1.The effect of Huangqi injectionon theimmune function and myocardial enzymes of the children with viral myocarditis
International Journal of Traditional Chinese Medicine 2016;38(4):333-335
ObjectiveTo investigate the effect of Huangqiinjection on the immune function of cardiomyocytes and myocardial enzymes of the children with viral myocarditis.MethodsA total of 86 patients who met the inclusion criteria of viral myocarditis were randomized into two groups. Fourty-onepatients in the control group took 1, 6 Fructose Diphosphate (FDP), and 86 patients of the treatment group tookHuangqi injection based on the intervention of control group. Both groups were treated for three weeks. The main outcomes were myocardial enzymes and immune function of cardiomyocytes.ResultsTotal effective rate of treatment group was significantly higher than the control group (95.56%vs. 80.49%;χ2=4.740,P<0.05). After treatment, the levels of CD3+ (64.9% ± 8.8%vs. 52.7% ± 8.2%,t=6.633), CD4+ (41.7% ± 6.5%vs.37.3% ± 7.2%,t=2.978), CD8+ ( 28.9% ± 4.2%vs.26.4% ± 4.3%,t=2.726) of treatment group were siginificantly higher than the control group (P<0.05). The CK (129.7 ± 29.8 U/Lvs. 167.7 ± 34.5 U/L,t=-5.479), CK-MB (12.7 ± 4.2 U/L vs.18.9 ± 6.2 U/L,t=-5.472), LDH (165.3± 38.4 U/Lvs.197.2 ± 46.3 U/L,t=-3.489), cTnⅠ(0.129 ± 0.012μg/Lvs. 0.204 ± 0.071μg/L,t=-6.981) of treatment group were significantly lower than the control group (P<0.05). Conclusion Huangqiinjection can significantly improve the clinical efficative rates, the immune function of cardiomyocytes and reduce the myocardial enzymes of children with viral myocarditis.
2.Improved automated method for isolation of canine pancreatic islets
Jun XING ; Yanbo CHENG ; Jianyu WU ; Yi ZHOU ; Chun SONG ; Chunfang SONG
Chinese Journal of General Surgery 1993;0(03):-
Objective To study an improved automated method for isolation and purification of large amounts of human pancreatic islets from large mammals,and try to create conditions for preparation and isolation of large amounts of human islets.Methods An improved automated system was used to isolate and purify panreatic islets of sogs.Under the general anaesthesia(GA) condition,the pancreas of the dogs was via in situ vascular perfused using cold HC-A solution and then removed en bloc with duodenum and spleen.Then they were placed in cold UW aolutian.Intraductal collagenase-Ⅴ and pefabloc(4 ℃) was delivered with controlled perfusion.lslets were dissociated in system of Ricordi Chamber and purified islets separated with Ficoll density gradient centrifugation under controlled temperature.Digestion time,islets remaining trapped in exocrine tissue,final islet purity,insulin and C-pep secretory activity,and islet recovery were observed.The purified islets were observed under light microscope and electronic microscope after 24 h culture.Results The digestion time rate was(25.0?6.0) min,islets remaining trapped in exocrine tissue was(9.4?2.4)%,final islet purify rate was(89.7?3.5)%,islet recovery after digestion was(17.2?3.6)?104 IEQ/pancreas.Islet recovery after purification was(8.3?2.0)?104IEQ/pancreas.Insulin and C-pep secretory activity of the purified islets and their ultrastructure after 24 h culture were ideal.Conclusions Our improved automated method and facilities for isolation of canine pancreatic islets are reliable,The morphology and function of the procured islets are excellent and they can foreseeably be used for large-scale preparation of huma islets for clinical use.
3.Effects of losartan on oxygen free radicals,cell apoptosis and Bcl-2 expression in ischemia-reperfusion injury of pancreas in rats
Jun XING ; Ping XU ; Desen LIANG ; Yanbo CHEN ; Aidong LI ; Chun SONG ; Chunfang SONG
Chinese Journal of General Surgery 1997;0(06):-
Objective To investigate the protective effect of losartan on acute ischemia-reperfusion(I/R)(injury) of pancreas in rats.Methods Seventy-two Wister rats were randomly divided into 3 groups:(1)(Control group);(2)Ischemia-reperfusion group:the anterior mesenteric artery and the celiac artery were(occluded) for 15 min,30min and 60min followed by 6 hours reperfusion;(3)Losartan group:losartan(40mg/kg)were administered by gavage at 12h and 1h before arterial occlusion.The pathologic changes of pancreatic tissue were observed under light microscopy;TUNEL was used to detect apoptosic of pancreatic cells;Bcl-2 expression in the pancreatic cells of rats was analyzed by immunohistochemistry technique.(Results) Losartan treatment reversed the histological abnormalities including infiltration of inflammatory cells and atrophy of acinar cells.Compared with losartan group,pancreatic tissue of I/R group exhibited increased MDA[((20.1?1.2))nmol/g and((34.9?2.6)) vs(17.9?2.1)nmol/g and(25.2?3.3)nmol/g,P
4.Directed evolution of aflatoxin detoxifzyme in vitro by error-prone PCR.
Sai ZHANG ; Keke XING ; Yadong HU ; Chunfang XIE ; Daling LIU ; Dongsheng YAO
Chinese Journal of Biotechnology 2011;27(7):1100-1108
The experiment was conducted by directed evolution strategy (error-prone PCR) to improve the activity of aflatoxin detoxifzyme with the high-throughput horse radish peroxidas and recessive brilliant green (HRP-RBG) screening system. We built up a mutant library to the order of 10(4). Two rounds of EP-PCR and HRP-RBG screening were used to obtain three optimum mutant strains A1773, A1476 and A2863. We found that mutant A1773 had upper temperature tolerance of 70 degrees C and that its enzyme activity was 6.5 times higher than that of the parent strain. Mutant strains A1476 worked well at pH 4.0 and its enzyme activity was 21 times higher than that of the parent strain. Mutant A2863 worked well at pH 4.0 and pH 7.5, and its enzyme activity was 12.6 times higher than that of the parent strain. With DNA sequencing we found that mutant A1773 revealed two amino acid substitutions, Glu127Lys and Gln613Arg. Mutant A1476 revealed four amino acid substitutions: Ser46Pro, Lys221Gln, Ile307Leu and Asn471lle. Mutant A2863 revealed four amino acid substitutions: Gly73Ser, Ile307Leu, Va1596Ala and Gln613Arg. The results provided a useful illustration for the deep understanding of the relationship between the function and structure of aflatoxin detoxifzyme.
Aflatoxin B1
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antagonists & inhibitors
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chemistry
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Amino Acid Substitution
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Directed Molecular Evolution
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Enzyme Activation
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Enzyme Stability
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Multienzyme Complexes
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genetics
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metabolism
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Mutant Proteins
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genetics
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metabolism
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Point Mutation
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Polymerase Chain Reaction
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methods
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Protein Engineering
5. Comparison on the 10 years risk for ischemic cardiovascular disease among Han, Uygur, Kazak population from Xinjiang Uygur Autonomous Region
Xing LI ; Chunfang SHAN ; Fen LIU ; Jun WANG ; Xiaomei LI ; Yitong MA ; Xiang XIE ; Zixiang YU ; Yining YANG
Chinese Journal of Cardiology 2019;47(6):486-491
Objective:
To compare the 10 years risk for ischemic cardiovascular disease among Han, Uygur, Kazak nationality residents of Xinjiang Uygur Autonomous Region.
Methods:
From October 2007 to October 2010,14 618 adult (aged ≥35 years) Han (