1.Study on the pretreatment of the series of HPD macroporous adsorption resin.
Cun-Qin JIA ; Yang-Chun LI ; Peng-Fei TU ; Hong-Quan ZHANG
China Journal of Chinese Materia Medica 2005;30(18):1425-1470
OBJECTIVETo develop a method for the pretreatment of the series of HPD macroporous adsorption resin (MAR).
METHODThe effect of 2% NaOH to pretreatment of the series of HPD MAR was studied by gas chromatography and UV spectrometery.
RESULTThe eluting effect by ethanol was better after the MAR was marinated and eluted by 2% NaOH.
CONCLUSIONThe pretreatment of the series of HPD MAR was: after marinated and eluted by 2% NaOH, the series of HPD MAR were eluted by ethanol at 2 BV x h(-1) at 60 degrees C for 3-4 bed volumes (BV). At then the UV absorbance of eluate was 0.2-0.5. Benzene was not detected and the other residues less than 10 mg x L(-1) in eluted-MAR by GC. And the MARs match to the standard of medicine.
Adsorption ; Chromatography, Gas ; Drug Contamination ; Ethanol ; Naphthalenes ; analysis ; Resins, Synthetic ; chemistry ; Sodium Hydroxide ; Spectrophotometry, Ultraviolet ; Toluene ; analysis
2.Study on detection of samples of Rh-weak D and Del.
Xiao-Zhu WANG ; Jiong-Cai LAN ; Xu-Hua WU ; Hua-You ZHOU ; Wei-Jia LIU ; Dan LIU ; Cun-Sheng QI ; Feng-Qin ZENG ; Ke-Qing DU
Journal of Experimental Hematology 2005;13(3):509-511
To study the detection of weak D and Del from samples initially screened RhD(-), RhD phenotype was initially screened by routine serological test, out of which weak D phenotype was detected by indirect antiglobulin test (IAT) and Del phenotype was detected by chloroform-trichloroethylene absorption-elution test. The results showed that 56 samples were RhD(-) confirmed by routine serology test, which were screened out of 26 200 donors, among them 5 samples were typed as weak D by IAT and 9 cases samples were typed as Del by absorption-elution test. In conclusion, the samples which typed as RhD(-) by routine serological test must be identified by IAT and chloroform-trchloroethylene absorption test is order to detect weak D and Del phenotype. It is important for clinical transfusion safely.
Blood Donors
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Blood Grouping and Crossmatching
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methods
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standards
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Epitopes
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immunology
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Erythrocytes
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immunology
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Humans
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Rh-Hr Blood-Group System
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blood
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immunology
3.Based on EMR for design of telemedical regional healthcare platform.
Qi LIU ; Cheng-Yong QIN ; Xi-Yu ZHANG ; Jia-Jun DU ; Xiao-Lin SUN ; Qing-Lai GAO ; Zong-Yong CHEN ; Ping WANG ; Cun-Xiang WANG
Chinese Journal of Medical Instrumentation 2009;33(5):347-350
According to international medical information standard and Chinese healthcare management criterion,this paper study EMR features which focus on standard documents exchange and sharing.Tele Regional Healthcare Platform is established by EMR in order to realize medical resource sharing between big hospital in the situation of China, one solution is offered to stave difficulty and high expense of medical service in countryside.
Computer Communication Networks
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Medical Records Systems, Computerized
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Software Design
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Telemedicine
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instrumentation
;
methods
4.Protective effect and mechanism of Ershiwuwei Zhenzhu Pills on cerebral apoplexy rats.
Zhi-Jia LIU ; Cun-Ping WANG ; Bin YANG ; Nan WANG ; Qin WANG ; Jian GU ; Rui TAN
China Journal of Chinese Materia Medica 2022;47(8):2064-2073
To study the protective effect of Ershiwuwei Zhenzhu Pills on ischemic stroke rats. Ninety 4-weeks-old SPF male SD rats were randomly divided into 6 groups(n=15):sham operation group, model group, nimodipine group(12 mg·kg~(-1)), Ershiwuwei Zhenzhu Pills high-dose group(400 mg·kg~(-1)), Ershiwuwei Zhenzhu Pills medium-dose group(200 mg·kg~(-1)), Ershiwuwei Zhenzhu Pills low-dose group(100 mg·kg~(-1)).The permanent middle cerebral artery occlusion model(PMCAO) was established in the model group, nimodipine group, and Ershiwuwei Zhenzhu Pills groups by the improved thread plug method, while the sham operation group did not insert the thread plug.Nimodipine group and Ershiwuwei Zhenzhu Pills groups were given intragastric administration once a day for 24 days before the modeling operation, and once 1 hour before the modeling operation, while sham operation group and model group were given equal volumes of distilled water.The neuroethology of the surviving rats was measured; The volume of cerebral infarction in rats was measured by TTC method; The histopathology of rat brain was observed by HE method; The expression levels of tumor necrosis factor α(TNF-α),interleukin-1β(IL-1β),interleukin-6(IL-6),malondialdehyde(MDA),superoxide dismutase(SOD) and catalase(CAT) in serum were detected by ELISA;The mRNA expressions of Notch 1,Jagged 1,Hes 1 and Bcl-2 in rat brain were detected by RT-PCR;Western blot was used to detect the expression levels of caspase-3 protein in rat brain; the expression levels of vascular endothelial growth factor(VEGF) and CD34 positive cells in rat brain were detected by immunofluorescence.The low, medium and high dose groups of Ershiwuwei Zhenzhu Pills and nimodipine group could significantly reduce the neurobehavioral score and cerebral infarction volume of rats with permanent middle cerebral artery occlusion, reduce the morphological changes of nerve cells, decrease the expression of TNF-α,IL-1β and IL-6 in rat serum, increase the activity of SOD and CAT,and reduce the level of MDA.Furthermore, the expression levels of Notch l, Jagged l, Hes l and Bcl-2 mRNA were significantly increased, and the expression level of caspase-3 protein was decreased.Meanwhile, the number of VEGF and CD34 positive cells increased in the treatment group.The differences were statistically significant. Ershiwuwei Zhenzhu Pills has a protective effect on ischemic stroke rats, and its mechanism may be related to anti-inflammation, anti-oxidation, promotion of nerve cell proliferation, inhibition nerve cell apoptosis and promotion of angiogenesis.
Animals
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Caspase 3/metabolism*
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Drugs, Chinese Herbal/pharmacology*
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Infarction, Middle Cerebral Artery/drug therapy*
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Interleukin-6/metabolism*
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Ischemic Stroke/drug therapy*
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Male
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Nimodipine/pharmacology*
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Proto-Oncogene Proteins c-bcl-2/metabolism*
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RNA, Messenger
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Rats
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Rats, Sprague-Dawley
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Superoxide Dismutase/metabolism*
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Tumor Necrosis Factor-alpha/metabolism*
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Vascular Endothelial Growth Factor A/metabolism*
5.TRAF6 promotes Bacillus Calmette-Guérin-induced macrophage apoptosis through the intrinsic apoptosis pathway.
Qin Mei MA ; Li LIU ; Jia Lin YU ; Zhao Qian GONG ; Xiao Ping WANG ; Xiao Ling WU ; Guang Cun DENG
Journal of Southern Medical University 2022;42(9):1279-1287
OBJECTIVE:
To investigate the role of tumor necrosis factor receptor-associated factor 6 (TRAF6) in regulating Bacillus Calmette-Guérin (BCG)-induced macrophage apoptosis.
METHODS:
The expression of TRAF6 in peripheral blood samples of 50 patients with active tuberculosis (TB) and 50 healthy individuals were detected using quantitative real-time PCR (qPCR). RAW264.7 macrophages were infected with BCG at different MOI and for different lengths of time, and the changes in expressions of Caspase 3 and TRAF6 were detected with Western blotting and qPCR. In a RAW264.7 cell model of BCG infection with TRAF6 knockdown established using RNA interference technique, the bacterial load was measured and cell apoptotic rate and mitochondrial membrane potential (MMP) were determined with flow cytometry. The expression levels of TRAF6, Caspase 3, PARP, BAX and Bcl-2 in the cells were detected using Western blotting, and the expressions of TRAF6 and Caspase 3 were also examined with immunofluorescence assay.
RESULTS:
The expression of TRAF6 was significantly upregulated in the peripheral blood of patients with active TB as compared with healthy subjects (P < 0.001). In RAW264.7 cells, BCG infection significantly increased the expressions of Caspase 3 and TRAF6, which were the highest in cells infected for 18 h and at the MOI of 15. TRAF6 knockdown caused a significant increase of bacterial load in BCG-infected macrophages (P=0.05), lowered the cell apoptotic rate (P < 0.001) and reduced the expressions of Caspase 3 (P=0.002) and PARP (P < 0.001). BCG-infected RAW264.7 cells showed a significantly increased MMP (P < 0.001), which was lowered by TRAF6 knockdown (P < 0.001); the cells with both TRAF6 knockdown and BCG infection showed a lowered BAX expression (P=0.005) and an increased expression of Bcl-2 (P=0.04).
CONCLUSION
TRAF6 promotes BCG-induced macrophage apoptosis by regulating the intrinsic apoptosis pathway.
Apoptosis
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BCG Vaccine
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Caspase 3/metabolism*
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Humans
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Intracellular Signaling Peptides and Proteins
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Macrophages
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Mycobacterium bovis/metabolism*
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Poly(ADP-ribose) Polymerase Inhibitors
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TNF Receptor-Associated Factor 6/metabolism*
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bcl-2-Associated X Protein/metabolism*
6.A novel robust nomogram based on peripheral monocyte counts for predicting lymph node metastasis of prostate cancer.
Jia-Wei ZHOU ; Yun-Hua MAO ; Yang LIU ; Hai-Tao LIANG ; Chandni Chandur SAMTANI ; Yue-Wu FU ; Yun-Lin YE ; Gang XIAO ; Zi-Ke QIN ; Cun-Dong LIU ; Jian-Kun YANG ; Qi-Zhao ZHOU ; Wen-Bin GUO ; Kang-Yi XUE ; Shan-Chao ZHAO ; Ming-Kun CHEN
Asian Journal of Andrology 2021;23(4):409-414
Accurate methods for identifying pelvic lymph node metastasis (LNM) of prostate cancer (PCa) prior to surgery are still lacking. We aimed to investigate the predictive value of peripheral monocyte count (PMC) for LNM of PCa in this study. Two hundred and ninety-eight patients from three centers were divided into a training set (n = 125) and a validation set (n = 173). In the training set, the independent predictors of LNM were analyzed using univariate and multivariate logistic regression analyses, and the optimal cutoff value was calculated by the receiver operating characteristic (ROC) curve. The sensitivity and specificity of the optimal cutoff were authenticated in the validation cohort. Finally, a nomogram based on the PMC was constructed for predicting LNM. Multivariate analyses of the training cohort demonstrated that clinical T stage, preoperative Gleason score, and PMC were independent risk factors for LNM. The subsequent ROC analysis showed that the optimal cutoff value of PMC for diagnosing LNM was 0.405 × 109 l