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Biomedical subjects

T Hongo

Publications and source records attributed to T Hongo.

At least 163 records · Page 9Linked to original sources
PubMed1978

Pattern of projections of individual pyramidal tract neurons to the spinal cord of the monkey.

The results suggest : (1) that PT neurons sending axons to motor nuclei innervating distal forelimb muscles branch less than other PT neurons; (2) that a group of PT neurons located close together may influence various species of motoneurons, but that this influence is the strongest on motoneurons of one species; (3) that individual PT neurons terminate only on a small fraction of a given motoneuron group.

Efferent Pathways↗
PubMed1977

Peripheral vascular effects of glucagon, acetylocholine and dopamine with an implanted total artificial heart (TAH).

Three vasoactive drugs--glucagon, acetylcholine and dopamine were used in calves with an implanted TAH to study their mere vascular effects. We noticed that glucagon, besides being a potent vasodilator, affected the vascular system gradually rather than instantly. Also, it allowed for the gradual recovery of the system, thus avoiding sudden fluctuations in systemic and pulmonary blood pressures. Glucagon was found to have a unique capability of decreasing vascular resistance with only a slight drop in systolic pressure. Acetylcholine action was rather instant, exhibiting a sudden fall in both systolic and diastolic blood pressures. In animals with a TAH, dopamine seemed to work differently from that in subjects with an intact natural heart. While many investigators failed to see any change in pulmonary vascular resistance due to dopamine injection in subjects with an intact natural heart, we noticed about 20% increase in pulmonary vascular resistance (with a dose of 10 muGm/Kg). However, at low dosages of dopamine, we did not notice any appreciable change in pulmonary vascular resistance, which suggests that its action is dose dependent. We tend to believe that glucagon offers promising results in controlling the pulmonary hypertension in calves with a TAH. It is, also, our opinion that further investigation on the vascular effects of dopamine would reveal more pertinent and interesting results and solve the existing discrepancies.

Acetylcholine↗
PubMed1975

The vestibulospinal tract: crossed and uncrossed effects on hindlimb motoneurones in the cat.

Effects produced by stimulation of Deiters' nucleus on contralateral hindlimb motoneurones were investigated in the cat with intracellular and monosynaptic reflex recording. Polysynaptic PSPs were evoked in all species of motoneurone examined. The minimal synaptic linkage was found to be disynaptic in the excitatory path and prisynaptic in the inhibitory path. Experiments with various lesions to the spinal funiculus and those with mapping of the stimulated sites in the brain stem showed that the effects were evoked almost exclusively via the lateral vestibulospinal tract of the stimulated side. The crossed effects were excitatory in extensor motoneurones of all species studied except for hip extensors (ABSm) in which EPSPs and/or IPSPs were evoked. The effects on flexors, by contrast, were not simple and consisted of EPSPs, IPSPs or a mixture of both. The difference in effects depended, though not entirely, on the species of motor nucleus. Between the excitatory and inhibitory effects on knee flexor (PBSt) motoneurones the former predominated under chloralose and the latter under pentobarbital anaesthesia. By recording PSPs evoked from the two vestibulospinal tracts in the same motoneurone, the convergence pattern and the magnitude of effects from the two tracts were studied. The interneuronal organization of the crossed vestibulo-motoneuronel pathway and its functional significance are discussed.

Animals↗
PubMed1975

Inhibition of hepatic drug-metabolizing enzymes by thiophaophate insecticides and its toxicological evaluation.

Thiophosphate insecticides, fenitrothion, diazinon and methylparathion, inhibit hepatic drug-metabolizing enzyme activity which was assayed using aminopyrine and aniline as substrates. About 50% inhibition was observed 4 hrs after the injection of fenitrothion into mice in a dose of 25 mg/kg. The addition in vitro of thiophosphates into a reaction mixture of drug metabolizing enzyme also produced an effective inhibition and IC50 was around 10(-5)M for fenitrothion. DDVP and oxygenated metabolite of fenitrothion did not show any inhibiting effect either in vitro or in vivo. The inhibition of thiophosphates in vitro was competitive while the kinetics of in vivo inhibition was shown as non-competitive. The drug metabolism in the rat liver preparation was also inhibited by thiophosphate in vitro, but in vivo treatment to male rats resulted in only slight inhibition. Female rats exhibited the similar response as mice. The administration of fenitrothion to mice prolonged the hexobarbital sleeping time and, consequently, suppressed the oxidative metabolism of parathion in liver preparation. These effects reveal that the biological half life of thiophosphate insecticides could be altered by the mode of administration or by co-existing thiophosphates.

Aminopyrine N-Demethylase↗