HUANG Jie-ling, ZHONG Ming, YU Sheng-min. Effects of Total Alkaloids from on Proliferation of Human Hepatic Stellate Cells and Collagen,Cytokines Related to Hepatic Fibrosis[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(13): 283-286.
HUANG Jie-ling, ZHONG Ming, YU Sheng-min. Effects of Total Alkaloids from on Proliferation of Human Hepatic Stellate Cells and Collagen,Cytokines Related to Hepatic Fibrosis[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(13): 283-286. DOI: 10.11653/syfj2013130283.
Objective:To observe the effect of total alkaloids from Phyllodium pulchellum on proliferation of human hepatic stellate cell line Lx-2 and the impact on secretion of collagen and cytokines which are related to liver fibrosis. Method: After recovery
Lx-2 cells in logarithmic growth were diluted to a concentration of 1×105/mL
and inoculated 0.1 mL in hole in incubator at 37 ℃
blank control group was set up
the concentration of the drug administered in an order of 100
75
55
40
30
20
15
10 mg·L-1. After 48 h of administration
MTT assay was used to detect cell proliferation. Similarly
after recovery
Lx-2 cells in logarithmic growth were diluted to a concentration of 1×105/mL
and inoculated 0.1 mL/hole in incubator at 37 ℃
blank control group and Colchicine group (6.25 mg·L-1) were set up. After 48 h of administration
ELISA method was used to detect Lx-2 cell supernatant for type I collagen (COL I)
type III collagen (COL III)
type IV collagen (COL Ⅳ)
transforming growth factor β1(TGF β1) and platelet-derived growth factor (PDGF) content. Result: Compared with the control group
Lx-2 cell proliferation was inhibited by the total alkaloids in a concentration-dependent manner with inhibition rates of 49.4%
25.9%
24.7%
15.3%
15.3%
12.9%
2.35% and 1.18% accordingly. Compared with the control group
the total alkaloids of 40 mg·L-1 could significantly inhibit COL I
COL Ⅲ
COL Ⅳ
TGF-β1 and PDGF secretion ( P<0.05 or P <0.01). Conclusion: The total alkaloids from P. pulchellum can inhibit the proliferation of Lx-2 cells and the secretion of COLⅠ