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1.
J Agric Food Chem ; 64(45): 8491-8498, 2016 Nov 16.
Article in English | MEDLINE | ID: mdl-27771954

ABSTRACT

This study was done to identify pesticide-biodegrading microorganisms and to characterize degradation rates. Bacillus safensis strain FO-36bT, Bacillus subtilis subsp. inaquosorum strain KCTC13429T, and Bacillus cereus strain ATCC14579T were isolated from pesticide-polluted soil in Sudan, separately incubated with each pesticide with periodic samples drawn for GC and GC-MS. Pesticide biodegradation followed a biphasic model. α and ß half-lives (days) of chlorpyrifos, malathion, and dimethoate in B. safensis culture were 2.13, 4.76; 2.59, 5.66; and 9.5, 11.0, respectively. Values in B. subtilis and B. cereus cultures were 4.09, 9.45 and 4.33, 9.99 for chlorpyrifos; 2.99, 5.36 and 2.43, 4.71 for malathion; and 9.53, 15.11 and 4.16, 9.27 for dimethoate. No metabolite was detected in B. subtilis cultures, whereas a few were detected from B. safensis and B. cereus cultures. Bacterial efficiency can be ordered as B. safensis > B. subtilis > B. cereus for chlorpyrifos and B. cereus > B. subtilis > B. safensis for malathion and dimethoate.


Subject(s)
Bacillus cereus/metabolism , Bacillus/metabolism , Chlorpyrifos/metabolism , Dimethoate/metabolism , Malathion/metabolism , Pesticides/metabolism , Soil Microbiology , Soil Pollutants/metabolism , Bacillus/classification , Bacillus/genetics , Bacillus/isolation & purification , Bacillus cereus/classification , Bacillus cereus/genetics , Bacillus cereus/isolation & purification , Biodegradation, Environmental , Phylogeny , Sudan
2.
Clin Radiol ; 69(6): e285-90, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24630134

ABSTRACT

AIM: To assess the relationship between chest computed tomography (CT) findings of patients with toxocariasis and levels of serological markers. MATERIALS AND METHODS: A total of 38 cases of patients diagnosed with toxocariasis by enzyme-linked immunosorbent assay (ELISA), CT, and serological markers were retrospectively reviewed. The presence of nodule with or without ground-glass opacity (GGO) halo, consolidation, focal GGO, pleural effusion, and lymphadenopathy at chest CT were evaluated. Statistical analysis was performed with the Fisher's exact test. RESULTS: The most common chest CT findings were nodule (n = 12, 31.6%) and focal GGO (n = 12, 31.6%). In patients with normal eosinophil levels, focal GGO (n = 9, 37.5%) was the most common finding. In contrast, nodule with a GGO halo (n = 7, 50%) was the most common finding in the eosinophilia group. Nodule with a GGO halo was more common in the eosinophilia group, with a statistically significant difference (p = 0.017). Nodule was more common in the eosinophilia group, and focal GGO was more common in the normal eosinophil group. CONCLUSION: The most common chest CT findings in toxocariasis were nodule with or without GGO halo, and focal GGO. In the eosinophilia group, nodule with a GGO halo was significantly more frequent. Other CT findings did not show a statistically significant relationship with serological markers.


Subject(s)
Lung Diseases, Parasitic/diagnostic imaging , Toxocariasis/diagnostic imaging , Adult , Aged , Aged, 80 and over , Biomarkers/blood , Enzyme-Linked Immunosorbent Assay , Eosinophils , Female , Humans , Immunoglobulin E/blood , Leukocyte Count , Male , Middle Aged , Multidetector Computed Tomography , Retrospective Studies , Solitary Pulmonary Nodule , Young Adult
3.
Vet J ; 193(1): 222-7, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22130461

ABSTRACT

Regulatory T cells (Treg) cells play a crucial role in tumor progression by suppressing anti-tumor immunity, but are not well-documented in veterinary oncology. To identify the characteristics of Treg cells in tumor microenvironments, the numbers of Treg cells were analyzed and compared with histological prognostic factors and molecular biomarkers in canine mammary carcinoma (MC) tissues (n=37). Abundant Treg cells were associated with high histological grade and lymphatic invasion. The numbers of Treg cells infiltrating intratumoral areas markedly increased in tumors with poor prognostic factors, such as high histological grade, lymphatic invasion, and necrosis. These findings suggest that Treg cells play a role in canine MC progression. Furthermore, Treg cell numbers in intratumoral compartments may provide a potential prognostic factor when assessing canine MCs, which may in turn lead to the development of new immunologic therapeutics.


Subject(s)
Biomarkers, Tumor/immunology , Carcinoma/physiopathology , Dog Diseases/physiopathology , Forkhead Transcription Factors/immunology , Mammary Neoplasms, Animal/physiopathology , T-Lymphocytes, Regulatory/immunology , Animals , Biomarkers, Tumor/metabolism , Carcinoma/genetics , Carcinoma/immunology , Disease Progression , Dog Diseases/genetics , Dog Diseases/immunology , Dogs , Epidermal Growth Factor/immunology , Epidermal Growth Factor/metabolism , Female , Forkhead Transcription Factors/metabolism , Mammary Neoplasms, Animal/genetics , Mammary Neoplasms, Animal/immunology , Prognosis , Receptors, Estrogen/immunology , Receptors, Estrogen/metabolism , T-Lymphocytes, Regulatory/cytology , T-Lymphocytes, Regulatory/metabolism
4.
Osteoporos Int ; 19(11): 1579-87, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18437273

ABSTRACT

UNLABELLED: This study investigated regional variations in the 3D microstructure of trabecular bone in human proximal femur, with respect to aging. The results demonstrate that age-related changes in trabecular microstructure significantly varied from different sub-regions of the proximal femur. INTRODUCTION: We hypothesize that the age-related changes in trabecular bone microstructure appear to be varied from specific anatomic sub-regions of the proximal femur followed by non-uniform bone loss. The purpose of this study was therefore to explore regional variations in the 3D microstructure of trabecular bone in human proximal femur, with respect to aging. METHODS: A total of 162 trabecular bone cores from six regions of 27 femora of male cadaver donors were scanned using micro-computed tomography (micro-CT). The following microstructural parameters were calculated: bone volume fraction (BV/TV), trabecular number (Tb.N), thickness (Tb.Th) and separation (Tb.Sp), structure model index (SMI), and degree of anisotropy (DOA). RESULTS: Age-related changes in trabecular microstructure varied from different regions of the proximal femur. There was a significant decrease in bone volume fraction and an almost identical decrease in trabecular thickness associated with aging at any region. Regional analysis demonstrated a significant difference in BV/TV, Tb.Th, Tb.Sp, Tb.N and DOA between superior and inferior neck, as well as a significant difference in BV/TV, Tb.Sp, Tb.N, SMI and DOA between superior and inferior trochanter. CONCLUSIONS: Age-related changes in bone loss and trabecular microstructure within the male proximal femur are not uniform in this cadaveric population.


Subject(s)
Aging/pathology , Femur/ultrastructure , Adult , Aged , Aged, 80 and over , Anisotropy , Femur/diagnostic imaging , Femur Head/diagnostic imaging , Femur Head/ultrastructure , Femur Neck/diagnostic imaging , Femur Neck/ultrastructure , Humans , Imaging, Three-Dimensional/methods , Male , Middle Aged , X-Ray Microtomography/methods
5.
Neurosci Lett ; 290(3): 201-4, 2000 Sep 01.
Article in English | MEDLINE | ID: mdl-10963898

ABSTRACT

To elucidate possible mechanisms of phorbol 12-myristate 13-acetate (PMA) induced in vitro invasiveness of glioblastoma cells, we examined expression levels of membrane-type 1 matrix metalloproteinase (MT1-MMP), MMP-2, MMP-9 and tissue inhibitor of metalloproteinase (TIMP)-1 and TIMP-2 using Western blotting and gelatin zymography assay, and found that PMA induced the secretion of MMP-9, activated MMP-2 proenzyme to fully active form of 59 kDa, down-regulated the TIMP-1 and TIMP-2 secretion, and increased MT1-MMP on the cell surface. However, PKC inhibitor Go 6983 reversed all of these effects brought about by PMA. We, therefore, conclude the activation of PKC by PMA in these cells plays a critical role in the regulation of MMPs/TIMPs system, which has a major role in tumor invasion and metastasis.


Subject(s)
Brain Neoplasms/enzymology , Glioblastoma/enzymology , Matrix Metalloproteinases/metabolism , Neoplasm Invasiveness/physiopathology , Phorbol Esters/pharmacology , Protein Kinase C/metabolism , Tissue Inhibitor of Metalloproteinases/metabolism , Brain Neoplasms/drug therapy , Brain Neoplasms/physiopathology , Glioblastoma/drug therapy , Glioblastoma/physiopathology , Humans , Phorbol Esters/metabolism , Protein Kinase C/drug effects , Tetradecanoylphorbol Acetate/analogs & derivatives , Tetradecanoylphorbol Acetate/metabolism , Tetradecanoylphorbol Acetate/pharmacology , Tumor Cells, Cultured
6.
J Korean Med Sci ; 15(3): 309-14, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10895974

ABSTRACT

To evaluate possible roles of matrix metalloproteinase (MMP)-1, -2, tissue inhibitor of metalloproteinase (TIMP)-1, -2 and membrane-type-1 matrix metalloproteinase (MT1-MMP) in invasion of human gliomas, expressions of these proteins were investigated in ten cases of human glioma and two meningioma tissues and eight human glioma cell lines. In gelatin zymography, MMP-2 activities of glioblastomas were higher than astrocytomas. The activated form of MMP-2 was seen in five of six cases of glioblastomas, but not in astrocytomas. MMP-9 activity was detected in all cases of malignant astrocytomas but the reactivity of MMP-9 was weaker than that of MMP-2. MT1-MMP mRNA expression in glioblastomas was higher than that in astrocytomas. Five cases of glioblastomas with activated form of MMP-2 had MT1-MMP expressions. In vitro, human glioma cell lines with high expression of MT1-MMP also showed high MMP-2 activity. TIMP-1 transcripts were constitutively present in almost all glioma tissues and cell lines, whereas TIMP-2 mRNA were weak especially in malignant gliomas. Imbalance of TIMP-2/MMP-2 was observed using immunoprecipitation analysis in a glioma cell line. High expression of MMP-2 and MT1-MMP is possibly involved in invasiveness of malignant glioma.


Subject(s)
Brain Neoplasms/enzymology , Gene Expression Regulation, Enzymologic , Glioma/enzymology , Matrix Metalloproteinase 2/genetics , Metalloendopeptidases/genetics , Animals , Blotting, Northern/methods , Brain/pathology , Brain Neoplasms/pathology , Enzyme Activation , Glioma/pathology , Humans , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/metabolism , Matrix Metalloproteinases, Membrane-Associated , Papio , Tissue Inhibitor of Metalloproteinase-1/genetics , Tissue Inhibitor of Metalloproteinase-2/genetics , Tumor Cells, Cultured
7.
Planta Med ; 64(6): 500-3, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9741293

ABSTRACT

Ginseng saponin metabolites produced by human intestinal bacteria were evaluated for antigenotoxic properties by testing their effects on benzo[a]pyrene (B[a]P)-induced mutagenicity and clastogenicity. They include 20-O-(beta-D-glucopyranosyl)-20(S)-protopanaxadiol (IH-901), 20-O-(alpha-D-arabinopyranosyl(1-->6)-beta-D-glucopyranosyl]- 20(S)-protopanaxadiol (IH-902) and 20-O-[alpha-D-arabinofuranosyl(1-->6)-beta-D-glucopyranosyl]-20(S)- protopanaxadiol (IH-903). IH-901, IH-902 and IH-903 inhibited the mutagenicity of B[a]P in a dose-dependent manner. In the chromosome aberration assay, IH-901 and IH-903 reduced the frequency of chromosome aberration induced by B[a]P. These results suggest that the ginseng saponin metabolites tested in the present study have potential as chemopreventive agents.


Subject(s)
Antimutagenic Agents/chemistry , Antimutagenic Agents/pharmacology , Benzo(a)pyrene/toxicity , Chromosome Aberrations , Intestines/microbiology , Microsomes, Liver/metabolism , Panax , Plants, Medicinal , Salmonella typhimurium/genetics , Saponins/metabolism , Saponins/pharmacology , Animals , Benzo(a)pyrene/antagonists & inhibitors , Cell Line , Cricetinae , Cricetulus , Humans , Lung , Male , Mutagenicity Tests , Rats , Rats, Sprague-Dawley , Salmonella typhimurium/drug effects , Sister Chromatid Exchange
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