OBJECTIVETo research the influence of gilt to the retention of the complete metal crown.

METHODSSixty Ni-Cr alloy complete metal crown were divided into three groups, control group (common Ni-Cr alloy complete metal crown), whole gold-plating group (whole gilding on the tissue surface of the inner Ni-Cr alloy complete metal crown), partial gold-plating group (gilding on the tissue surface of 1/3 cervical inner Ni-Cr alloy complete metal crown). The retention force of complete metal crown was measured by tensile force/pressure ergograph.

RESULTSThe retention force of control group, partial gold-plating group, whole gold-plating group were (657 +/- 151) N, (632 +/- 139) N, (569 +/- 103) N, respectively. There were significant differences between control group and whole gold-plating group, whole gold-plating group and partial gold-plating group (P < 0.05). There was no significant difference between control group and partial gold-plating group (P > 0.05).

CONCLUSIONThe force of retention would decrease after gilding on the tissue surface of the inner Ni-Cr alloy complete metal crown, but have no influence to normal retention requirement of complete crown. Although the retention of partial gold-plating complete metal crown had somewhat decrease, it could be ignored.

Animals ; Chromium Alloys ; Crowns ; Female ; Gold ; Humans ; Swine

OBJECTIVETo evaluate wear resistance and hardness of three kinds of new composite resins.

METHODSThree kinds of new composite resins, Solidex, Spectrum, Filtek Z350, were tested. Enamel as control group. A refited MG-200 wear machine was used in this study. Scanning electron microscope (SEM) was used to observe the friction surface of each tested material. Hardness of each tested material was determined by Vickers indentation technique. The data of wear and hardness were analyzed by Mann-Whitney test and 1-way ANOVA. The relationship between the hardness of the composites and the amount of wear of them was determined by a regression analysis method.

RESULTSFiltek Z350 showed the lowest volumetric wear and highest Vickers hardness in the composites (P < 0.05). No significant differences in wear and hardness were observed between Solidex and Spectrum (P > 0.05). Significant relationships were observed between the hardness of the composites and the amount of wear of them (r = 0.968 6) (P < 0.05). Different wear characters of the friction surface of the tested materials were observed by SEM.

CONCLUSIONNanofilled composite was superior to the hybrid composite in wear resistance and hardness.

Composite Resins ; Dental Enamel ; Dental Materials ; Dental Restoration Wear ; Hardness ; In Vitro Techniques ; Materials Testing ; Surface Properties

OBJECTIVETo evaluate the clinic effects of alginate impression and agar/alginate combined impression.

METHODS237 patients of fixed partial denture were collected and divided into group A and group B. Group A was taken impression by aglinate impression, including 81 patients (207 abutments). Group B was taken impression by agar/alginate combined impression, include 156 patients (392 abutments). The impressions were observed by megaloscope, and the number of abutment, the types and number of defect were recorded.

RESULTSIn the aglinate impressions, 57.0 percent of abutment had some defect. But in the agar/alginate combined impressions, 36.0 percent of abutment had some defect. There were significant difference between group A and group B in the abutment, air bubbles in cervical margin, unsharpness of the gingival sulcus and shoulders (P<0.05). There were no significant difference between group A and group B in the split and defect of the impressions on the cervical margin.

CONCLUSIONThere were less defects in the agar/alginate combined impression than in the alginate impression.

Alginates ; Dental Impression Materials ; Dental Impression Technique ; Dental Models ; Denture, Partial, Fixed ; Gingiva ; Glucuronic Acid ; Hexuronic Acids ; Humans

Objective:To determine the differential expressions of long non-coding RNA(lncRNA)and messenger RNA(mRNA)in normal and asthenospermia(AS)men and analyze their biological significance in AS.Methods:We isolated and ex-tracted total RNAs from 9 normal and 9 AS sperm samples,determined the expressions of RNAs in the sperm using the DNBSEQ se-quencing platform,and analyzed their relevant functions by gene ontology enrichment(GO)and Kyoto encyclopedia of genes and ge-nomes pathway(KEGG)analyses.Results:An average of 10.64G data was generated per group,with 282 185 RNAs detected,in-cluding 107 009 lncRNAs.Among the total number of lncRNAs,15 157 were differentially expressed,2 190 upregulated and 12 967 downregulated;and among the 19 514 mRNAs,13 736 were differentially expressed,4 995 upregulated and 8 741 downregulated.Differentially expressed genes were enriched mainly in the sperm cell membrane and the pathways related to the ion channel functions,sperm development and fertilization.Conclusion:Differentially expressed lncRNAs and mRNAs can be identified by sequencing a-nalysis of AS and normal sperm.Regulation of sperm function through membrane ion channels may contribute to the development of AS,which provides a molecular basis for further research on AS.

[Abstract] Objective To investigate the protective effect of exogenous hydrogen sulfide (H

To investigate the effect of notoginsenoside Ft1(Ft1) on proliferation, migration and apoptosis of breast cancer cells, we conducted several assays including CCK-8 assay, EdU staining, single cell migration assay and Hoechst 33258 staining. The effect of Ft1 on expression of apoptosis related proteins, HIF-1α, PI3K/Akt/mTOR/p70S6K and MAPK pathways was examined with Western blot. Ft1 could significantly reduce cell survival and inhibit cell proliferation in breast cancer cells in a dose-dependent manner. Ft1 also increased chromatin condensation of MDA-MB-231 cells. Furthermore, Ft1 decreased protein expression of Bcl-2 and HIF-1α and increased expression of cleaved caspase 3 in MDA-MB-231 cells after 12 h treatment. Ft1 significantly down-regulated the levels of p-Akt, p-mTOR and p-p70S6K as well as p-ERK1/2, but up-regulated that of p-JNK. Ft1 significantly inhibited the level of p-EGFR (Tyr1068) and p-EGFR (Ser1046/1047) in MDA-MB-231 cells. Finally, Ft1 significantly inhibited the migration path length and velocity of HS578T cells when used at the concentration without affecting cell viability. Thus, Ft1 exhibited multiple antitumor effects including inhibition of cell survival and migration, promotion of cell apoptosis in breast cancer cells. Suppression of HIF-1α via Akt/mTOR/p70S6K and MAPK pathways may be involved in the pharmacological effect of Ft1 on cell proliferation and apoptosis of breast cancer cells.

Due to the negative autopsy and without cardiac structural abnormalities, unexpected sudden cardiac death （USCD） is always a tough issue for forensic pathological expertise. USCD may be associated with parts of fatal arrhythmic diseases. These arrhythmic diseases may be caused by disorders of cardiac ion channels or channel-related proteins. Caveolin can combine with multiple myocardial ion channel proteins through its scaffolding regions and plays an important role in maintaining the depolarization and repolarization of cardiac action potential. When the structure and function of caveolin are affected by gene mutations or abnormal protein expression, the functions of the regulated ion channels are correspondingly impaired, which leads to the occurrence of multiple channelopathies, arrhythmia or even sudden cardiac death. It is important to study the effects of caveolin on the functions of ion channels for exploring the mechanisms of malignant arrhythmia and sudden cardiac death.
Arrhythmias, Cardiac/physiopathology* ; Autopsy ; Caveolins/metabolism* ; Channelopathies/genetics* ; Death, Sudden, Cardiac/pathology* ; Forensic Pathology ; Humans ; Ion Channels/metabolism* ; Mutation ; Myocardium

OBJECTIVES: To explore the genetic variation sites of caveolin （CAV） and their correlation with sudden unexplained death （SUD）. METHODS: The blood samples were collected from SUD group （71 cases）, coronary artery disease （CAD） group （62 cases） and control group （60 cases）, respectively. The genome DNA were extracted and sequencing was performed directly by amplifying gene coding region and exon-intron splicing region of CAV1 and CAV3 using PCR. The type of heritable variation of CVA was confirmed and statistical analysis was performed. RESULTS: A total of 4 variation sites that maybe significative were identified in SUD group, and two were newfound which were CAV1： c.45C>T （T15T） and CAV1：c.512G>A （R171H）, and two were SNP loci which were CAV1：c.246C>T （rs35242077） and CAV3：c.99C>T （rs1008642） and had significant difference （P<0.05） in allele and genotype frequencies between SUD and control groups. Forementioned variation sites were not found in CAD group. CONCLUSIONS The variants of CAV1 and CAV3 may be correlated with a part of SUD group.
Caveolins/genetics* ; Coronary Artery Disease ; Death, Sudden/etiology* ; Exons ; Genotype ; Humans ; Male ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide