دورية أكاديمية

Levosimendan inhibits disulfide tau oligomerization and ameliorates tau pathology in TauP301L-BiFC mice

التفاصيل البيبلوغرافية
العنوان: Levosimendan inhibits disulfide tau oligomerization and ameliorates tau pathology in TauP301L-BiFC mice
المؤلفون: Sungsu Lim, Seulgi Shin, Yoonsik Sung, Ha Eun Lee, Kyu Hyeon Kim, Ji Yeon Song, Gwan-Ho Lee, Hira Aziz, Nataliia Lukianenko, Dong Min Kang, Nicolette Boesen, Hyeanjeong Jeong, Aizhan Abdildinova, Junghee Lee, Byung-Yong Yu, Sang Min Lim, Jun-Seok Lee, Hoon Ryu, Ae Nim Pae, Yun Kyung Kim
المصدر: Experimental and Molecular Medicine, Vol 55, Iss 3, Pp 612-627 (2023)
بيانات النشر: Nature Publishing Group, 2023.
سنة النشر: 2023
المجموعة: LCC:Medicine
LCC:Biochemistry
مصطلحات موضوعية: Medicine, Biochemistry, QD415-436
الوصف: Alzheimer’s disease: A tool for preventing toxic tangles The discovery that an already approved drug can disrupt tau protein aggregation in cultured cells and live mice could guide the development of new therapies for Alzheimer’s. Tau plays an important role in organizing the internal structure of neurons, but in neurodegenerative disease is seen to form abnormal assemblies that are toxic to cells. Researchers led by Ae Nim Pae and Yun Kyung Kim at the Korea Institute of Science and Technology, Seoul, South Korea have devised an assay that allowed them to identify agents that actively interfere with this process. Levosimendan, a drug approved for heart failure, broke up tau aggregates in cell culture and reduced cognitive symptoms in a mouse model of tau-induced neurodegeneration. Further investigation of levosimendan’s mode of action could yield interventions that slow or prevent Alzheimer’s progression.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2092-6413
Relation: https://doaj.org/toc/2092-6413
DOI: 10.1038/s12276-023-00959-5
URL الوصول: https://doaj.org/article/41f48540f4264ce39a8946491a2dbb86
رقم الأكسشن: edsdoj.41f48540f4264ce39a8946491a2dbb86
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20926413
DOI:10.1038/s12276-023-00959-5