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Biomedical subjects

J Ono

Publications and source records attributed to J Ono.

At least 73 records · Page 4Linked to original sources
PubMed1998

Effects of adrenal steroids on basal ganglia neuropeptide mRNA and tyrosine hydroxylase radioimmunoreactive levels in the adrenalectomized rat.

To investigate the effects of type I (mineralocorticoid) and type II (glucocorticoid) receptor activation on striatal neuropeptide [preproenkephalin (PPE), preprotachykinin (PPT), and preprodynorphin (DYN)] mRNA and midbrain cholecystokinin (CCK) mRNA as well as striatal tyrosine hydroxylase radioimmunoreactivity (TH-RIC) levels, we administered either replacement levels of corticosterone (CORT; 0.5 mg/kg/day, s.c.) or pharmacological levels of deoxycorticosterone acetate (DOCA; a mineralocorticoid steroid with ability to bind to type I and type II receptors; 5 mg/kg, s.c.) to adrenalectomized adult male rats. After 1 week of recovery from adrenalectomy surgery, animals were injected daily with sesame oil or CORT for 1, 3, or 7 days or DOCA for 3 or 7 days and killed 16 h after the last injection. Adrenalectomy resulted in a decrease in all three striatal neuropeptide mRNA levels, compared with sham-operated rats. CORT replacement resulted in recovered PPE and PPT mRNA levels after 1 day and elevated PPE mRNA levels over those in sham-operated controls after 3 days. In contrast, DYN mRNA levels showed recovery after 7 days of CORT replacement. Results after DOCA treatment largely paralleled those after CORT replacement. There were no significant treatment effects on indirect markers of midbrain dopaminergic activity, i.e., CCK mRNA and TH-RIC. From these results we conclude that compared with striatal tachykinin and dynorphinergic neurons, enkephalinergic cells show greater sensitivity, whereas the dopaminergic system, including mesencephalic CCK, demonstrates an insensitivity to physiological CORT and to pharmacological DOCA treatment.

Adrenalectomy↗
PubMed1998

Analysis of the expression of CagA and VacA and the vacuolating activity in 167 isolates from patients with either peptic ulcers or non-ulcer dyspepsia.

OBJECTIVES: The goals of this study were: 1) to examine the prevalence of cytotoxin-associated protein (CagA), vacuolating cytotoxin (VacA), and the vacuolating cytotoxin activity (VCA) in vitro of infecting Helicobacter pylori isolates and 2) to clarify the relation between the expression of these virulence factors and the occurrence of peptic ulceration. METHODS: One hundred sixty-seven clinical isolates of H. pylori from patients with peptic ulcer disease (gastric ulcer, 62 cases; duodenal ulcer, 48 cases) and nonulcer dyspepsia (57 cases) were studied regarding their genetic and phenotypic properties. RESULTS: Type 1 bacteria, which had both CagA and VCA, and type 2 bacteria, which did not express either CagA or VCA, represented 62.9% and 7.8%, respectively; the remaining 29.4% had an intermediate phenotype, expressing either CagA independent of the presence of VCA (CagA+VCA-) or vice versa (CagA-VCA+). CagA+VCA- and CagA-VCA+ bacteria represented 17.4 % and 12.0%, respectively, both of which were more numerous than the type 2 category. The proportion of the CagA-positive isolates was significantly higher in both the duodenal ulcer (97.9%) and gastric ulcer (83.9%) patients than in the non-ulcer dyspepsia patients (61.4%) (p < 0.01). On the other hand, the proportion of VacA/VCA-positive isolates was not significantly different between peptic ulcer disease and non-ulcer dyspepsia. CONCLUSIONS: The currently used classification of this bacterium based on the concomitant expression of CagA and VacA/VCA into the two major types is not adequate. The CagA-positive phenotype thus may be important as a virulence marker for peptic ulcer disease independent of the presence of VacA/VCA.

Adult↗
PubMed1998

[Clinical analysis on 127 cases of fungemia in Fukuoka University Hospital between 1984 and 1994].

A clinical analysis on 127 cases out of 140 cases presenting with fungemia at Fukuoka University Hospital between 1984 and 1994 was done. The number of the positive blood cultures during the same period was 1188 and the rate of fungemia was 11.8%. The rates generally increased in recent years, 9.0% (1984-1986), 10.2% (1987-1989) and 13.6% (1990-1994), but decreased after 1992. C. albicans has shown a tendency to decrease while C. parapsilosis and C. glabrata have increased in recent years thus suggesting the effect of the prevalence of intravenous hyperalimentation (IVH) and azole antifungal agents. Only 3.9% of the fungemia were preceded by bacteremia. In addition to the known risk factors for fungemia such as IVH (89.0%) and the antibacterial agents, H2-receptor antagonists were used in 58.3% of the cases. 14 cases of the fungemia were observed during the prophylactic use of antifungal drugs. Therefore, fungemia should always be kept in mind regarding the differential diagnosis for bacteremia when an indwelling venous catheter is used. The prompt extubation of the catheter in addition to the adjustment of the dosage of antifungal drugs in response to the status of the host defense system are thus considered to be important in the treatment of fungemia.

Adolescent↗
PubMed1998

Intermittent rhythmic delta activity (IRDA) in a patient with band heterotopia.

We report a patient with band heterotopia whose electroencephalogram (EEG) showed typical morphological features of intermittent rhythmic delta activity (IRDA). This 18-year-old woman had complex partial seizures. Neuropsychometry revealed mental dysfunction. Magnetic resonance imaging (MRI) showed bilaterally symmetrical layer of heterotopic gray matter in deep white matter over the frontal, parietal and occipital regions. This case is the first report of IRDA detected in band heterotopia.

Adolescent↗
PubMed1998

[Electroencephalography and prognosis in stroke patients].

Electroencephalography (EEG) and its relationship to prognosis were studied in 105 patients with cerebrovascular disease in the acute to subacute stages. Twenty cases had normal EEG, and most of them recovered well. Fifty-five cases had mildly to moderately abnormal EEG with focal asymmetric or slow waves in the unilateral hemisphere. Among them, 41 cases (75%) recovered to the extent of being capable of independent walking, 38 cases (69%) recovered sufficiently to engage in independent activities of daily livings (ADL) and 42 cases (76%) returned home. On the other hand 30 cases who had severely abnormal EEG with diffuse slow waves in the unilateral or bilateral hemispheres showed a poor prognosis. Among them, 18 cases (60%) were confined to bed, 20 cases (69%) remained in totally dependent ADL, and 4 cases (13%) died. Thus, EEG is shown to reflect well functional recovery in stroke patients.

Activities of Daily Living↗
PubMed1998

Sigmoid sinus dural arteriovenous malformation resulting from jugular foramen schwannoma--case report.

A 69-year-old male presented with a jugular foramen schwannoma occluding the sigmoid sinus and associated with sigmoid sinus dural arteriovenous malformation. The patient presented with dizziness and pulsatile tinnitus following an extended period of hearing loss beginning several years before. Both lesions were resected successfully after transarterial embolization of the malformation. The sequence of symptom development suggests the dural sinus thrombosis caused the dural arteriovenous malformation.

Aged↗
PubMed1998

Serial magnetic resonance imaging of acute spontaneous thrombosis of a giant intracranial aneurysm--case report.

A 46-year-old female presented with decreased bilateral visual acuity due to an unruptured non-thrombosed giant aneurysm arising from the left internal carotid artery. After admission, acute thrombosis of the aneurysm occurred spontaneously. Her consciousness and visual acuity temporarily worsened. Serial T2-weighted magnetic resonance (MR) imaging showed the size of the low intensity area near the orifice increased, and the aneurysm ruptured thereafter. Trapping of the aneurysm with a high-flow bypass was performed. Serial MR imaging findings clearly demonstrated the intraluminal structure of the thrombosed giant aneurysm. The aneurysm grew in size after thrombosis. The enlarging signal-void area on T2-weighted MR images were indicative of aneurysmal rupture. MR imaging is quite helpful to evaluate the changes of intraluminal thrombosis and size in giant aneurysms.

Acute Disease↗
PubMed1998

Angioarchitecture related to hemorrhage in cerebral arteriovenous malformations.

A retrospective study was conducted to determine the angioarchitecture related to hemorrhage in patients with cerebral arteriovenous malformations (AVMs), who underwent conservative treatment and long-term follow-up. The average observation period was 9.3 years, and the annual bleeding rate was estimated at 3.6%. In all cases angiographic findings were reviewed in detail. The average AVM grade by Spetzler-Martin was 3.5. Higher bleeding rate was observed in large AVM (5.4%) compared with small (2.1%) or medium AVM (2.9%). Deep venous drainage (8.6%/year) was strongly correlated to hemorrhage. Concerning location of nidus, hemorrhage was frequently found in insular, callosal, and cerebellar AVMs. Venous ectasia, feeder aneurysm, and external carotid supply were commonly demonstrated on angiograms. Comparison of annual bleeding rate revealed that AVMs with intranidal aneurysm (8.5%) and venous stenosis (5.5%) had a high propensity to hemorrhage. Therapeutic strategy should be focused on these potentially hazardous lesions by the use of endovascular embolization or stereotactic radiosurgery, even if surgical resection is not indicated.

Adolescent↗
PubMed1998

Effects of troglitazone on the growth and differentiation of hematopoietic cell lines.

Troglitazone (Tro), one of the thiazolidinediones, is a novel antidiabetic agent for patients with type 2 diabetes mellitus. Tro is a specific ligand of PPARgamma, the nuclear receptor that regulates the growth and differentiation of cells at the transcriptional level. We attempted to investigate the effect of Tro on HL-60 and other hematopoietic cell lines and thus found HL-60 cells to be arrested at the G1 phase and to differentiate into monocytes. In addition, apoptosis was also induced by Tro at higher concentrations. The G1 arrest was induced in all the hematopoietic cell lines examined while differentiation into the monocytic lineage was observed not only in the myelogenous and promonocytic cell lines but also in an erythroleukemia cell line.

Animals↗
PubMed1998

[Squatting test].

Explore the source record for details and available documents.

Autonomic Nervous System↗
PubMed1998

SPECT findings in mitochondrial encephalomyopathy.

UNLABELLED: We investigated the alterations in regional cerebral blood flow (rCBF) in mitochondrial encephalomyopathy (MEM), using [123I]N-isopropyl-p-iodoamphetamine (IMP) or 99mTc-hexamethyl propyleneamine oxime SPECT in 10 MEM patients. METHODS: Four of the patients had MEM with lactic acidosis and strokelike episodes (MELAS), 2 had Kearns-Sayre syndrome (KSS), 1 had myoclonic epilepsy with ragged red fibers (MERRF) and 3 had cytochrome C oxidase deficiency (CCOD). Cerebral perfusion reserve was obtained from 6 patients (3 MELAS, 1 MERRF, 1 KSS, 1 CCOD) for a comparative analysis using the split-dose 123I-IMP SPECT method before and after the injection of acetazolamide. RESULTS: All patients with MELAS showed focal hypoperfusion in the parietal and/or occipital lobes. Follow-up studies (3 MELAS patients) revealed extension or improvement in the abnormal perfusion. The hypoperfused lesions were correlated with abnormal CT/MRI findings. Perfusion was normal in 1 MERRF, 2 KSS and 3 CCOD patients, whereas CT/MRI findings in 1 MERRF, 1 KSS and 1 CCOD patient were abnormal. The cerebral perfusion reserve in 3 MELAS patients was decreased significantly compared with that in patients with other types of MEM (MELAS 7.4%, other MEM 33.8%; p < 0.05). CONCLUSION: The rCBF was altered specifically in patients with MELAS, suggesting that brain perfusion SPECT will be useful in diagnosing and assessing such patients. The decreased cerebral perfusion reserve in patients with MELAS may represent an important feature of the pathogenesis of the strokelike episodes. The SPECT findings of patients with other types of MEM (MERRF, KSS and CCOD) were normal.

Adolescent↗
PubMed1998

[Venous system playing a key role in transpetrosal approach].

A case with a large vertebrobasilar junction aneurysm developed a venous infarction in the temporal lobe after an operation using the transpetrosal approach. Although little of the literature has been concerned with venous complications after the transpetrosal approach, the case prompted us to study the venous system as playing a key role in the transpetrosal approach. Analyzing 30 carotid and 15 vertebral angiograms of 15 patients who underwent preoperative cerebral angiography using digital subtraction angiography (DSA), we investigated the venous system near the junction of the superior petrosal sinus, the transverse sinus and the sigmoid sinus (STS junction) which may play a key role in the transpetrosal approach. Drainage pathways of the superficial middle cerebral vein (SMCV) were classified into four types; sphenoparietal, sphenobasal, sphenopetrosal and undeveloped. In the sphenopetrosal type (4/30: 13%), the drainage of SMCV passes back along the floor of the middle fossa to drain into the transverse sinus. The lateral temporal vein (LTV) and the temporobasal vein (TBV) drain into the transverse sinus. The LTV emptied into the transverse sinus either directly (20/30: 67%) or indirectly through the tentorial sinus (10/30: 33%). The entry of the LTV into the transverse sinus (venous point) was usually located in the lateral third of the transverse sinus (14/20: 70%), but sometimes in the middle third (6/20: 30%). The TBV, observed in 8/30 (27%), also often emptied into the tentorial sinus to drain into the transverse sinus. Atresia of a unilateral transverse sinus and a large LTV emptying into the distal sigmoid sinus was observed in 2/15 cases. The venous system near the STS junction may be interrupted by the incision of the tentorium and the middle fossa dura mater and by the retraction of the sigmoid sinus. Since the transpetrosal approach may cause venous complication by compromising the venous system near the STS junction, it is necessary to evaluate of the venous system preoperatively using DSA and to set up a surgical strategy preserving the venous system.

Aneurysm↗
PubMed1998

[Relationship between visual field loss and retinal nerve fiber layer thickness in open-angle glaucoma].

We studied the correlation between retinal nerve fiber layer thickness and visual field loss in 117 eyes of 62 patients with open angle glaucoma using the Aulhorn Classification as modified by Greve. We divided the peripapillary area into four quadrants [superior (S), inferior (I), temporal (T), nasal (N)] and the total (T0), and measured the peripapillary retinal nerve fiber layer thickness (NFLT) with a confocal scanning laser polarimeter (Nerve Fiber Analyzer). We also obtained the relative ratios (mean ratios) of the total circumference to the nasal quadrant (T0/N), the superior to the nasal quadrant (S/N), the temporal to the nasal quadrant (T/N), the inferior to the nasal quadrant (I/N), the total to the temporal quadrant (T0/T), the superior to the temporal quadrant (S/T), the nasal to the temporal quadrant (N/T), and the inferior to the temporal quadrant (I/T). Significant decreases were observed in the mean ratios to the temporal quadrant, i.e., T0/T, S/T, and I/T, in stages I to VI when compared with stage 0. However, no significant differences were observed among stages I to VI. These results suggest that these parameters may not precisely reflect the progression of the disease, but may aid differential diagnosis of the early stage (stage 0) from the middle and late stages (stages I to VI).

Female↗
PubMed1998

[A case of juvenile type dentatorubral-pallidoluysian atrophy (DRPLA) with psychomotor retardation since infancy].

We report here a case of an 11-year-old boy with juvenile type of dentatorubral-pallidoluysian atrophy (DRPLA). His psychomotor development has been delayed since infancy and cerebellar ataxia was noted at the age of 2 years, indicating an early onset. At the age of 6 years, he had progressive myoclonus epilepsy (PME) and underwent a series of neuroradiological, electrophysiological and pathological examinations, which failed to reveal the etiology. Gene analysis performed at the age of 11 years revealed an expanded CAG repeat at the DRPLA locus in both the patient and his asymptomatic father. In the absence of a positive family history, a diagnosis of DRPLA may be difficult due to its clinical variability. We conclude that DRPLA should be taken into account in the differential diagnosis of childhood PME and that gene analysis should be performed to confirm a diagnosis of DRPLA.

Anticipation, Genetic↗
PubMed1998

[Relationship between the retinal nerve fiber layer thickness and the effect of aging in normal eyes].

We studied the correlation between the thickness of the retinal nerve fiber layer and the role of age in 155 normal eyes of 83 subjects without significant ocular diseases. Subjects with a refractive error exceeding +/- 5 diopters were excluded. We divided the peripapillary area into four quadrants: superior (S), inferior (I), temporal (T), and nasal (N). We measured peripapillary retinal nerve fiber layer thickness (NFLT) in these four quadrants and in the total area (T(o)) using a confocal scanning laser polarimeter (Nerve Fiber Analyzer), and determined the correlation coefficients. The retinal nerve fiber layer thickness of the total area and of the four quadrants was not significantly associated with an increase in age. Since changes in the thickness were small in the nasal and temporal quadrants, we measured the relative ratios of the thickness in each quadrant to that in the nasal and temporal quadrants. The ratio of the total area to the nasal quadrant (T(o)/N), the superior to the nasal quadrant (S/N), the inferior to the nasal quadrant (I/N), the total area to the temporal quadrant (T(o)/T), the superior to the temporal quadrant (S/T), and the inferior to the temporal quadrant (I/T) was significantly associated with an increase in age. Multiple comparison in each age group revealed no age-related significant decreases in any of the parameters. These findings suggest that these parameters may reflect the degree of aging in normal eyes, but age-related abnormality in the retinal nerve fiber layer thickness may be small.

Adult↗
PubMed1997

Differentiation of dys- and demyelination using diffusional anisotropy.

We attempted differential diagnosis of dysmyelination and demyelination in childhood using magnetic resonance diffusion weighted imaging. Pelizaeus-Merzbacher disease, one of the dysmyelination disorders, demonstrated diffuse high intensity of the cerebral white matter on T2-weighted images, which demonstrated diffusional anisotropy on diffusion weighted images. On the other hand, high intensity lesions on T2-weighted images in Krabbe disease, one of the demyelination disorders, lost diffusional anisotropy. Another demyelination disorder, Alexander disease-related disorder, also lost its diffusional anisotropy. In contrast to relatively high signal of the lesions on diffusion-weighted images in Krabbe disease (high signal type), the lesions in Alexander disease-related disorder showed low signal on diffusion-weighted images (low signal type). These results suggest that diffusion-weighted images will be clinically useful to differentiate dysmyelination from demyelination; both of them demonstrate similar high intensity lesions of the white matter on T2-weighted images.

Adult↗
PubMed1997

Regional cortical dysplasia associated with suspected hypomelanosis of Ito.

A 15-year-old girl with epilepsy, whose skin lesions were reminiscent of hypomelanosis of Ito, is reported. She manifested hypopigmented linear streaks on her upper and lower limbs. Brain magnetic resonance imaging examinations demonstrated poor differentiation of cerebral gray and white matter of her left occipital lobe, with accompanying gliosis. This region also revealed narrowing of sulci, considered to be mass effect. In this region, almost continuous spike discharges were evident on electroencephalograms, and low-perfusion status was observed on single photon emission computed tomography at rest. She also manifested right lower homonymous quadrant anopsia, which may have its origin in the lesion detected, which appeared to be a migration disorder of neuroblasts in our patient, suggesting that the spectrum of hypomelanosis of Ito might be involved.

Adolescent↗