This paper introduces the working principle of the blood circle treatment system outside the body. A monitoring instrument of plasma leakage suited for the blood circle treatment system outside the body is developed based on the absorption spectrum experiments of plasma leakage. Photoelectric detection technology and virtual instrumentation are utilized in the development. A series of detecting experiments of waste solution containing plasma with continuously changing concentration show the monitoring system possesses a relatively high sensitivity. Moreover, the experiments of continual detection with plasma concentration at one certain point indicate the monitoring system has a quite good stability. The monitoring instrument is adapted to dynamically detecting the plasma leakage when the blood circle treatment system outside the body is working.

Objective To investigate the relationship between Helicobacter pylori (H. pylori) infection and concentration of reactive oxygen species (ROS) in AGS cells. Methods AGS cells were cultured with either Hp11638 (CagA~+ , VacA~+ ) extract or Hp11638 mutant (CagA~+ , VacA~-) extract for 48 hours, then the cells and supernatants were collected. The concentration of ROS in AGS cells was measured by flow cytometry. The eytochrome C reduction was detected by spectrophotometer at 550 nm. Results The ROS levels in the AGS cells were correlated with two H. pylori strains in a concentration- and time-dependent manner. The ROS levels in AGS cells treated with Hp11638 extract in different concentrations or times were correspondingly higher than those treated with Hp11638 mutant extract. Similar results were found in examination of cytochrome C reduction. Conclusion The elevation of ROS in AGS cells is related to effects of H. pylori proteins, and the VaeA protein involves in the process.

Objective To investigate the influence of application of local anesthesia with lidocaine on bronchial lavage fluid (BLF) pseudomonas aeruginosa culture and drug sensitivity in cases with lung infection .Methods Two hundred and seventy speci-men of BLF were collected from 135 patients with infection of lung .And BLF were collected directly from right-broncho in control group ,and from left-broncho in lidocaine group .The outcome of pseudomonas aeruginosa culture and drug sensitivity were com-pared in the two groups .Results Fourty-two cases were postitive in BLF pseudomonas aeruginosa culture in the control group ,and 40 cases were postitive in lidocaine group .The positive rates were 31 .11% and 29 .63% ,respectively .There were no significance between the two groups (P<0 .001) .Compared with the control group ,the sensitive strains of pseudomonas aeruginosa were obvi-ously less and the drug tolerance strains were much more in lidocaine group for Ciprofloxacin and Levofloxacin (P<0 .05) .Howev-er ,there were no influence for drugs such as Piperacillin/Tazobactam and Ceftazidime ,etc .Conclusion 2% lidocaine has no influ-ence on the outcome of BLF pseudomonas aeruginosa culture .But it may reduce the drug sensitivity of Ciprofloxacin and Levofloxa-cin in cases with infection of lung .

OBJECTIVE：To stud y the effects of Zhitong shunqi capsule on JAK/STAT signaling pathway of chronic atrophic gastritis（CAG）model rats ，and to provide reference for clarifying its mechanism of improving CAG. METHODS ：Totally 60 SD rats were randomly divided into blank group ，model group ，positive control group [vitacoenzyme ，0.09 g/（kg·d）]，Zhitong shunqi capsule low-dose ，medium-dose and high-dose groups [ 0.75，1.5，3 g/（kg·d）]，with 10 rats in each group. Except for blank group，other groups were given N-methyl-N′-nitro-N-nitrosoguanidine freely drinking combined with abnormal ingestion method to induce CAG model. After end of modeling ，administration groups were given relevant medicine intragastrically ，blank group and model group were given constant volume of water intragastrically ，for consecutive 28 d. After end of medication ，ELISA method was used to determine the serum levels of IL- 1β and IL-6；the gastric mucosa tissue pathologic change was observed by HE staining；mRNA and protein expressions of JAK 1，STAT3，SOCS-3 and c-Myc in gastric mucosa tissue were detected by real-time PCR and Western blotting assay. RESULTS ：Compared with blank group ，the sparse and irregular glands with deep staining cell nucleus could be seen in the gastric mucosa of rats in model group ；serum levels of IL- 1 β and IL-6，mRNA and protein expressions of JAK 1，STAT3 and c-Myc in gastric mucosa tissue were increased significantly （P＜0.05），while mRNA and protein expression of SOCS- 3 in gastric mucosa tissue were decreased significantly （P＜0.05）. Compared with model group ， glandular arrangement of gastric mucosa was more orderly and the number of heavy stained cells was less in administration groups；serum level of IL- 6 and mRNA expression of c-Myc in gastric mucosa of rats was decreased significantly in Zhitong shunqi capsule low-dose group （P＜0.05），while the protein expression of SOCS- 3 was increased significantly （P＜0.05）； serum levels of IL- 1β and IL-6，mRNA expressions of JAK 1，STAT3 and c-Myc in gastric mucosa tissue ，protein expression of JAK1 were decreased significantly in Zhitong shunqi capsule medium-dose group （P＜0.05），while mRNA and protein expression of SOCS- 3 was increased significantly in gastric mucosa tissue （P＜0.05）；above indexes were improved significantly in positive control group and Zhitong shunqi capsule high-dose group （P＜0.05）. Compared with positive control group ，mRNA and protein expression of STAT 3 in gastric mucosa tissue were decreased significantly in Zhitong shunqi capsule high-dose group （P＜0.05）. CONCLUSIONS：Zhitong shunqi capsule can improve CAG model rat to certain extent ，the mechanism of which may be associated with the down-regulation of mRNA and protein of JAK 1，STAT3 and c-Myc ，and up-regulation of mRNA and protein of SOCS-3.