result 2861 件
JaLCDOI | 10.18926/AMO/30753 |
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FullText URL | fulltext.pdf |
Author | Nakatani, Satoru| Naito, Ichiro| Momota, Ryusuke| Hinenoya, Noriko| Horiuchi, Kanji| Nishida, Keiichiro| Ohtsuka, Aiji| |
Abstract | We attempted to prepare colloidal iron within tissues by means of microwave irradiation. Mouse tissue blocks were fixed with a mixture of paraformaldehyde and ferric chloride in a cacodylate buffer, immersed in a cacodylate buffered ferric chloride solution, and irradiated in a microwave processor. Colloidal iron was prepared within tissues or cells, and was observed in the form of electron dense fine granules (1-2 nm in diameter) by transmission electron microscopy. Collagen fibrils in the connective tissue showed colloidal iron deposition at regular periodical intervals. Cells in the splenic tissue showed that fine colloidal granules were deposited on the ribosomes but not on the nuclear chromatin. This finding suggests that ferric ions could not diffuse into the nucleus, which was surrounded by the nuclear envelope. The podocyte processes of the renal glomerulus were stained diffusedly. Though this microwave in situ colloidal iron preparation method has some limitations, it is convenient for use in biomedical specimen preparation in transmission electron microscopy. |
Keywords | colloidal iron microwave histochemistry transmission electron microscopy |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-02 |
Volume | volume60 |
Issue | issue1 |
Publisher | Okayama University Medical School |
Start Page | 59 |
End Page | 64 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16508690 |
Web of Science KeyUT | 000235538900007 |
JaLCDOI | 10.18926/AMO/30752 |
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FullText URL | fulltext.pdf |
Author | Yamamoto, Shin| Kitamura, Yoshihiro| Yamada, Norihito| Nakashima, Yoshihiko| Kuroda, Shigetoshi| |
Abstract | Previous EEG studies have shown that transcendental meditation (TM) increases frontal and central alpha activity. The present study was aimed at identifying the source of this alpha activity using magnetoencephalography (MEG) and electroencephalography (EEG) simultaneously on eight TM practitioners before, during, and after TM. The magnetic field potentials corresponding to TM-induced alpha activities on EEG recordings were extracted, and we attempted to localize the dipole sources using the multiple signal classification (MUSIC) algorithm, equivalent current dipole source analysis, and the multiple spatio-temporal dipole model. Since the dipoles were mapped to both the medial prefrontal cortex (mPFC) and anterior cingulate cortex (ACC), it is suggested that the mPFC and ACC play an important role in brain activity induced by TM. |
Keywords | transcendental meditation magnetoencephalography(MEG) source analysis medial prefrontal cortex anterior cingulate cortex |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-02 |
Volume | volume60 |
Issue | issue1 |
Publisher | Okayama University Medical School |
Start Page | 51 |
End Page | 58 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16508689 |
Web of Science KeyUT | 000235538900006 |
JaLCDOI | 10.18926/AMO/30751 |
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FullText URL | fulltext.pdf |
Author | Kitajima, Takuji| Nishii, Kenji| Ueoka, Hiroshi| Shibayama, Takuo| Gemba, Kenichi| Kodani, Tsuyoshi| Kiura, Katsuyuki| Tabata, Masahiro| Hotta, Katsuyuki| Tanimoto, Mitsune| Sobue, Tomotaka| |
Abstract | To evaluate recent improvements in lung cancer screening, we compared the results of recently conducted lung cancer screening with those of a previous screening. This study compared the survival of lung cancer patients detected by lung cancer screening conducted between 1976 and 1984 (early period) with that conducted between 1989 and 1997 (late period). Two hundred seventy-six patients with lung cancer were detected in the early period and 541 patients with lung cancer were detected in the late period. The median survival time (late : 49.8 vs. early : 27.8 months) and the 5-year survival rate (late : 47.8 vs. early : 34.8%) of the patients with lung cancer detected in the late period were significantly better than those in the early period (p = 0.0054). Among patients undergoing resection, the proportion of pathological stage I patients in the late period was significantly higher than that in the early period (late : 60.8 vs. early : 54.9%, p = 0.005). Multivariate analysis showed that the screening time period was a significant prognostic factor (hazard ratio = 0.685, 95% confidence interval : 0.563-0.832, p = 0.0002). These results were consistent with the findings of case-control studies of lung cancer screening programs in the late period recently conducted in Japan, which also showed a greater efficacy for screening than for previous case-control studies in the early period. |
Keywords | lung cancer screening survival lung cancer mortality |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 173 |
End Page | 179 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838046 |
Web of Science KeyUT | 000238503600005 |
JaLCDOI | 10.18926/AMO/30750 |
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FullText URL | fulltext.pdf |
Author | Hiraki, Akio| Murakami, Tomoyuki| Aoe, Keisuke| Matsuda, Eisuke| Maeda, Tadashi| Umemori, Yoshiki| Ueoka, Hiroshi| |
Abstract | We describe here a patient with a recurrent hemangiopericytoma of the superior mediastinum 23 years after an initial complete resection. In the current biopsy specimen, the tumor cells were much more anaplastic than those seen 23 years ago. Although the patient was treated with chemotherapy, which consisted of ifosfamide and epirubicin, the tumor was unresponsive and he died 6 months later from disease progression. Careful long-term follow-up is mandatory for patients with hemangiopericytomas because recurrence with greater malignancy can develop following an extended disease-free interval. |
Keywords | primary hemangiopericytoma recurrence mediastinal tumor |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 197 |
End Page | 200 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838049 |
Web of Science KeyUT | 000238503600008 |
JaLCDOI | 10.18926/AMO/30749 |
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FullText URL | fulltext.pdf |
Author | Komiyama, Takamitsu| Nishida, Keiichiro| Yorimitsu, Masanori| Doi, Hideyuki| Miyazawa, Shinichi| Kitamura, Ai| Yoshida, Aki| Nasu, Yoshihisa| Abe, Nobuhiro| Ozaki, Toshifumi| |
Abstract | Ossification disturbance in femoral head reportedly is seen in the Spontaneously Hypertensive rats (SHR) between ages of 10 and 20 weeks. We investigated serum and tissue levels of insulin-like growth factor-1 (IGF-1) and vascular endothelial growth factor (VEGF) in SHR relevant to the ossification disturbance and osteonecrosis of the femoral head. Serum levels of IGF-1 and VEGF were significantly lower in SHR than in Wistar Kyoto rats (WKY) at weeks 5, 10, 15 and 20 (p<0.005). The incidence of histological ossification disturbance of the femoral head was higher in SHR (59%) than in WKY (40%) at week 20. Lower serum and local levels of VEGF in SHR appeared to be related to the incomplete ossification of the femoral heads. Immunohistochemical study showed significantly lower numbers of IGF-1 and VEGF positive chondrocytes in the femoral epiphyseal cartilage of SHR than in those of WKY at weeks 10, 15 and 20. Our results suggest that local and/or systemic levels of IGF-1 and VEGF between ages of 5 and 20 weeks might play roles in the pathogenesis of ossifi cation disturbance of the femoral head in SHR. |
Keywords | spontaneous hypertensive rats insulin like growth factor-1 vascular endothelial growth factor ossification disturbance osteonecrosis |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 141 |
End Page | 148 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838042 |
Web of Science KeyUT | 000238503600001 |
JaLCDOI | 10.18926/AMO/30748 |
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FullText URL | fulltext.pdf |
Author | Tamesue, Kiyokazu| Ichiba, Shingo| Nawa, Sugato| Shimizu, Nobuyoshi| |
Abstract | This study was carried out to determine whether an extracorporeal membrane oxygenation (ECMO) support could be sufficiently conducted by the right ventricle alone from the viewpoint of the hemodynamics and blood gas state. Six infant dogs underwent a bypass between the left pulmonary artery and left atrium with an in-line oxygenator after a left pneumonectomy. Partial ECMO support was conducted simply by opening the circuit, and total ECMO support was conducted by ligating the right pulmonary artery. After the establishment of partial ECMO, approximately one-third of the right ventricular output was passively shunted through the bypass circuit, and the cardiac index and central venous pressure did not change. The mean pulmonary arterial pressures increased significantly. After a complete ligation of the right pulmonary artery, all 6 dogs survived for 12 h, but the cardiac output and blood pressure decreased significantly. The blood gas state was sufficiently maintained throughout the experiment. The results suggest the possibility of using the pumpless ECMO support. However, the flow resistance of the membrane oxygenator proved to still be too high for use in a total pumpless ECMO. Further studies on long-term ECMO and the development of a membrane oxygenator with a considerably low flow-resistance are needed. |
Keywords | pumpless ECMO implantable artificial lung pulmonary bypass |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 167 |
End Page | 172 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838045 |
Web of Science KeyUT | 000238503600004 |
JaLCDOI | 10.18926/AMO/30747 |
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FullText URL | fulltext.pdf |
Author | Redsch, Oliver| Miyaishi, Satoru| Heinemann, Axel| Fiedler, Georg| Puschel, Klaus| Yamamoto, Hideki| Ishizu, Hideo| |
Abstract | The authors designed a questionnaire to investigate the differences in German and Japanese general practitioners? (GP) awareness of suicide and attitudes toward patients with suicidal ideation in their respective societies. The purpose of this study was to obtain insights leading to a better means of suicide prevention in primary care in Japan. The background for conducting the study was declining suicides in the past 20 years and the lower suicide rate in Germany compared with the present situation in Japan, where the number of suicides has in recent years continued to exceed 30,000, resulting in a suicide rate approximately 2 times higher than that in Germany. The questionnaire was randomly mailed to GPs in Okayama-Prefecture (western Japan) and Hamburg-State (northern Germany) and was collected in the same way. The patterns of answers were compared between the 2 countries, and the differences were statistically analyzed. Japanese GPs seem to have a lower will to prevent suicide in daily practice compared to German GPs and a great lack of knowledge about treatment of suicidal patients. These observations suggest that improving GPs? interest in the problem of suicide and providing training programs for the treatment of patients with suicidal intentions might be a means of achieving better suicide prevention in Japan. |
Keywords | suicide prevention general practitioner Japan Germany |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 159 |
End Page | 165 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838044 |
Web of Science KeyUT | 000238503600003 |
JaLCDOI | 10.18926/AMO/30746 |
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FullText URL | fulltext.pdf |
Author | Matsuo, Toshihiko| |
Abstract | We report herein the disappearance of macular hard exudates after the introduction of hemodialysis in diabetic patients. A 62-year-old woman and a 52-year-old man with diabetes mellitus showed hard exudates in the macula of the left eyes. Both patients had previously undergone panretinal photocoagulation in both eyes. During the follow-up, hemodialysis was introduced for deteriorating chronic renal failure caused by diabetic nephropathy. Half a year later, macular hard exudates in the left eyes disappeared dramatically in both patients, but the visual acuity remained the same. No additional laser treatment was done during the observation period. Hemodialysis is considered to have accelerated the resolution of macular hard exudates in both patients. The deposition of macular hard exudates in diabetic patients is due in part to concurrent poor renal function. |
Keywords | hemodialysis diabetic retinopathy hard exudates macular edema |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 201 |
End Page | 205 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838050 |
Web of Science KeyUT | 000238503600009 |
JaLCDOI | 10.18926/AMO/30745 |
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FullText URL | fulltext.pdf |
Author | Norii, Mika| Yamamura, Masahiro| Iwahashi, Mitsuhiro| Ueno, Akiko| Yamana, Jiro| Makino, Hirofumi| |
Abstract | The inflamed synovial tissue (ST) of rheumatoid arthritis (RA) is characterized by the selective accumulation of interferon gamma-producing Th1-type CD4+ T cells. In this study, we investigated whether the predominance of Th1-type CD4+ cells in the ST lesion is mediated by their selective recruitment through Th1 cell-associated chemokine receptors CXCR3 and CCR5. The lymphocyte aggregates in the ST of RA contained a large number of CD4+ T cells, which mostly expressed both CXCR3 and CCR5, but not CCR4. In contrast, the frequencies of CD4+ and CD8+ T cells expressing CXCR3 and CCR5 in the blood were significantly decreased in RA patients, compared with healthy controls (HC), although there was no difference in the frequencies of CCR4-expressing CD4+ and CD8+ T cells between RA and HC. CXCR3, CCR5, and CCR4 expression in blood CD4 + T cells and CXCR3 expression in CD8+ T cells were increased after interleukin-15 (IL-15) stimulation. Therefore, the distribution of Th1-type CD4+ T cells into the ST from the blood in RA may be associated with the local expression of chemokines, both CXCR3 and CCR5 ligands, and IL-15 may play a role in enhancing these chemokine receptors on CD4+ T cell infiltrates. |
Keywords | CXCR3 CCR5 CD4+ T cells interleukin-15 rheumatoid arthritis |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 149 |
End Page | 157 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838043 |
Web of Science KeyUT | 000238503600002 |
JaLCDOI | 10.18926/AMO/30744 |
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FullText URL | fulltext.pdf |
Author | Ogawa, Aiko| Emori, Tetsuro| Sumita, Wakako| Watanabe, Atsuyuki| Fujio, Hideki| Miyaji, Katsumasa| Ohe, Tohru| |
Abstract | A 52-year-old obese woman was admitted to our institution for evaluation of dyspnea and pulmonary hypertension (PH). Polysomnography revealed severe obstructive sleep apnea (OSA) with an apnea hypopnea index of 99.8. Treatment with nocturnal continuous positive airway pressure (CPAP) resulted in correction of daytime hypoxemia, hypercapnia, and near-normalization of pulmonary artery pressure. To our knowledge, this is the most severe case of OSA-associated PH (approximately70 mmHg) reported to date, and it was successfully treated with nocturnal CPAP. This case demonstrates that OSA should be considered and polysomnography performed in all patients with PH, irrespective of severity, and that nocturnal CPAP has therapeutic effects on both OSA and daytime PH. |
Keywords | continuous positive airway pressure polysomnography secondary pulmonary hypertension sleep apnea syndrome |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 191 |
End Page | 195 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838048 |
Web of Science KeyUT | 000238503600007 |
JaLCDOI | 10.18926/AMO/30743 |
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FullText URL | fulltext.pdf |
Author | Sumiyoshi, Hideaki| Matsuo, Noritaka| Shin, Toshitaka| Shirabe, Komei| Yoshioka, Hidekatsu| |
Abstract | Type III collagen is found in fetal skin and blood vessels. Previously, we characterized the proximal promoter of the human alpha1(III) collagen gene (COL3A1) using the human rhabdomyosarcoma cell line, A204, and NIH3T3 cells (Yoshino et al., Biochim Biophys Acta, 2005). In the present study, we further analyzed this promoter using additional cell lines, namely a human embryonal rhabdomyosarcoma cell line (RD) and bovine vascular smooth muscle cells (vSMCs), both of which show high expression of type III collagen. Using a luciferase assay, electrophoretic mobility shift assays (EMSA), and DNase footprinting assay, 2 types of multifactor complexes were shown to bind to the DNA region in the vicinity of the B element (- 80 to - 58), depending on the cell type. Next, we used cells stably transfected with a GFP-linked type III collagen promoter fragment for analysis of promoter expression. Usually, transfected cells retained the characteristics of the original cells. However, in several clones derived from RD cells, promoter expression as well as cell shape changed to patterns characteristic of the A204 cell line. Nuclear factors expressed by these clones were also characteristic of the A204 line. |
Keywords | type III collagen promoter transcription DNA binding protein |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-06 |
Volume | volume60 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 181 |
End Page | 189 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16838047 |
Web of Science KeyUT | 000238503600006 |
JaLCDOI | 10.18926/AMO/30742 |
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FullText URL | fulltext.pdf |
Author | Tajiri, Takuma| Tate, Genshu| Iwaku, Takeshi| Takeyama, Nobuyuki| Fusama, Shigeyoshi| Sato, Shuichi| Kunimura, Toshiaki| Mitsuya, Toshiyuki| Morohoshi, Toshio| |
Abstract | Right pleural effusion was diagnosed in a 36-year-old woman with right upper quadrant pain and fever. Enhanced pelvic computed tomography performed because of irregular genital bleeding revealed the pelvic inflammatory disease. Upon further questioning, the patient confirmed that she had recently undergone therapy for Chlamydia trachomatis infection. Therefore she was given an injection of tetracycline because we suspected Fitz-Hugh-Curtis syndrome (FHCS), a pelvic inflammatory disease characterized by perihepatitis associated with chlamydial infection. A remarkable clinical response to antibiotics was noted. The right upper quadrant pain was due to perihepatitis, and the final diagnosis was FHCS. Right pleural effusion may be caused by inflammation of the diaphragm associated with perihepatitis. Once chlamydial infection reaches the subphrenic liver, conditions in the closed space between the liver and diaphragm due to inflammatory adhesion may be conductive to chlamydial proliferation. The possibility of FHCS should be considered in patients and carefully distinguished from other abdominal diseases. |
Keywords | perihepatitis right pleural eff usion Fitz-Hugh-Curtis syndrome chlamydial infection pelvic inflammatory disease |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-10 |
Volume | volume60 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 289 |
End Page | 294 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 17072375 |
Web of Science KeyUT | 000241509000005 |
JaLCDOI | 10.18926/AMO/30741 |
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FullText URL | fulltext.pdf |
Author | Nagasaka, Takeshi| Goel, Ajay| Matsubara, Nagahide| Tanaka, Noriaki| |
Abstract | Aberrant promoter methylation, an 'epigenetic' form of genomic instability that leads to transcriptional silencing of tumor suppressor genes, is increasingly being recognized as a crucial component in the evolution of human cancers. With our limited knowledge of the molecular basis and timing of the initiation of altered methylation events in the stepwise progression of cancers, the biggest challenge we currently face is to identify novel biomarkers and technologies for the timely screening of patients carrying such alterations. One such strategy would be to develop tests for the detection of fecal DNA methylation patterns that will improve the sensitivity of noninvasive screening tests for colorectal neoplasia, and moreover, will decrease both mortality and the incremental costs of treating colorectal cancers. |
Keywords | fecal DNA colorectal cancer methylation epigenetics |
Amo Type | Review |
Publication Title | Acta Medica Okayama |
Published Date | 2006-10 |
Volume | volume60 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 249 |
End Page | 256 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 17072371 |
Web of Science KeyUT | 000241509000001 |
JaLCDOI | 10.18926/AMO/30740 |
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FullText URL | fulltext.pdf |
Author | Une, Tomoka| Yokoyama, Yuji| Ninomiya, Shinsuke| Shinozuka, Masako| Maruyama, Hidehiko| Morishima, Tsuneo| |
Abstract | Some marker chromosomes and chromosome rearrangements are difficult to identify using G-bands by Giemsa staining after trypsin treatment (G-banding) alone. Molecular cytogenetic techniques, such as spectral karyotyping (SKY) and fluorescence in situ hybridization (FISH), can help to detect chromosomal aberrations precisely. We analyzed the karyotypes in 6 cases of multiple congenital abnormalities and 1 case of spontaneous abortion (case 2). Three cases (cases 1, 6, and 7) had marker chromosomes, and 4 cases (cases 2-5) had chromosomal rearrangements. The karyotypes in cases 1, 2, and 3 were determined using FISH with probes based on the clinical findings and family histories. Spectral karyotyping (SKY) analysis in cases 4-7 showed that this method is useful and saves time. The combination of SKY and FISH analyses defi ned the range of the ring chromosome in case 7. We demonstrated that a combination of G-banding, FISH, and SKY can be applied effectively to the investigation of chromosomal rearrangement and to the detection of marker chromosome origins. We suggest the use of these methods for prenatal diagnosis, in which the inherent time limitations are particularly important. |
Keywords | spectral karyotyping fluorescence in situ hybridization molecular cytogenetics marker chromosome chromosome rearrangement |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-10 |
Volume | volume60 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 279 |
End Page | 287 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 17072374 |
Web of Science KeyUT | 000241509000004 |
JaLCDOI | 10.18926/AMO/30739 |
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FullText URL | fulltext.pdf |
Author | Aiga, Ayako| Asaumi, Koji| Lee, You Jin| Kadota, Hiroaki| Mitani, Shigeru| Ozaki, Toshifumi| Takigawa, Masaharu| |
Abstract | The localization and expression of neurotrophins and their receptors during distraction osteogenesis was investigated in 72 male rat femurs (11 weeks old) to further clarify the concurrence of cellular and molecular events of new bone formation. After osteotomy, a 7-day lag phase was followed by distraction at the rate of 0.25 mm/12 h for 21 days (distraction phase), and a 7-day consolidation phase. The localization of neurotrophins (NGF, BDNF and NT-3) and their receptors tropomyosinrelated kinases (TRKA, TRKB and TRKC) by immunostaining showed positive staining in bone forming cells in each stage, although the presence and staining intensity varied by cell type and phase. The expressions of NGF, BDNF and NT-3 by real-time polymerase chain reaction (real-time PCR) showed that the peak of the mRNA expression of NGF occurred 10 days after distraction. NT-3 increased during bone extension, but decreased when distraction stopped. In contrast, BDNF continued to increase gradually throughout the distraction and consolidation phases. These findings suggest that neurotrophins and their receptors may play different roles in endochondral and intramembranous ossification in distraction osteogenesis. The tension stress caused by distraction may stimulate the expression of neurotrophins and their receptors, and promote osteogenesis. |
Keywords | neurotrophin Trk distraction osteogenesis mechanical stress |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-10 |
Volume | volume60 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 267 |
End Page | 277 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 17072373 |
Web of Science KeyUT | 000241509000003 |
JaLCDOI | 10.18926/AMO/30738 |
---|---|
FullText URL | fulltext.pdf |
Author | Ohtani, Yuu| Aoe, Motoi| Hara, Fumikata| Tao, Hiroyuki| Koshimune, Ryuichiro| Hirami, Yuuji| Hanabata, Tetsuro| Shimizu, Nobuyoshi| |
Abstract | To investigate the suppressive effect of human recombinant TIMP-1 (rh-TIMP-1) on tumor proliferation using an in vivo xenograft system, HT29 was suspended in 0.1 ml phosphate buffered saline (PBS) and then subcutaneously injected in the back of female mice (BALB/C nu/nu). The mice were divided into 2 groups an and the tumor diameter was measured after rh-TIMP-1 (2 mg/kg) (rh-TIMP-1 group) or PBS (control group) was administered injections according to the following schedules. Schedule 1 : Beginning 2 weeks after the subcutaneous injection of HT29, an intraperitoneal injection of rh-TIMP-1 or PBS were performed twice a day (every 12 h) for 14 consecutive days. Schedule 2 : Beginning 1 week after the subcutaneous injection of HT29, an intraperitoneal injection was performed twice a day for 14 consecutive days. Schedule 3 : Intraperitoneal injections were started simultaneously with the subcutaneous injection of HT29, and then performed twice a day for 21 consecutive days. The mice were sacrificed and the tumors extirpated for immunohistochemical investigation. In addition, gelatin zymography and a cell proliferation assay were performed. With Schedule 1, the changes in the tumor diameter in the rh-TIMP-1 group followed the same course as those in the control group, and no suppressive effect on tumor proliferation was observed. However, with Schedule 3, a remarkable suppressive effect was observed throughout the treatment period. In immunostaining, more cases negative for MMP-9 were observed in the rh-TIMP-1 group than in the control group. Cases negative for CD34 were significantly more observed in the rh-TIMP-1 group than in the control group with Schedule 3. All of the results were obtained through the suppressive effect of rh-TIMP-1 on angiogenesis. |
Keywords | MMP-2 MMP-9 TIMP-1 molecular targeting therapy angiogenesis |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-10 |
Volume | volume60 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 257 |
End Page | 266 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 17072372 |
Web of Science KeyUT | 000241509000002 |
JaLCDOI | 10.18926/AMO/30737 |
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FullText URL | fulltext.pdf |
Author | Suzaki, Noriyuki| Hiraki, Akio| Takigawa, Nagio| Ueoka, Hiroshi| Tanimoto, Yasushi| Kozuki, Toshiyuki| Tabata, Masahiro| Kanehiro, Arihiko| Kiura, Katsuyuki| Tanimoto, Mitsune| |
Abstract | A 71-year-old Japanese man with adenocarcinoma of the lung developed interstitial pneumonia after treatment with paclitaxel. The patient had acute chills and fever on the fourth day after the second exposure to paclitaxel, rapidly got worse despite empiric therapies, and developed prolonged respiratory failure requiring mechanical ventilation. Four months later, he died of respiratory failure due to progression of both interstitial pneumonia and lung cancer. This is the first case developing fatal paclitaxel-induced pulmonary toxicity to date. Interstitial pneumonia should be considered one of the possible life-threatening complications during treatment with paclitaxel. |
Keywords | paclitaxel adverse effect lung cancer interstitial pneumonia |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-10 |
Volume | volume60 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 295 |
End Page | 298 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 17072376 |
Web of Science KeyUT | 000241509000006 |
JaLCDOI | 10.18926/AMO/30736 |
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FullText URL | fulltext.pdf |
Author | Inukai, Yoshihide| Takahashi, Kayo| Wang, Da-Hong| Kira, Shohei| |
Abstract | This study assessed total and segmental distribution of fat mass (FM) in athletes with spinal cord injury (SCI) and examined the relationships between segmental distribution of fat mass and age, injury level, athletic history, and training load in order to provide useful information for improvements in their physical strength and training. Twenty-five male athletes with SCI participated in the study. The whole bone composition was measured by a dual-energy X-ray absorptiometry (DXA) method for the calculation of bone minerals, FM, and fat-free mass. The percent fat of the trunk, arms, and legs was also calculated. The percent fat in the legs was highest in comparison with that in the trunk and arms (p < 0.001), and the percent fat in the trunk was higher than that in the arms (p < 0.001). The body fat (p < 0.01), waist circumference (p < 0.01), and waist-to-hip ratio (p < 0.0001) were higher in the group aged 40 or older in comparison with that aged 39 or younger. Path analysis revealed that training load was a factor decreasing the percent fat on the arms and trunk (p < 0.01), and athletic history was a factor reducing the percent fat on the arms (p < 0.05). Our study suggests that exercise is effective in reducing the waist circumference, waist-to-hip ratio, and percent body fat of SCI individuals, and that such effects can help to enhance athletic performance and likely to protect against development of metabolic syndromes resulting from a sedentary lifestyle. |
Keywords | body composition percentage of fat DXA spinal cord-injured athletes path analysis |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-04 |
Volume | volume60 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 99 |
End Page | 106 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16680186 |
Web of Science KeyUT | 000237001900005 |
JaLCDOI | 10.18926/AMO/30735 |
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FullText URL | fulltext.pdf |
Author | Alptekin, Davut| Luleyap, Husnu Umit| Yilmaz, Levent| Demirhindi, Hakan| Gokel, Yuksel| Pazarbasi, Ayfer| Dokur, Mehmet| Kasap, Mulkiye| Kasap, Halil| |
Abstract | This study included 45 patients with intentional insecticide intoxication and 21 with accidental intoxication who were treated at the First-Aid and Emergency Department of Balcali Hospital at the Faculty of Medicine in the Cukurova University, Adana, Turkey, while the control group consisted of 25 people selected from university personnel known to be healthy. Patients with a history of X-ray exposure in the last 6 months or of any virus disease as well as continuous drug users and smokers were excluded, leaving a total of 49 patients. Acetylcholine esterase (Pseudocholinesterase) enzyme (AchE), sister-chromatid exchanges (SCE), the mitotic index (MI), and the replication index (RI) were evaluated. Blood samples were cultured for SCE evaluation and sera separated for AchE levels. Insecticide exposure was generally intentional for suicide in adolescents and at older ages, but accidental for children. AchE levels were found to be significantly lower in organophosphorus (OP) and carbamated (CB) insecticide poisoning groups in comparison with the control group (p<0.001), while the pyrethroid (PY) group was not statistically different for the AchE effect (p>0.05). SCE was found to be significantly higher in OP and CB groups (p<0.001), while the PY and control groups were statistically similar for SCE levels (p>0.05). This study showed an increase in SCE in response to orally ingested insecticides. These findings indicate that insecticide exposure results in cell abnormalities, with resulting impediments to the division and replication of cells, as suggested by MI decreases and RI increases, while the speed of the division cycles of stimulated cells increases. |
Keywords | insecticide intoxication acetylcholine esterase enzyme (AchE) sister-chromatid exchanges (SCE) |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-04 |
Volume | volume60 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 121 |
End Page | 126 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16680189 |
Web of Science KeyUT | 000237001900008 |
JaLCDOI | 10.18926/AMO/30734 |
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FullText URL | fulltext.pdf |
Author | Sugimoto, Seiichiro| Doihara, Hiroyoshi| Ogasawara, Yutaka| Aoe, Motoi| Sano, Shunji| Shimizu, Nobuyoshi| |
Abstract | A 61-year-old man, who was diagnosed with superior vena cava syndrome by papillary thyroid carcinoma, was referred to our hospital. A bulky thyroid tumor with tracheal invasion extended from the left neck to the right atrium without distant metastases. The risk of sudden death due to airway occlusion, tumor embolism or obstruction of the tricuspid valve led us to elect surgery. Extended resection of thyroid cancer was performed with cardiopulmonary bypass. Peritoneal dissemination was found via laparotomy. A histological diagnosis of anaplastic carcinoma arising from transformation of papillary carcinoma was made. After the operation, bilateral ureteral occlusion by peritoneal dissemination and multiple lung metastases were detected. The patient died with acute renal failure on postoperative day 12. Intraatrial extension of thyroid cancer is rare, and only 12 cases have been reported in the literature. We present a case of thyroid cancer with intraatrial extension. |
Keywords | superior vena cava syndrome thyroid cancer cardiopulmonary bypass |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2006-04 |
Volume | volume60 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 135 |
End Page | 140 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 16680191 |
Web of Science KeyUT | 000237001900010 |