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Biomedical subjects

K Nakai

Publications and source records attributed to K Nakai.

At least 361 records · Page 20Linked to original sources

Innervation of the cerebral veins as compared with the cerebral arteries: a histochemical and electron microscopic study.

The distribution of nerve fibers in the cerebral veins was studied by catecholamine fluorescence simultaneously with acetylcholinesterase (AChE) histochemistry. A comparison of nerve fibers in the cerebral arteries was made. The ultrastructure of terminal boutons in the veins fixed with potassium permanganate was also studied. In the adventitia of the cerebral artery, green fluorescent aminergic fibers and brownish AChE-reactive (probably cholinergic) fibers were observed. In contrast, the cerebral venous system showed no AChE-positive fibers. Catecholamine fluorescent varicose fibers were detected in the dural sinus, the internal cerebral vein, and the superficial vein of Labbé. The highest density of aminergic fibers was found in the dural sinus and the second highest in the internal cerebral vein. Most of the terminal boutons in the adventitia of the cerebral veins were found adjacent to a muscle-like cell and showed only cored vesicles under electron microscopy. Results of our study suggest that the cerebral venous system has a neurogenic innervation, mainly from aminergic fibers, which is different from the neurogenic supply to the cerebral arterial system.

Animals↗

Visual afferents to norepinephrine-containing neurons in cat locus coeruleus.

A total of 208 single neurons were extracellularly recorded in the locus coeruleus (LC) of 11 cats. In later histofluorescence studies, greenish fluorescent LC neurons, from which we believed to have recorded well-isolated action potentials, were always found in or close to the center of red fluorescent halo due to an injected dye which marked the recording site. One hundred twelve of these 208 neurons were further subjected to electrical stimulation of the dorsal bundle of ascending axons originating from the norepinephrine (NE)-containing LC neurons and thus activated antidromically with a mean latency of 8.9 ms (the remaining neurons were lost before this examination). The mean conduction velocity was 1.2 m/s. Furthermore, it is suggested that 22% of thus antidromically identified NE neurons in the cat LC had an ascending axon of the conduction velocity faster than 2.4 m/s. This finding may be related with an electron-microscopic observation which indicated the presence of myelinated catecholamine (CA) axons, though not many in number, in the cat visual cortex. Responses by the NE-containing LC neurons to various natural visual stimuli, such as flashlight, moving and stationary light-slit, multiple spots, and gratings were examined. It turned out, however, that flash alone was effective to activate LC neurons. The latency of flash evoked activity was between 48 and 96 ms (N = 12; mean: 60 ms). Furthermore, the following areas in the central visual pathway were electrically stimulated to activate LC neurons orthodromically: the optic chiasm (OX), the dorsal lateral geniculate nucleus (LGN), the superior colliculus (SC), and the visual cortex (VC). The range and the mean of the latency for orthodromic responses were as follows: OX (N = 36, 8.4-42 ms; mean: 21 ms); LGN (N = 17, 6.0-17 ms; mean: 8.1 ms); SC (N = 12, 3.6-12 ms; mean: 5.6 ms); VC (N = 10, 7.8-40 ms; mean: 16.4 ms). The long latency of these orthodromic responses and its wide distribution suggest that afferents to the LC from the above-mentioned visual structures are most likely polysynaptic in nature. The extensive input convergence, including acoustic and nociceptive afferents, and the polysynaptic connection in each afferent pathway indicated a strong similarity between the afferent connectivity of NE-containing LC neurons revealed in the present study and that known for reticular formation neurons. Then, we would like to suggest that visual signals from the eyes impinge upon the NE-containing LC neurons via the reticular formation and that the afferents from the LGN, the SC, and the VC also join this common path through the reticular formation to reach the LC.

Animals↗

In vivo release of testosterone from protein--vinyl polymer composites.

Hydrophilic vinyl polymer-protein composites containing testosterone were made by means of thermal denaturation of albumin after radiation-induced polymerization of 2-hydroxyethylmethacrylate (HEMA) at--78 degrees C. The albumin-HEMA mixed polymer can be considerably digested with trypsin. The degree of digestion was smaller than that expected from calculation. It was deduced that the digestion of the albumin component was retarded in the presence of HEMA. The same tendency was observed in in vivo experiments. At the same time, in vivo release of testosterone was depressed in albumin-HEMA mixed polymer composite in accordance with the weight decrease of polymer composite resulting from digestion. The effect of testosterone on the weight of ventral prostate was investigated using composites in castrated Wistar rats. The effect was larger in the controlled slow release from implanted composites rather than that of dosage by injection. The microscopic observation showed that the inflammation and foreign body reaction in rat tissue were retarded in albumin-HEMA mixture polymer composite compared with 100% albumin composite.

Animals↗

Gas chromatographic--mass fragmentographic determination of homopantothenic acid in plasma.

A gas chromatographic--mass fragmentographic method was developed for the determination of homopantothenic acid in plasma. Acidified plasma was deproteinized by extraction with chloroform and subsequently the aqueous layer was extracted with ethyl acetate. The organic layer containing homopantothenic acid was reduced to dryness, and the resulting residue was redissolved in N,O-bis(trimethylsilyl)trifluoroacetamide--pyridine solution to allow trimethylsilylation. Aliquots of this solution were injected into the gas chromatograph--mass spectrometer and analyzed by the selected ion monitoring method using L-ascorbic acid as an internal standard. The detection limit for homopantothenic acid was 5 ng/ml of plasma. A precise and sensitive assay for the determination of homopantothenic acid in plasma was established.

Chromatography, Gas↗

Comparative anatomy of the distribution of catecholamines within the inferior olivary complex from teleosts to primates.

The distribution of catecholamine (CA) in the inferior olivary complex (IO) of various vertebrate (from fish to monkey) was investigated by means of the histofluorescence technique. In addition, using rats, a further attempt was made to elucidate the origins of CA in the IO. The IO of the lower vertebrates (from fish to birds) was in general poorly innervated by the CA neuron system. IO in the lower mammals, such as insectivora and bats, contained only a few CA nerve terminals, while that in the higher mammals such as rat, guinea pig, rabbit, cat, and monkey revealed quite a number. In these animals, species-species patterns of CA nerve terminals were found. In the rat, the highest concentration was observed in the dorsal lamella of the principal nucleus and in guinea pig ventral lamella. In the rabbit and cat, maximum CA nerve terminals were detected in the dorsal accessory nucleus, while in the monkey, they were detected in the medial accessory nucleus. The retrograde tracer technique of horseradish peroxidase (HRP) suggested that the main source of the abundant CA terminals in IO of the rat might be A1, A2, and A3 noradrenaline neurons, though not locus coeruleus and not dopaminergic ones.

Animals↗

Study on the absorption and protein binding of carbaryl, dieldrin and paraquat in rats fed on protein diet.

Carbaryl was well absorbed from the small intestine of rats. In the cytosol fraction of intestinal mucosa, it was bound to a smallmolecular component (M. W. 2,200 daltons). In serum, carbaryl was bound mainly to albumin and partly to globulins. Dieldrin was slowly absorbed from small intestine. The peak of dieldrin concentration in blood was observed 2.5 hr after the administration. Binding of dieldrin to mucosal protein in cytosol was not detectable. In serum, dieldrin was bound to lipoproteins, globulins and partly to albumin. Absorption of paraquat from the small intestine was more rapid than that of dieldrin in situ study. However, in vivo study, the absorption of paraquat was the lowest among these three chemicals. In the cytosol fraction of intestinal mucosa, paraquat was bound to a small-molecular component (M. W. 3,100 daltons). In serum, it was present in unbound fraction. In the comparative studies with protein diets, absorption of paraquat from small intestine in situ was higher in low protein diet rats than that in high protein diet rats. However, difference in absorption in vitro and in histopathological study was not noted between low protein diet rats and high protein diet rats.

Animals↗