critical factor contributing to cognitive dysfunction in obese mice after sevoflurane exposure.

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Medicine Pub Date : 2024-10-16 DOI:10.1186/s10020-024-00954-0
John Man Tak Chu, Suki Pak Wing Chiu, Jiaqi Wang, Raymond Chuen Chung Chang, Gordon Tin Chun Wong
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Abstract

Background: The number of major operations performed in obese patients is expected to increase given the growing prevalence of obesity. Obesity is a risk factor for a range of postoperative complications including perioperative neurocognitive disorders. However, the mechanisms underlying this vulnerability are not well defined. We hypothesize that obese subjects are more vulnerable to general anaesthesia induced neurotoxicity due to reduced levels of adiponectin. This hypothesis was tested using a murine surgical model in obese and adiponectin knockout mice exposed to the volatile anaesthetic agent sevoflurane.

Methods: Obese mice were bred by subjecting C57BL/6 mice to a high fat diet. Cognitive function, neuroinflammatory responses and neuronal degeneration were assessed in both obese and lean mice following exposure to 2 h of sevoflurane to confirm sevoflurane-induced neurotoxicity. Thereafter, to confirm the role of adiponectin deficiency in, adiponectin knockout mice were established and exposed to the sevoflurane. Finally, the neuroprotective effects of adiponectin receptor agonist (AdipoRon) were examined.

Results: Sevoflurane triggered significant cognitive dysfunction, neuroinflammatory responses and neuronal degeneration in the obese mice while no significant impact was observed in the lean mice. Similar cognitive dysfunction and neuronal degeneration were also observed in the adiponectin knockout mice after sevoflurane exposure. Administration of AdipoRon partially prevented the deleterious effects of sevoflurane in both obese and adiponectin knockout mice.

Conclusions: Our findings demonstrate that obese mice are more susceptible to sevoflurane-induced neurotoxicity and cognitive impairment in which adiponectin deficiency is one of the underlying mechanisms. Treatment with adiponectin receptor agonist ameliorates this vulnerability. These findings may have therapeutic implications in reducing the incidence of anaesthesia related neurotoxicity in obese subjects.

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脂肪连接蛋白缺乏是导致肥胖小鼠在七氟烷暴露后出现认知功能障碍的关键因素。
背景:随着肥胖症发病率的上升,肥胖患者接受大型手术的数量预计也会增加。肥胖是导致一系列术后并发症(包括围手术期神经认知障碍)的风险因素。然而,这种脆弱性的内在机制还不十分明确。我们假设,肥胖受试者由于脂肪连接蛋白水平降低,更容易受到全身麻醉诱导的神经毒性的影响。我们利用肥胖小鼠和脂肪连接蛋白基因敲除小鼠的手术模型,在暴露于挥发性麻醉剂七氟醚的情况下对这一假设进行了验证:方法:用高脂肪饮食饲养 C57BL/6 小鼠,从而培育出肥胖小鼠。对肥胖小鼠和瘦小鼠暴露于七氟烷 2 小时后的认知功能、神经炎症反应和神经元变性进行评估,以确认七氟烷诱导的神经毒性。之后,为了证实脂肪连接蛋白缺乏在七氟烷诱导的神经毒性中的作用,建立了脂肪连接蛋白基因敲除小鼠并将其暴露于七氟烷。最后,还研究了脂肪连接素受体激动剂(AdipoRon)对神经的保护作用:结果:七氟烷在肥胖小鼠中引发了明显的认知功能障碍、神经炎症反应和神经元变性,而在瘦小鼠中未观察到明显影响。脂肪连接素基因敲除小鼠在暴露于七氟烷后也出现了类似的认知功能障碍和神经元退化。服用 AdipoRon 可部分防止七氟烷对肥胖小鼠和脂肪连接蛋白基因敲除小鼠的有害影响:我们的研究结果表明,肥胖小鼠更容易受到七氟醚诱导的神经毒性和认知障碍的影响,而脂肪连接蛋白缺乏是其潜在机制之一。使用脂联素受体激动剂可改善这种易感性。这些发现可能对降低肥胖者麻醉相关神经毒性的发生率具有治疗意义。
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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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