دورية أكاديمية

Clinic serum levels of Plin5 is therapeutic target of spinal cord injury and Plin5 reduced inflammation in spinal cord injury via silent information regulator 1 dependent inhibition of NLRP3 inflammasome

التفاصيل البيبلوغرافية
العنوان: Clinic serum levels of Plin5 is therapeutic target of spinal cord injury and Plin5 reduced inflammation in spinal cord injury via silent information regulator 1 dependent inhibition of NLRP3 inflammasome
المؤلفون: WU, Binqiang, LIANG, Xiao, ZHAO, Feng, FAN, Wei, LI, Chunjiang, ZHAO, Bin, REN, Jie
المصدر: Food Science and Technology. January 2022 42
بيانات النشر: Sociedade Brasileira de Ciência e Tecnologia de Alimentos, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Plin5, SIRT1, NLRP3, spinal cord injury
الوصف: The study investigated that clinic significance and molecular mechanism of Plin5 in spinal cord injury (SCI). Serum levels of Plin5 was down-regulated and there is a negative correlation between Plin5 and IL-1β levels in patients with SCI,. Human Plin5 protein could reduce inflammation, and prevented spinal cord injury in rat model of SCI. Over-expression of Plin5 reduced inflammation divisors via activation of SIRT1 and suppression of NLRP3 in vitro model of SCI; down-regulation of Plin5 promoted inflammation divisors via inactivation of SIRT1 and induction of NLRP3 in vitro model of SCI. SIRT1 is important targets of Plin5 in inflammation divisors of SCI. The inhibition of SIRT1 reduced the effects of Plin5 on inflammation divisors of SCI. The activation of NLRP3 also reduced the effects of Plin5 on inflammation divisors of SCI. We concluded that clinic Serum levels of Plin5 is therapeutic target of SCI and Plin5 reduced inflammation in SCI via SIRT1 dependent suppression of NLRP3 Inflammasome.
نوع الوثيقة: article
وصف الملف: text/html
اللغة: English
تدمد: 0101-2061
DOI: 10.1590/fst.51121
URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612022000100715
حقوق: info:eu-repo/semantics/openAccess
رقم الأكسشن: edssci.S0101.20612022000100715
قاعدة البيانات: SciELO
الوصف
تدمد:01012061
DOI:10.1590/fst.51121