Antidiabetic Micro-/Nanoaggregates from Ge-Gen-Qin-Lian-Tang Decoction Increase Absorption of Baicalin and Cellular Antioxidant Activity In Vitro.
Antidiabetic Micro-/Nanoaggregates from Ge-Gen-Qin-Lian-Tang Decoction Increase Absorption of Baicalin and Cellular Antioxidant Activity In Vitro.
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葛根芩连汤汤中的抗糖尿病微/纳米聚集体可增加黄芩苷的吸收和细胞体外抗氧化活性
DOI:
10.1155/2017/9217912
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发表时间:
2017
影响因子:
--
通讯作者:
Rao P
中科院分区:
文献类型:
--
作者:
Lin D;Du Q;Wang H;Gao G;Zhou J;Ke L;Chen T;Shaw C;Rao P
The antidiabetic effects of Ge-Gen-Qin-Lian-Tang decoction (GQD) have been proven clinically. In a pharmacological study conducted on STZ-induced diabetic rats, the constitutive aggregates/sediments of Ge-Gen-Qin-Lian-Tang decoction exhibited stronger hypoglycemic and antioxidant activities compared to the soluble compositions. This study aims to demonstrate the pharmacological properties of aggregates derived from GQD by measuring permeability of the active monomer phytochemicals (e.g., baicalin) in a Caco-2 cell monolayer and determine the cellular viability, intracellular redox status (MDA and SOD), and insulin secretion of pancreatic β-cell line, INS-1, following STZ-induced oxidative stress. The aggregates were separated into three fractions, namely, “MA (microaggregates),” “400 g supernatant,” and “MNA (micro-/nanoaggregates),” by centrifugation at 400 ×g and 15000 ×g, respectively. Aggregates in the sediment increased baicalin absorption, showed little toxicity to β-cells, elevated intracellular SOD levels, and significantly suppressed oxidative damage effects on cellular viability and functions. The “MA” fraction had a larger particle size and provided higher antioxidant cellular protection than “MNA” in vitro, implying that the sediments may be the active components in the herbal decoction. The actions of these micro-/nanoaggregates may provide a new perspective for understanding the antidiabetic effects of herbal decoctions and aid in interpretation of synergistic actions between the multiple components.
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DOI:
10.1038/ismej.2014.177
发表时间:
2015-03
期刊:
The ISME journal
影响因子:
--
作者:
通讯作者:
--
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Zhou, Ji-Yin;Zhou, Shi-Wen
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Zhou, Shi-Wen
DOI:
10.1186/1756-9966-31-48
发表时间:
2012-05-20
期刊:
Journal of experimental & clinical cancer research : CR
影响因子:
--
作者:
Huang Y;Hu J;Zheng J;Li J;Wei T;Zheng Z;Chen Y
通讯作者:
Chen Y
DOI:
10.1016/j.bbamcr.2011.05.003
发表时间:
2011-08
期刊:
Biochimica et biophysica acta
影响因子:
--
作者:
Takahashi H;Chen MC;Pham H;Angst E;King JC;Park J;Brovman EY;Ishiguro H;Harris DM;Reber HA;Hines OJ;Gukovskaya AS;Go VL;Eibl G
通讯作者:
Eibl G
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5.4
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Lau, Kit-Man;Lai, Kwok-Kin;Lau, Clara Bik-San
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Lau, Clara Bik-San