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1.
J Helminthol ; 89(4): 439-45, 2015 Jul.
Article in English | MEDLINE | ID: mdl-24739959

ABSTRACT

The liver fluke, Opisthorchis viverrini, and the minute intestinal fluke, Haplorchis taichui, are prevalent in many Asian countries. This study analysed the patterns of infections of O. viverrini and H. taichui in Lahanam and Thakhamlien villages (Savannakhet Province, Lao PDR), in two cross-sectional investigations. Out of a total of 207 human participants, post-anthelmintic treatment positivity rates for expelled worms were 170 (82.1%) for H. taichui and 65 (31.4%) for O. viverrini. Both these species co-exist in the study villages. When each parasite was analysed separately, H. taichui infections reached a plateau among people aged >20 years. Opisthorchis viverrini infection rates were highest in the age group 21-30 years, with decreasing infection rates after the age of 30. Our findings indicated that fish-borne trematode infections were more prevalent among adults. Fish, common intermediate hosts, were acquired in the study area for analysis. The examination of 35 species of fish as intermediate hosts found O. viverrini metacercariae in only six species, and these were found mostly during the month of November. Many farmers who live on the rice fields obtain their food from their immediate environment, including these intermediate-host fish, potentially putting them at greater risk of O. viverrini infection. By contrast, H. taichui metacercariae were found in three species of fish obtained from the market, meaning that anyone could consume them and become infected. If people who work in rice fields limit the species of fish they consume, or avoid consuming raw fish during the month of November, they may reduce their risk of O. viverrini infection.


Subject(s)
Trematoda/classification , Trematode Infections/parasitology , Adolescent , Adult , Animals , Child , Child, Preschool , DNA, Helminth/genetics , Female , Humans , Infant , Laos/epidemiology , Male , Middle Aged , Opisthorchis , Trematoda/genetics , Trematode Infections/epidemiology , Young Adult
2.
Gynecol Obstet Invest ; 66(1): 12-3, 2008.
Article in English | MEDLINE | ID: mdl-18230909

ABSTRACT

A rare case of a 31-year-old woman is reported who had massive intraperitoneal bleeding caused by ovarian hemorrhage as the first manifestation of acute leukemia. Preoperative laboratory findings revealed severe anemia (Hb 6.6 g/dl) and thrombocytopenia (1.5 x 10(4)/mm(3)) but normal leukocyte count (3.9 x 10(3)/mm(3)). After surgery, blast cells were found in her peripheral blood and she was diagnosed with M0 type acute myeloid leukemia. In addition, histopathology revealed infiltration of leukemic cells in the resected ovary.


Subject(s)
Hemoperitoneum/etiology , Leukemia, Myeloid, Acute/pathology , Ovarian Neoplasms/secondary , Adult , Female , Humans , Ovarian Neoplasms/surgery
3.
Placenta ; 28(2-3): 192-8, 2007.
Article in English | MEDLINE | ID: mdl-16638616

ABSTRACT

Id-1, a member of the helix-loop-helix transcription factor family, inhibits the differentiation of Rcho-1 cells, which were derived from rat choriocarcinoma and consist of trophoblast stem cells. Id-1 is expressed at a high level in undifferentiated trophoblast stem cells and then down-regulated during early differentiation, and is thought to be a key regulator in the trophoblast giant-cell differentiation pathway. In this study, we analyzed the signaling mechanism regulating the high expression levels of Id-1 in undifferentiated Rcho-1 cells. Promoter deletion analysis revealed that a 31-bp sequence (Box-2 region), located between -200 and -169bp in the Id-1 promoter is necessary for the promoter activity. Electrophoretic mobility shift assays and DNA affinity precipitation assays showed that Box-2-binding activity was decreased during differentiation and that Sp-1 protein bound to this sequence. The protein level of Sp-1 was decreased during the differentiation. These results suggest that the Sp-1 protein level may regulate the Box-2-binding activity and the trophoblast giant-cell differentiation.


Subject(s)
Cell Differentiation/physiology , Inhibitor of Differentiation Protein 1/physiology , Sp1 Transcription Factor/physiology , Trophoblasts/physiology , Animals , Cell Line , Electrophoresis, Polyacrylamide Gel , Electrophoretic Mobility Shift Assay , Gene Expression Regulation , Inhibitor of Differentiation Protein 1/genetics , Promoter Regions, Genetic , Rats , Signal Transduction/physiology , Trophoblasts/cytology
4.
Anal Biochem ; 207(2): 255-60, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1481979

ABSTRACT

Menadione-catalyzed H2O2 production by viable cells is proportional to viable cell number. The correlations between the viable cell number and the concentration of H2O2 produced are determined with the rapid chemiluminescent assay (S. Yamashoji, T. Ikeda, and K. Yamashoji, 1989, Anal. Biochem. 181, 149-152). This chemiluminescent assay of viable cells requires only 10 min and is much faster than NR (neutral red) inclusion and MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) reduction assays, which require 3-5 h. When viable cells are incubated with antitumor drugs, detergents, mycotoxins, and glycoalkaloids for 24-48 h, a decrease in menadione-catalyzed H2O2 production in a dose- or incubation time-dependent manner is observed. In general, the 50% inhibition concentration determined by the chemiluminescent assay is lower than that determined by NR inclusion and MTT reduction assays, and the order of relative cytotoxic effects of agents is the same among these assays. Furthermore, clear cytotoxic effects are observed by the chemiluminescent assay after 1 h exposure of trypsinized cells to toxic compounds. Therefore, the chemiluminescent assay is expected to be more useful for the rapid detection of cytotoxic compounds than NR inclusion and MTT reduction assays.


Subject(s)
Antineoplastic Agents/pharmacology , Cell Survival/drug effects , Hydrogen Peroxide/metabolism , Vitamin K/pharmacology , 3T3 Cells , Adenocarcinoma , Animals , Cell Count/methods , Cell Line , Coloring Agents , Humans , Indicators and Reagents , Luminescent Measurements , Male , Mice , Prostatic Neoplasms , Tetrazolium Salts , Thiazoles , Tomatine/pharmacology , Tumor Cells, Cultured
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