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Pantothenate-encapsulated liposomes combined with exercise for effective inhibition of CRM1-mediated PKM2 translocation in Alzheimer's therapy.
Chen, Yisheng; Huang, Lei; Luo, Zhiwen; Han, Dan; Luo, Wei; Wan, Renwen; Li, Yan; Ge, Yunshen; Lin, Wei-Wei; Xie, Yuchun; Sun, Mingming; Wang, Qian; Li, Zhiwei; Chen, Shiyi; Yang, Yi; Huang, Bin; Xu, Yuzhen.
Afiliação
  • Chen Y; Department of Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China; Department of Medical Sciences, Ningde Normal University College of Medical Sciences, No. 1 Xueyuan Road, Jiaocheng District, Ningde City, Fujian, China.
  • Huang L; Department of Molecular, Cell, and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, 01605, MA, USA. Electronic address: lei.huang@umassmed.edu.
  • Luo Z; Department of Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Han D; Department of Emergency Medicine and Intensive Care, Songjiang Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Luo W; Department of Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Wan R; Department of Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Li Y; School of Basic Medical Sciences, Ningxia Medical University, Yinchuan 750004, China.
  • Ge Y; Department of Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Lin WW; Department of Neurosurgery, Second Affiliated Hospital of Zhejiang University School of Medicine, Zhejiang University, 88 Jiefang Road, Hangzhou 310009, Zhejiang, China.
  • Xie Y; Jiangsu Province Geriatric Hospital, China.
  • Sun M; Laboratory Animal Center, Guangxi Medical University, Nanning, Guangxi, China.
  • Wang Q; Department of Central Laboratory, The Affiliated Taian City Central Hospital of Qingdao University, Taian, Shandong, China.
  • Li Z; Clinical Laboratory Center, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, Xinjiang, PR China.
  • Chen S; Department of Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China. Electronic address: yschen21@m.fudan.edu.cn.
  • Yang Y; School of Basic Medical Sciences, Ningxia Medical University, Yinchuan 750004, China. Electronic address: yangyi@nxmu.edu.cn.
  • Huang B; The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China. Electronic address: binhuang9294@gmail.com.
  • Xu Y; Department of Rehabilitation, The Second Affiliated Hospital of Shandong First Medical University, Taian, Shandong, China. Electronic address: xuyuzhen@sdfmu.edu.cn.
J Control Release ; 373: 336-357, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38996921
ABSTRACT
Alzheimer's disease (AD) is a complex neurodegenerative condition characterized by metabolic imbalances and neuroinflammation, posing a formidable challenge in medicine due to the lack of effective treatments. Despite considerable research efforts, a cure for AD remains elusive, with current therapies primarily focused on symptom management rather than addressing the disease's underlying causes. This study initially discerned, through Mendelian randomization analysis that elevating pantothenate levels significantly contributes to the prophylaxis of Alzheimer's disease. We explore the therapeutic potential of pantothenate encapsulated in liposomes (Pan@TRF@Liposome NPs), targeting the modulation of CRM1-mediated PKM2 nuclear translocation, a critical mechanism in AD pathology. Additionally, we investigate the synergistic effects of exercise, proposing a combined approach to AD treatment. Exercise-induced metabolic alterations share significant similarities with those associated with dementia, suggesting a potential complementary effect. The Pan@TRF@Liposome NPs exhibit notable biocompatibility, showing no liver or kidney toxicity in vivo, while demonstrating stability and effectiveness in modulating CRM1-mediated PKM2 nuclear translocation, thereby reducing neuroinflammation and neuronal apoptosis. The combined treatment of exercise and Pan@TRF@Liposome NP administration in an AD animal model leads to improved neurofunctional outcomes and cognitive performance. These findings highlight the nanoparticles' role as effective modulators of CRM1-mediated PKM2 nuclear translocation, with significant implications for mitigating neuroinflammation and neuronal apoptosis. Together with exercise, this dual-modality approach could offer new avenues for enhancing cognitive performance and neurofunctional outcomes in AD, marking a promising step forward in developing treatment strategies for this challenging disorder.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Citoplasmáticos e Nucleares / Carioferinas / Doença de Alzheimer / Proteína Exportina 1 / Lipossomos Limite: Animals / Humans / Male Idioma: En Revista: J Control Release / J. control. release / Journal of controlled release Assunto da revista: FARMACOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Citoplasmáticos e Nucleares / Carioferinas / Doença de Alzheimer / Proteína Exportina 1 / Lipossomos Limite: Animals / Humans / Male Idioma: En Revista: J Control Release / J. control. release / Journal of controlled release Assunto da revista: FARMACOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China