<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>719</id><JournalTitle>NHIBITION OF YIGANKANG, A COMBINATION OF CHINESE  HERBS, ON PROLIFERATION OF RAT HEPATIC STELLATE CELLS  INDUCED BY INTERLEUKIN-1Î’</JournalTitle><Abstract>Chinese blood-activating and stasis-eliminating herbal medicines have been used to treat liver fibrosis and have been 
reported to inhibit rat hepatic stellate cells (HSCs) proliferatio n. To study the mechanism of the proliferation inhibition of rat 
HSCs  when  using  herbal  medicine,  the  present  study  tried  to  evaluate  the  inhibition  of  Yigankang  Decoction  on  c-Jun  Nterminal kinase (JNK) and Activator protein-1 (AP-1) of rat hepatic stellate cells induced by interleukin-1Î² (IL-1Î²). 
The  present  study  tried  to  evaluate  the  inhibition  of  Yigankang  Decoction  which  contains  blood-activating  and  stasiseliminating Chinese herbs such as large doses of Radix Salviae Miltiorrhizae (RSM) and Radix  Angelicae Sinensis (RAS) on 
JNK and AP-1 in rat HSCs induced by IL-1Î². Interleukin-1Î² up-regulated the proliferation of rat HSCs. After stimulation of IL -Î² for 24 h, the proliferation of rat HSCs increased significantly  than the corresponding values in the  control group  (1.573 Â± 
0.026 vs. 1.390 Â± 0.073, p < 0.01). After pretreated with the different concentrations  of the JNK pathwayâ€™s inhibitor SP600125
(10  Î¼mol/L,  1.427  Â±  0.113; 20  Î¼mol/L,  0.772  Â±  0.093;  40  Î¼mol/L,  0.675  Â±  0.074),  the  proliferation  of  rat  HSCs  that  were 
induced by IL-1Î² decreased significantly than the corresponding values in the control group  (1.560Â±0.110) (p < 0.05; p < 0.01; 
p < 0.01). IL-1Î² activated the JNK pathway in a time-dependent manner in rat HSCs. After stimulation of IL-1Î² for 0, 5, 15, 30, 
60 and 120 min, the JNK activities were 0.982 Â± 0.299, 1.501 Â± 0.720, 2.133 Â± 0.882, 3.360 Â± 0.452, 2.181 Â± 0.789, 1.385 Â± 
0.368, respectively. In comparison with the group without IL-1Î², the JNK activities differed significantly at 15, 30 and 60 min 
(p < 0.01, p < 0.01,  p < 0.01). Yigankang Decoction inhibited the activities of JNK (1.610 Â± 0.242  vs. 3.360 Â± 0.452, p < 0.01) 
and AP-1 activity (342.43 Â± 85.77  vs.  597.70 Â± 83.96,  p  < 0.01) obviously.  IL-1Î² can stimulate the proliferation of rat  HSCs, 
and JNK/AP-1 signaling pathway is involved in the process. Therefore, Yigankang Decoction can inhibit HSCs proliferation, 
can be explained, in part, through JNK/AP-1 pathway</Abstract><Email>yapingzhang@aliyun.com</Email><articletype>Research</articletype><volume>7</volume><issue>2</issue><year>2016</year><keyword>Activator protein,Yigankang Decoction,c-Jun N-terminal kinase,Hepatic stellate cells,Proliferation</keyword><AUTHORS>Xue-Mei Ai,Ya-Ping Zhang,Ning Tang,Ze-Yu Liu,Xi-Xian Yao</AUTHORS><afflication>Department of Pediatrics, Third Hospital of Hebei Medical University, Shijiazhuang 050051, Hebei Province, PR China,Department of Pediatrics, Third Hospital of Hebei Medical University, Shijiazhuang 050051, Hebei Province, PR China,Department of Pediatrics, Third Hospital of Hebei Medical University, Shijiazhuang 050051, Hebei Province, PR China,Department of Pediatrics, Third Hospital of Hebei Medical University, Shijiazhuang 050051, Hebei Province, PR China,Department of Gastroenterology, The Second Hospital of Hebei Medical University, Shijiazhuang 050000, Hebei Province,  PR China</afflication></Article></Articles>