Academic Journal

Oxymatrine attenuates amyloid beta 42 (Aβ 1–42 )-induced neurotoxicity in primary neuronal cells and memory impairment in rats

التفاصيل البيبلوغرافية
العنوان: Oxymatrine attenuates amyloid beta 42 (Aβ 1–42 )-induced neurotoxicity in primary neuronal cells and memory impairment in rats
المؤلفون: Dong, Peiliang, Ji, Xiaomeng, Han, Wei, Han, Hua
المصدر: Canadian Journal of Physiology and Pharmacology ; volume 97, issue 2, page 99-106 ; ISSN 0008-4212 1205-7541
بيانات النشر: Canadian Science Publishing
سنة النشر: 2019
الوصف: Amyloid beta 42 (Aβ 1–42 )-induced oxidative stress causes the death of neuronal cells and is involved in the development of Alzheimer’s disease. Oxymatrine (OMT) inhibits oxidative stress. In this study, we investigated the effect of OMT on Aβ 1–42 -induced neurotoxicity in vivo and in vitro. In the Morris water maze test, OMT significantly decreased escape latency and increased the number of platform crossings. In vitro, OMT markedly increased cell viability and superoxide dismutase activity. Moreover, OMT decreased lactate dehydrogenase leakage, malondialdehyde content, and reactive oxygen species in a dose-dependent manner. OMT upregulated the ratio of Bcl-2/Bax and downregulated the level of caspase-3. Furthermore, OMT inhibited the activation of MAP kinase (ERK 1/2, JNK) and nuclear factor κB. In summary, OMT may potentially be used in the treatment of Alzheimer’s disease.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1139/cjpp-2018-0299
الاتاحة: http://dx.doi.org/10.1139/cjpp-2018-0299
http://www.nrcresearchpress.com/doi/full-xml/10.1139/cjpp-2018-0299
http://www.nrcresearchpress.com/doi/pdf/10.1139/cjpp-2018-0299
Rights: http://www.nrcresearchpress.com/page/about/CorporateTextAndDataMining
رقم الانضمام: edsbas.82A95BF3
قاعدة البيانات: BASE