دورية أكاديمية

Anti-neuroinflammatory activity of elephantopus scaber L. via activation of Nrf2/HO-1 signaling and inhibition of p38 MAPK pathway in LPS-induced microglia BV-2 cells

التفاصيل البيبلوغرافية
العنوان: Anti-neuroinflammatory activity of elephantopus scaber L. via activation of Nrf2/HO-1 signaling and inhibition of p38 MAPK pathway in LPS-induced microglia BV-2 cells
المؤلفون: Chan, Chim Kei, Tan, Loh Teng Hern, Andy, Shathiswaran N., Kamarudin, Muhamad Noor Alfarizal, Goh, Bey Hing, Kadir, Habsah Abdul
المصدر: Chan , C K , Tan , L T H , Andy , S N , Kamarudin , M N A , Goh , B H & Kadir , H A 2017 , ' Anti-neuroinflammatory activity of elephantopus scaber L. via activation of Nrf2/HO-1 signaling and inhibition of p38 MAPK pathway in LPS-induced microglia BV-2 cells ' , Frontiers in Pharmacology , vol. 8 , 397 . https://doi.org/10.3389/fphar.2017.00397Test
سنة النشر: 2017
مصطلحات موضوعية: Anti-inflammatory, Antioxidant, Elephantopus scaber L., NF-κB, Nrf2
الوصف: Elephantopus scaber L. (family: Asteraceae) has been traditionally utilized as a folkloric medicine and scientifically shown to exhibit anti-inflammatory activities in various in vivo inflammatory models. Given the lack of study on the effect of E. scaber in neuroinflammation, this study aimed to investigate the anti-neuroinflammatory effect and the underlying mechanisms of ethyl acetate fraction from the leaves of E. scaber (ESEAF) on the release of pro-inflammatory mediators in lipopolysaccharide (LPS)-induced microglia cells (BV-2). Present findings showed that ESEAF markedly attenuated the translocation of NF-κB to nucleus concomitantly with the significant mitigation on the LPS-induced production of NO, iNOS, COX-2, PGE 2 , IL-1β, and TNF-α. These inflammatory responses were reduced via the inhibition of p38. Besides, ESEAF was shown to possess antioxidant activities evident by the DPPH and SOD scavenging activities. The intracellular catalase enzyme activity was enhanced by ESEAF in the LPS-stimulated BV-2 cells. Furthermore, the formation of ROS induced by LPS in BV-2 cells was reduced upon the exposure to ESEAF. Intriguingly, the reduction of ROS was found in concerted with the activation of Nrf2 and HO-1. It is conceivable that the activation promotes the scavenging power of antioxidant enzymes as well as to ameliorate the inflammatory response in LPS-stimulated BV-2 cells. Finally, the safety profile analysis through oral administration of ESEAF at 2000 mg/kg did not result in any mortalities, adverse effects nor histopathologic abnormalities of organs in mice. Taken altogether, the cumulative findings suggested that ESEAF holds the potential to develop as nutraceutical for the intervention of neuroinflammatory disorders.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
DOI: 10.3389/fphar.2017.00397
الإتاحة: https://doi.org/10.3389/fphar.2017.00397Test
https://research.monash.edu/en/publications/f0eada41-1734-4677-8bea-d6b28fa13b9fTest
https://researchmgt.monash.edu/ws/files/345531204/341388597_oa.pdfTest
http://www.scopus.com/inward/record.url?scp=85021089099&partnerID=8YFLogxKTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.77B4225
قاعدة البيانات: BASE