|1.||Lee, Ching-Kuo: 1 article (06/2015)|
|2.||Juan, Shu-Hui: 1 article (06/2015)|
|3.||Chang, Chih-Cheng: 1 article (06/2015)|
|4.||Wang, Yu-Shiou: 1 article (06/2015)|
|5.||Chou, Hsiu-Chu: 1 article (06/2015)|
|6.||Cheng, Kur-Ta: 1 article (06/2015)|
|7.||Lin, H: 1 article (05/2013)|
|8.||Lin, W-C: 1 article (05/2013)|
|9.||Wu, J-B: 1 article (05/2013)|
|10.||Hsiao, H-B: 1 article (05/2013)|
02/01/2011 - "In the present study, we reported that kinsenoside, a major component of Anoectochilus formosanus, inhibited inflammatory reactions in mouse peritoneal lavage macrophages and protects mice from endotoxin shock. "
02/01/2011 - "Kinsenoside isolated from Anoectochilus formosanus suppresses LPS-stimulated inflammatory reactions in macrophages and endotoxin shock in mice."
|3.||Body Weight (Weight, Body)
11/01/2007 - "Our study showed that this compound exhibited significantly antihyperglycemic activity at the dose of 15mg/kg body weight, which is speculated to be partially attributed to modulating the activity of enzymatic antioxidants, scavenging free radicals, and reducing the content of factor NO. Much more intact beta cells in the islets of Langerhans with denser insulin in kinsenoside-treated groups than the negative control were observed, which greatly supported the morphological and functional elucidation. "
|5.||Diabetic Angiopathies (Diabetic Angiopathy)