Objective:To evaluate the effect of reduction by leverage with minimally invasive and internal fixation with Ideal Compression Screw to treat fracture of calcaneus.Methods:13 patients(17 fee)twith fracture of calcaneus were treated by reduction by leverage with minimally invasive and internal fixation with Ideal Compression Screw.According to Sanders'classification,10 sides were classified as typeⅡfracture and 7 sides as typeⅢfracture.Results:The post-operative functional evaluation by American Orthopaedic Foot and Ankle Society ankle score system revealed excellent outcomes in 12 feet(70.6%),good in 3(17.6%),fair in 2(11.8%).The excellent rate was 88.2%.Conclusion:Reduction by leverage with minimally invasive and internal fixation with Ideal Compression Screw to treat fracture of calcaneus is an effective and micro-invasive method in treatment of fractures of calcaneus.The technique can contribute to sta-ble fixation,low operation complication and high rate of excellent to good outcomes,et al.

To serve as carriers of cells and bioactive molecules, three-dimensional scaffolds play a key role in bone defect repair. The chemical component and microstructure of the scaffold can affect the mechanical properties and seed cells. A variety of fabrication techniques have been used in producing scaffolds, some made random porous structure, some created well-designed structure using rapid prototyping methods, and others prepared bio-derived materials as scaffolds. However, scaffolds may vary in their inner structure, mechanical properties and repairing efficiency as well because of different manufacturing methods. In this review, we overview the main achievements concerning the effects of material and microstructure on the mechanical performance, seed cells and defect repair of bone scaffolds.
Biocompatible Materials ; Bone and Bones ; Porosity ; Tissue Scaffolds

Based upon Ju and Swanson's studies on the eytoarchitecture of the bed nuclei of stria terminalis (BST) of the rat, the present work studies in detail the distribution of serotonin-immunoreactive fibers and terminals (5-HT-ir fibers) in the BST of the rat with ABC or PAP technique visualized with glucose oxidase-DAB-nickel method. The results are as followsithree types of 5-HT-ir fibers were identified in the BST, viz. thick fibers, thin fibers and varicose fibers. Only varicose fibers were found in the stria extension of the BST, whereas the rest of the BST contained other types as well. In the oval nucleus, juxitacapsular nucleus, fusiform nucleus, posterior dorsal nucleus and principle nucleus,all three types of 5-HT-ir fibers were observed, while the remaining parts of the BST were occupied with thin and varicose fibers. These fibers were distributed unevenly in the BST, with highest density in the ventromedial part of the anterior ventral area and the ventrolateral part of the posterior division; moderate density in the anterior dorsal area, the ventrolateral part of the anterior ventral area and the dorsolateral part of the posterior division; and were scattered in the anterior lateral area and the medial part of the posterior division. The difference in density of 5-HT-ir fibers among various areas of the BST corresponds generally with the sequence of ontogenesis of the BST. Mismatch of the distribution of 5-HT-ir fibers and 5-HT receptors in the BST of the rat is also discussed.

The present work studies the origin of serotonin-immunoreactive fibers and terminals (5-HT-ir fibers) in the bed nuclei of the stria terminalis (BST) of the rat, with combined retrograde tracing and 5-HT immunoperoxidase methods. The results are as follows: 5-HT-ir fibers in the main part of the BST originate mainly from the dorsal and median raphe nuclei in addition to the region adjacent to the medial lemniscus and the caudal linear nucleus raphe. About one third of HRP-labelled neurons in every above-mentioned raphe nucleus are also 5-HT immunoreactive and innervate mainly the ipsilateral BST, and they are constituted by part of every type of 5-HT-ir cells in most regions of these nuclei.

In our previous studies, substance P-like immunoreactive varicose nerve fibers have been demonstrated in the pars distalis of the adenohypophysis of the dog. They were found, at light microscopical level, to be closely related to gland cells. In the present study, the ultrastructure of substance P-like immunoreactive nerve fibers and their relationship with the gland cells of the pars distalis in the dog were investigated by use of pre-embedding immuno-electron microscopy. Direct contacts could be ascertained on every cell type of the gland, including folliculo-stellate cells. Typical synapses were identified on somatotropes and corticotropes, more on the latter. Most of them were of asymmetrical type with round to oval small clear vesicles and scattered large dense cored vesicles. It is considered morphologically proved that the substance P-like immunoreactive nerve fibers have effector role in the pars distalis of the dog.

Based upon Ju and Swanson's recent studies on the cytoarchitecture of the bed nuclei of the stria terminalis (BST) in the rat, the present work studied in detail the distribution of GABA-immunoreactive (GABA-ir) neurons and fibers in the BST of the rat with ABC immunohistochemical method. A large number of GABA-ir neurons were distributed in the dorsal regions of the anterolateral (AL) and anterodorsal (AD) areas as well as the ventral regions of the anteroventral (AV) area and posterior part of the BST, whereas the other regions contained relatively less numbers of GABA-ir cells. GABA-ir neurons which were displayed moderate to high densities in the oval and juxitacapsular nuclei of the AL, the parastrial and fusiform nuclei of the AV, and the principal nucleus of the posterior part were limited within the extent of these nuclei, while the remained regions of the BST were scattered by GABA-ir cells; GABA-ir fibers were concentrated mainly in the dorsal regions of the AL and AD, the parastrial and fusiform nuclei of the AV, and the dorsal regions of the posterior part. In the strial terminalis, numerous GABA-ir fibers were located chiefly in the ventrolateral and ventromedial angles of it. Combined with the results of availlable studies, the above mentioned results indicate that all the fibers which project, by way of the stria terminalis, from the oval nucleus of the BST to the ipsilateral amygdaloid central nucleus (Ce), or from the Ce and amygdaloid medial nucleus to the ipisilateral oval and principal nuclei of the BST may be GABAergic, and among them, the GABAergic projections from the oval nucleus of the BST to the Ce may play an important role in the generation and propagation of epilepsy.

Objective To explore the effects of puerarin on proliferation ,invasion ,migration and tube formation in human endo-thelial cells and its possible mechanism .Methods The effect of puerarin on cell proliferation was determined using methyl thiazolyl tetrazolium(MTT) assay .Invasion was evaluated with transwell chamber .Migration was performed by the wound healing method . Endothelial tube formation was performed by tube formation assay .The expressions of phosphorylase Akt(p-Akt) and phosphoryl-ase nitric oxide synthase(p-eNOS) protein were determined by western blot .Results Puerarin promote the proliferation ,invasion , migration and tube formation of human endothelial cells(P<0 .05) .The expression of p-Akt and p-eNOS were increased signifi-cantly(P<0 .05) .Conclusion Puerarin can promote the proliferation ,invasion ,migration and tube formation of human endothelial cells .Up regulation of p-AKT and p-eNOS protein may be one of its mechanisms .

The determination of tumor markers is of great value for esophageal squamous cell carcinoma. This article reviews the application status of routine tumor markers and the progression on the role of tumor markers in early diagnosis, predicting chemotherapy or radiotherapy response, monitoring disease recurrence and evaluation of prognosis in esophageal squamous cell carcinoma.

Objective To investigate the role of glucocorticoid-induced tumor necrosis factor ligand (GITRL) in regulating the inflammatory reaction of kupffer cells.Methods The kupffer cells and T cells of mice were isolated and divided into 6 groups after being co-cultured:control group,kupffer cells and T cells were cultured in DMEM only; lipopolysaccharide (LPS) group,kupffer cells and T cells were cultured in media with LPS (1 mg/L) ; LPS + GITRL siRNA group,kupffer cells and T cells were cultured in media as the LPS group after transfected with GITRL siRNA ; LPS + control siRNA group,kupffer cells and T cells were cultured in media as the LPS group after transfected with control siRNA; LPS + pEGFP-N1 GITRL group,kupffer cells and T cells were cultured in media as the LPS group after transfected with pEGFP-N1 GITRL plasmid; LPS + pEGFP-N1 control group,kupffer cells and T cells were cultured in media as the LPS group after transfected with control plasmid.After 24 hours of treatment,the expressions of GITRL and PDL1 of kupffer cells were detected by immunofluorescence and western blot,respectively.The proliferation and apoptosis of T cells were measured by MTF assay and Annexin V/PI flow cytometry,respectively.The expression of tumor necrosis factor (TNF-α) in the supernatant fluid was measured by ELISA.All data were analyzed using the independent t test and one-way analysis of variance.Results The transfection efficiencies of GITRL siRNA and pEGFP-N1 GITRL were 90％ and 85％,respectively.Compared with normal kupffer cells,the protein expression of GITRL of kupffer cells transfected with GITRL siRNA was significantly decreased,while the protein expression of GITRL of kupffer cells transfected with pEGFP-N1 GITRL was significantly increased (t =41.72,13.10,P ＜ 0.05).There was no significant difference in the protein expressions of GITRL between normal kupffer cells and those in the control groups (F =2.27,P ＞ 0.05).The fluorescence intensity of GITRL in the LPS group was significantly higher than that in the control group (t =49.29,P ＜ 0.05).Compared with LPS group,the activation of GITRL expression by the LPS was significantly suppressed in the LPS + GITRL siRNA group (t =9.84,P ＜ 0.05),while the expression of GITRL in the LPS + pEGFP-N1 GITRL group was significantly increased (t =5.78,P ＜ 0.05).There was no significant difference in the GITRL expression among the LPS + control siRNA group,LPS + pEGFP-N1 control group and LPS group (F =0.86,P ＞ 0.05).The expression of PDL1 in the LPS group was significantly lower than that in the control group (t =18.83,P ＜0.05).Compared with LPS group,the expression of PDL1 in the LPS + pEGFP-N1 GITRL group was significantly suppressed (t =11.79,P ＜ 0.05),while the expression of PDL1 in the LPS + GITRL siRNA group was significantly stronger (t =19.08,P ＜ 0.05).There was no significantly difference in the expression of PDL1 in the LPS + control siRNA group,LPS + pEGFP-N1 control group and LPS group (F =2.22,P ＞ 0.05).The proliferation of T cells was increased and the number of apoptotic T cell was decreased in the LPS group when compared with control group (t =49.43,40.11,P ＜ 0.05).Compared with LPS group,the proliferation and apoptosis of T cells in the LPS + pEGFP-N1 GITRL group had the same trend (t =5.77,12.64,P ＜0.05); while the proliferation of T cells was decreased and the apoptosis of T cells was increased in the LPS + GITRL siRNA group (t =17.00,49.90,P ＜ 0.05).There was no significant difference in the proliferation and apoptosis of T cells among the LPS + control siRNA group,LPS + pEGFP-N1 control group and LPS group (F =1.87,1.35,P ＞ 0.05).The expression of TNF-α was significantly higher in the LPS group than that in the control group (t =125.68,P ＜ 0.05).Compared with the LPS group,the expression of TNF-α was significantly decreased in the LPS + GITRL siRNA group (t =119.65,P ＜ 0.05),while the expression of TNF-α in the LPS + pEGFP-N1 GITRL group was significantly increased (t =147.70,P ＜ 0.05).There was no significant difference in the TNF-α expression among the LPS + control siRNA group,LPS + pEGFP-N1 control group and LPS group (F =0.14,P ＞ 0.05).Conclusion Kupffer cells suppress the expression of PDL1 by upregulating GITRL,and thus activate the proliferation of T cells and promote the inflammatory reaction.The immunologic balance may be recovered after the interference of GITRL to restrain the inflammatory reaction.

Objective To study the protective mechanism of S-adenosylmethionine ( SAM) underlying liver injury induced by lipopolysaccharides ( LPS). Methods One hundred BABL/c mice were randomly divided into LPS group and SAM group. Mice in LPS group were intraperitoneally injected with 10 mg/kg LPS,and the mice in SAM group were injected with 100 mg/kg SAM 2 h before receiving the same dose of LPS. The survival rate of mice in 2 groups was recorded in 24,48,72 and 120 h after LPS injection. Histopathological changes in liver of mice were examined in 0,1,3,6,12 and 24 h after LPS injection. Tumor necrosis factor-? ( TNF-?) and interleukin-10 ( IL-10) levels in serum were measured by ELISA analysis at above time points. Expression of Toll-like receptor 4 ( TLR4) and liver X receptor ? ( LXR?) in hepatic tissues was detected by immunohistochemistry and Western blotting. Results SAM increased the survival rate of mice from 50. 0% ,40. 0% ,30. 0% ,and 30. 0% before LPS injection to 80. 0% ,70. 0% ,60. 0% ,and 50. 0% after its injection ( P