27 P = 0.039, P < 0.05), There were n difference of occurrence degree. Conclusion: The new method of calcium supplement can reduce incidence of citrate intoxication. Through the study suggested that picker to preventive use of calcium supplements before collection, Reducing the occurrence of the CI. At the same time continue to selleck kinase inhibitor observe whether reducing reaction symptoms. Key Word(s): 1. blood stem cell; 2. Collect; 3. citrate intoxication; 4. calcium, Ca; Presenting Author: QIANG ZHAO Additional Authors: GANGWEI CHEN, ZHENG YONG, QIANG REN, NING ZHANG, FANG LIU, HAO LIU Corresponding Author: QIANG ZHAO Affiliations: Department of Gastroenterology, First Affiliated Hospital

of the Medical College, Shihezi University, Shihezi, Xinjiang Objective: Hydrogen sulfide (H2S) has been considered as the third gasotransmitter, and affects multiple physiopathological progresses. Some researches report that PI3K/Akt signal pathway is a target of H2S. In present study, we aimed to investigate the effects of H2S donor–sodium hydrosulfide (NaHS) and the PI3K/Akt signal pathway inhibitor–LY294002 respectively on liver tissue morphology and collagen deposition and detect the relationship between H2S and PI3K/Akt signal pathway for better understanding the mechanism of hydrogen sulfide on hepatic fibrosis rats. Methods: Therefore,

the hepatic fibrosis Selleckchem DAPT rat models were established by hypodermic injection of carbon tetrachloride mixed with cottonseed oil at the concentration of 40%, feeding high-fat, high-cholesterol diet and drinking ethanol. The rats were randomly divided into five groups after six weeks: hepatic fibrosis group (group HF), DMSO group (group D), LY294002 group (group L), NaHS group (group S), and

LY294002+NaHS group (group LS), and the rats in group HF, group D, group LY and group S were intraperitoneally infused with physiologic saline, 2‰ DMSO solution, LY294002 solution (0.3 mg/kg●d), and NaHS solution (56 μmol/kg●d) separately for 12 times, at the same time, the rats in group LS were intraperitoneally infused with LY294002 solution (0.3 mg/kg●d) and NaHS solution (56 μmol/kg●d) simultaneously for 12 times. All rat livers were collected after all above treatments. Hepatic fibrosis pathology stages were determined O-methylated flavonoid by HE staining. The depositions of collagen fiber were observed by Masson staining. The expressions of type I and III collagen were tested by RT-PCR and immunohistochemisty. The expressions of PI3K and p-Akt were tested by western blot. HE staining was used to determine hepatic fibrosis stages. Results: Compares with group N, the stage of hepatic fibrosis raised apparently in group HF and group D. Compared with group HF and group HF and group D, the stage of hepatic fibrosis in group S and group LY were decreased. But there was no obvious difference among group LY, group S and group LS.