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Dive into the research topics where Hideomi Fukuda is active.

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Featured researches published by Hideomi Fukuda.


European Journal of Pharmacology | 1975

The chloride-dependent depression by GABA in the frog spinal cord☆

Yoshihisa Kudo; Norio Abe; Satoko Goto; Hideomi Fukuda

Spontaneous activities from ventral and dorsal roots of the isolated perfused spinal cord of the bullfrog were inhibited by GABA. beta-Alanine showed a strong and glycine a weaker inhibitory effect. The inhibitory effect of GABA was markedly reduced in a chloride-free medium, whereas glycine and beta-alanine still showed an inhibitory effect similar to that seen in normal medium. Employing the sucrose-gap method, a marked depolarization in the dorsal root and a small but obvious hyperpolarization in the ventral root were found by the application of GABA. These results support the view that GABA is one of the transmitters involved in pre- and postsynaptic inhibition of the spinal cord. The postsynaptic hyperpolarizing effect of GABA on motoneurones would be caused directly through increased permeability of the membrane to chloride ion. The depolarizing effect of GABA on primary afferent terminals is discussed in connection with chloride dependency.


European Journal of Pharmacology | 1974

Excitation of rat muscle spindle afferents by lyoniol-A

Hideomi Fukuda; Yoshihisa Kudo; Hideki Ono

Abstract The effect of lyoniol-A, a diterpenoid from an Ericaceous plant, on the de-efferented muscle spindle was studied to elucidate the mechanism responsible for abnormal behaviours in mammals resulting from administration of the agent. Increase in the frequency of afferent discharges in response to lyoniol-A (200–300 Hz) was much greater than that obtained on stretching the muscle or after suxamethonium. The result showed that lyoniol-A did not affect the extrafusal fibres nor intrafusal fibres and that adaptation, one of the characteristics of a muscle spindle, did not appear after an administration of the agent. In conclusion, lyoniol-A is a potent muscle spindle excitant that is likely to be a pharmacologically useful tool, and this action may largely responsible for the abnormal behaviours resulting from an administration of lyoniol-A. The experiment also dealt with lyoniol-B (deacetyl-lyoniol-A), grayanotoxin-I and veratridine.


European Journal of Pharmacology | 1969

Depression by strychnine of afferent discharges from the muscle spindle of the bullfrog in vitro

Hideomi Fukuda; Kazuo Watanabe; Yoshihisa Kudo

Abstract Strychnine (1.25 × 10−5 − 1 × 10−4M) caused a reduction in the rate of afferent discharge from the muscle spindle of the isolated M. extensor longus dig. IV from the bullfrog subjected to stretch. The possible site of action of the drug is discussed.


Brain Research | 1979

Decrease in the extracellular potassium activity of the frog spinal cord during the application of aliphatic anions

Yoshihisa Kudo; Yasuo Nagai; Hideomi Fukuda

Ionic mechanisms of physiological and pharmacological phenomena have been investigated by substituting the extracellular ions with the other inactive foreign ionsl,2,s,10,1L In these studies selected ions were expected to have little or no pharmacological effects by themselves. Thus, the resultant alterations in the physiological functions were analyzed as the consequences of lack of removed ions. We reported that the potential in dorsal and ventral roots of isolated frog spinal cord measured by a sucrose-gap method was markedly hyperpolarized during the perfusion with Ringer solution in which chloride ion was substituted by propionate s. On the other hand, Barker and Nicoll 1, who employed isethionate as a main anion, reported that the perfusion of hemisected frog spinal cord with chloride-free medium caused a depolarization in root potentials. This discrepancy may be attributable to the undesired actions of employed foreign anions on the neuronal membrane. In the present study, the alterations ofextracellular potassium activity during the application of popular monovalent anions, which have frequently been employed as main anions in replacing extracellular chloride ion, were examined. Experiments were carried out on the isolated perfused spinal cord 9 of the bullfrog (Rana catesbeiana) weighing 80-150 g. Procedures for preparing isolated perfused spinal cord, drug application, and a sucrose-gap method were the same as described elsewhere 6-s. Potassium-sensitive microelectrodes were prepared according to the technique described by Walked 4 and Vysko~il and K[i~ ~3. The potassium-sensitive microelectrode was filled with 0.5 M KC1, with about 500/zm column of Corning ion exchanger resin (477317) in its tip, and a reference electrode was filled with solution of 0.15 M NaCI. Tips of these electrodes were assembled under microscopic observation


Japanese Journal of Pharmacology | 1976

ALTERATION OF EXTRACELLULAR K+-ACTIVITY INDUCED BY AMINO ACIDS IN THE FROG SPINAL CORD

Yoshihisa Kudo; Hideomi Fukuda


Chemical & Pharmaceutical Bulletin | 1970

Some Observations on the Cardiovascular Effects of 9-Substituted Berberines

Hideomi Fukuda; Kazuo Watanabe; Yoshihisa Kudo


Japanese Journal of Pharmacology | 1974

Rigidity in rats due to anemic decerebration and the effect of chlorpromazine.

Hideomi Fukuda; Tsugutaka Ito; Satoe Hashimoto; Yoshihisa Kudo


Japanese Journal of Pharmacology | 1972

SPONTANEOUS ELECTRICAL ACTIVITY OF THE BULLFROG SPINAL CORD AND SUSCEPTIBILITY TO SOME CENTRALLY ACTING DRUGS AND AMINO ACIDS

Yoshihisa Kudo; Hideomi Fukuda


Chemical & Pharmaceutical Bulletin | 1974

Structure-activity relationship of lyoniol-A and related compounds in association with the excitatory effect on muscle spindle afferents.

Hideomi Fukuda; Yoshihisa Kudo; Hideki Ono; Masaiti Yasue; Jinsaku Sakakibara; Takeshi Kato


Chemical & Pharmaceutical Bulletin | 1976

Pharmacological study on the aortic arch baroreceptors in the rabbit.

Junichi Ishiko; Hideomi Fukuda

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Hideki Ono

Nagoya City University

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Norio Abe

Nagoya City University

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