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H Haraguchi

Publications and source records attributed to H Haraguchi.

At least 73 records · Page 4Linked to original sources

Comparisons between discrete lever-press and shuttle avoidance responses in mice: acquisition processes and effects of psychoactive drugs.

Acquisition processes of discrete lever-press (L-type) and shuttle (S-type) avoidance responses as well as effects of psychoactive drugs thereon were investigated in dd strain mice. The mice showed a more rapid acquisition of S-type avoidance than L-type. However, the mean avoidance rates and occurrences of good-performing mice (showing an avoidance rate of higher than 75%) were almost the same in both types when the training was carried out for more than 15 sessions of 1 hr each. The response rate of L-type avoidance was 2.5-3 times as high as that of S-type avoidance. Methamphetamine and cocaine increased the response rate in almost the same grade in both types of avoidance. Chlorpromazine, haloperidol, pilocarpine and physostigmine suppressed both L-type and S-type avoidance responses. However, the L-type showed a higher sensitivity than the S-type to the avoidance-suppressing effect of these drugs. Atropine, scopolamine and morphine suppressed L-type avoidance response, while they facilitated S-type avoidance. The drug-induced changes in the response rate of the S-type were well correlated with those in the ambulatory activity. The changes in the response rate of the L-type were also consistent with those in the ambulatory activity after administration of methamphetamine, cocaine, chlorpromazine, haloperidol, pilocarpine and physostigmine, but inconsistent after atropine, scopolamine and morphine. The present results suggest that L-type and S-type avoidance responses in mice sometimes show a different change after administration of psychoactive drugs.

Animals↗

Effects of diazepam and pentobarbital on discrete lever-press avoidance response in mice: baseline-dependent changes.

Effects of diazepam (0.5, 1, 2 and 4 mg/kg, sc) and pentobarbital (5, 10, 20 and 30 mg/kg, sc) on discrete lever-press avoidance response in the dd strain mice were investigated in consideration of the baseline avoidance levels. The dose-effect relations were obtained with 4 groups of mice showing the baseline avoidance rates of 0-24% (Group 1), 25-49% (Group 2), 50-74% (Group 3) and 75-100% (Group 4). In Group 1, both diazepam (0.5-2 mg/kg) and pentobarbital (5-20 mg/kg) increased the avoidance rate without a marked change in the response rate (frequency of lever-pressings). A significant increase in the avoidance rate was observed when 1 mg/kg of diazepam and 10 mg/kg of pentobarbital were administered. In contrast, both diazepam and pentobarbital decreased the response and avoidance rates in Groups 2-4. These results suggest that the effects of diazepam and pentobarbital on the avoidance response in mice vary depending on the baseline avoidance levels.

Animals↗

[Clinical experience with aztreonam in the field of obstetrics and gynecology].

Aztreoman (SQ 26,776, AZT), a synthetic monobactam antibiotic, was applied clinically in the field of obstetrics and gynecology. AZT was administered by intravenous drip infusion for 6 to 8 days at a daily dose of 2 g divided in 2 times to 5 cases. Klebsiella in 1 case with puerperal endometritis, Enterococcus, Propionibacterium and Bacteroides in each 1 case with pyometra was isolated. The clinical effect of Klebsiella was excellent. Bacteroides in 1 not-examined case was good. Enterococcus and Bacteroides with pyometra was not effective. Side effects were observed in 2 cases. One case with eclampsia arised LDH and A1-P in serum and 1 case with hepatitis arised GOT and GPT in serum.

Adolescent↗

Determination of methylthio and methylsulphone polychlorinated biphenyls in tissues of patients with 'yusho'.

The liver, lung and mesenteric adipose tissue of three patients with 'yusho', polychlorinated biphenyl (PCB) poisoning, and two control persons were analysed for methylthio and methylsulphone metabolites of PCBs by gas chromatography with electron capture detection, gas chromatography-mass spectrometry and mass fragmentography. The tissues were shown to contain two congeners of methylthio PCBs with four chlorine atoms, and 16 congeners of methylsulphone PCBs with three, four, five or six chlorine atoms. The concentrations of methylthio PCBs in the liver, lung and adipose tissue of the yusho patients were 0.1-0.5, 0.2-1.4 and 0.5-1.0 micrograms/kg, respectively, and those of methylsulphone PCBs were 0.3-0.7, 1.0-2.5 and 0.7-1.0 micrograms/kg, respectively. The concentration ratios of methylthio and methylsulphone PCBs to unchanged PCBs were 1-2% in the liver, 4-8% in the lung and 0.1-0.2% in the adipose tissue for yusho patients, indicating that these metabolites accumulate slightly more in the lung and liver than in the adipose tissue, relative to PCBs. The tissue levels of the PCB metabolites in control persons were about one tenth of those in yusho patients.

Adipose Tissue↗

Physiological activity of warburganal and its reactivity with sulfhydryl groups.

Warburganal, a unique dialdehyde sesquiterpene isolated from East African Warburgia plants, showed a strong antifungal activity. However, this growth inhibition in Saccharomyces cerevisiae was reversed with L-cysteine. In addition, warburganal inhibited the alcoholic fermentation of S. cerevisiae while L-cysteine reversed this inhibition. When alcohol dehydrogenase, a sulfhydryl enzyme, was incubated with warburganal, the enzyme activity decreased with time. The decrease was more rapid at alkaline pH. L-Cysteine prevented this enzyme inhibition by warburganal but could not restore the enzyme activity lost already due to warburganal. Warburganal lost its characteristic ultraviolet absorption spectrum in the presence of L-cysteine. The change in absorbance was favored at alkaline pH, indicating Michael reaction type addition of L-cysteine to warburganal. Based on these observations, a variety of physiological activities due to warburganal appear to result from its irreversible reactivity with sulfhydryl groups.

Alcohol Oxidoreductases↗

[Laboratory and clinical studies on latamoxef in the field of obstetrics and gynecology].

Latamoxef (LMOX) is a new antibiotic synthesized by Shionogi Research Laboratory. Chemically LMOX is especially unique with a sulfur atom replacing the oxygen atom in the 1 position of the conventional cephalosporin nucleus, and in addition, this antibiotic has a cephamycin-like structure. The antibacterial activity of LMOX shows high potency against Gram-negative bacteria, but tends to be weak against Gram-positive bacteria. The tissue levels of LMOX in humans after intravenous injection of 1 g were examined. The levels in uterine and adnexa uteri tissue at 1 hour after administration were 25.4 and 27.4 micrograms/g respectively. LMOX was administered to 147 cases in infections of obstetric and gynecological field. The clinical effect according to disease was 94.6% for intrauterine infections, 95.0% for adnexitis, 87.0% intrapelvic infections, and 100% for external genital organ infections, making a total of 92.5%. The rate of occurrence of side effects or abnormal laboratory findings was similar to or slightly less than that seen with other beta-lactam antibiotics.

Adult↗

[Homocystinuria].

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Amino Acid Metabolism, Inborn Errors↗