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1.
Chinese Medical Journal ; (24): 1845-1849, 2016.
Article in English | WPRIM | ID: wpr-251293

ABSTRACT

<p><b>BACKGROUND</b>During craniotomies using the transpetrosal-presigmoid approach, exposure of the sigmoid sinus remains an essential but hazardous step. In such procedures, accurate localization of the anterosuperior point of the transverse-sigmoid sinus junction (ASTS) is very important for reducing surgical morbidity. This study aimed to create an accurate and practical method for identifying the ASTS.</p><p><b>METHODS</b>On the lateral surfaces of 40 adult skulls (19 male skulls and 21 female skulls), a rectangular coordinate system was defined to measure the x and y coordinates of two points: the ASTS and the squamosal-parietomastoid suture junction (SP). With the coordinate system, the distribution characteristics of the ASTS were statistically analyzed and the differences between the ASTS and SP were investigated.</p><p><b>RESULTS</b>For ASTS-x, significant differences were found in different sides (P = 0.020); the ASTS-x in male skulls was significantly higher on the right side (P = 0.017); there was no significant difference between the sides in female skulls. There were no significant differences in gender or interaction of gender and side for ASTS-x, and for ASTS-y, there were no significant differences in side, gender, or interaction of gender and side. For both sides combined, the mean ASTS-x was significantly higher than the mean SP-x (P = 0.003) and the mean ASTS-y was significantly higher than the mean SP-y (P = 0.011).</p><p><b>CONCLUSIONS</b>This reference coordinate system may be an accurate and practical method for identifying the ASTS during presigmoid craniotomy. The SP might be difficult to find during presigmoid craniotomy and, therefore, it is not always a reliable landmark for defining the ASTS.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Cranial Sinuses , Craniotomy , Skull , Transverse Sinuses
2.
National Journal of Andrology ; (12): 708-712, 2015.
Article in Chinese | WPRIM | ID: wpr-276033

ABSTRACT

<p><b>OBJECTIVE</b>To explore the correlation of the gene polymorphisms of Toll-like receptor 2 ( TLR2) and TLR4 with the susceptibility and recurrence of condyloma acuminatum (CA).</p><p><b>METHODS</b>Using Snapshot, we detected the gene polymorphisms of TLR2 597(T/C), 1350(T/C), 15607(A/G), and 2258(G/A) and TLR4 896(A/G) and 1196(C/T) in the peripheral blood of 140 CA patients and 105 HPV-negative controls. We made comparisons between the CA patients and controls as well as between the cases of recurrent CA and those of non-recurrence at 6 months after treatment.</p><p><b>RESULTS</b>There were 72, 48, and 20 cases of genotype TT, TC, and CC of TLR2 597 (T/C), respectively, in the CA patients, as compared with 71, 31, and 3 cases in the controls. The gene frequency of mutant C was 31. 43% in the patients, significantly higher than 17.62% in the controls (χ2 = 12.04, P < 0.01), and it was 38.68% in the recurrent cases, remarkably higher than 27.01% in the non-recurrent cases (χ2 = 4.16, P < 0.05). There were 74, 49, and 17 cases of genotype TT, TC, and CC of TLR2 1350( T/C), respectively, in the CA patients, as compared with 73, 29, and 3 cases in the controls. The gene frequency of mutant C was 29. 64% in the patients, significantly higher than 16. 67% in the controls (χ2 =11.05, P < 0.01), and it was 36.79% in the recurrent cases, markedly higher than 25. 29% in the non-recurrent cases (χ2 = 4.18, P < 0.05). There were 44, 66, and 30 cases of genotype AA, AG, and GG of TLR2 15607(A/G), respectively, in the CA patients, as compared with 26, 58, and 21 cases in the controls. There was no significant difference in the gene frequencies of mutant G between the two groups (χ2 = 0.33, P > 0.05). No mutant genes of TLR2 2508 (G/A) or TLR4 896(A/G) and 1196(C/ T) were detected in either the CA patients or the controls. Linkage disequilibrium analysis showed a tight linkage between TLR2 597 (T/C) and 1350(T/C) (D' = 1, r2 = 0.93).</p><p><b>CONCLUSION</b>TLR2 597(T/C) is tightly linked to 1350(T/C), which is correlated with both the susceptibility and the recurrence of condyloma acuminatum.</p>


Subject(s)
Aged , Humans , Case-Control Studies , Condylomata Acuminata , Genetics , Gene Frequency , Genetic Linkage , Genetic Predisposition to Disease , Genotype , Polymorphism, Genetic , Recurrence , Toll-Like Receptor 2 , Genetics , Toll-Like Receptor 4 , Genetics
3.
Singapore medical journal ; : 346-352, 2015.
Article in English | WPRIM | ID: wpr-244781

ABSTRACT

<p><b>INTRODUCTION</b>Herpes simplex virus type 2 (HSV-2) is the most common cause of genital herpes. Glycoprotein G (gG) is a prototype antigen for type-specific serodiagnosis distinguishing between HSV type 1 (HSV-1) and HSV-2 infections. As immunological diagnosis kits for accurate differentiation between HSV-1 and HSV-2 antibodies can be expensive, there is a need to develop a convenient, sensitive, specific and cost-effective serodiagnostic kit.</p><p><b>METHODS</b>We successfully expressed a fragment of gG comprising residues 321-580 of HSV-2 with histidine tag (gG(321-580His)) in a Bac-to-Bac baculovirus expression system, which had an antigenicity similar to its native counterpart. An indirect enzyme-linked immunosorbent assay (ELISA) was developed using gG(321-580His) as the diagnostic antigen and evaluated by comparison with a commercial HerpeSelect 2 ELISA immunoglobulin G kit as reference.</p><p><b>RESULTS</b>In testing 318 field serum samples, the diagnostic relative sensitivity and specificity of the developed gG(321-580His)-ELISA test in qualitative comparison with the commercial kit were 93.81% and 96.74%, respectively, and the accuracy was 94.65%.</p><p><b>CONCLUSION</b>The study indicates that gG(321-580His) has a high diagnostic potential for HSV-2 virus serodiagnosis in humans.</p>


Subject(s)
Adult , Female , Humans , Male , Antibodies, Viral , Blood , Enzyme-Linked Immunosorbent Assay , Herpes Genitalis , Diagnosis , Virology , Herpes Simplex , Diagnosis , Virology , Herpesvirus 1, Human , Herpesvirus 2, Human , Immunoglobulin G , Chemistry , Polymerase Chain Reaction , Reagent Kits, Diagnostic , Reference Values , Reproducibility of Results , Sensitivity and Specificity , Serologic Tests , Methods
4.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 477-480, 2014.
Article in English | WPRIM | ID: wpr-812245

ABSTRACT

AIM@#To study the chemical constituents of the fruits of Illicium henryi.@*METHOD@#Chromatographic separations on silica gel, Sephadex LH-20 gel and MCI gel were used to isolate the compounds. The structures were elucidated based on extensive spectroscopic data analyses.@*RESULTS@#Seven compounds were obtained and their structures were identified as 10-benzoyl-cycloparvifloralone (1), cycloparvifloralone (2), 2α-hydroxycycloparviforalone (3), henrylactone B (4), merrillianone (5), henrylactone C (6) and 7, 14-ortholactone- 3-hydroxyfloridanolide (7).@*CONCLUSION@#Compound 1 is a new sesquiterpene lactone. The tested compounds showed weak anti-HBV activities on HBV surface antigen (HBsAg) secretion and HBV e antigen (HBeAg) secretion using Hep G2.2.15 cell line.


Subject(s)
Humans , Antiviral Agents , Chemistry , Pharmacology , Fruit , Chemistry , Hep G2 Cells , Hepatitis B virus , Illicium , Chemistry , Molecular Structure , Plant Extracts , Chemistry , Pharmacology , Sesquiterpenes , Chemistry , Pharmacology
5.
Chinese Journal of Experimental and Clinical Virology ; (6): 199-201, 2010.
Article in Chinese | WPRIM | ID: wpr-316924

ABSTRACT

<p><b>OBJECTIVE</b>To explore the inhibition effect of RNA interference on the ICP4 expression and DNA replication of herpes simplex virus type 2 (HSV2).</p><p><b>METHODS</b>Four pairs of siRNA targeted to HSV2 ICP4 gene and negative control siRNA were synthetized by chemical method, named as siRNA-1, siRNA-2, siRNA-3, siRNA-4 and siRNA-N respecticely. HSV2 HG52 was used to attack Vero cell after transfection overnight. Vero cell and supernatant were collected at 1d, 2d, 3d, 4d and 5d after virus attacking. Flurogenic quantitative reverse transcription polymerase chain reaction (FQ-RT-PCR)was used to detect the expression of HSV2 ICP4 mRNA, flurogenic quantitative polymerase chain reaction(FG-PCR) was used to detect the expression of HSV2 DNA and Western-Blot was used to detect the expression of HSV2 ICP4 protein.</p><p><b>RESULTS</b>All the four pairs of siRNA could significantly inhibit the expression of HSV2 ICP4 mRNA and protein, especially siRNA-2. The above siRNAs could significantly decrease HSV2 DNA copy number,too.</p><p><b>CONCLUSION</b>siRNAs targeted to HSV2 ICP4 gene could significantly inhibit expression of HSV2 ICP4 mRNA and protein, and decrease HSV2 DNA copy number, suggesting that siRNA can inhibit HSV2 DNA replication through silencing ICP4 gene.</p>


Subject(s)
Gene Expression Regulation, Viral , Genetics , Gene Silencing , Physiology , Herpesvirus 2, Human , Genetics , RNA Interference , Allergy and Immunology , RNA, Small Interfering , Pharmacology , RNA, Viral , Metabolism , Reverse Transcriptase Polymerase Chain Reaction
6.
National Journal of Andrology ; (12): 391-393, 2006.
Article in Chinese | WPRIM | ID: wpr-338287

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the social factors of patients with genital herpes (GH) relapsing and guide GH patients to avoid the related social factors.</p><p><b>METHODS</b>To select 96 case of patients with recurrent genital herpes of final diagnosis and detailedly record the related social factors before relapsing. The social factors were compared between male and female GH patients, and compared between frequently recurrent (> 6/year) and non-frequently recurrent GH patients (< or = 6/year) too.</p><p><b>RESULTS</b>65.6% (63/96) of recurrent GH patients have certain social factors before relapsing. The main social factors are overtiredness, mental stress and excessive sexual contact. Staying up late and excessive drinking are common social factors, too. There was no significant difference of social factors between male and female GH patients (P >. 05), and also no significant difference between frequently recurrent and non-frequently recurrent GH patients (P > 0.05), too.</p><p><b>CONCLUSION</b>Overtiredness, mental stress and excessive sexual are the main social elements during inducing genital herpes relapsing. It is important to reduce GH relapsing and spreading of HIV and syphilis by guiding recurrent genital herpes patients to avoid related social elements.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Fatigue , Epidemiology , Herpes Genitalis , Epidemiology , Recurrence , Sexual Behavior , Stress, Psychological , Epidemiology
7.
Chinese Journal of Experimental and Clinical Virology ; (6): 4-7, 2006.
Article in Chinese | WPRIM | ID: wpr-305559

ABSTRACT

<p><b>BACKGROUND</b>To investigate the epidemiological characteristics of human papillomavirus (HPV) infection in men attending a sexually transmitted diseases (STD) clinic in Hangzhou area.</p><p><b>METHODS</b>The enrolled individuals were men aged 18-70 years attending the STD clinic. Penile swabs were assessed for HPV DNA using polymerase chain reaction with the consensus primers MY09/11. The HPV genotypes of positive PCR products were determined by restriction fragment length polymorphisms and direct sequence analysis.</p><p><b>RESULTS</b>Of 375 swabs collected, 305 (81.3%) yielded sufficient DNA for the subsequent HPV analysis. Among the 305 subjects, the prevalence of HPV was 13.8%. Low risk HPV types were found in 8.5% (26/305) of the enrolled individuals, high risk types were found in 4.3% (13/305) of the enrolled individuals, and multiple types were found in 1.0% (3/305) of participants. The prevalence of HPV infection was higher in participants from urban area than in those from rural area (P<0.05). The prevalence was also higher in those who had received less years of education (P<0.05) and those who had more sex partners (P<0.05).</p><p><b>CONCLUSION</b>HPV infection among men at high risk is not uncommon. The detection rate of HPV DNA was significantly related to some sociodemographic factors, such as residence, educational level and the number of sex partners.</p>


Subject(s)
Adolescent , Adult , Aged , Humans , Male , Middle Aged , Young Adult , Alphapapillomavirus , Genetics , Capsid Proteins , Genetics , China , Epidemiology , DNA, Viral , Genetics , Genotype , Oncogene Proteins, Viral , Genetics , Outpatients , Papillomavirus Infections , Epidemiology , Virology , Polymerase Chain Reaction , Sexually Transmitted Diseases , Epidemiology , Surveys and Questionnaires
8.
Biomedical and Environmental Sciences ; (12): 153-157, 2006.
Article in English | WPRIM | ID: wpr-229710

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the epidemiological characteristics of human papillomavirus (HPV) infection in men attending a sexually transmitted diseases (STD) clinic in Hangzhou area.</p><p><b>METHODS</b>Male subjects (n=375) aged 18-70 years, attending the STD clinic were recruited. Urethral swabs were assessed for HPV DNA using polymerase chain reaction (PCR) with the consensus primers MY09/11. HPV genotypes of positive PCR products were determined by restriction fragment length polymorphisms and direct sequence analysis.</p><p><b>RESULTS</b>Of the 375 swabs collected, 305 (81.3%) yielded sufficient DNA for the subsequent HPV analysis. Among the 305 subjects, the prevalence of HPV was 13.8%. Nononcogenic HPV types were found in 8.5% (26/305) of subjects, oncogenic types in 4.3% (13/305), and multiple types in 1.0% (3/305). The prevalence of HPV infection was higher in subjects from urban area than in those from rural area (P < 0.05). The prevalence was also higher in those who received fewer years of education (P < 0.05) and those who had more sex partners (P < 0.05).</p><p><b>CONCLUSIONS</b>HPV infection among men at high risk is not uncommon. The detection rate of HPV DNA is significantly related to some sociodemographic factors, such as residence, educational level and the number of sex partners.</p>


Subject(s)
Adolescent , Adult , Aged , Humans , Male , Middle Aged , Ambulatory Care Facilities , China , Epidemiology , Papillomaviridae , Classification , Genetics , Papillomavirus Infections , Diagnosis , Epidemiology , Virology , Polymerase Chain Reaction , Sequence Analysis, DNA , Sexually Transmitted Diseases
9.
China Journal of Chinese Materia Medica ; (24): 1961-1965, 2006.
Article in Chinese | WPRIM | ID: wpr-246041

ABSTRACT

<p><b>OBJECTIVE</b>To study the chemical constituents of the leaves of Isatis indigotica.</p><p><b>METHOD</b>The leaves of I. indigotica were extracted with 80% ethanol. The EtOH extract was dispersed in H20 and extracted with petroleum, EtOAc and BuOH successively. The EtOAc fraction was isolated and purified by column chromatography on silica gel, Sephadex LH -20 and Rp-8, Rp-18. All the compounds were identified on the basis of spectral analyses (including MS, 1H-NMR, 13 C-NMR) , RESULT: Eleven compounds were isolated from the leaves of I. indigotica, and structures were characterized as 10H-indolo [3, 2-b] quinoline (1), indirubin (2), 4 (3H)-quinazo-linone (3), (E)-3-(3', 5'-dimethoxy-4'-hydroxybenzylidene) -2-indolinone (4), 2, 3-dihydropyrrolo [2, 1-b] quinazolin-9(1H) -one (5) , benzoic acid (6) , o-droxy-benzoic acid (7), ( - ) -lariciresinol (8) , ( + ) -isolariciresinol (9), isovitexin (10), 6-f-D-glucopyranosyldiosmetin (11).</p><p><b>CONCLUSION</b>1, 4, 5, 8, 9, 11 were obtained from the leaves of I. indigotica for the first time.</p>


Subject(s)
Furans , Chemistry , Indole Alkaloids , Chemistry , Isatis , Chemistry , Lignans , Chemistry , Lignin , Chemistry , Naphthols , Chemistry , Plant Leaves , Chemistry , Plants, Medicinal , Chemistry , Quinolines , Chemistry
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