Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 57
Filter
Add more filters










Publication year range
1.
Sci Rep ; 13(1): 14487, 2023 Sep 02.
Article in English | MEDLINE | ID: mdl-37660183

ABSTRACT

The transient photocurrent is one of the key parameters of the spatial radiation effect of photoelectric devices, and the energy level defect affects the transient photocurrent. In this paper, by studying the deep level transient spectrum of a self-designed Schottky diode, the defect properties of the interface region of the anode metal AlCu and Si caused by high-temperature annealing at 150 â„ƒ, 200 â„ƒ and 300 â„ƒ for 1200 h have been quantitatively analyzed. The study shows that the defect is located at the position of + 0.41 eV on the valence band, the concentration is 2.8 [Formula: see text] 1013/cm2, and the capture cross section is [Formula: see text] = 8.5 [Formula: see text] 1017. The impurity energy level mainly comes from the diffusion of Al atom in anode metal. We found that the defect did not cause the electrical performance degradation and obvious morphology change of the device, but the transient photocurrent increased significantly. The reason is that the high temperature treatment results in a growth in the density of states at the interface between AlCu-Si. The more mismatched dislocations and recombination center increased the reverse current of the heterojunction. The above view is proved by the TCAD simulation test.

2.
Zhonghua Yu Fang Yi Xue Za Zhi ; 56(4): 479-485, 2022 Apr 06.
Article in Chinese | MEDLINE | ID: mdl-35488547

ABSTRACT

Objective: To investigate the epidemiological characteristics of Yersinia enterocolitica in patients with diarrhea in Pudong New Area, Shanghai. Methods: Active surveillance of diarrhea was conducted in 14 sentinel hospitals (three tertiary-level hospitals, nine secondary-level hospitals, and two primary-level hospitals) from January 2013 to December 2019 in Pudong New Area of Shanghai, China base on their location, catchment area, and patient volume. Cold enrichment method was used to isolate Y. enterocolitica and further detection of bioserotype, virulence genes and antimicrobial susceptibility of the isolates were conducted. The difference of rates was determined using chi-square test or Fisher's exact test. Results: A total of 12 941 diarrhea cases were included, and 0.7% (88/12 941) cases were confirmed with Yersinia enterocolitica infection. 67.0% (59/88) cases were single infection, 33.0% (29/88) cases were mixed infections. Detection rates of Y. enterocolitica increased annually (0.3%-1.2%) and were highest in children<5 years of age (1.1%, 37/3 218) and in spring (1.1%, 32/2 998) (χ2 were 18.64 and 9.76, respectively, P<0.05). 58.0% (51/88) cases had watery diarrhea, 15.9% (14/88) had fever and 14.8% (13/88) had vomiting. The predominant bioserotypes were 3/O:3 (53.4%, 47/88), followed by 1A/O:8 (15.9%, 14/88) and 1A/O:5(6.8%, 6/88), respectively. Bioserotype 3/O:3 counted for the highest proportions (89.2%, 33/37) in children <5 years of age. All the strains of bioserotype 3/O:3 harbored ail, ystA, yadA and virF genes, which encoded pathogenic Y. enterocolitica. 11/14 strain of 1A/O:8 and 4/6 strains of 1A/O:5 harbored ystB gene. Most strains were resistant to ampicillin (80.7%,71/88) and amoxicillin/clavulanic acid (71.6%,63/88), and 63.8% (56/88) strains were multidrug resistance (MDR). The difference of antimicrobial resistance rates between 3/O:3 and non 3/O:3 was statistically significant in ampicillin, cefoxitin, nalidixic acid, tetracycline and ampicillin/sulbactam (χ2 was 14.68, 43.80, 41.86, 30.54 and 5.07, respectively, P<0.05). Conclusion: The detection rate of Yersinia enterocolitica was higher in children than in adults in Pudong New Area, Shanghai. The predominant bioserotype was pathogenic 3/O:3 with multidrug resistance.


Subject(s)
Yersinia enterocolitica , Ampicillin , Anti-Bacterial Agents/pharmacology , Child , China/epidemiology , Diarrhea/epidemiology , Humans
3.
J Biol Regul Homeost Agents ; 33(2): 531-536, 2019.
Article in English | MEDLINE | ID: mdl-30972997

ABSTRACT

The aim of this study was to evaluate the effects of rehabilitative aerobic exercise on blood pressure, serum inflammatory factors, endothelin and quality of life in patients with hypertension. Ninety patients with mild hypertension visiting West China Hospital of Sichuan University from June 2017 to December 2017 were enrolled and randomly divided into an experimental group and a control group. Patients in both groups were given a low-salt diet, and the experimental group was given an extra three-month treadmill training. Systolic blood pressure (SBP), diastolic blood pressure (DBP), serum tumor necrosis factor α (TNF-α), serum interleukin-6 and endothelin-1, body mass index (BMI), triglyceride (TG) and other indicators were examined in both groups before and after exercise, SF-36 scale was used to evaluate the quality of life. The results showed that after 3 months of exercise, SBP and DBP in the experimental group were significantly lower than those in the control group (P less than 0.05). Compared with the control group, the concentrations of TNF-α, interleukin-6 and endothelin-1 in the experimental group were significantly decreased (P less than 0.05). Correlation analysis showed that IL-6 was positively correlated with SBP (P less than 0.05), and TNF-α and ET-1 were positively correlated with diastolic blood pressure (P less than 0.05). The general health status, energy, mental health, social function, emotional function and health changes of the experimental group were significantly improved compared with before exercise (P less than 0.05). In conclusion, rehabilitative aerobic exercise can lower blood pressure and improve the overall quality of life in mild hypertension patients by inhibiting vascular inflammation and lowering plasma endothelin-1.


Subject(s)
Blood Pressure , Endothelin-1/blood , Exercise Therapy , Hypertension/blood , Hypertension/therapy , Humans , Interleukin-6/blood , Quality of Life , Triglycerides/blood , Tumor Necrosis Factor-alpha/blood
4.
Zhonghua Liu Xing Bing Xue Za Zhi ; 40(3): 354-359, 2019 Mar 10.
Article in Chinese | MEDLINE | ID: mdl-30884618

ABSTRACT

Objective: To investigate the antimicrobial resistance and molecular epidemiology of foodborne Yersinia (Y.) enterocolitica in Pudong New District of Shanghai. Methods: Four kinds of raw food samples were collected in retail circulation sites in Pudong from 2012 to 2016. Cold enrichment method was used to isolate Y. enterocolitica and further detection of biotype, serotype, virulent genes, antimicrobial susceptibility of the isolates and pulsed field gel electrophoresis (PFGE) were conducted. Results: A total of 3 900 raw food samples were collected during this period, including poultry product (n=590), livestock product (n=1 074), aquatic product (n=1 488), vegetable (n=748), in which 111 (2.8%) were contaminated by Y. enterocolitica. The detection rates of Y. enterocolitica in poultry product samples (5.3%, 31/590) and livestock product samples (4.5%, 48/1 074) were higher than those in aquatic product samples (1.6%, 24/1 488) and vegetable samples (1.1%, 8/748). The predominant biotype was 1A (95.5%) and predominant serotype was O∶8 (42.3%). All the strains lacked ail, ystA, yadA and virF genes, which encoded pathogenic Y. enterocolitica. Seventy six (68.5%) strains harbored ystB gene, in which 35 (31.5%) belonged to 1A/O∶8/ystB pattern. Most strains were resistant to ampicillin (74.8%) and amoxicillin/clavulanic acid (70.3%), and non-sensitive rate to Cefoxitin was over 50.0%. No third generation cephalosporin or fluoroquinolone resistant strains were detected, but 38.7% (43/111) strains were multidrug resistant (MDR). Serotype O∶8 and O∶5 strains had 44 and 18 PFGE patterns, respectively. Conclusions: The main foodborne exposure sources of Y. enterocolitica in raw food were poultry and livestock products in Pudong New District. 1A/O∶8/ystB was the predominant pattern with potential pathogenicity despite lacks of typical pathogenic virulent genes. The antimicrobial resistant rates of Y. enterocolitica were at a low level, but MDR strains still existed. Molecular types of the isolates showed highly genetic diversity.


Subject(s)
Drug Resistance, Bacterial , Food Microbiology , Raw Foods/microbiology , Yersinia enterocolitica , Anti-Bacterial Agents/pharmacology , Bacterial Typing Techniques , China/epidemiology , Humans , Molecular Epidemiology , Serogroup , Yersinia enterocolitica/classification , Yersinia enterocolitica/drug effects , Yersinia enterocolitica/genetics , Yersinia enterocolitica/isolation & purification
5.
Genet Mol Res ; 16(1)2017 Feb 16.
Article in English | MEDLINE | ID: mdl-28218780

ABSTRACT

Alzheimer's disease (AD) is a neurodegenerative disorder, and is the most common type of dementia in the elderly population. Growing evidence indicates that microRNAs (miRNAs) play a crucial role in neuroinflammation associated with AD progression. In this study, we analyzed the expression of microRNA-139 (miR-139) as well as the learning and memory function in AD. We observed that the miR-139 expression was significantly higher in the hippocampus of aged senescence accelerated mouse prone 8 (SAMP8) mice (2.92 ± 0.13) than in the control mice (1.49 ± 0.08). Likewise, the overexpression of miR-139 by means of hippocampal injection impaired the hippocampus-dependent learning and memory formation. In contrast, the downregulation of miR-139 in mice improved learning and memory function in the mice. The level of cannabinoid receptor type 2 (CB2), a potential target gene of miR-139, was inversely correlated with the miR-139 expression in primary hippocampal cells. Furthermore, we demonstrated that miR-139 inversely modulated the responses to proinflammatory stimuli. Together, our findings demonstrate that miR-139 exerts a pathogenic effect in AD by modulating CB2-meditated neuroinflammatory processes.


Subject(s)
Alzheimer Disease/psychology , Hippocampus/cytology , MicroRNAs/genetics , Receptor, Cannabinoid, CB2/genetics , Alzheimer Disease/genetics , Alzheimer Disease/metabolism , Animals , Cells, Cultured , Cytokines/metabolism , Disease Models, Animal , Gene Expression Regulation , Hippocampus/metabolism , Hippocampus/pathology , Humans , Maze Learning , Mice , MicroRNAs/metabolism , Receptor, Cannabinoid, CB2/metabolism
6.
J Biomech ; 44(11): 2040-6, 2011 Jul 28.
Article in English | MEDLINE | ID: mdl-21665208

ABSTRACT

Fluid flow in the bone lacuno-canalicular network can induce dynamic fluctuation of intracellular calcium concentration ([Ca(2+)](i)) in osteoblasts, which plays an important role in bone remodeling. There has been limited progress in the mathematical modeling of this process probably due to its complexity, which is controlled by various factors such as Ca(2+) channels and extracellular messengers. In this study we developed a mathematical model to describe [Ca(2+)](i) response induced by fluid shear stress (SS) by integrating the major factors involved and analyzed the effects of different experimental setups (e.g. [Ca(2+)](i) baseline, pretreatment with ATP). In this model we considered the ATP release process and the activities of multiple ion channels and purinergic receptors. The model was further verified quantitatively by comparing the simulation results with experimental data reported in literature. The results showed that: (i) extracellular ATP concentration has more significant effect on [Ca(2+)](i) baseline (73% increase in [Ca(2+)](i) with extracellular ATP concentration varying between 0 and 10 µM), as compared to that induced by SS (25% variation in [Ca(2+)](i) with SS varying from 0 to 3.5 Pa); (ii) Pretreatment with ATP-medium results in different [Ca(2+)](i) response as compared to the control group (ATP-free medium) under SS; (iii) Relative [Ca(2+)](i) fluctuation over baseline is more reliable to show the [Ca(2+)](i) response process than the absolute [Ca(2+)](i) response peak. The developed model may improve the experimental design and facilitate our understanding of the mechanotransduction process in osteoblasts.


Subject(s)
Calcium/metabolism , Models, Biological , Osteoblasts/metabolism , Adenosine Triphosphate/metabolism , Calcium Signaling , Cells, Cultured , Ion Channels/metabolism , Mechanotransduction, Cellular , Receptors, Purinergic/metabolism , Shear Strength
7.
Lett Appl Microbiol ; 50(2): 168-72, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20002577

ABSTRACT

AIMS: To investigate whether Vibrio vulnificus metalloprotease (VvpE) can induce the production of specific anti-VvpE antibody to confer effective protection against Vibrio vulnificus infection and to evaluate the possibility of VvpE as a potential vaccine candidate against disease caused by V. vulnificus. METHODS AND RESULTS: The gene encoding the 65-kDa VvpE of V. vulnificus was amplified by PCR and cloned into the expression vector pET21(b). The recombinant VvpE of V. vulnificus was expressed in Escherichia coli BL21(DE3). This His(6)-tagged VvpE was purified and injected intramuscularly into mice to evaluate its ability to stimulate immune response. Specific antibody levels were measured by ELISA. The 75% protective efficacy of recombinant VvpE was evaluated by active immunization and intraperitoneal challenge with V. vulnificus in mice. CONCLUSIONS: The recombinant His(6)-tagged VvpE of V. vulnificus is capable of inducing high antibody response in mice to confer effective protection against lethal challenge with V. vulnificus. VvpE might be a potential vaccine candidate to against V. vulnificus infection. SIGNIFICANCE AND IMPACT OF THE STUDY: This study uses His(6)-tagged VvpE to act as vaccine that successfully induces effective and specific anti-VvpE antibody and offers an option for the potential vaccine candidate against V. vulnificus infection.


Subject(s)
Antigens, Bacterial/immunology , Bacterial Proteins/immunology , Bacterial Vaccines/immunology , Metalloproteases/immunology , Vibrio Infections/prevention & control , Vibrio vulnificus/immunology , Animals , Antibodies, Bacterial/blood , Antibodies, Bacterial/immunology , Antigens, Bacterial/biosynthesis , Antigens, Bacterial/genetics , Antigens, Bacterial/pharmacology , Bacterial Proteins/biosynthesis , Bacterial Proteins/genetics , Bacterial Proteins/pharmacology , Bacterial Vaccines/biosynthesis , Bacterial Vaccines/genetics , Bacterial Vaccines/pharmacology , Female , Immunization/methods , Metalloproteases/biosynthesis , Metalloproteases/genetics , Metalloproteases/pharmacology , Mice , Mice, Inbred BALB C , Recombinant Proteins/biosynthesis , Recombinant Proteins/genetics , Recombinant Proteins/immunology , Recombinant Proteins/pharmacology , Vibrio Infections/enzymology , Vibrio Infections/genetics , Vibrio Infections/immunology , Vibrio vulnificus/enzymology , Vibrio vulnificus/genetics
8.
Oncogene ; 27(3): 332-8, 2008 Jan 10.
Article in English | MEDLINE | ID: mdl-17621266

ABSTRACT

The ribosomal acidic P0 protein, an essential component of the eukaryotic ribosomal stalk, was found to interact with the helix-loop-helix protein human Grap2 and cyclin D interacting protein (GCIP)/D-type cyclin-interacting protein 1/human homolog of MAID protein. Using in vivo and in vitro binding assays, we show that P0 can interact with the N and C termini of GCIP via its N-terminal 39-114 amino-acid residues. Although the P0-GCIP complex was detected mainly in cytoplasmic fraction, polysome profile analysis indicated that the P0-GCIP complex did not coelute with either polysomes or 60S ribosomes, suggesting that GCIP associates with the free form of P0 in the cytoplasm. Transfection of GCIP into MCF-7 cells resulted in decreased levels of pRb phosphorylation. Cotransfection of P0 with GCIP, however, resulted in GCIP-mediated reduction of pRb phosphorylation level which was repressed by P0. Furthermore, overexpression of P0 in breast cancer and hepatocellular cancer cell lines promoted cell growth and colony formation compared to control transfectants. Overexpression of P0 also increased cyclin D1 expression and phosphorylation of pRb at Ser780. Interestingly, P0 mRNA was overexpressed in 12 of 20 pairs of breast cancer/ normal breast specimens (60%). Together, these data indicate that P0 overexpression may cause tumorigenesis in breast and liver tissues at least in part by inhibiting GCIP-mediated tumor suppression.


Subject(s)
Breast Neoplasms/pathology , Carcinoma, Hepatocellular/pathology , Cell Transformation, Neoplastic/metabolism , Hepatocytes/pathology , Ribosomal Proteins/metabolism , Transcription Factors/metabolism , Breast Neoplasms/metabolism , Carcinoma, Hepatocellular/metabolism , Cell Line, Tumor , Cell Proliferation , Hepatocytes/metabolism , Humans , Phosphorylation , Protein Interaction Domains and Motifs , Protein Interaction Mapping , Up-Regulation
9.
Oncol Rep ; 17(1): 35-9, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17143475

ABSTRACT

The mammalian Janus kinase (JAK) family consists of four members, namely JAK1, JAK2, JAK3 and TYK2, which play a critical role in cytokine/growth factor signaling and is increasingly associated with human cancers. Aberrant activation of these non-receptor tyrosine kinases may contribute to carcinogenesis. Herein, we focused on exploring the potential role of p-JAK1 in breast cancer. The expression profiles of p-JAK1 were analyzed in 68 pairs of cancer and non-cancer breast tissues from the same infiltrating ductal carcinoma case by using immunoblotting technique. The results obtained were further correlated with clinicopathological characteristics. Intriguingly, p-JAK1 expression was decreased in 55.9% of breast cancer tissues as compared to the matched non-cancer tissues. Further immunohistochemistry study showed an intense p-JAK1 staining predominantly in adjacent normal breast tissues but not the matched cancer lesions. Decreased p-JAK1 expression in breast cancer tissues was significantly correlated with positive estrogen receptor (ER) status and increased tumor size (p=0.010 and 0.009). We also found that p-JAK1 expression was high in ERalpha-negative breast cancer cell lines but was low in ERalpha-positive breast cell lines. Transfection of ERalpha-positive MCF-7 cells with an ERalpha-specific siRNA upregulated the expression of p-JAK1. In summary, our results indicated that an altered p-JAK1 expression might be involved in the development of breast infiltrating ductal carcinoma in an ERalpha-related manner.


Subject(s)
Breast Neoplasms/metabolism , Carcinoma, Ductal, Breast/metabolism , Janus Kinase 1/biosynthesis , Receptors, Estrogen/metabolism , Breast Neoplasms/enzymology , Breast Neoplasms/pathology , Carcinoma, Ductal, Breast/enzymology , Carcinoma, Ductal, Breast/pathology , Enzyme Activation , Humans , Immunoblotting , Immunohistochemistry , Janus Kinase 1/metabolism , Neoplasm Staging , Phosphorylation
10.
Vet Res Commun ; 30(6): 645-54, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16838206

ABSTRACT

The effects of hexachlorocyclohexane (HCH) on growth performance and immune and oxidative stress in growing/finishing pigs were studied. Seventy-two pigs, with equal numbers of barrows and gilts, of the same genotype (Duroc x Landrace x Large White), were randomly assigned to three groups receiving the same basal diet, exposed to 0, 0.4 and 0.8 mg/kg technical HCH, respectively, for 90 days. Six pigs from each group were randomly picked out and slaughtered on a finishing feeding trial. The result showed that addition of HCH did not affect the growth performance significantly but increased the weight of kidney and thymus significantly. Total serum IgG and IgM were elevated significantly, but there were no significant differences in serum IgA, C3 and C4 among the groups. Addition of HCH to feedstuff reduced superoxide dismutase (SOD), glutathione S-transferase (GST), glutathione reductase (GR) and glutathione peroxidase (GSH-Px) activities in liver, reduced serum catalase (CAT) activity, and increased serum malondialehyde (MDA). Moreover, the activities of serum alanine aminotransferase and alkaline phosphatase were increased significantly. Addition of 0.4 mg/kg or 0.8 mg/kg HCH did not affect the growth performance but affected the immune and antioxidant potential.


Subject(s)
Hexachlorocyclohexane/toxicity , Insecticides/toxicity , Liver/metabolism , Organ Size/drug effects , Oxidative Stress/drug effects , Swine/growth & development , Alanine Transaminase/metabolism , Alkaline Phosphatase/metabolism , Animals , Dose-Response Relationship, Drug , Female , Food Contamination , Immunoglobulin G/blood , Immunoglobulin M/blood , Lipid Peroxidation , Liver/drug effects , Liver/enzymology , Male , Oxidative Stress/immunology , Random Allocation , Weight Gain/drug effects
11.
J Neuropathol Exp Neurol ; 62(9): 917-26, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14533781

ABSTRACT

Aged individuals with Down syndrome (DS) develop senile plaques and neurofibrillary tangles consistent with Alzheimer disease (AD). Prior to or in parallel with AD pathology, compensatory growth responses may occur. Immunohistochemistry and confocal microscopy studies in the hippocampus from 15 individuals ranging in age from 5 months to 67 years compared markers of normal and abnormal tau accumulation (phosphorylated tau [AT8, MC-1], tau-1, N-terminal tau) with the extent and location of neuronal growth marker immunoreactivity (BDNF, GAP-43, MAP-2). In middle age (30-40 years), prior to entorhinal neuron loss, the earliest tau accumulation occurred in the outer molecular layer (OML), which was consistent with both pathological and compensatory fetal tau expression. These events were followed at a later age, associated with entorhinal neuron loss, by an increase in GAP-43. Hilar neurons exhibiting a sprouting morphology were also noted. Age-dependent observations in the DS brain in the current study parallel hippocampal compensatory responses described in entorhinal cortex lesion studies in rodents. Thus, compensatory growth responses may occur in DS prior to extensive AD pathology and may be one mechanism underlying observations in PET studies of hypermetabolism in the entorhinal cortex of individuals with DS.


Subject(s)
Down Syndrome/metabolism , Down Syndrome/pathology , tau Proteins/metabolism , Adolescent , Adult , Age Factors , Age of Onset , Aged , Child , Child, Preschool , Entorhinal Cortex/metabolism , Entorhinal Cortex/pathology , Female , Gene Expression Regulation/physiology , Hippocampus/metabolism , Hippocampus/pathology , Humans , Infant , Male , Middle Aged , Phosphorylation
12.
Toxicol In Vitro ; 17(2): 139-43, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12650666

ABSTRACT

Exposure to arsenic has been reported to cause DNA damage and eventually the occurrence of bladder, lung and skin cancers. A previous report has demonstrated that arsenite-induced phosphorylation of Mre11, a protein involved in the repair of DNA double strand breaks (DSBs), is M phase-dependent and requires the Nijmegen breakage syndrome (NBS) protein, NBS1 [DNA Repair 1 (2002) 137]. Furthermore, arsenite treatment arrests cells at the M phase and the cells eventually go through apoptosis [Biochemical Pharmacology 60 (2000) 771]. Here we demonstrate that arsenite treatment enhances the generation of nitric oxide (NO), and that the enhanced NO generation is dominant at the G2/M phase. Arsenite-induced NO generation is impaired in DSB repair-defective NBS cells, but not in NBS1-reconstituted NBS cells, suggesting NBS1 is required for effective NO generation. In summary, our study showed, for the first time, that arsenite-induced NO generation is cell-cycle- and NBS1-dependent.


Subject(s)
Arsenites/toxicity , Cell Cycle Proteins/metabolism , G2 Phase/drug effects , Mitosis/drug effects , Nitric Oxide/metabolism , Nuclear Proteins/metabolism , Cell Cycle Proteins/physiology , Cells, Cultured , DNA-Binding Proteins/metabolism , Fibroblasts/cytology , Fibroblasts/metabolism , Humans , MRE11 Homologue Protein , Nuclear Proteins/physiology , Phosphorylation , Tumor Cells, Cultured/cytology , Tumor Cells, Cultured/metabolism
13.
Aust N Z J Obstet Gynaecol ; 42(3): 259-63, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12230059

ABSTRACT

OBJECTIVE: To assess whether total hysterectomy is associated with increased postoperative vesicourethral abnormalities. SAMPLE: Forty-five patients had a laparoscopic hysterectomy and 36 patients had a total abdominal hysterectomy. DESIGN: Before and after hysterectomy, patients underwent a urinalysis, a personal interview, and an urodynamic study. RESULTS: Of the laparoscopic hysterectomy group, 27 patients (60%) exhibited urinary symptoms preoperatively, and 22 patients (48.9%) remained symptomatic following surgery. There was no significant change in the number of women with one or more urinary symptoms, but the incidence of urinary frequency and stress incontinence decreased significantly following hysterectomy (p < 0.05). Of the total abdominal hysterectomy group, preoperative voiding symptoms were present in 22 patients (61.1%). After surgery, urinary symptoms were present in 19 patients (52.8%). Some patients did not complain of any urinary frequency or stress incontinence following hysterectomy, but this figure did not differ significantly (p > 0.05). Maximal urethral closure pressure and maximal cystometric capacity demonstrated significant increases for both groups following surgery. CONCLUSIONS: The results indicated that total hysterectomy, either laparoscopic or total abdominal hysterectomy, did not significantly increase the subjective and objective incidence of vesicourethral dysfunction. On the contrary, some patients experience a substantial improvement of pre-existing urinary frequency or stress incontinence, partly as a result of an increase in the maximal urethral closure pressure and total bladder capacity following hysterectomy.


Subject(s)
Hysterectomy/methods , Urination , Female , Humans , Postoperative Period , Urethra/physiopathology , Urinary Bladder/physiopathology , Urinary Incontinence/physiopathology , Urodynamics
14.
Kaohsiung J Med Sci ; 17(7): 381-4, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11593966

ABSTRACT

Scar endometriosis remains quite rare and there is only one case report in the literature of plastic surgery. We present a case of endometrioma appearing on the cesarean section scar. The classic symptom was a painful scar that became swollen and more tender during menstruation. The cause of surgical scar endometriosis is believed to be iatrogenic transplantation of endometrium to the surgical wound. Surgical excision remains the treatment of choice. This entity must be kept in mind by plastic surgeons evaluating patients who present with soft-tissue masses of the abdominal wall in the setting of previous combined hysterectomy and abdominoplasty.


Subject(s)
Cesarean Section/adverse effects , Cicatrix/complications , Endometriosis/etiology , Adult , Endometriosis/pathology , Endometriosis/surgery , Female , Humans , Pregnancy
15.
Biochem Biophys Res Commun ; 287(2): 359-65, 2001 Sep 21.
Article in English | MEDLINE | ID: mdl-11554735

ABSTRACT

The blue fluorescent protein (BFPVV) gene bfpvv from Vibrio vulnificus CKM-1 was cloned and sequenced. The transformants exhibited blue fluorescence when irradiated by UV source. Nucleotide sequence analysis predicted an ORF of 717 bp encoding a 239-amino-acid polypeptide with a calculated molecular mass of 25.8 kDa. The nucleotide sequence of the bfpvv gene and its deduced amino acid sequence showed significant homology to those of the short-chain dehydrogenase/reductase (SDR) family proteins from various organisms. Some functionally important residues in SDR were strictly conserved in BFPVV, such as an active-site Tyr145, a catalytic site Lys149, and a common GlyXXXGlyXGly pattern in the N-terminal part of the molecule. By changing three amino acid residues, Tyr145, Lys149, and Gly9 to Phe, Ile, and Val, respectively, it was found that the G9V mutant did not generate blue fluorescence, while mutants Y145F and K149I have 126 and 68.5% fluorescence compared with the wild-type BFPVV.


Subject(s)
Bacterial Proteins/genetics , Luminescent Proteins/genetics , Vibrio/genetics , Amino Acid Sequence , Bacterial Proteins/chemistry , Cloning, Molecular , DNA, Bacterial/analysis , Electrophoresis, Polyacrylamide Gel , Fluorescence , Luminescent Proteins/chemistry , Molecular Sequence Data , Mutagenesis, Site-Directed , Sequence Homology, Amino Acid , Vibrio/chemistry
16.
Kaohsiung J Med Sci ; 17(5): 278-81, 2001 May.
Article in English | MEDLINE | ID: mdl-11517868

ABSTRACT

Endometriosis is a common disease found in reproductive age women, but pulmonary endometriosis is rare. We present a 21-year-old female with catamenial chest pain, chest tightness, severe cough, and hemoptysis. Though we could not find any definite intrapulmonary endometriotic lesion by computed tomography and bronchoscope, she was diagnosed to have pulmonary endometriosis due to the typical clinical symptoms. After 6 months of GnRH agonist application, the symptoms were completely relieved. She has been followed up and has been symptoms free for at least 6 months after administration of GnRH agonist.


Subject(s)
Endometriosis/drug therapy , Leuprolide/therapeutic use , Lung Diseases/drug therapy , Adult , Female , Humans
17.
Brain Res ; 898(2): 350-7, 2001 Apr 20.
Article in English | MEDLINE | ID: mdl-11306022

ABSTRACT

Several studies have suggested that activated caspase-3 has properties of a cell death executioner protease. In this study, we examined the expression of activated caspase-3 in AD and aged control brains. Activated caspase-3 immunoreactivity was seen in neurons, astrocytes, and blood vessels, was elevated in AD, and exhibited a high degree of colocalization with neurofibrillary tangles and senile plaques. These data suggest that activated caspase-3 may be a factor in functional decline and may have an important role in neuronal cell death and plaque formation in AD brain.


Subject(s)
Aging/metabolism , Aging/pathology , Alzheimer Disease/enzymology , Alzheimer Disease/pathology , Brain/enzymology , Brain/pathology , Caspases/metabolism , Aged , Alzheimer Disease/physiopathology , Amyloid beta-Peptides/metabolism , Antibodies/metabolism , Astrocytes/enzymology , Astrocytes/pathology , Blood Vessels/enzymology , Blood Vessels/pathology , Brain/physiopathology , Caspase 3 , Cell Count , Humans , Immunohistochemistry , Neurofibrillary Tangles/enzymology , Neurofibrillary Tangles/pathology , Neurofilament Proteins/metabolism , Neurons/enzymology , Neurons/pathology , Plaque, Amyloid/enzymology , Plaque, Amyloid/pathology
18.
J Nat Prod ; 64(3): 318-23, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11277747

ABSTRACT

Four new briarane diterpenes, briaexcavatolides K-N (1-4), along with a known diterpene, 5, have been isolated from the Taiwanese gorgonian Briareum excavatum. The structures of the new metabolites were established by extensive spectral analyses. Furthermore, the structure, including the relative configuration of briaexcavatolide K (1), was confirmed by a single-crystal X-ray analysis. Briaexcavatolides K and L (1 and 2) are the only briarane diterpenes known to possess hydroxyl groups at the C-8beta and C-17alpha positions, respectively. Cytotoxicity of these metabolites toward various cancer cell lines also is described.


Subject(s)
Cnidaria/chemistry , Diterpenes/isolation & purification , Animals , Crystallography, X-Ray , Diterpenes/chemistry , Molecular Structure , Taiwan
19.
Neurobiol Aging ; 22(2): 195-207, 2001.
Article in English | MEDLINE | ID: mdl-11182469

ABSTRACT

To understand the extent and specificity of astrocyte pathology in sporadic frontotemporal dementia (FTD), we examined several FTD cases for molecular and morphologic characteristics of astrocyte degeneration. We quantified reactive and degenerating astrocytes in sections of frontal, temporal, parietal, and occipital cortex identified using glial fibrillary acidic protein (GFAP) immunoreactivity, terminal deoxynucleotidyl transferase (TdT) labeling, and morphological characteristics and compared them with nondemented, age-matched control brains. Conventional and confocal microscopy revealed that a subpopulation of GFAP(+) astrocytes exhibited positive TdT labeling and beading of their processes in the frontal, temporal, and parietal cortices in 5 of 7 FTD cases that also exhibited gliosis. This morphology was reproduced in cultured astrocytes using ischemic insults. Degenerating astrocytes in FTD correlated inversely with cerebral blood flow as measured by single photon emission computed tomography (SPECT) analysis of (133)Xe inhalation (r = 0.55, p < 0.05). Furthermore, areas of significant astrogliosis corresponded to areas of SPECT hypoperfusion, suggesting that astrocytes may be affected by or perhaps have a causal role in the disturbances of cerebral perfusion in FTD.


Subject(s)
Astrocytes/pathology , Cerebral Cortex/blood supply , Cerebral Cortex/pathology , Cerebrovascular Circulation , Dementia/pathology , S100 Proteins , Aged , Aged, 80 and over , Alzheimer Disease/pathology , Astrocytes/chemistry , Calcium-Binding Proteins/analysis , DNA Fragmentation , DNA Nucleotidylexotransferase/analysis , Dementia/diagnostic imaging , Female , Glial Fibrillary Acidic Protein/analysis , Gliosis/pathology , Humans , Male , Microscopy, Confocal , Middle Aged , Nerve Growth Factors/analysis , S100 Calcium Binding Protein beta Subunit , Tomography, Emission-Computed, Single-Photon
20.
Am J Pathol ; 158(1): 189-98, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11141492

ABSTRACT

Although evidence suggests that neurofibrillary tangles (NFTs) and neuronal cell loss are prominent features of Alzheimer's disease (AD), the relationship between the two remains unknown. In the present study, the relationship between the activation of apoptotic mechanisms and NFT formation in AD was investigated using a caspase-cleavage site-directed antibody to fodrin, an abundant neuronal cytoskeleton protein. This antibody recognized cleavage products of fodrin after digestion by caspase-3, but did not recognize full-length fodrin. In vitro analysis of this fodrin caspase-cleavage product (CCP) antibody demonstrates that it is a specific probe for the detection of apoptotic but not necrotic pathways in cultured neurons. To determine whether caspases cleave fodrin in vivo, tissue sections from controls and AD were immunostained for fodrin (CCPs). Although no staining was observed in control cases, labeling of neurons was observed in the hippocampus of all AD cases, which increased as a function of disease progression. To determine a possible relationship between caspase activation and NFT formation, double-labeling experiments with fodrin CCP and PHF-1 were performed. Co-localization of these markers was observed in many neurons, and quantitative analysis showed that as the extent of NFT formation increased, there was a significant corresponding increase in fodrin CCP immunolabeling (r = 0.84). Taken together, these results provide evidence for the activation of apoptotic mechanisms in neurons in the AD brain and suggest that there is an association between NFT formation and the activation of apoptotic pathways in AD.


Subject(s)
Alzheimer Disease/metabolism , Caspases/metabolism , Neurofibrillary Tangles/metabolism , Adult , Aged , Aged, 80 and over , Alzheimer Disease/pathology , Animals , Apoptosis , Blotting, Western , Brain/metabolism , Brain/pathology , Carrier Proteins/immunology , Carrier Proteins/metabolism , Cell-Free System , Cells, Cultured , Dogs , Enzyme Activation , Female , Hippocampus/chemistry , Hippocampus/pathology , Humans , Immunohistochemistry , Male , Microfilament Proteins/immunology , Microfilament Proteins/metabolism , Microscopy, Confocal , Middle Aged , Neurons/chemistry , Rats , Rats, Sprague-Dawley , Tumor Cells, Cultured
SELECTION OF CITATIONS
SEARCH DETAIL
...