Protection of Differentiating Neuronal Cells from Amyloid β Peptide-induced Injury by Alkaline Extract of Leaves of Sasa senanensis Rehder

被引:15
|
作者
Sakagami, Hiroshi [1 ]
Tsuji, Mayumi [2 ]
Tomomura, Mineko [1 ]
Masuda, Yoshiko [1 ]
Iwama, Soichi [1 ]
Nakagawa, Mika [1 ]
Suzuki, Hayato [1 ]
Tanaka, Kenta [1 ]
Abe, Tomoyuki [1 ]
Tamura, Nobuaki [1 ]
Tomomura, Akito [1 ]
Yokose, Satoshi [1 ]
Takeshima, Hiroshi [1 ]
Natori, Takenori [3 ]
Horiuchi, Misaki [4 ]
Fujisawa, Tomohiro [4 ]
Kiuchi, Yuji [2 ]
Oguchi, Katsuji [2 ]
Yasui, Toshikazu [1 ]
Oizumi, Hiroshi [4 ]
Oizumi, Takaaki [4 ]
机构
[1] Meikai Univ, Sch Dent, Sakado, Saitama, Japan
[2] Showa Univ, Sch Med, Tokyo, Japan
[3] Teikyo Heisei Univ, Fac Pharmaceut Sci, Tokyo, Japan
[4] Daiwa Biol Res Inst Co Ltd, Kawasaki, Kanagawa, Japan
来源
IN VIVO | 2018年 / 32卷 / 02期
基金
日本学术振兴会;
关键词
Nerve cell; NGF; differentiation; amyloid beta-peptide; protection; hormesis; bamboo leaf extract; PC12; CELLS; ALZHEIMERS-DISEASE; TAU-PROTEIN; APOPTOSIS; MEDICINE; GROWTH;
D O I
10.21873/invivo.11229
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: We have previously reported the protection of doxorubicin-induced keratinocyte toxicity by alkaline extract of the leaves of Sasa senanensis Rehder (SE). In order to extend the generality of the cell protective effect of SE, we investigated whether it also protects rat PC12 and human SH-SY5Y neuron model cells from amyloid beta-peptide (A beta)-induced injury. Materials and Methods: Viability of cells was determined by the MTT method. Cytotoxicity was evaluated by the concentration that reduces the cell viability by 50% (CC50). Protection from A beta-induced cytotoxicity was evaluated by the concentration that reversed the A beta-induced reduction of viability by 50% (EC50). The selectivity index (SI) of neuroprotective activity was defined as the ratio of EC50 to CC50. A beta(1-42) aggregation was assayed using A beta(1-42) ammonium hydroxide. Results: SE showed hormetic growth stimulation at lower concentrations in both neuron precursors and differentiated cells. SE reproducibly inhibited A beta-induced cytotoxicity against both undifferentiated and differentiated neuron cells. Both the extent of differentiation induction and viability depended on the cell density, suggesting the release of growth and differentiation stimulation substances into culture supernatant. Higher concentrations of SE partially reduced the A beta(1-42) aggregation. Conclusion: Hormetic growth stimulation and inhibition of aggregation may be involved in the neuroprotective activity of SE.
引用
收藏
页码:231 / 239
页数:9
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