دورية أكاديمية

Cycloastragenol Is a Potent Telomerase Activator in Neuronal Cells: Implications for Depression Management

التفاصيل البيبلوغرافية
العنوان: Cycloastragenol Is a Potent Telomerase Activator in Neuronal Cells: Implications for Depression Management
المؤلفون: Fanny C.F. Ip, Yu Pong Ng, H.J. An, Ying Dai, Hai Hong Pang, Yue Qing Hu, Allison C. Chin, Calvin B. Harley, Yung Hou Wong, Nancy Y. Ip
المصدر: Neurosignals, Vol 22, Iss 1, Pp 52-63 (2014)
بيانات النشر: Cell Physiol Biochem Press GmbH & Co KG
سنة النشر: 2014
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: cAMP response element binding, NGF, Astragalus membranaceus, Saponin, Telomere, Telomerase reverse transcriptase, Neurology. Diseases of the nervous system, RC346-429, Neurophysiology and neuropsychology, QP351-495
الوصف: Cycloastragenol (CAG) is an aglycone of astragaloside IV. It was first identified when screening Astragalus membranaceus extracts for active ingredients with antiaging properties. The present study demonstrates that CAG stimulates telomerase activity and cell proliferation in human neonatal keratinocytes. In particular, CAG promotes scratch wound closure of human neonatal keratinocyte monolayers in vitro. The distinct telomerase-activating property of CAG prompted evaluation of its potential application in the treatment of neurological disorders. Accordingly, CAG induced telomerase activity and cAMP response element binding (CREB) activation in PC12 cells and primary neurons. Blockade of CREB expression in neuronal cells by RNA interference reduced basal telomerase activity, and CAG was no longer efficacious in increasing telomerase activity. CAG treatment not only induced the expression of bcl2, a CREB-regulated gene, but also the expression of telomerase reverse transcriptase in primary cortical neurons. Interestingly, oral administration of CAG for 7 days attenuated depression-like behavior in experimental mice. In conclusion, CAG stimulates telomerase activity in human neonatal keratinocytes and rat neuronal cells, and induces CREB activation followed by tert and bcl2 expression. Furthermore, CAG may have a novel therapeutic role in depression. © 2014 S. Karger AG, Basel
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1424-862X
1424-8638
العلاقة: http://www.karger.com/Article/FullText/365290Test; https://doaj.org/toc/1424-862XTest; https://doaj.org/toc/1424-8638Test; https://doaj.org/article/781e1268950a4ddeafda8b6cf96d14d3Test
DOI: 10.1159/000365290
الإتاحة: https://doi.org/10.1159/000365290Test
https://doaj.org/article/781e1268950a4ddeafda8b6cf96d14d3Test
رقم الانضمام: edsbas.4B3D7315
قاعدة البيانات: BASE
الوصف
تدمد:1424862X
14248638
DOI:10.1159/000365290