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Biomedical subjects

A Sawa

Publications and source records attributed to A Sawa.

At least 73 records · Page 4Linked to original sources

The effects of droperidol and diazepam on the neural excitation of ketamine hydrochloride.

The effects of neuroleptics (droperidol and diazepam) were studied on the neural excitation by ketamine hydrochloride by means of the c-fiber reflex, in the spinal cat and the intact cat. Results can be summarized as follows: 1) Ketamine hydrochloride 125-500 micrograms/Kg i.v. facilitated the neural activity on the c-fiber reflex of the intact cat, but it depressed that of the spinal cat. 2) Droperidol 50-250 micrograms/Kg i.v. and diazepam 50-250 micrograms/Kg i.v. did not influence the neural activity on the c-fiber reflex of the intact cat, but it depressed that of the spinal cat. 3) Droperidol 125 micrograms/Kg i.v. followed by ketamine hydrochloride 125 micrograms/Kg i.v. facilitated the neural activity of the intact cat c-fiber reflex. 4) Diazepam 50 micrograms/Kg i.v. followed by ketamine hydrochloride 250 micrograms/Kg i.v. did not influence the neural activity of the intact cat c-fiber reflex. These data suggested that the neural excitation of ketamine hydrochloride was depressed by diazepam and that a small dose of droperidol did not depress the neural excitation of the intact cat.

Animals↗

Evidence that dynorphin-(1-13) acts as an agonist on opioid kappa-receptors.

The study concerned the opioid-receptor subtype on which dynorphin-(1-13) acts in in vitro isolated preparations. The potency of dynorphin-(1-13) relative to that of ethylketocyclazocine (Mr 2266), a representative kappa-receptor agonist, in inhibiting the electrically evoked contractions of the guinea-pig ileum was found to be similar to that found with either mouse was deferens or rabbit ileum. Moreover, Mr 2266 was found to be several-fold more effective than naloxone to antagonize the agonist actions of both kappa-receptor agonists such as ethylketocyclazocine, ketocyclazocine and bremazocine, and dynorphin-(1-13) either in the guinea-pig ileum, mouse vas deferens, or in rabbit ileum. Additionally, dynorphin-(1-13) was found to have a significant inhibitory action on the rabbit vas deferens which had been shown to contain kappa-receptors exclusively. The data indicate that dynorphin-(1-13) acts as an endogenous agonist on kappa-receptors.

Animals↗

Calcium requirements for electrically-induced release of an endogenous opiate receptor ligand from the guinea-pig ileum.

Calcium requirements for electrically-induced release of an endogenous opiate receptor ligand in the myenteric plexus-longitudinal muscle strip of the guinea-pig ileum were studied. The naloxone-reversible depression of the electrically evoked contraction caused by stimulation at 10 Hz in normal Krebs solution was markedly reduced by decreasing the calcium concentration in the solution. The depression was greatly diminished by increasing the magnesium concentration in the solution. These results show that the electrically-induced release of an opiate-like material requires calcium ions.

Animals↗

Effects of narcotic analgesics on serotonin metabolism in brain of rats and mice.

The effects of narcotic analgesics on the brain 5-hydroxytryptamine (5-Ht) and 5-hydroxyindoleacetic acid (5-HIAA) levels of rats and mice were investigated in relation to our preceding data on the effect of humoral modulatorents. The results suggest that morphine accelerates the release of brain 5-HT both in rats and mice, and that neither methadone nor pethidine alters the brain 5-HT and 5-HIAA levels in rats. The morphine-induced increase in brain 5-HT turnover is likely to be involved in the morphine-induced decrease in locomotor activity and hypothermia in rats. The activity-decreasing effects of methadone or pethidine, on the other hand, are mediated by mechanisms different from those which mediate the effects of morphine. In contrast, an increase in brain 5-HT turnover in mice apparently does not play an important role on activity-increasing effects of morphine but rather participates in other pharmacological effects of morphine.

Analgesics, Opioid↗