4.4 Article

Mulberry fruit improves memory in scopolamine-treated mice: role of cholinergic function, antioxidant system, and TrkB/Akt signaling

期刊

NUTRITIONAL NEUROSCIENCE
卷 24, 期 12, 页码 940-950

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/1028415X.2019.1696613

关键词

Akt; antioxidant enzymes; apoptosis; brain-derived neurotrophic factor; hippocampal neuronal cells; memory impairment; mulberry fruit; tropomyosin-related kinase receptor B

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2017R1D1A3B03027867]
  2. National Research Foundation of Korea [2017R1D1A3B03027867] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Research showed that mulberry fruit extract (MFE) protected neuronal cells by improving cell viability, reducing oxidative stress, suppressing apoptosis, regulating protein expression, and upregulating BDNF and antioxidant enzymes. This neuroprotective effect was achieved by stabilizing the activation of the TrkB/Akt pathway. Such findings suggest the potential of MFE as a food supplement for preventing and treating neurodegenerative diseases.
Objectives: Although mulberry fruit possesses some biological activities, it is not known how it protects neuronal cells in neurodegenerative diseases. Here, we examined whether mulberry fruit extract (MFE) protected neuronal cells against oxidative stress-induced neurodegeneration. Methods: In this experiments, glutamate challenged hippocampal neuronal HT-22 cell lines as an in vitro model and scopolamine-induced memoty-impairment mice model were used. Results: MFE improved cell viability and glutathione level as well as reducing reactive oxygen species level in glutamate-treated HT-22 cells. Additionally, MFE suppressed apoptotic bodies and mitochondrial depolarization through regulating expression of apoptosis-related proteins. Furthermore, MFE elevated expression of p-TrkB, p-Akt, p-CREB, BDNF, and antioxidant enzymes as well as nuclear translocation of Nrf2. In contrast, the inclusion of K252a, a TrkB inhibitor, or MK-2206, an Akt selective inhibitor, neutralized the neuroprotective actions of MFE. Separately, MFE attenuated scopolamine-induced amnesia via regulating the activities of enzymes related with cholinergic function and the antioxidant system in mice. Additionally, MFE protected neuronal cells in the hippocampal CA1 and CA3 regions in brain of mice. Conclusions: MFE protects neuronal cells against oxidative stress-induced apoptosis through upregulating the expression of BDNF and antioxidant enzymes by stabilizing the activation of the TrkB/Akt pathway. Such an effect of MFE, which includes rich polyphenols, may provide information for its application as a food supplement for the prevention and treatment of neurodegenerative diseases.

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