Proceedings of the 8th Neurological Disorders Summit (NDS-2023)

L. Ju, Jiepei Zhu, T. Morey, N. Gravenstein, C. Seubert, T. Vasilopoulos, A. Martynyuk, Chisato Kinoshita, K. Aoyama, T. Nakaki, E. Spinazzi, Mychael Delgardo, Andrés Pascual-Leones, Colby T Joncas, G. Mandigo, S. Lavine, J. Grinband, E. Sander, I. Khaliulin, Maryam Kartawy, H. Amal, Juliana Condoleo, Hu Wang, C. K. Bullen, Xiaoli Rong, Hao Fang, Senthilkumar S. Karuppagounder, Yongxing Gao, T. Dawson, V. Dawson, Jin-chong Xu, Jong-Hyun Son, Amanda K. Gerenza, Gabrielle M. Bingener, J. Bonkowsky, Kharon Grimmet, L. Gangwani, LouAnne E. Boyd, S. Upreti, Madhumita P. Ghosh, M. Podda, Saviana Antonella, Barbati, Chiara D'Amelio, Ida Nifo Sarrapocchiello, S. Fusco, Claudio Grassi, Matea Drlje, Sara Trnski, Andrija Štajduhar, Mihaela Bobić-Rasonja, Davide di Cenco, Eugene Kim, Eilidh MacNicol, K. Ilić, D. Cash, S. Škokić, N. Milošević, M. Youdim, Ofira Einstein Presenter, A. Katz, T. Ben-Hur, R. Howell, M. Lloyd-Puryear, Rabea Iris Pantelatos, K. Moen, A. Vik, T. Skandsen, René Daniel, S. Efrati, A. Hadanny, S
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Abstract

Introduction: Preexisting neurodegenerative diseases, perioperative stress, and inflammation play an essential role in accelerated neurocognitive decline after general anesthesia (GA) and surgery, termed perioperative neurocognitive disorder (PND). PND is an important public health problem potentially affecting millions of patients. Because neurodegenerative diseases pre-vail and worsen with age, PND is most readily detectable and studied in the aging population. Traumatic brain injury (TBI), with >50 million cases/year, is a dominant cause of disability in young adults. Similar to PND, the pathophysiology of TBI involves lasting dysregulation of stress response systems, neuroinflammation, and cognitive decline. Patients with a history of TBI may also require GA/surgery or sedation to treat conditions unrelated to TBI, or injuries sustained at the time of TBI. Here we tested whether the effects of GA/surgery, TBI, and subsequent repeated exposure to the general anesthetic sevoflurane (SEVO) interact to induce neurological and neuroendocrine abnormalities in the exposed young adult male rats (an animal model of PND) and/or in their future offspring (intergenerational PND). Methods: All animal procedures were approved by IACUC. Sprague-Dawley
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第八届神经系统疾病高峰会议论文集(NDS-2023)
先前存在的神经退行性疾病,围手术期应激和炎症在全麻(GA)和手术后加速神经认知衰退中起重要作用,称为围手术期神经认知障碍(PND)。PND是一个重要的公共卫生问题,可能影响数百万患者。由于神经退行性疾病随着年龄的增长而发生和恶化,PND在老年人群中最容易被发现和研究。外伤性脑损伤(TBI)是导致年轻人残疾的主要原因,每年约有5000万例。与PND相似,创伤性脑损伤的病理生理包括持续的应激反应系统失调、神经炎症和认知能力下降。有TBI病史的患者也可能需要GA/手术或镇静来治疗与TBI无关的疾病,或TBI时持续的损伤。在这里,我们测试了GA/手术、TBI和随后反复暴露于全身麻醉剂七氟醚(SEVO)的影响是否会在暴露的年轻成年雄性大鼠(PND的动物模型)和/或它们未来的后代(代际PND)中引起神经和神经内分泌异常。方法:所有动物实验均经IACUC批准。Sprague-Dawley
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