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Biomedical subjects

Y Ishimoto

Publications and source records attributed to Y Ishimoto.

17 recordsLinked to original sources

A study on the brain structures related to conditioned emotional response by means of [14C]2-deoxy-D-glucose method.

Brain structures activated during conditioned emotional response were studied by means of the [14C]2-deoxyglucose method. The experimental (CSE) animals were conditioned with paired 25 25-sec-long flicker sequences (CS) and 1-sec-long 150 V AC electric shocks (US), while the control (CSC) animals were given only 25 CS sequences. Average densities of a unit square (200 microns x 200 microns) of 47 nuclei or cortical areas in the left hemisphere were obtained from an autoradiogram and the optical density ratio (ODR), which is the relative optical density of each structure to that of the corpus callosum, was calculated. Comparison of ODRs of each structure from both groups revealed a significant increased uptake of [14C]2-deoxyglucose (P less than 0.05, Mann-Whitney U-test) in the caudal portion of area 10, area 2, area 18 and the hippocampal formation.

Animals

Electroencephalographic changes during and after water intoxication.

A case of water intoxication with remarkable hyponatremia was investigated with a special reference to EEG changes during and after the episode. The patient recovered his EEG as his consciousness disturbance had improved through an intravenous infusion of high osmolality saline, correlating with the serum sodium level. Further, the clinical importance of recording EEG for water intoxication was stressed.

Adult

Evoked potentials of self-interrupted Jacksonian epilepsy.

We describe a female case of Jacksonian epilepsy who can interrupt the spreading of her march by grasping her fingers firmly with her right hand. Neurophysiologically, Somatosensory evoked potential (SEP) was remarkably decreased in amplitude with pressure stimulation similar to her method. Such a change in SEP was observed also in a healthy subject. Accordingly, it is suggested that the stimulation only to the proprioceptor of fascia suppresses the activity in the cortex.

Aged

Comparative anatomical studies on the cerebellar nuclei of the pangolins.

The configurations and volumes of the cerebellar nuclei of left and right 10 sides of 5 cases of the pangolins (Manis pentadactyla) were examined with sagittal myelin sheath and toluidine blue stained serial sections and reconstruction models based upon these serial sections respectively. The cerebellar nuclei of the pangolins, same as in other mammals can be divided into four nuclei, nucleus medialis (M), nucleus interpositus posterior (P), nucleus interpositus anterior (A) and nucleus lateralis (L). In all cases from medially to laterally, M, P, A and L appear in order and disappear M, A, P and L in order respectively. The volume of each nucleus in the total volume of the cerebellar nuclei is: M; 5.3-7.9% P; 27.1-31.2% A; 17.6-22.9% L; 42.4-46.2% In right and left each cerebellar nuclei significant difference is not recognized as p is less than 0.05. The posterior protuberance of the nucleus medialis protrudes remarkably in 4 cases of No. 1, No. 2, No. 3 and No. 4 but in only 1 case of No. 5 it protrudes slightly. In nucleus interpositus posterior the ventrolateral protuberance protrudes slightly in 4 cases of No. 1, No. 3, No. 4 and No. 5 but in only 1 case of No. 2 it protrudes remarkably. The anterior protuberance protrudes remarkably in all cases and the superior protuberance protrudes remarkably in 3 cases of No. 2, No. 3 and No. 4 but in 2 cases of No. 1 and No. 5 it protrudes slightly. In sulci, sulcus b and sulcus a' are distinct in all cases and sulcus a, sulcus c, sulcus b' and sulcus c' are considerably remarkable. In the toluidine blue stained serial sections, the nucleus medialis is composed of close small nerve cells, nucleus interpositus posterior is composed of the diffuse medium-sized nerve cells, nucleus interpositus anterior is composed of the close medium-sized nerve cells and nucleus lateralis is composed of the diffuse large nerve cells. In projection pictures of each subnuclei to the cerebellar cortex in each directions in the dorsal view the nucleus medialis is projected to the medial part of the folium vermis, the medial part of the nucleus interpositus posterior to the lateral part of the folium vermis and partly caudolateral part of the declive, and the lateral part of it to the crus II of the lobulus ansiformis.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals

Transaminative pathway of cysteine metabolism in rat tissues.

Enzyme activities of the transaminative pathway of cysteine metabolism in various rat tissues were examined. Liver was found the most active tissue, followed by kidney and heart. Liver and kidney were more pronounced in mercaptopyruvate sulfurtransferase activity than in cysteine transaminase activity; heart was more active in the latter. Red blood cells, which have pronounced sulfurtransferase activity, exhibited no transaminase activity, indicating the pathway is negligible in this tissue.

Animals

Desulfuration of l-cysteine through transamination and transsulfuration in rat liver.

Desulfuration of L-cysteine by rat liver via a pathway of transamination followed by transsulfuration was studied using cyanide as a sulfur acceptor. More than a 5-fold increase in formation of thiocyanate from L-cysteine and cyanide was observed in the presence of 2-oxoglutarate and pyruvate. L-Cysteine aminotransferase and 3-mercaptopyruvate sulfurtransferase activities in the same preparations were also determined. It was concluded that L-cysteine was desulfurated through transamination and transsulfuration of the resulting 3-mercaptopyruvate, and that the rate-limiting step appears to be the transamination reaction.

Animals

Transaminase of L-cysteine in rat liver mitochondria.

Transamination of L-cysteine in rat liver was examined. Specific activity of the reaction in mitochondria was found higher than that in cytosol. The mitochondrial reaction was shown to be catalyzed by two different enzymes. The first was active with 2-oxoglutarate and inactivated by heating at 60 degrees C for 10 minutes; the activity was protected from heat inactivation by the presence of 2-oxoglutarate. The second enzyme was active with pyruvate and more stable than the first under heat treatment; 2-oxoglutarate had little protective effect on this second enzyme. The two enzyme activities were separated by heat treatment and ammonium sulfate fractionation.

Animals