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Biomedical subjects

S Ono

Publications and source records attributed to S Ono.

At least 667 records · Page 37Linked to original sources
PubMed1987

Age-related brain atrophy enhanced by smoking: a quantitative study with computed tomography.

We examined the chronic effect of smoking on brain atrophy quantitatively with computed tomography (CT). Study was performed on 159 smokers and 194 non-smokers from 40 to 69 years old with neither neurological nor focal abnormality in brain CT. Brain atrophy index (BAI) which was a quantitative marker of brain atrophy reported previously, was calculated from each pixel of brain CT. There was a significant age dependent increase of BAI in both non-smokers and smokers. Smokers showed a significant increase in BAI (atrophic) compared to non-smokers in three age groups, 50-54, 55-59 (p less than 0.01, both) and 65-69 (p less than 0.05). In the male, the mean BAI became high when the smoking index increased (p less than 0.01). The systolic blood pressure and serum triglycerides of smokers were significantly higher than the non-smokers (p less than 0.05 and p less than 0.01). It was suggested that age-related brain atrophy was increased by chronic smoking through advanced atherosclerosis.

Adult↗
PubMed1987

Difference in the effects of phenobarbital and 3-methylcholanthrene treatment on subunit composition of hepatic glutathione S-transferase in male and female rats.

Male rats more than seven weeks old showed significantly higher activity of hepatic cytosolic glutathione S-transferase (GST) than females. This sex-related difference in GST activities might be explained by the difference in subunit composition of the enzymes between males and females. The relative proportion of subunit composition of GST between adult male and female rats was as follows: Ya, female greater than male; Yb(Yb'), male much greater than female; Yc, female greater than male. Since phenobarbital (60 mg/kg, i.p. for seven days) induced the Yb subunit as well as Ya subunit, the enzyme activity was more increased in males than in females and the sex difference became more marked. 3-Methylcholanthrene (20 mg/kg, i.p. three times) caused an increase of Ya subunit alone, and then the increased extent was greater in females than in males, and resulted in the disappearance of sex difference.

Aging↗
PubMed1987

Photosensitized acceleration of riboflavin on the formation of lenticular HMW-protein aggregation.

The percentage of high molecular weight protein aggregates obtained by Sepharose 6B column chromatography was increased significantly at pH 9.0 as compared to that of at pH 4.0 and 7.0, especially by exposure to light. The authors suggest that aggregation of lens protein is induced by light-exposure in the presence of riboflavin at higher pH's and that riboflavin acts as a photosensitizer to form high molecular weight protein aggregates in the lens.

Animals↗
PubMed1987

[Left ventricular isovolumic relaxation time estimated by the aortic root echocardiogram].

Dual echocardiogram was recorded simultaneously with phonocardiogram (PCG) to analyze the isovolumic relaxation time (IRT) of the left ventricle (LV) in 85 patients with various heart diseases and in 23 normal subjects. The measurements used were time intervals from the onset of the aortic component of the second heart sound (IIA) to the onset of the posterior deflection of the posterior aortic wall in the aortic root echocardiogram (X) (IIA-X interval), and to the onset of the most rapid opening motion of the anterior mitral leaflet (D') (IIA-D' interval) during early diastole. 1. The IIA-X interval was directly proportional to the IIA-D' interval in the entire study population. 2. The IIA-X interval was prolonged with advancing age in normal subjects. 3. The IIA-X interval was significantly increased in patients with hypertensive heart disease, old myocardial infarction, hypertrophic cardiomyopathy, and dilated cardiomyopathy, but significantly decreased in patients with mitral stenosis. Thus, the IIA-X interval, which was measured easily and noninvasively from the aortic root echocardiogram is a reliable indicator of the isovolumic relaxation time of the left ventricle, as well as of the IIA-D' interval.

Adolescent↗
PubMed1987

Polyclonal B-cell activation by a B-cell differentiation factor B151-TRF2. IV. B151-TRF2-responsive F1 B cells consist of two separate populations capable of recognizing only one of the parental I-A products expressed on B cells.

Polyclonal IgM PFC responses of unstimulated B cells induced by a B cell differentiation factor, B151-TRF2, have been shown to involve an Ia-dependent process which is inhibitable by anti-Ia monoclonal antibody (mAb). Moreover, we have demonstrated that when T cell-depleted (B10 x B10.BR)F1 (H-2b/k) spleen cells are fractionated based on their ability to bind to a B10 (H-2b) monolayer, the B151-TRF2 responses of the adherent and nonadherent cell fractions are markedly inhibited by anti-I-Ab and anti-I-Ak mAbs, respectively. From these results, we hypothesized that B cell-recognition of self-I-A products expressed on B cells is involved in the B151-TRF2-induced polyclonal B cell activation. The present study examined the genetic and cellular requirements for the successful separation of F1 B cells with parental monolayers in order to prove recognition by B cells of self-I-A products expressed on B cells. The experiments utilizing monolayers from H-2 congenic strains revealed that identity at the I-A subregion of the H-2 complex between responding F1 B cells and monolayer cells was necessary and sufficient for the successful separation of F1 B cells. In support of this conclusion, purified B cells and B cell lines expressing only parental I-A products on the surface could function effectively as monolayers. Masking of I-A determinants expressed on the monolayer with anti-I-A mAb almost completely abolished the successful separation of F1 B cells, whereas pretreatment of Ia antigens on responding F1 B cells with anti-Ia mAbs did not affect the subsequent separation, indicating involvement of receptor-I-A product interaction rather than like-like interaction in the separation of F1 B cells by the monolayer. The B151-TRF2 responses of purified B cells obtained from athymic nude mice were specifically inhibited by the relevant anti-I-A mAb but not by anti-L3T4 and anti-LFA-1 mAbs, both of which were inhibitory to the Ia-restricted T cell responses. In addition, anti-Thy1.2 mAb plus complement-treated spleen cells from athymic F1 nude mice were successfully fractionated with parental monolayer into two separate populations with restriction specificity for only one of parental I-A products. These results negate the involvement of Ia-restricted T cells in the Ia-dependent process of the B cell activation. Finally, it was demonstrated that there was no apparent difference in the expression of respective parental I-A products between F1 B cell subpopulations adherent and nonadherent to parental monolayers.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗