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Biomedical subjects

H Tsuruta

Publications and source records attributed to H Tsuruta.

At least 109 records · Page 6Linked to original sources
PubMed1985

The stereochemical configuration of the natural 1 alpha,25-dihydroxyvitamin D3-26,23-lactone.

Four possible diastereoisomers of 1 alpha,25-dihydroxyvitamin D3-26,23-lactone were chemically synthesized and compared with the natural metabolite by high-pressure liquid chromatography. The four synthetic diastereoisomers of 1 alpha,25-dihydroxyvitamin D3-26,23-lactone could be separated into three peaks by high-pressure liquid chromatography. The naturally occurring 1 alpha,25-dihydroxyvitamin D3-26,23-lactone isolated from dog serum and in vitro incubation of chick kidney homogenates comigrated with 23(S)25(R)-1 alpha,25-dihydroxyvitamin D3-26,23-lactone. The four diastereoisomers of 1 alpha,25-dihydroxyvitamin D3-26,23-lactone were tested against naturally occurring 1 alpha,25-dihydroxyvitamin D3-26,23-lactone to determine their relative competition in the 1 alpha,25-dihydroxyvitamin D3-specific cytosol receptor binding assay for 1 alpha,25-dihydroxyvitamin D3. 23(S)25(S)-1 alpha,25-Dihydroxyvitamin D3-26,23-lactone was the best competitor followed by 23(R)25(R)-1 alpha,25-dihydroxyvitamin D3-26,23-lactone and 23(R)25(S)-1 alpha,25-dihydroxyvitamin D3-26,23-lactone, and 23(S)25(R)-1 alpha,25-dihydroxyvitamin D3-26,23-lactone was the poorest competitor. Natural 1 alpha,25-dihydroxyvitamin D3-26,23-lactone isolated from dog serum had almost the same binding affinity as that of 23(S)25(R)-1 alpha,25-dihydroxyvitamin D3-26,23-lactone. These data unequivocally demonstrate that the stereochemistry of the natural 1 alpha,25-dihydroxyvitamin D3-26,23-lactone has the 23(S) and 25(R) configuration.

Animals↗
PubMed1985

Partial insomnia, hyperactivity and hyperdipsia induced by repeated administration of toluene in rats: their relation to brain monoamine metabolism.

In an attempt to examine chronic effects of toluene on sleep, spontaneous locomotor activity and drinking behavior, rats were repeatedly administered toluene i.p. at doses of 100 and 200 mg/kg body weight for 14 consecutive days. The 200-mg/kg injections induced a decrease in total sleep on Day 1, an increase in locomotor activity on Days 1 through 4 and an increase in drinking activity on Days 0 through 6 after discontinuation of the daily injections. Both the reduced sleep and the increased locomotor activity appeared during the light period, whereas the drinking activity increased during the dark period. In order to find neurochemical correlates of the toluene-induced changes in behavior, regional concentrations of brain monoamines and their metabolites were determined. The toluene-induced partial insomnia and hyperactivity were associated with lowered concentrations of serotonin in frontal cortex, hippocampus and midbrain and 5-hydroxyindoleacetic acid in midbrain and hypothalamus. The increased drinking activity was associated with increased concentrations of striatal 3,4-dihydroxy-phenylacetic acid and homovanillic acid and hypothalamic noradrenaline and 3-methoxy-4-hydroxyphenylethyleneglycol. Central monoaminergic mechanisms were implicated in the toluene-induced partial insomnia, hyperactivity and hyperdipsia.

Animals↗
PubMed1984

Acute effects of toluene on circadian rhythms of sleep-wakefulness and brain monoamine metabolism in rats.

Acute effects of a single i.p. injection of toluene on circadian rhythms of sleep-wakefulness were investigated in rats which were chronically implanted with EEG and EMG electrodes for polygraphic recordings. The toluene injection produced an initial increase in wakefulness (W) and a subsequent increase in slow-wave sleep (SWS) during the dark period. In an attempt to clarify mechanisms of these biphasic effects of toluene on sleep-wakefulness rhythms, brain monoamines and their metabolites were determined at the times of the initial increase in W and the increased SWS. The initial increase in W was associated with an increase in cortical NA, MHPG and 5-HT together with a decrease in cortical 5-hydroxyindoleacetic acid (5-HIAA), while the increased SWS during the dark period was associated with an increase in 5-HIAA and a concomitant decrease in 3-methoxy-4-hydroxyphenylglycol (MHPG). The toluene-induced changes in sleep-wakefulness seemed to be manifested at lower blood levels of toluene than the behavioral signs of central nervous system (CNS) depression. These biphasic effects of toluene on circadian sleep-wakefulness rhythms are discussed in terms of the reciprocal interactions between central 5-HT and NA neurons.

Animals↗