Objective To explore the effect of different cold ischemia (CI) time on the changes of early intragraft cytokines (TNF-α and IL-6) and their correlation with regeneration after small-for-size (30% standard volume) liver transplantation (LT) in rats. Methods A model of Lewis rat 30% standard volume liver transplantation was established. The rats were divided into 3 groups: 1 h CI group, 8 h CI group and 16 h CI group (n= 20 in each group) according to the CI time of donor livers stored in UW solution. Survival rate at day 7 after LT in each group was recorded and specimens were collected at predetermined intervals from 90 min, 1, 2, 4 h and 7 day post-reperfusion. Expression patterns of TNF-αand IL-6 were determined and compared in 30% liver grafts with different CI time following transplantation. Progression of DNA synthesis of hepatocytes was confirmed by BrdU uptake. Morphological assessment of the liver grafts was also made. Results Operative success rate of LT was 100% in all groups. Mean survival rate in 1 h and 8 h CI group was 100% respectively (＞ 7 day). Mean survival rate in 16 h CI group was low, and no recipient animals survived on the postoperative day 7. Compared with 1 h CI group, IL-6 expression in 30% liver grafts stored for 8 h and 16 h was markedly increased post-transplantation (F=184.12, P<0.05). TNF-α expression in 30% liver grafts in 8 h and 16 h CI groups was markedly increased post-reperfusion (F=58.81, P< 0.05). There was no statistically significant difference in the expression of TNF-α and IL-6 between 8 h CI and 16 h CI groups. Number of positively stained nuclei in 1 h CI group was greater than that in 8 h CI group at 24 h after transplantation (t=5.59, P<0.05). At 24 h after transplantation histology showed mild injury in grafts of CI 1 h group. CI 8 h led to mild sinusoidal dilatation and inflammation.Grafts stored for 16 h demonstrated focal congestion, hepatocyte collapse and necrosis. Conclusion At the early stage of small-for-size liver transplantation, up-regulation of cytokines (TNF-α and IL-6) is an important factor in the liver regeneration. The early initiating signals for the regenerative response are present in the small-for-size liver grafts with different CI time.

Objective To screen antarctic bacteria producing EPA and analyse its composition of fatty acids.Methods Two hundred strains of bacteria were isolated from ice and soil of the Antarctic.The total lipid was extracted by using a modified one-phase Bligh and Dyer extraction,and screened by means of GC using fish oil as standard.In the end,eight strains of bacteria were screened which had high content of EPA or DHA.Among them,one bacterium(NJ136) which had the highest content of EPA was obtained,its total lipid was extracted by means of Soxhlet extractor,and the compositions of fatty acids were analysed by means of GC-MS.Results and conclusion The relative contents of EPA and total unsaturated fatty acids of NJ136 were 6.66% and(51.92%) respectively,the content of total fat,EPA and unsaturated fatty acids of dry bacteria weight were 7.94%,5.3 mg?g~(-1) and 41.2 mg?g~(-1),respectively.

Objective To observe the effects of intrathymic islet transplantation or renal subcapsule islet transplantation on the graft survival.Methods C57BL/6 mice were used as recipients and BALB/c as donors The recipients receiving intrathymic or renal subcapsule islet transplantation were divided into simple transplantation groups and the group intraperitoneally receiving rabbit antithymocyte serum(ATS) at the time of islet transplantation.Results The median survival time (MST) of simple intrathymic allografts were 19.5 days,longer than that of allografts implanted beneath the renal capsule.Administration of ATS at the time of islet transplantation delayed rejection of islets transplanted to the renal subcapsute(MST,43.0 days),and intrathymic allografts were superior(MST,93.8 days).Six of 8 intrathymic grafts with administration of ATS survived permanently.especially a state of donor-specific unresponsiveness was induced.Conclusion The thymus may be an immunoprivileged site for islet transplantation and may play an important role during the induction of immune tolerance.

Objective To explore the molecular mechanisms involved in liver regeneration after different cold ischemic (CI) times for the liver graft in 30% volume rat liver transplantation. Methods A model of 30% volume Lewis to lewis rat liver transplantation with hepatic artery reconstruction was established. Rats were grouped as follows: 1 h CI group (n =25), 8 h CI group (n =25) and 16h CI group (n = 25). Survival rate of rats in each group and liver regeneration were observed. Specimen were collected at predetermined intervals from 90 min, 1,4 and 7 d post-reperfusion. TNF-α and IL-6 expression, STAT3 activation were determined in liver grafts. Expression of cyclin D1 and hepatocyte replication with BrdU uptake were studied by immunohiatochemistry. Statistical analysis was used to compare BrdU positively stained hepatoeytes at 1 d post- reperfusion in each group. Results 30% liver transplantation was performed in a total of 75 rats. Compared with rats in 1 h CI group, TNF-α and IL-6 expression in 8 h CI and 16 h CI groups were markedly increased after 30% liver transplantation. STAT3 activity in 8 h CI and 16 h CI groups was significantly increased. Cyclin D1 expression in 8 CI group was demonstrated with cytoplasmic and nuclear staining. Grafts in 16 h CI group showed large areas with no cyclin D1 expression. Number of hepatoeytes with positively stained neclei in 1 h CI group was more than that in 8 h CI group at 1 d after transplantation (t = 6.14, P < 0.05). Conclusion Liver regeneration following 30% liver graft transplantation may be through TNF-α/IL-6/STAT3/ Cyclin D1/DNA synthesis pathways. The reason for 30% liver graft failure with significant cold ischemic injury is that hepatocytes may not respond to initiating signals for liver graft regeneration.

Objective To identify the molecular characteristics on nucleotide and amino acid in E gene through the comparative analysis of differences between genotype 3 Japanese encephalitis virus(JEV)in China and the live attenuated vaccine(SA14-14-2).Methods Obtained the E gene nucleotide sequence of Japanese encephalitis virus from GenBank.Multiple alignment and amino acid(AA)analysis were carried out by Clustal X(1.81),DNAStar and GENEDOC(3.2).According to the ribbon diagram of the E protein structure based on the model of the soluble fragment of tick-borne encephalitis virus(TBEV)as a template for Japanese encephalitis virus E protein amino acid sequence analysis.Results Compared different regions and different host genotype 3 JEV with SA14-14-2 the nucleotide sequence homology was,up 96%and 95% and the amino acid homology was up 95%and 94%,respectively.The nucleotide and amino acid homology was higher among the same area and the same host.Ten common amino acid variations and five special variations(E160 in domain Ⅰ,E123 and E227 in domain Ⅱ,E441 and E487 in non-structural domain)were found between genotype 3 JEV and SA14-14-2.Conclusion The homology in E gene was higher between genotype 3 JEV in China and SA14-14-2.Five special amino acid differences were found in genotype 3 JEV.The existing live attenuated vaccine strain is theoretically possible to protect genotype 3 JEV in China.

Objective:To study the influence of occlusal force change on apoptosis of periodontal ligament fibroblast(PDLF) and expression of proliferating nuclear antigen(PCNA) in the fibroblasts,so as to explore the possible mechanism for remodeling of periodontal ligament.Methods:Animal model of occlusal force change was established by extracting the right first,second and third maxillary molars in male SD rats.The rats were sacrificed at 6,12 hours and day 1,2,3,5,7,14,and 28 d after extracting the teeth(n=6),and their alveolar bone tissues were harvested.H-E staining was used to observe the morphologic changes of the alveolar bone tissues.TUNEL method and immunohistochemistry were used to detect apoptosis and PCNA expression in PDLF.The rats with normal occlusal forces were used as control(n=6).The results were assigned a mean score based on the percentage and the intensity of cells positively stained for TUNEL and PCNA.Results:Animal model of occlusal force change was successfully established.H-E staining showed that the control group had more pycnotic periodontal ligament,orderly fibres,and flatter alveolar bone than the model group.TUNEL result showed that the cell apoptosis reached its peak at 12 h after extracting the teeth(252.67?6.62),significantly higher than that of control group(7.17?2.32,P

Tumor is still an unresolved health problem for human.The main obstacle for tumor cure is that precise diagnosis of tumor at the early stage can't be realized,which leads to the mortality increased year by year due to missing the best time of the treatment.Furthermore,lack of targeted ability and serious side effects of the medicine used for tumor treatment also limit the clinical application.Therefore,it is urgent to design and develop a novel targeted drug delivery vehicle.Recent studies show that targeted nanomaterials are superior on tumor-specific diagnosis and target therapy.This review will highlight the current advances in the targeted nanomaterials effect on tumor diagnosis and treatment in recent years and prospect the foreground of future development.

Objective To investigate the clinical curative effect of“Qing Dynasty Palace manipulation” in combination with plaster immobilization and foot bath with traditional Chinese medicine for acute soft tissue sprain of the ankle.Method A total of 90 patients with acute soft tissue sprain of the ankle from emergency department of WangJing Hospital, CACMS were recruited from July 2013 to April 2014 and randomly divided into two groups with 45 patients in each. The patients in the treatment group were treated with the court manipulation, plaster and Chinese herbs washing, and those in the control group were only treated with cast immobilization. The clinical curative effect was evaluated using Baird-Jackson score system(excellent: 96-100; good: 91-95; fair: 81-90; poor: 0-80).Result At the second, third week after treatment, the excellent/good rates in the treatment group were significantly higher than those in the control group(at week 2: 73.3%vs. 44.4%;χ2=11.468,P<0.01; at week 3: 86.7%vs.60.0%;χ2=6.875,P<0.05). At week 2 and 3, Baird-Jackson scores in the treatment group(87.41±14.12, 93.16±9.51)and in the control group(76.32±11.41, 82.54±9.22)were significantly higher than those before treatment(treatment group: 72.11±12.61; control group: 71.67±13.12, allP<0.05); at week 3, Baird-Jackson score in the treatment group were significantly higher than that in the control group(P<0.05).Conclusion“Qing Dynasty Palace manipulation” in combination with plaster immobilization and foot bath with traditional Chinese medicine can increase Baird-Jackson score and aid recovery of the ankle function in patients with acute soft tissue sprain of the ankle.

Objective To study the molecular mechanisms of hepatoeyte regeneration following different cold preservation (CP) durations after rat partial liver transplantation. Methods Mate inbred Lewis rats were used as donors and recipients. Donor liver was kept in 4℃ UW solution for 1 h (coldisehemia 1 h group, CI 1 h group), 8 h (CI 8 h group) and 16 h (CI 16 h group) and then implantedorthotopieally. 50% liver graft transplantation model was established by ligating the left portion ofmedian lobe, left lateral lobe and caudate lobe with 3-O silk suture prior to reperfusion. Survival rate ofeach group and hepatoeyte regeneration were recorded after grafting. Reverse transcription-polymerasechain reaction was used to detect the expression of IL-6 and TNF-α in the liver tissues. Western blotanalysis was done to measure STAT3 activation in the liver. Immunohistoehemistry was conducted toanalyze the expression of cyclin D1 and hepatocyte replication with BrdU uptake in the graft. ResultsOperative success rate in all groups was 100%. Compared with CI 1 h group, the TNF-α and IL-6expression (F=67.45 for TNF-a comparison, P<0.05 and F=287.73 for IL-6 comparison,P<0.05 respectively) in 8 h CI and 16 h CI groups was markedly increased after partial grafttransplantation. STAT3 activity in 8 h C1 and 16 h C1 groups was also significantly increased ascompared with that in 1 h CI group. Cyclin D1 expression in 8 CI group was demonstrated withcytoplasmic and nuclear staining at 24 h after transplantation. Grafts in 16 h CI group showed largeareas with no cyclin D1 expression. Number of hepatocytes with BrdU positively stained neclei in 8 hCI group was more than that in 16 h C1 group at 24 h after transplantation (t=19.40, P<0.05).Conclusion Hepatocytes regeneration was present following rat partial transplantation in the graftspreserved for limited time, which may be regulated by TNF-α/IL-6' STAT3/ Cyelin D1/DNAsynthesis pathways; Hepatocytes could not respond to early signals for liver graft regeneration when50%liver graft preserved for 16 h.

Objective To explore the microsurgical techniques in establishing an orthotopic rat liver transplantation model of 20% small-for-size graft. Methods A rat liver transplantation model of 20% small-for-size liver graft was orthotopically performed. Forty male Lewis rats were used as 20 donors and 20 recipients. Donor liver was perfused with 4℃ UW solution via donor portal vein. Su-prahepatic inferior vena cava was anastomosed end-to-end with running suture. Infrahepatic inferior vena cava and portal vein were reconstructed by cuff technique. A sleeve anastomosis for hepatic artery was used. Continuity of the bile duct was established with an end-to-end intraluminal stent. Survival rate of the recipients was recorded and immunohistochemical analysis of hepatocyte replication con-firmed by bromodeoxyuridine (BrdU) uptake. Results Totally 20 liver transplantations of 20% par-tial liver graft were successfully performed. The successful rate of the operation was 100%. Survival rate of the recipients with 20% liver grafts was 93.8% (＞14 d). Histological examination showed normal liver structure with limited injury after transplantation. The number of positively stained nuclei was significantly increased at 72 h after transplantation. Conclusion The 20Z% small-for-size liver grafts initiate and complete the process of liver regeneration after transplantation. Skillful microsur-gery is the key to success of the transplantation model. The stable model is suitable for basic research in partial liver transplantation.