1.Comparison of the effect of interlocking minimally invasive percutaneous plating and interlocking intramedul-lary nailing in the treatment of tibial fractures of the lower tibia
Chinese Journal of Primary Medicine and Pharmacy 2016;23(16):2469-2472
Objective To observe the effect of interlocking minimally invasive percutaneous plating and interlocking intramedullary nailing in treating fractures of the lower tibia,thus to guide clinical treatment.Methods A retrospective analysis of 70 patients with tibial fractures of the lower tibia were made.All the patients were divided into interlocking minimally invasive percutaneous plating group (A group)and interlocking intramedullary nailing group (B group),35 cases in each group.The operative time,blood loss,fracture healing time,hospitalization time were compared,the ankle score after 1 month,3 months,6 months,9 months,12 months were recorded,the complica-tions(loose,broken nails,deep infection,superficial infection,delayed union,malunion,joint pain)were observed,the Johner Wruh method was used to evaluate the clinical efficacy of postoperative tibial functional recovery.Results The operative time of A group and B group were (130.2 ±40.1)min and (96.4 ±30.5)min,A group was signifi-cantly longer than B group (t =3.853,P <0.05).There were no differences between A group and B group in bleed-ing amount,fracture healing time,hospitalization time (t =0.336,0.228,1.743,all P >0.05).There were no differ-ences between A group and B group in the ankle score after 1 month,3 months,6 months,9 months,12 months(t =0.855,1.315,1.527,0.787,0.885,both P >0.05).The clinical efficacy of tibia functional recovery in A group and B group were 97.14% and 94.29%,the difference was not statistically significant (χ2 =0.354,P >0.05).The inci-dence rates of loose,broken nails,deep infection,superficial infection,delayed healing in A group and B group had no difference (χ2 =0,0.348,1.014,3.134,0.348,all P >0.05),the incidence rates of malunion and joint pain in A group and B group were 2.86% and 20%,25.71% and 48.57%,which of A group were significantly lower than B group,the differences were statistically significant (χ2 =5.081,3.916,all P <0.05).Conclusion Interlocking min-imally invasive percutaneous plating and interlocking intramedullary nailing have exact effect in treatment of tibial fractures of the lower tibia,the effect of both methods has no difference,but interlocking minimally invasive percutane-ous plating has lower rate of malunion and knee pain,and suits for fracture patients with good soft tissue condition,but interlocking intramedullary nailing suits for fracture patients with poor soft tissue condition,fracture patients with good soft tissue condition and simple fracture,should master surgical indications of both surgery.
2.Protease-activated receptor 1 challenges human lung epithelial cells to produce MCP-1
Haiyan WANG ; Shaoheng HE ; Yanshan ZHENG
Journal of Third Military Medical University 2003;0(17):-
Objective To investigate the actions of PAR1 agonists and thrombin on the secretion of monocyte chemoattractant protein (MCP)-1 from human lung epithelial cells. Methods A549 cells were cultured in a 12-well culture plate. The challenge was performed by addition of various concentrations of PAR1 agonist peptides SFLLR and its reverse peptides RLLFS, thrombin or thrombin inhibitor named hirudin into each well, respectively. After 2 h or 16 h, the reactions were terminated by removal of the supernatant from each well. A sandwich ELISA was used to determine the levels of MCP-1 in supernatants. Results Following 16 h incubation, SFLLR could induce concentration-dependent secretion of MCP-1. The maximum release of MCP-1 was nearly 12-fold more than baseline release. The reverse PAR1 agonists had little effects on MCP-1 release. Thrombin could induce concentration-dependent secretion of MCP-1. As low as 3 000 U/L thrombin could induce MCP-1 release from epithelial cells, and the maximum of accumulated release of MCP-1 was observed with 10 000 U/L thrombin, which was 5-fold more than baseline release. Thrombin inhibitor hirudin could inhibit thrombin induced secretion of MCP-1. The time course showed that the actions of PAR1 agonist peptides SFLLR and thrombin initiated at 2 h and reached their peak at 16 h. Conclusion PAR1 agonist peptides and thrombin are potent secretogogue of MCP-1 release from cultured human lung epithelial cells, and PAR1 antagonists and thrombin inhibitor may possess the ability to inhibit airway inflammation.
3.Development of cell model of polymer/liquid crystal and effect of their elasticity on adhesion of rBM-MSCs
Yanshan GUO ; Hao WU ; Liheng ZHENG ; Yupan SHANG ; Mei TU ; Jiaqing ZHANG
Chinese Journal of Pathophysiology 2015;(6):1064-1069
[ ABSTRACT] AIM:To develop the cell model of polymer/liquid crystal and to study the effect of their elasticity on the adhesion of rat bone marrow mesenchymal stem cells (rBM-MSCs).METHODS: Using the method of solvent e-vaporation induced phase separation, the cell model of polymer/liquid crystal was constructed.The surface morphology and phase separation structure were determined by polarized optical microscopy ( POM) , scanning electron microscopy ( SEM) and small angle X-ray scattering ( SAXS ) .rBM-MSCs were separated and expanded by adherent culture.The surface markers of rBM-MSCs were detected by flow cytometry.The cells were induced to osteogenic differentiation and adipogenic differentiation for 2 weeks.After 3 passages, the cells were divided into 4 groups, including total PU control group, 10%membrane group, 30%membrane group and 50%membrane group.The cells were then incubated with rhodamine phalloi-din for cytoskeleton staining and were observed under the confocal laser scanning microscope after cultured for 24 h.RE-SULTS:The cell model of polymer/liquid crystal was constructed successfully using the method of solvent evaporation in-duced phase separation.Flow cytometry results showed that the rBM-MSCs positively expressed CD29, CD44 and CD90, and negatively expressed CD34 and CD45.After stained with alizarin red S and oil red O, the calcium nodule and lipid droplets in rBM-MSCs were observed obviously.The cytoskeleton staining result indicated that the area in total PU control group, 10%membrane group and 30%membrane group were greater, and the actin microfilaments were also clearer than
that in 50%membrane group.CONCLUSION:The cell model with suitable content of liquid crystal made a contribution to the rBM-MSCs’ adhesion, but too much liquid crystal inhibits cell adhesion.
4.Construction of Hi FGF2 eukaryotic expression plasmids and its over-expression induced cell apoptosis
Zhonglin CHEN ; Hongyan JIANG ; Xiaobing HONG ; Zhonghua CHEN ; Yanshan ZHENG ; Han XU ; Ganggang SHI ; Zhanqin HUANG
Chinese Pharmacological Bulletin 2014;(11):1535-1538
Aim To construct eukaryotic expressing plasmid of hi FGF2 ( high molecular weight isoform fi-broblast growth factor-2,hi FGF2) gene and to investi-gate its effect on apoptosis after its overexpression in HEK293 cells. Methods The DNA template primer was designed and synthesized. The pDsRed1-N1 plas-mids were digested by the restriction enzymes of Nhel and Hind III. The hi FGF2 was ligated with linearized pDsRed1-N1 by T4 DNA Ligase. The recombinant plasmid was identified by endonuclease digestion and sequenced. The recombinant hi FGF2 plasmid was transient transfected into HEK293 cells by Lipofectami-neTM 2000 Reagent. The transfection efficiency was de-tected by fluorescence inversion microscope. The cell apoptosis was detected by Annexin V-FITC/PI apopto-sis detection kit with flow cytometry analysis. Results The pDsRed1-N1 eukaryotic expression vector was consistent with the design. The recombinant hi FGF2 plasmid was transfected in HEK293 cells. The trans-fection rate was more than 70%. The FITC/PI dyeing rate in hi-FGF2 over-expression HEK297 cells was a-bout ( 29. 12 ± 2. 81 )%. Conclusions pDsRed1-N1 eukaryotic expression vector is successfully constructed and transfected into HEK293 cells. Over-expression of hi FGF2 induces cell apoptosis.
5.Three-dimensional reconstruction of carp brain tissue and brain electrodes for biological control.
Yong PENG ; Aidi WANG ; Tingting WANG ; Jinglong LI ; Zhanqiu WANG ; Yang ZHAO ; Zilin WANG ; Zheng ZHAO
Journal of Biomedical Engineering 2020;37(5):885-891
In order to accurately implant the brain electrodes of carp robot for positioning and navigation, the three-dimensional model of brain structure and brain electrodes is to be proposed in the study. In this study, the tungsten electrodes were implanted into the cerebellum of a carp with the aid of brain stereotaxic instrument. The brain motor areas were found and their three-dimensional coordinate values were obtained by the aquatic electricity stimulation experiments and the underwater control experiments. The carp brain and the brain electrodes were imaged by 3.0 T magnetic resonance imaging instrument, and the three-dimensional reconstruction of carp brain and brain electrodes was carried out by the 3D-DOCTOR software and the Mimics software. The results showed that the brain motor areas and their coordinate values were accurate. The relative spatial position relationships between brain electrodes and brain tissue, brain tissue and skull surface could be observed by the three-dimensional reconstruction map of brain tissue and brain electrodes which reconstructed the three-dimensional structure of brain. The anatomical position of the three-dimensional reconstructed brain tissue in magnetic resonance image and the relationship between brain tissue and skull surface could be observed through the three-dimensional reconstruction comprehensive display map of brain tissue. The three-dimensional reconstruction model in this study can provide a navigation tool for brain electrodes implantation.
Animals
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Brain/diagnostic imaging*
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Carps
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Electrodes
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Electrodes, Implanted
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Imaging, Three-Dimensional
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Magnetic Resonance Imaging
6.Intermuscular coupling based on wavelet packet-cross frequency coherence.
Yihao DU ; Xiaolin BAI ; Wenjuan YANG ; Lin ZHENG ; Ping XIE
Journal of Biomedical Engineering 2020;37(2):288-295
Human motion control system has a high degree of nonlinear characteristics. Through quantitative evaluation of the nonlinear coupling strength between surface electromyogram (sEMG) signals, we can get the functional state of the muscles related to the movement, and then explore the mechanism of human motion control. In this paper, wavelet packet decomposition and : coherence analysis are combined to construct an intermuscular cross-frequency coupling analysis model based on wavelet packet- : coherence. In the elbow flexion and extension state with 30% maximum voluntary contraction force (MVC), sEMG signals of 20 healthy adults were collected. Firstly, the subband components were obtained based on wavelet packet decomposition, and then the : coherence of subband signals was calculated to analyze the coupling characteristics between muscles. The results show that the linear coupling strength (frequency ratio 1:1) of the cooperative and antagonistic pairs is higher than that of the nonlinear coupling (frequency ratio 1:2, 2:1 and 1:3, 3:1) under the elbow flexion motion of 30% MVC; the coupling strength decreases with the increase of frequency ratio for the intermuscular nonlinear coupling, and there is no significant difference between the frequency ratio : and : . The intermuscular coupling in beta and gamma bands is mainly reflected in the linear coupling (1:1), nonlinear coupling of low frequency ratio (1:2, 2:1) between synergetic pair and the linear coupling between antagonistic pairs. The results show that the wavelet packet- : coherence method can qualitatively describe the nonlinear coupling strength between muscles, which provides a theoretical reference for further revealing the mechanism of human motion control and the rehabilitation evaluation of patients with motor dysfunction.
Adult
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Algorithms
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Electromyography
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Humans
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Movement
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Muscle Contraction
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Muscle, Skeletal
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physiology
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Range of Motion, Articular