1.Implement innovation of scientific research administration based on human being
Chinese Journal of Medical Science Research Management 2008;21(3):139-140
The human oriented concept is the new principle of scientific research administration. According to the character of scientific research administration. the nlain task of its innovation is to change administrator's concept. to make administrative management becoming service, as well as to enhance service consciousness. It is needed to establish high-qualified scientifie research administrative team with seeking truth from facts and human oriented concept. on the basis of the hospital administration. Meanwhile, improring continuously the administrator's quality is also important measure for adaptation of knowledge economic era
2.EXPRESSION OF DENDRITIC CELL MOLECULE MARKER AND ITS RELATION WITH T CELL IN HUMAN BREAST CANCER
Acta Anatomica Sinica 1953;0(01):-
Objective To investigate the numbers and distribution of dendritic cells and the expressive intensity of CD1c,S-100,HLA-DR and its relation with T cell in human breast cancer tissues,and to discuss the relationship between dendritic cell(DCs) and developing of breast cancer.The study can provide the experimental data in the further biological therapy of breast cancer. Methods The human breast cancer tissues and relatively normal breast tissues were collected from surgical operation and the samples of 20 patients with breast cancer were analyzed by immunocytochemistry and computer imaging techniques. Results The result showed that the expressive intensity of CD1c,S-100,HLA-DR was dramatically weaker in breast cancer tissues than in those of relatively normal breast tissues(P
4.Effect of prokinetic agents on the electrical activity of stomach and duodenum in rats
Fujun LI ; Yiyou ZOU ; Tianhui HUANG
Journal of Central South University(Medical Sciences) 2009;34(7):599-602
Objective To determine the effect of prokinetic agents such as domperidone, mo-sapride, clarithromycin, and itopride on the electrical activity of the stomach and duodenum in SD rats, and also to explore the mechanism. Methods The organism functional experiment system BL-420E was used to record the myoelectrical activity in the stomach and duodenum of SD rats in all groups using domperidone, mosapride, itopride, clarithromycin, and physiological saline on the inter-digestive phase. The effect of the prokinetic agents on the amplitude and freqency of gastric and duo-denal electromyologram in the SD rats was compared. The antagonists such as atropine, phento-lamine, and propranolol were added to investigate the mechanism of action with all prokinetic agents. Results All prokinetic agents increased the amplitude and frequency of gastric and duodenal fast waves in the SD rats (P<0.05). The effect of itopride was the most obvious among the 3 groups (P<0.05), and clarithromycin had the weakest effect (P<0.05). The amplitude and frequency of gastric and duodenal fast waves in the SD rats in the groups of clarithromycin, domperidone, mosa-pride, itopride, and physiological saline were inhibited by atropine (P<0.05) , but not by phento-lamine and propranolol. Conclusion Itopride, mosapride, domperidone, and clarithromycin can in-crease the amplitude and frequency of gastric and duodenal fast waves in the SD rats. The mechanism may be related to cholinergic receptors, but not adrenergic receptors.
5.Current Diagnosis and Therapy Advancement of Solid Pseudopapillary Tumor of The Pancreas
Chinese Journal of Bases and Clinics in General Surgery 2003;0(05):-
Objective To summarize the current diagnostic and therapeutic advancement of solid pseudopapillary tumor of the pancreas.Methods Relevant literatures about the diagnosis and treatment of solid pseudopapillary tumor of the pancreas,which were published recently domestic and abroad were collected and reviewed.Results Solid pseudopapillary tumor of the pancreas is now considered to be a low-grade malignancy with characteristic clinical,imaging and pathological features.Resection is considered to be the optimal choice with favourable prognosis.Conclusion An awareness of the features may guide us to a correct diagnosis and treatment of this rare neoplasm,but the deep understanding of the disease needs the accumulation of more cases and fundamental research.
6.The influence of large volume slow speed paracentesis on kidney blood flow in patients with cirrhosis
Fujun LI ; Huixiang YANG ; Yiyou ZOU
Chinese Journal of Practical Internal Medicine 2002;0(08):-
Objective To study investigate the influence of large volume slow speed paracentesis on kidney blood flow in patients with cirrhosis.Methods Plasma rennin(PRA),angiotensin-Ⅱ,aldosterone(ALD)and blood pressure,pulse were detected before and 1 hour after large volume slow speed paracentesis in 15 paients.Results After paracentesis,patients had significant reductions in diastolic pressure[(76.0?7.9)mm Hg vs(70.7?8.0)mm Hg,P
7.The Relationship of Gene Expression Levels of Proinflammation Cytokines, Tyrosine Hydroxylase of Schizophrenic and PANSS Score
Liang LIU ; Fujun JIA ; Hengfen LI
Chinese Mental Health Journal 1989;0(03):-
0.05), but each gene expression level was higher in schizophrenic or siblings than in normal controls (P
8.Interleukin-6 Inhibits the Expression of Apolipoprotein M in HepG2 Cells
Li LI ; Gang GUO ; Yunzhao TANG ; Fujun SUN ; Daiqing LI
Tianjin Medical Journal 2010;38(3):216-218
Obiective:To investigate the effect of interleukin-6(IL-6)on apolipoprotein(apo)M expression in a human hepatoblastoma cell line(HepG2).Methods:HepG2 cells were cultured and incubated with different concentrations of IL-6 (0,1.25,2.5,5,10,20,40 and 80 μg/L)for 24 hours.After the incubations,total RNAs were extracted and applied to reverse transcript PCR and real-time quantitative PCR to detect the expression levels of apoM and apoA-I.The effect of IL-1α on apoM expression was also determined.Results:IL-6 significantly inhibited the expression of apoM(F=10.778,P < 0.01).Whereas IL-6 did not influence the expression of apoA-I(F=2.004,P > 0.05).IL-1α(0,1.25,2.5,5,10,20,40 and 80 μg/L)did not decrease the expression of apoM(F=2.038,P > 0.05).Cooclusion:IL-6 inhibits apoM mRNA transcription,which may contribute to the pathogenesis of abnormal lipid metabolism and macrovascular complications in type 2 diabetes.
9.An in vivo study on pharmacodynamics of 4-aminosalicylic acid oral colon-specific delivery coated tablets
Yan LI ; Hongjian LI ; Yukui MA ; Fujun SUN
Chinese Journal of New Drugs and Clinical Remedies 2007;26(1):6-11
AIM: To examine the pharmacodynamics of a self-developed oral colon-specific delivery coated tablets of 4-aminosalicylic acid (4-ASA) on rats. METHODS: Ulcerative colitis rat model was developed by intrarectal administration of 2, 4, 6-trinitrobenzenesulfonic acid (TNBS) in alcohol. Rats were divided randomly into healthy control group, TNBS control group, TNBS + lower dose (coated tablets) group, TNBS +medium dose (coated tablets) group, TNBS + higher dose (coated tablets) group, TNBS + sulfasalazine (SASP) group, TNBS + medium dose non-coated tablet group. Several indices including macroscopic change,histological damage, and tissue myeloperoxidase (MPO) activity were examined after 5 consecutive oral drug administration to assess pharmacodynamics of the coated tablets. RESULTS: An experimental ulcerative colitis in rats was induced by TNBS. Compared with 4-ASA non-coated tablet group, decreased macroscopic and histological damage score and lower MPO activity were observed after the oral administration of 4-ASA coated tablets or SASP. There was no significant difference between the effects on the indices of higher dose of coated tablets and SASP (P > 0.05) CONCLUSION: The self-made 4-ASA oral colon-specific delivery coated tablet showes higher effect than non-coated tablets to treat ulcerative colitis in rats.
10.Effects of titanium ions on the proliferation and activation of T lymphocytes in vitro
Fujun CHEN ; Donghui CHEN ; Qian YANG ; Chang LI ; Li TANG
Chinese Journal of Tissue Engineering Research 2016;20(52):7781-7787
BACKGROUND:Titanium ions have been proved to stimulate the secretion of bone remodeling-related factors from T lymphocytes;however, the effects of titanium ions on the early activation, intermediate activation, and cel cycle of T lymphocytes remain unclear. OBJECTIVE:To investigate the effects of titanium ions on the proliferation and activation of T lymphocytes in vitro. METHODS:Cel proliferation and cycle test:Jurkat E6-1 T lymphocytes in logarithmic phase were col ected and cultured in the medium containing 0 (control), 25 (low concentration), 50 (middle concentration), and 100μmol/L (high concentration) titanium ions for 24 hours to detect the cel relative proliferation rate and cel cycle. Cel activation trial:Jurkat E6-1 T lymphocytes were divided into two groups that were subdivided into four groups containing 0, 25, 50, and 100μmol/L titanium ions, respectively with or without phytohemagglutinin (PHA) pre-stimulation. The expressions of CD69 and CD25 were measured after cultured for 24 hours. RESULTS AND CONCLUSION:Titanium ions enhanced T lymphocytes proliferation in a concentration-dependent manner (P<0.05). Compared with the control group, the percentages of G0/G1 phase decreased and the proportions of cel s in S and G2/M phase increased significantly in the low, middle and high concentration groups (P<0.05). The proportion of G0/G1-phase cel s in the high concentration group was less and the proportion of G2/M phase cel s was higher than those in the middle and low concentration groups (P<0.05). With PHA pre-stimulation, the expression of CD69 in the high concentration group was higher than that in the middle and low concentration groups (P<0.05);whereas the difference of CD25 expression was not significant among four subgroups. Titanium ions promoted the expression of CD69 in a concentration-dependent manner (P<0.05), but there was no CD25 expression in each subgroup without PHA pre-stimulation. To conclude, titanium ions can significantly promote T lymphocyte proliferation and early activation in vitro, and moreover, induce S and G2/M phase arrest in T lymphocytes.