result 18185 件
JaLCDOI | 10.18926/AMO/32111 |
---|---|
FullText URL | fulltext.pdf |
Author | Mori, Akitane| Yokoi, Isao| Noda, Yasuko| Willmore, L James| |
Abstract | Head injury or hemorrhagic cortical infarction results in extravasation of blood and breakdown of red blood cells and hemoglobin. Iron liberated from hemoglobin, and hemoglobin itself, are associated with the generation of reactive oxygen species (ROS) and reactive nitrogen species (RNS). ROS and RNS have been demonstrated to be involved in the mechanism of seizures induced by iron ions in the rat brain, an experimental animal model for posttraumatic epilepsy (PTE). ROS are responsible for the induction for peroxidation of neural lipids, i.e., an injury of neuronal membranes, and also could induce disorders in the excitatory and inhibitory neurotransmitters. Antioxidants, such as a phosphate diester of vitamin E and C (EPC-K1) and antiepileptic zonisamide, have been known to prevent the epileptogenic focus formation, or to attenuate seizure activities in the iron-injected rat brain. Natural antioxidants, such as alpha-tocopherol, and condensed tannins, including (-)-epigallocatechin and (-)-epigallocatechin-3-O-gallate, adenosine and its derivative, melatonin, uyaku (Lindera Strychnifolia), fermented papaya preparations, Gastrodia elata BI., and Guilingji, have been demonstrated to scavenge ROS and/or RNS and to be prophylactic for the occurrence of epileptic discharge in the iron-injected rat brain. |
Keywords | posttraumatic epilepsy iron-induced epileptic seizures antioxidant reactive oxygen species reactive ?nitrogen species |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-06 |
Volume | volume58 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 111 |
End Page | 118 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15471432 |
Web of Science KeyUT | 000222273300001 |
JaLCDOI | 10.18926/AMO/32110 |
---|---|
FullText URL | fulltext.pdf |
Author | Shinji, Toshiyuki| Kyaw, Yi Yi| Gokan, Katsunori| Tanaka, Yasuhito| Ochi, Koji| Kusano, Nobuchika| Mizushima, Takaaki| Fujioka, Shin-ichi| Shiraha, Hidenori| Lwin, Aye Aye| Shiratori, Yasushi| Mizokami, Masashi| Khin, Myo| Miyahara, Masayuki| Okada, Shigeru| Koide, Norio| |
Abstract | The prevalence of hepatitis C virus (HCV) genotypes in Myanmar in comparison with the rest of Southeast Asia is not well known. Serum samples were obtained from 201 HCV antibody-positive volunteer blood donors in and around the Myanmar city of Yangon. Of these, the antibody titers of 101 samples were checked by serial dilution using HCV antibody PA test II and Terasaki microplate as a low-cost method. To compare antibody titers by this method and RNA identification, we also checked HCV-RNA using the Amplicor 2.0 test. Most high-titer groups were positive for HCV-RNA. Of the 201 samples, 110 were successfully polymerase chain reaction (PCR) amplified. Among them, 35 (31.8%) were of genotype 1, 52 (47.3%) were of genotype 3, and 23 (20.9%) were of type 6 variants, and phylogenetic analysis of these type 6 variants revealed that 3 new type 6 subgroups exist in Myanmar. We named the subgroups M6-1, M6-2, and M6-3. M6-1 and M6-2 were relatively close to types 8 and 9, respectively. M6-3, though only found in one sample, was a brand-new subgroup. These subtypes were not seen in Vietnam, where type 6 group variants are widely spread. These findings may be useful for analyzing how and when these subgroups were formed. |
Keywords | hepatitis C virus(HCV)genotype type 6 variant Myanmar Southeast Asia phylogenetic analysis |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-06 |
Volume | volume58 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 135 |
End Page | 142 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15471435 |
Web of Science KeyUT | 000222273300004 |
JaLCDOI | 10.18926/AMO/32109 |
---|---|
FullText URL | fulltext.pdf |
Author | Sato, Kyoko| Kawakami, Norito| Ohtsu, Tadahiro| Tsutsumi, Akizumi| Miyazaki, Shougo| Masumoto, Takeshi| Horie, Seichi| Haratani, Takashi| Kobayashi, Fumio| Araki, Shunichi| |
Abstract | Previous in vitro and animal experiments have shown that sulforaphane, which is abundant in broccoli, inhibits Helicobacter pylori (H. pylori) infection and blocks gastric tumor formation. This suggests that broccoli consumption prevents chronic atrophic gastritis (CAG) introduced by H. pylori infection and, therefore, gastric cancer. For an epidemiological investigation of the relationship between the broccoli consumption and CAG, a cross-sectional study of 438 male employees, aged 39 to 60 years, of a Japanese steel company was conducted. CAG was serologically determined with serum cut-off values set at pepsinogen I < or = 70 ng/ml and a ratio of serum pepsinogen I/pepsinogen II < or = 3.0. Broccoli consumption (weekly frequency) and diet were monitored by using a 31-item food frequency questionnaire. The prevalence of CAG among men who ate broccoli once or more weekly was twice as high as that among men who consumed a negligible amount (P < 0.05). Multiple logistic regression analysis indicated that broccoli consumption once or more weekly significantly increased the risk for CAG (odds ratio, 3.06; 95% confidence interval, 1.12-8.38; P < 0.05), after controlling for age, education, cigarette smoking, and alcohol consumption. The present study failed to show an expected association between frequent broccoli consumption and a low prevalence of CAG. |
Keywords | broccoli sulforaphane chronic atrophic gastritis pepsinogen Helicobacter pylori (H. pylori) |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-06 |
Volume | volume58 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 127 |
End Page | 133 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15471434 |
Web of Science KeyUT | 000222273300003 |
JaLCDOI | 10.18926/AMO/32108 |
---|---|
FullText URL | fulltext.pdf |
Author | Nagai, Kazunobu| Aoe, Motoi| Shimizu, Nobuyoshi| |
Abstract | Hepatocyte growth factor (HGF) is a multifunctional factor implicated in tissue regeneration, wound healing, and angiogenesis. HGF was initially thought to be liver-specific, but it has become clear that HGF acts on alveolar type II cells and bronchial epithelial cells. This study was conducted to determine the role of HGF in pulmonary ischemia in a rat model. The first increase of the plasma HGF level was noted 30 min after pulmonary ischemia, and reached a peak at 12 h. Real-time reverse transcription polymerase chain reaction (Real-time RT-PCR) revealed that the HGF messenger RNA (mRNA) expression in the injured left lung was markedly increased at 1, 6, and 12 h after pulmonary ischemia (P < 0.05). The interleukin-1beta (IL-1beta) mRNA expression, one of the inflammatory cytokines which induces HGF expression, was markedly increased at 1 h in the injured left lung (P = 0.0007). Therefore, we considered that HGF might be mainly induced by paracrine mechanisms in pulmonary ischemia. In conclusion, we have shown that the expression of HGF was induced in pulmonary ischemia, and may be a useful biological marker for the early diagnosis. |
Keywords | hepatocyte growth factor (HGF) interleukin-1? (IL-1?) pulmonary ischemia enzyme-linked im-munosorbent assay(ELISA) real-time reverse transcription polymerase chain reaction (real-time RT-PCR) |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-06 |
Volume | volume58 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 119 |
End Page | 125 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15471433 |
Web of Science KeyUT | 000222273300002 |
JaLCDOI | 10.18926/AMO/32107 |
---|---|
FullText URL | fulltext.pdf |
Author | Onoda, Keisuke| Satoh, Toru| Tsuchimoto, Shouji| Katsumata, Atsushi| |
Abstract | Angiography is gold standard technique as preoperative examination for unruptured aneurysmal surgery. Neurosurgeons have observed the unexpected irregular shape and size of the aneurysmal dome and neck in many cases of unruptured cerebral aneurysms during aneurysmal microsurgery, and known the discrepancy between the findings of angiography and operative view. We could not find out the report described the preoperative evaluation of outer-wall (contour) of aneurysm. In the present study, we attempted to evaluate the outer-wall of an unruptured cerebral aneurysm using three-dimensional CT cisternogram (3D-CTC) to provide useful preoperative information. The study was performed on three cases of unruptured cerebral aneurysm that were identified incidentally by MR angiography. We performed three-dimensional CT aniography (3D-CTA) and 3D-CTC for each patient. In the present study, we visualized the contours of vessels and aneurysms using a 3D-CTC in three cases of unruptured cerebral aneurysm. We found the discrepancy between the 3D-CTC contour image and the intra-luminal image 3D-CTA image. This method may be useful for the decision of the surgical approach and have the potential to evaluate the anatomical structure of aneurysmal dome and neck preoperatively. |
Keywords | three-dimensional CT cisternogram three-dimensional CT angiogram unruptured cerebral aneurysm contour of cerebral aneurym |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-06 |
Volume | volume58 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 157 |
End Page | 162 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15471438 |
Web of Science KeyUT | 000222273300007 |
JaLCDOI | 10.18926/AMO/32106 |
---|---|
FullText URL | fulltext.pdf |
Author | Yokoyama, Teruhiko| Tsugawa, Masaya| Nagai, Atsushi| Kumon, Hiromi| |
Abstract | We retrospectively evaluated the subjective and objective treatment results of transurethral microwave thermotherapy (TUMT) for benign prostatic hyperplasia (BPH) and explored the difference in effectiveness between 30- and 60-min single treatments. From June 1997 through March 2003, 58 men with BPH underwent TUMT using the Targis device. Twenty-seven and 31 patients each received a single treatment of 60 or 30 min, respectively. Evaluations after treatment included a clinical determination of the International Prostate Symptom Score, urodynamic assessments by peak flow rate, and magnetic resonance imaging (MRI). In the 60-min treatment, the symptom score improved significantly, from 17.9 to 9.5 after 2 months. Similarly, there was a significant improvement in peak flow rate, from 6.7 to 11.2 ml/sec after 2 months. In the 30-min treatment, the symptom score also improved significantly, from 18.4 to 13.4 after 2 weeks. Similarly, there was a significant improvement in the peak flow rate, from 6.4 to 11.7 ml/sec after 1 month. MRI imaging showed necrosis of the prostate gland 2 weeks after either treatment. These results demonstrated that both the 60-min and the 30-min treatments were effective for patients with BPH. Moreover, the 30-min treatment led to quicker improvement than the 60-min treatment. Thus, a 30-min TUMT protocol is considered recommendable for this treatment. |
Keywords | prostate benign prostatic hyperplasia microwave thermotherapy MRI |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-06 |
Volume | volume58 |
Issue | issue3 |
Publisher | Okayama University Medical School |
Start Page | 151 |
End Page | 156 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15471437 |
Web of Science KeyUT | 000222273300006 |
JaLCDOI | 10.18926/AMO/32105 |
---|---|
FullText URL | fulltext.pdf |
Author | Asanuma, Masato| Miyazaki, Ikuko| Diaz-Corrales, Francisco J| Ogawa, Norio| |
Abstract | Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by dopaminergic neuron-specific degeneration in the substantia nigra. A number of gene mutations and deletions have been reported to play a role in the pathogenesis of familial PD. Moreover, a number of pathological and pharmacological studies on sporadic PD and dopaminergic neurotoxin-induced parkinsonism have hypothesized that mitochondrial dysfunction, inflammation, oxidative stress, and dysfunction of the ubiquitin-proteasome system all play important roles in the pathogenesis and progress of PD. However, these hypotheses do not yet fully explain the mechanisms of dopaminergic neuron-specific cell loss in PD. Recently, the neurotoxicity of dopamine quinone formation by auto-oxidation of dopamine has been shown to cause specific cell death of dopaminergic neurons in the pathogenesis of sporadic PD and dopaminergic neurotoxin-induced parkinsonism. Furthermore, this quinone formation is closely linked to other representative hypotheses in the pathogenesis of PD. In this article, we mainly review recent studies on the neurotoxicity of quinone formation as a dopaminergic neuron-specific oxidative stress and its role in the etiology of PD, in addition to several neuroprotective approaches against dopamine quinone-induced toxicity. |
Keywords | dopamine quinone quinoprotein Parkinson’sdisease oxidative stress neurotoxin |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-10 |
Volume | volume58 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 221 |
End Page | 233 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15666991 |
Web of Science KeyUT | 000224708800001 |
JaLCDOI | 10.18926/AMO/32104 |
---|---|
FullText URL | fulltext.pdf |
Author | Savranlar, Ahmet| Ustundag, Yucel| Ozer, Tulay| Bayraktaroglu, Taner| Demircan, Nejat| Ozdemir, Huseyin| Borazan, Ali| |
Abstract | Granulocytic sarcoma or chloroma is a tumor seen in myelocytic leukemia. Spinal epidural onset is rare and is generally seen before or together with the onset of myelocytic leukemia. An epidural mass located at the 2nd-5th thoracic levels in an 18-year-old male patient was pathologically diagnosed as granulocytic sarcoma. Radiotherapy was performed after surgical intervention. Ten months later, he was re-admitted with abdominal pain. At this time, an epidural mass at the 6th-9th thoracic levels was detected on magnetic resonance imaging, and acute promyelocytic leukemia was diagnosed. After systemic chemotherapy, partial remission was achieved. We aimed to present this rare case with its remarkable follow-up findings. |
Keywords | chloroma acute promyelocytic leukemia epidural mass thoracicspine |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-10 |
Volume | volume58 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 251 |
End Page | 254 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15666994 |
Web of Science KeyUT | 000224708800004 |
JaLCDOI | 10.18926/AMO/32103 |
---|---|
FullText URL | fulltext.pdf |
Author | Nishida, Atsushi| Sugiyama, Shinsaku| Aoki, Shozo| Kuroda, Shigetoshi| |
Abstract | The authors conducted a study on children undergoing treatment at major school refusal treatment centers in Hiroshima Prefecture. On the whole, school refusal in the prefecture was found to peak between 13 and 14 years of age. By age group, the main reason for school refusal in elementary school group was parent-child relationship with separation anxiety. Given additional problems such as neglect at home and complicated social situations in their schools, junior high school students were found to present diverse symptoms from introversion and self-analysis to extroversion, neglect of studies, and delinquency. Among high school students, there were more cases suffering withdrawal and schizophrenia spectrum disorders. The major task regarding treatment seems to lie in how to treat complex cases combining different problems. We summarized herein the studies we have carried out and propose a model for a network therapy system based on functional liaisons between treatment centers. With this system, a child psychiatric medical facility plays the part of a liaison center for the overall network system. |
Keywords | school refusal characteristics of different age groups network therapy liaisons between treatment centers |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-10 |
Volume | volume58 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 241 |
End Page | 249 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15666993 |
Web of Science KeyUT | 000224708800003 |
JaLCDOI | 10.18926/AMO/32102 |
---|---|
FullText URL | fulltext.pdf |
Author | Hyodo, Tsuyoshi| Kanazawa, Susumu| Dendo, Shuichi| Kobayashi, Keita| Hayashi, Hirohide| Kouno, Yoshihiro| Fujishima, Mamoru| Hiraki, Yoshio| |
Abstract | We compared the thin-section CT findings of 11 intrapulmonary lymph nodes with pathological findings and evaluated the possibility of CT scan differential diagnosis from pulmonary metastatic nodules. First, we retrospectively reviewed CT scan and pathological findings of intrapulmonary lymph nodes. The median size of these nodules was 6.2 mm. The nodules appeared round (n=3) or angular (n=8) in shape with a sharp border, and they were found below the level of the carina. The median distance from the nearest pleural surface was 4.6 mm, and 3 of the 11 nodules were attached to the pleura. On thin-section CT scan, linear densities extending from the intrapulmonary lymph nodes were frequently visualized, and were pathologically proven to be ectatic lymphoid channels. We then compared the thin-section CT findings of 8 metastatic nodules less than 1 cm in diameter with those of the 11 intrapulmonary lymph nodes. The median size of these nodules was 6.8 mm, and the median distance from the nearest pleural surface was 16 mm. All nodules appeared round in shape. None of the nodules had linear densities extending from the nodules. The linear densities on thin-section CT scan may be the most useful characteristic of intrapulmonary lymph nodes, when differential diagnosis from metastatic nodules is necessary. |
Keywords | intrapulmonary lymph nodes thin-section CT scan pathological findings pulmonary metastatic nodules |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-10 |
Volume | volume58 |
Issue | issue5 |
Publisher | Okayama University Medical School |
Start Page | 235 |
End Page | 240 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15666992 |
Web of Science KeyUT | 000224708800002 |
JaLCDOI | 10.18926/AMO/32101 |
---|---|
FullText URL | fulltext.pdf |
Author | Zhang, Shan| Takeda, Yoshimasa| Hagioka, Shingo| Goto, Keiji| Morita, Kiyoshi| |
Abstract | To elucidate the mechanism by which hyperbaric oxygen (HBO2) induces electrical discharge, changes in the extracellular concentrations of GABA and glutamate were measured every 5 min using a microdialysis technique in rats during a period of exposure to HBO2 (5 atm abs). Electrical discharge was observed at 28 +/- 4 min after the onset of exposure. Though the extracellular concentrations of glutamate remained unchanged, the extracellular GABA concentrations (pre-exposure level, 0.026 +/- 0.005 microM in dialysate) began to decrease 15 min after the onset of exposure and reached their lowest level (74 +/- 14%, 0.019 +/- 0.004 microM) at the time of appearance of the discharge. There was a close logistic relationship between extracellular GABA concentrations and the discharge incidence, and the extracellular concentrations of GABA causing electrical discharge in 50% of the animals were estimated to be 80% of the pre-exposure level. These results suggest a possible mechanism that HBO2 exposure-induced discharge is caused by the decrease in extracellular concentration of GABA. |
Keywords | glutamic acid hyperbaric oxygenation gamma-aminobutyricacid microdialysis seizures |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-04 |
Volume | volume58 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 91 |
End Page | 95 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15255510 |
Web of Science KeyUT | 000221043700005 |
JaLCDOI | 10.18926/AMO/32099 |
---|---|
FullText URL | fulltext.pdf |
Author | Miyamoto, Noriyoshi| Senda, Masuo| Hamada, Masanori| Katayama, Yoshimi| Kinosita, Atsushi| Uchida, Kensuke| Inoue, Hajime| |
Abstract | Rheumatoid arthritis (RA) is often associated with deformities of the feet, and foot pain often arises in the talonavicular joint of patients with RA. The object of this study was to assess the relationship between magnetic resonance imaging (MRI) findings of the talonavicular joint and walking ability. The subjects were 35 RA patients (10 feet in 5 males and 56 feet in 30 females) aged 34-87 years (mean: 70 years +/- 12.1), with a disease duration from 1-54 years (mean: 14 years +/- 12.1). MRI findings were classified as follows: Grade 1, almost normal; Grade 2, early articular destruction; Grade 3, moderate articular destruction; Grade 4, severe articular destruction; and Grade 5, bony ankylosis dislocation. Walking ability was classified into one of 9 categories ranging from normal gait to bedridden status according to the system of Fujibayashi. As the grade of MRI images became higher the walking ability decreased, and these parameters showed a correlation by Spearman's rank correlation coefficient analysis (P = 0.003). Thus, in the present cohort group of patients with RA, the deterioration of walking ability increased with the severity of destruction of the talonavicular joint. |
Keywords | ?rheumatoid arthritis magnetic resonance imaging talonavicular joint walking ability |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-04 |
Volume | volume58 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 85 |
End Page | 90 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15255509 |
Web of Science KeyUT | 000221043700004 |
JaLCDOI | 10.18926/AMO/32098 |
---|---|
FullText URL | fulltext.pdf |
Author | Yamamoto, Yasuhiro| Okumura, Yoshihiro| Sato, Shuhei| Maki, Kumi| Mukai, Takashi| Mifune, Hirofumi| Akaki, Shiro| Takeda, Yoshihiro| Kanazawa, Susumu| Hiraki, Yoshio| |
Abstract | We studied the differentiation of thyroid nodules using fine-needle aspiration biopsy (FNA) and Tl-201 scintigraphy quantitative analysis. One-hundred and thirty-one thyroid nodules were examined: 83 follicular lesions (58 benign and 25 malignant lesions) and 48 non-follicular lesions (8 benign and 40 malignant lesions). During Tl-201 scintigraphy examinations, an early and a delayed image were acquired 10 and 120 min after an intravenous injection, respectively. The T/N ratio (counts of nodular lesion/counts of contralateral normal thyroid tissue) of each image was calculated quantitatively. We assessed the ability of the Tl-201 scintigraphy and of the FNA analysis to differentiate benign and malignant lesions and determined the cut-off levels for the assays. For the follicular lesions, the area under the ROC (Receiver Operating Characteristic) curve (Az) for the Tl-201 scintigraphy data was greater than that for the FNA data. For the non-follicular lesions, the Az for the FNA data was greater than that for the Tl-201 scintigraphy data. We set cut-off levels at 1.370 for follicular lesions, and 1.070 for non-follicular lesions. The sensitivity and specificity were 76% and 82.7% for follicular lesions, and 90% and 87.5% for non-follicular lesions, respectively. The overall accuracy of the analysis was 84.0%. |
Keywords | ?thyroid nodules fine-needle aspiration biopsy(FNA) Tl-201scintigraphy |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-04 |
Volume | volume58 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 75 |
End Page | 83 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15255508 |
Web of Science KeyUT | 000221043700003 |
JaLCDOI | 10.18926/AMO/32097 |
---|---|
FullText URL | fulltext.pdf |
Author | Koirala, Tirtha Raj| Hayashi, Kazuhiko| Jin, Zaishun| Onoda, Sachiyo| Tanaka, Takehiro| Oda, Wakako| Ichimura, Koichi| Ohara, Nobuya| Oka, Takashi| Yamada, Masao| Yoshino, Tadashi| |
Abstract | Epstein-Barr virus (EBV)-related herpesvirus (Si-IIA-EBV) was serially transmitted for 3 passages from rabbit to rabbit of the opposite sex by blood transfusion, which subsequently induced virus-associated rabbit lymphomas. The virus could be transmitted by transfusion with 15-20 ml of whole blood (7/7) or irradiated blood (1/6) from the EBV-related virus-infected rabbits, but there was no transmission with transfusion of cell-free plasma (0/6) from the infected rabbits. Passive anti-EBV-VCA IgG (x 20 approximately x 10) titers decreased during the first 1-2 weeks in the transfused rabbits. The virus-transmitted rabbits showed a gradual increase in antibody titers ranging from peak titers of x 640 to x 2560 after 3 weeks of transfusion. The recipient origin of malignant lymphoma that developed in the first rabbit transfused by infected blood was confirmed by chromosomal analysis. This rabbit model thus shows that EBV-related herpesvirus is serially transmissible by blood transfusion and that transmission can not be completely prevented by irradiation of blood, but removal of blood cells is the best way to prevent transmission of EBV-related virus. Therefore, this animal model provides a convenient in vivo system for studies of the prevention and therapy of transfusion-related transmission of EBV and EBV-associated lymphoproliferative diseases in immunocompromised human beings. |
Keywords | ?Epstein-Barr virus(EBV) rabbit lymphoproliferative diseases blood transfusion |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-04 |
Volume | volume58 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 67 |
End Page | 74 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15255507 |
Web of Science KeyUT | 000221043700002 |
JaLCDOI | 10.18926/AMO/32096 |
---|---|
FullText URL | fulltext.pdf |
Author | Erten, Nilgun| Saka, Bulent| Karan, M Akif| Parman, Yesin| Umman, Berrin| Tascioglu, Cemil| |
Abstract | A 34-year-old woman was admitted to our emergency room with a high fever, abdominal pain, dyspnea and confusion. High fever and abdominal pain had first occured after a cystocele operation 5 months earlier. Later, congestive heart failure with mural thrombus formation, peripheral polyneuropathy and ischemic cerebrovascular accident were identified in clinical follow-ups, and multiple arterial and venous thromboses were seen on cranial and abdominal magnetic resonance imaging angiography. The patient's symptoms improved with anticoagulant treatment. Antiphospholipid syndrome with elevated serum anticardiolipin IgG levels was diagnosed, and ischemic peripheral polyneuropathy with axonal degeneration was determined by sural nerve biopsy. In antiphospholipid syndrome, elevated anticardiolipin antibodies appear to be the most common acquired blood protein defect causing thrombosis. Disseminated vascular thrombosis in catastrophic antiphospholipid syndrome can result in multiorgan failure with increased morbidity and mortality. It rarely occurs secondary to various infections as in the case of our patient, who suffered postoperative intraabdominal infection. It is important to note that peripheral nervous system involvement is rare in antiphospholipid syndrome. |
Keywords | secondary antiphospholipid syndrome peripheral neuropathy |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-04 |
Volume | volume58 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 107 |
End Page | 110 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15255512 |
Web of Science KeyUT | 000221043700007 |
JaLCDOI | 10.18926/AMO/32093 |
---|---|
FullText URL | fulltext.pdf |
Author | Yata, Yutaka| Nakayama, Yoshihide| Takahara, Terumi| Yamazaki, Kunio| Masuyama, Kiichi| Sawataishi, Masaru| Suzuki, Shuichiro| Honma, Masanori| Ishizawa, Shin| Tanaka, Michio| Watanabe, Akiharu| Sugiyama, Toshiro| |
Abstract | We present a case of a primary advanced gastric tumor that was composed of 2 different pathological components: small cell carcinoma and moderately-differentiated adenocarcinoma. The patient was still alive four years after the surgery was performed, without recurrence. A large part of the tumor consisted of a diffuse sheet of small cell carcinoma, which transitioned into another small portion consisting of moderately-differentiated tubular adenocarcinoma components. Therefore, this case raised the possibility that small cell gastric carcinoma may originate from totipotential stem cells of the stomach. Although small cell carcinoma progresses aggressively, and patients with it have an extremely poor prognosis, this patient recovered uneventfully after the surgical resection, and has remained in good health, without any recurrences. |
Keywords | gastric tumor small cell carcinoma adenocarcinoma |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-12 |
Volume | volume58 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 275 |
End Page | 278 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15762296 |
Web of Science KeyUT | 000225959100004 |
JaLCDOI | 10.18926/AMO/32092 |
---|---|
FullText URL | fulltext.pdf |
Author | Kitamura, Yoshihisa| Araki, Hiroaki| Nagatani, Tadashi| Takao, Katsuyuki| Shibata, Kazuhiko| Gomita, Yutaka| |
Abstract | We studied the influence of imipramine on the duration of immobility in chronic forced-swim-stressed rats. Both single and chronic administration of imipramine potently shortened immobility in naive rats during forced-swim testing. However, chronic, 14-day forced-swim stress testing blocked the immobility-decreasing effect induced by a single administration of imipramine. When imipramine was administered for 14 days concurrently with forced-swim stress testing, immobility was shortened significantly. From the viewpoint of imipramine's effect, these findings suggest that chronic forced-swim stress testing in rats may be an effective animal model for depression. |
Keywords | stress depression imipramine forced-swim test animal model |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-12 |
Volume | volume58 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 271 |
End Page | 274 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15762295 |
Web of Science KeyUT | 000225959100003 |
JaLCDOI | 10.18926/AMO/32091 |
---|---|
FullText URL | fulltext.pdf |
Author | Kawabata, Masahiro| Kawabata, Teruyuki| Saeki, Kiyomi| |
Abstract | Because of the many superficial similarities between the immune system and the central nervous system, it has long been speculated that somatic DNA recombination is, like the immune system, involved in brain development and function. To examine whether or not the V(D)J recombination signals of the immune system work in an in vitro neural differentiation model, the P19 mouse embryonal carcinoma cell line was transfected with a reporter gene that is designed, when rearranged, to express bacterial beta-galactosidase, which was previously reported to exhibit somatic DNA recombination in the transgenic mouse brain. The cloned cells were then induced into neural cells by retinoic acid treatment. This neural induction treatment resulted in the cloning of a P19 cell line that showed a high incidence of beta-galactosidase-positive cells. Most of these beta-galactosidase-positive cells were immunocytochemically identified as either neurons, neuroepithelial cells, or astrocytes. The 5'-end sequences of the beta-galactosidase transcripts expressed in the induced cells were analyzed, and sequences were found that seemed to reflect DNA rearrangement through re-integration of the reporter gene into the host genome. However, the V(D)J recombination signals did not work in the in vitro model. These results suggested that DNA rearrangement activity though integration increased during neural differentiation of P19 cells. |
Keywords | DNA rearrangement neural differentiation retinoic acid P19 embryonal carcinoma cell |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-12 |
Volume | volume58 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 263 |
End Page | 270 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15762294 |
Web of Science KeyUT | 000225959100002 |
JaLCDOI | 10.18926/AMO/32090 |
---|---|
FullText URL | fulltext.pdf |
Author | Ando, Eiichi| Monden, Koichi| Mitsuhata, Ritsuko| Kariyama, Reiko| Kumon, Hiromi| |
Abstract | Staphylococci have been confirmed to form biofilms on various biomaterials. The purpose of this study was to investigate biofilm formation among methicillin-resistant Staphylococcus aureus (MRSA) isolates from patients with urinary tract infection (UTI) and to assess the relationship between biofilm-forming capacities and virulence determinants/clinical background. Over a 12-year period from 1990 through 2001, a total of 109 MRSA isolates were collected from patients (one isolate per patient) with UTI at the urology ward of Okayama University Hospital. We used the in vitro microtiter plate assay to quantify biofilm formation. We then investigated the presence of several virulence determinants by polymerase chain reaction assay and found eight determinants (tst, sec, hla, hlb, fnbA, clfA, icaA, and agrII) to be predominant among these isolates. Enhanced biofilm formation was confirmed in hla-, hlb-, and fnbA-positive MRSA isolates, both individually and in combination. Upon review of the associated medical records, we concluded that the biofilm-forming capacities of MRSA isolates from catheter-related cases were significantly greater than those from catheter-unrelated cases. The percentage of hla-, hlb-, and fnbA-positive isolates was higher among MRSA isolates from catheter-related cases than those from catheter-unrelated cases. Our studies suggest that MRSA colonization and infection of the urinary tract may be promoted by hla, hlb, and fnbA gene products. |
Keywords | methicillin-resistant Staphylococcus aureus urinary tract infection biofilm formation |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-08 |
Volume | volume58 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 207 |
End Page | 214 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15551758 |
Web of Science KeyUT | 000223559700005 |
JaLCDOI | 10.18926/AMO/32089 |
---|---|
FullText URL | fulltext.pdf |
Author | Iwatsuki, Keiji| Yamamoto, Takenobu| Tsuji, Kazuhide| Suzuki, Daisuke| Fujii, Kazuyasu| Matsuura, Hironori| Oono, Takashi| |
Abstract | Epstein-Barr virus (EBV), or human herpesvirus 4 (HHV-4), infects the vast majority of adults worldwide, and establishes both nonproductive (latent) and productive (lytic) infections. Host immune responses directed against both the lytic and latent cycle-associated EBV antigens induce a diversity of clinical symptoms in patients with chronic active EBV infections who usually contain an oligoclonal pool of EBV-infected lymphocyte subsets in their blood. Episomal EBV genes in the latent infection utilize an array of evasion strategies from host immune responses: the minimized expression of EBV antigens targeted by host cytotoxic T lymphocytes (CTLs), the down-regulation of cell adhesion molecule expression, and the release of virokines to inhibit the host CTLs. The oncogenic role of latent EBV infection is not yet fully understood, but latent membrane proteins (LMPs) expressed during the latency cycle have essential biological properties leading to cellular gene expression and immortalization, and EBV-encoded gene products such as viral interleukin-10 (vIL-10) and bcl-2 homologue function to survive the EBV-infected cells. The subsequent oncogenic DNA damage may lead to the development of neoplasms. EBV-associated NK/T cell lymphoproliferative disorders are prevalent in Asia, but quite rare in Western countries. The genetic immunological background, therefore, is closely linked to the development of EBV-associated neoplasms. |
Keywords | latent infection hydroa vacciniforme mosquito allergy chronic active EB virus infection hemophagocytic syndrome |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2004-08 |
Volume | volume58 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 169 |
End Page | 180 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 15551754 |
Web of Science KeyUT | 000223559700001 |