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Biomedical subjects

N Kudo

Publications and source records attributed to N Kudo.

At least 19 recordsLinked to original sources

Resetting from low threshold afferents of N-methyl-D-aspartate-induced locomotor rhythm in the isolated spinal cord-hindlimb preparation from newborn rats.

In this study we have investigated the effects of low threshold afferent stimulation on the centrally generated locomotor rhythm in an isolated spinal cord-hindlimb preparation from newborn (0-3 days old) rats. Locomotor activity was induced by bath application of N-methyl-D-aspartate (NMDA). Stimulation of low threshold afferents (below 2 times threshold (x T) for the incoming volley) in L2 and L3, but not L4 and L5 dorsal roots resets the ongoing rhythm. This is due to an abrupt excitation of the L2 and L3 ventral root bursts and an inhibition of the L5 ventral root burst on the ipsilateral side followed by reciprocal effects on the contralateral side. Similar effects were seen after stimulation of the quadriceps nerve with weak intensity (below 1.8 x T). We conclude that low threshold muscle afferents, possible group I afferents, have access to central pattern generators early in postnatal life and suggest that these findings may give an important opening in ontogenetic studies of how neural networks are assembled.

Afferent Pathways

Immunohistochemical study on development of serotonin-, substance P-, and enkephalin-positive fibers in the rat spinal motor nucleus.

Developmental changes in the coexistence of serotonin and substance P/enkephalin within single fibers of lamina IX of the rat lumbar spinal cord were examined by the use of a double-labelling immunohistochemical technique. On postnatal day (P) 0, 65.0% of immunoreactive varicosities contained only serotonin, and 21.3% of them had both serotonin and substance P. The coexistent ratio of serotonin and substance P in single fibers increased with development: 61.9% of serotonin positive varicosities co-contained substance P on P28, similar to the ratio found in adult animals (67.4%). The ratios of varicosities containing only substance P remained the same from P0 to adult stage (about 15%). Enkephalin positive immunoreactivity was not co-localized with serotonin positive varicosities at any stage of development. Although numerous serotonin positive fibers were found in lamina IX, only a few substance P and enkephalin positive fibers were observed in the same area on P0. The density of serotonin positive varicosities increased slightly by P28, whereas substance P and enkephalin positive fibers increased considerably by this age. Between P28 and the adult stage, the density of serotonin positive fibers decreased by about 50%. The cross sectional area of axonal varicosities containing serotonin- and substance P-like immunoreactivity was similar in both P0 and adult animals, whereas that of enkephalin positive fibers was different. We also examined the coexistence of serotonin and substance P within single neurons of the caudal raphe nuclei in P7 and adult animals, and found that the coexistent ratio significantly increased with development.

Aging

Inhibition of the liberation of arachidonic acid by cadmium ions in rabbit alveolar macrophages.

The effects of CdCl2 on the liberation of arachidonic acid (20:4) from membrane phospholipids of A23187-stimulated rabbit alveolar macrophages and on the activity of phospholipase A2 (PLA2) in a cytosolic fraction were studied. Alveolar macrophages were prelabeled with [3H]arachidonic acid (20:4) and then treated with A23187. This treatment resulted in a remarkable increase in the liberation of [3H]20:4 from their phospholipids. Exposure of cells to Cd2+ inhibited the liberation of [3H]20:4 in a dose-dependent manner. Liberation of [3H]20:4 from cell lipids was calcium dependent and the inhibitory effect of Cd2+ competed with the stimulatory effect of Ca2+. When Ca2+ was removed from the incubation medium, Cd2+ did not influence the liberation of [3H]20:4. Entry of 45Ca2+ into cells was enhanced by treatment of A23187. However, Cd2+ did not influence the cellular uptake of 45Ca2+. Treatment with A23187 markedly enhanced entry of 109Cd2+ into cells. The effect of Cd2+ on the activity of phospholipase A2 was determined with 1-palmitoyl-2-[14C]arachidonoyl-sn-glycero-3-phosphocholine as substrate. Calcium-dependent activation of PLA2 was observed and Cd2+ inhibited activation in a dose-dependent manner. These results suggest that exposure of alveolar macrophages to Cd2+ causes a reduction in the rate of liberation of 20:4 from cell lipids, as a possible result of the inhibition of PLA2 activity by Cd2+.

Animals

[Intrapleural treatment of breast cancer patients with pleural effusions: an analysis of 13 institutes in Kyoto and Shiga Prefectures. Kyoto and Shiga Breast Cancer Study Group].

Sixty-seven breast cancer patients with malignant pleural effusions underwent their first thoracentesis between 1980 and 1990 at 13 institutes in Kyoto and Shiga Prefectures. They received various intracavitary treatments including OK-432 and cultured effusion lymphocytes (n = 29, group A), OK-432 alone (n = 12), chemotherapeutic agents alone (n = 9), OK-432 and chemotherapy (n = 16) or other (n = 1, lentinan and tetracycline) therapy. Response rate and median survival time were 90%, 12 months for group A, respectively and 40% and 3 months for other treatments (group B, n = 38), resulting in significant differences. Multivariate analysis using Cox's proportional hazard model showed that the immunotherapy using cultured lymphocytes was the most important factor prolonging survival among several significant prognostic factors such as concomitant liver metastasis, disease-free period and laterality of effusion.

Antineoplastic Combined Chemotherapy Protocols

Species differences in the distribution and coexistence ratio of serotonin and substance P in the monkey, cat, rat and chick spinal cord.

Serotoninergic raphe-spinal motor neuron projections exhibit wide species differences in both innervation pattern and coexistence of serotonin and substance P. The coexistence ratios vary widely ranging from more than 80% (rat) to less than 1% (chick). Serotonin and substance P positive fibers are also unevenly distributed in the ventral horn of different species: dense clusters of serotonin and substance P positive fibers were preferentially located in the motor neuron pools of extensor muscles of the hip joint (chick) as well as antigravity muscles of the forelimb (cat and rat).

Animals

Serotonin-positive fibers within the spinal motor nucleus of the newborn rat, with special reference to co-localization of substance P.

Developmental changes of serotonin-positive fibers with special reference to co-localization with substance P was examined immunohistochemically in the ventral horn of rat lumbar spinal cord. Only about 20% of serotonin-positive fibers co-labelled with substance P on postnatal day (P) 0. The ratio of co-localization gradually increased, and reached the adult value by P28 (60-70%). Enkephalin-positive fibers were not co-localized with serotonin at any age examined. Although the densities of serotonin, substance P and enkephalin per unit area of the ventral horn gradually increased with development up to P28, the density of serotonin in the adult was decreased compared to P28 animals.

Afferent Pathways

Prevention by zinc of cadmium inhibition of stearoyl-CoA desaturase in rat liver.

Rats were fed a fat-free diet that contained zinc (50 ppm; ZA rats) or a fat-free diet without zinc (less than 2 ppm; ZD rats) for 16 days. Some rats in these two groups were injected subcutaneously with cadmium (Cd) at a dose of 0.01 mmol/kg body weight 48 h before they were killed. The treatment of ZD rats with Cd reduced the activity of liver microsomal stearoyl-CoA desaturase by 90% without any changes in the activity of NADH-cytochrome b5 reductase or in the microsomal level of cytochrome b5 whereas the activity of stearoyl-CoA desaturase was reduced by only 35% by the treatment of ZA rats with Cd. Exposure of ZD rats to Cd decreased the proportions of 18:1 (n-9) and 20:3 (n-9) in the major phospholipids of the liver, whereas the ZA rats showed few changes in fatty acid composition when they were treated with Cd. Although the changes in fatty acid composition were most marked in phosphatidylcholine among the various phospholipids, the activity of microsomal l-acylglycerophosphocholine (1-acyl GPC) acyltransferase was not affected by treatment with Cd. These results suggest that zinc is essential for the protection of hepatic stearoyl-CoA desaturase from challenges by Cd and that delta 9 desaturase plays a crucial role in the control of the acyl composition of hepatic phospholipids.

Animals

Effects of zinc deficiency on the fatty acid composition and metabolism in rats fed a fat-free diet.

The effects of dietary zinc deficiency (ZD) on the composition and metabolism of the fatty acyl chains of phospholipids in rat liver were investigated with a fat-free diet. The levels of (n - 9) fatty acids such as 18:1 and 20: 3(n - 9) in liver phospholipids (PL) were significantly lower in ZD-rats (19.4% and 5.4%, respectively) than in PF-rats (25.2 and 8.3%). On the other hand, the levels of (n - 6) acids such as 18:2 and 20:4 were higher in ZD-rats (3.3 and 19.1%, respectively) than in PF-rats (2.1 and 14.9%). In order to study the metabolism of fatty acids in vivo, 14C-18:0 or 14C-18:2 was intravenously injected, and then the conversion to the respective metabolite was examined. After the injection of 14C-18:0, the radioactivity was found in 18:0 (49.3% of the total), 18:1 (33.2%), and 20:3 (n - 9) (9.1%) in liver PL in PF-rats at 24 h. In ZD-rats, the radioactivity was dramatically lower in 18:1 (23.5%) and 20:3 (n - 9) (3.6%), suggesting that the conversion of 18:0 to 18:1 and 20:3 (n - 9) was strongly inhibited in ZD-rats. When 14C-18:2 was injected, the radioactivity was mainly found in 18:2, 20:3 (n - 6), and 20:4. The radioactivity in 20:4 in ZD-rats was slightly higher than that in control rats. These results indicate that zinc deficiency affects the fatty acid metabolism in liver, in particular, it causes a reduction in delta 9 desaturase activity, when rats are fed a fat-free diet.

Animals

The effect of cadmium on the composition and metabolism of hepatic fatty acids in zinc-adequate and zinc-deficient rats.

Exposure to cadmium (Cd) caused changes in the fatty acid composition of phospholipids, such as increases in levels of saturated and (n-6) fatty acids and decreases in levels of (n-9) fatty acids, in the liver phospholipids of rats fed a fat-free diet. These changes were similar to those caused by dietary zinc deficiency. The changes in fatty acid composition after administration of Cd were greater in zinc-deficient (ZD) rats than zinc-adequate (ZA) rats. When [14C]18:0 was injected intravenously in order to examine the metabolism of (n-9) fatty acids, a decrease in the rate of conversion of [14C]18:0 to [14C]18:1 was observed in liver phospholipids after treatment of ZD rats with Cd. These results suggested that Cd can affect the metabolism of fatty acids in relation to zinc status and, in particular, causes a reduction in the activity of delta 9-desaturase which converts 18:0 to 18:1.

Animals

Spatial patterns of reflex evoked by pressure stimulation of the foot pads in cats.

1. The spatial patterns of reflexes elicited by localized pressure stimulation of the foot skin were analysed by recording electromyographic activities of various hindlimb muscles or muscle nerve discharges in cats anaesthetized with sodium pentobarbitone. 2. Reflex discharges evoked by stimulation of the central pad occurred mainly in physiological toe extensors located in the foot. Stimulus-response relationships of single motor units revealed characteristically wide ranges of graded response and recruitment. 3. Within the central pad, the strongest excitation was evoked from the central lobe and was distributed to extensors of all four toes. Excitation from the medial and the lateral lobes was usually asymmetrical and weaker in toe muscles of the stimulated side. It is suggested that the weakness was in part due to concomitant inhibition. 4. Stimulation of a toe pad caused marked suppression of central pad-evoked activity of toe extensors with a highly specific spatial pattern. The inhibition was strongest in extensors of its own toe, and gradually weaker in the more distant toes. Weak excitation was occasionally evoked in extensors of the most medial or lateral toes, when the most lateral or the most medial toe-pad, respectively, was stimulated. 5. A similar pattern of relfex to that from the toe pad was evoked from the claw base and the hairy toe dorsum of each digit. 6. Reflex effects, both inhibitory and excitatory, from the central and toe pads, claw bases and toe dorsum were maintained during prolonged stimuli, indicating that slowly adapting receptors contributed to these reflexes. 7. It is concluded that stimulation of localized skin areas of the foot, particularly the pads, evokes highly specialized reflexes, which may be important in controlling movements of individual digits.

Animals

Cellular coaggregation of oral Streptococcus milleri with actinomyces.

Oral isolates of Streptococcus milleri were examined for their ability to coaggregate with actinomyces. Of the 68 S. milleri strains tested, including 3 reference strains, 40 strains coaggregated with Actinomyces naeslundii WVU45 (actinomyces coaggregation group B) and 36 strains coaggregated with Actinomyces viscosus T14V (actinomyces coaggregation group A). All S. milleri strains of serotypes b (4 strains), e (2 strains), and f (24 strains) coaggregated with both of the actinomyces. The coaggregation reactions between the S. milleri cells and A. naeslundii WVU45 cells were optimal at about pH 7.0 and were Ca2+ or Mg2+ dependent, but they were not inhibited by the presence of simple sugars or amino sugars, including lactose (up to 0.5 M). Treatment of the S. milleri cells with heat (100 degrees C, 3 min) or proteases (trypsin, 1.0 mg/ml; pronase, 0.25 mg/ml; 37 degrees C; 3 h) and of the actinomyces cells with periodate (0.01 M, 4 degrees C, 16 h) destroyed their coaggregating abilities. The coaggregations between cells of the S. milleri strains, we well as cells of the Streptococcus sanguis H1 (reference strain for streptococcus coaggregation group 2) and the actinomyces strains (WVU45 and T14V), were inhibited by AFH1 (a carbohydrate receptor on T14V cells for a lectin on H1 cells). These interactions were also inhibited by anti-AFH1 immunoglobulin G (IgG) and by anti-b, anti-e, and anti-f S. milleri IgG or anti-f IgG Fab fragments. These results suggest that S. milleri, at least strains of serotypes b, e, and f, belongs to streptococcus coaggregation group 2.

Actinomyces

An immunohistochemical study on the embryonic development of renin-containing cells in the mouse and pig.

The prenatal occurrence and distribution of renin-containing (RC) cells were investigated immunohistochemically in mouse and pig embryos. The RC cells of the mouse embryo were first observed at the 13th day of gestation at the walls of the renal, the mesonephric, the adrenal, the abdominal arteries, the adrenal glands and the testis. As the gestation of the mouse progressed, the RC cells had a tendency to localize in areas of the vascular pole of the metanephric glomerulus. In pig, when CRL was 0.8-2.0 cm, RC cells first appeared at the ventral walls of the dorsal aorta, the omphalo-mesenteric (i.e., the cranial mesenteric), the mesonephric, the mesonephric afferent glomerular arteries/arterioles and the inside of the mesonephric glomerulus. As the length of the pig embryo increased, no renin-immunoreactivity could be demonstrated at the degenerated mesonephros, while in the metanephros marked immunoreactivities were found only at the terminal regions of intralobular arteries, i.e., afferent arterioles or the vascular pole of the glomerulus.

Animals

Morphology of blood cells in carp (Cyprinus carpio L.).

The morphology of blood cells in the carp was investigated by light and electron microscopy. Erythrocytes, thrombocytes, lymphocytes, granulocytes and monocytes were identified as the peripheral blood cells. Thrombocytes were round to long oval, each containing vesicular and microtubular structures and an oval nucleus with abundant heterochromatins. Lymphocytes were divided into three types in size, small, medium and large. Some of the small and medium lymphocytes were alpha-naphthyl-acetate esterase (ANAE) positive, while large lymphocytes were pyroninophilic. Granulocytes were distinguished into three types (type I, type II and type III) according to the morphology of the nucleus and granules. Type I granulocytes possessed lobulated nuclei and a large number of cytoplasmic granules, each of which was oval and contained electron-dense materials and a crystalloid. Type II granulocytes had small eccentric nuclei and were subdivided into IIa and IIb granulocytes by electron microscopic analysis. Granules of type IIa granulocytes were furnished with an electron-dense rim. Granules of type IIb granulocytes were larger than those of type IIa, containing randomly distributed electron-dense and electron-lucent materials. Type III granulocytes possessed round nuclei and a few large granules. The granules were filled with regularly arranged fibriform materials and some needle-like structures. Monocytes were morphologically similar to those of mammals.

Animals

Histological study on seminal plasma absorption and spermiophagy in the epididymal region of domestic fowl.

Absorption of seminal plasma and spermiophagy in the fowl epididymal region were studied ultrastructurally and histochemically. Epithelial cells of the rete testis had sparse coated vesicles and rarely showed spermiophagy. Many macrophages in the lumen of the rete testis actively phagocytosed spermatozoa. Nonciliated cells in the proximal efferent ductules had well-developed microvilli, coated vesicles, numerous tubular structures, and lysosomes in their apical cytoplasm. They rarely contained fragments of spermatozoa. Intense alkaline phosphatase activity was observed at the luminal borders of these cells. Ciliated cells had no features indicating active absorption of seminal plasma. Epithelial cells of the connecting ductules and epididymal duct had numerous microvilli, a few vesicles, and small lysosomes. They did not contain spermatozoa. Intense acid phosphatase activity was observed on the luminal and lateral surfaces of the epithelial cells of the connecting ductules and epididymal duct. After injection of horseradish peroxidase into the excurrent ducts, a large amount of reaction product was detected in the vesicles and tubular structures of the nonciliated cells of the proximal efferent ductules. These results suggest that the absorption of seminal plasma occurred mainly in the efferent ductules, and that spermiophagy by macrophages occurred in the rete testis in the fowl epididymal region.

Absorption

Reduction of the adherence of Streptococcus sobrinus insoluble alpha-D-glucan by endo-(1----3)-alpha-D-glucanase.

Insoluble alpha-D-glucan, previously formed on a glass surface from sucrose by the action of cell-free D-glucosyltransferases of Streptococcus sobrinus OMZ176, was significantly removed by a purified preparation of endo-(1----3)-alpha-D-glucanase (mutanase) from a strain of Pseudomonas sp. Almost complete dissociation of adherent glucan occurred at the highest enzyme concentration (40 mU/mL) tested. Synthesis and de novo adherence on glass of the glucan was markedly inhibited by the presence of mutanase, even at low concentrations (4 mU/mL or less). When compared to native glucan, the mutanase-modified glucan samples (a) contained lower proportion of D-(1----3) linkages; (b) showed lower susceptibility to mutanase and higher susceptibility to (1----6)-alpha-D-glucanase (dextranase); (c) contained larger amounts of low-molecular-weight fractions; (d) had lower intrinsic viscosities; (e) showed higher S. sobrinus cell-agglutinating activities; and (f) consisted of looser entwinement of coalescent single-stranded fibrils (a major component) and shorter double-stranded fibrils (a minor one).

Adhesiveness

A morphological study on the obliteration processes of the ductus arteriosus in the horse.

The obliteration processes of the ductus arteriosus of equine foetuses and newborn foals were studied morphometrically and histologically. The length, internal and external diameters and circumference of the ductus in equine foetuses increased progressively and linearly up to 310 days with advancing foetal age, but the values, especially the internal diameter, decreased from 320 to 330 days. After birth, the ductal measurements decreased gradually and ductal closure was found in three of 14 foals examined on the first day post partum, in two of six on the second day and in nine of nine on the third day or later, suggesting that the ductus arteriosus closes physiologically within three days after birth. Microscopical findings of the ductus arteriosus were characterised by the rearrangement of smooth muscle cells in the inner media and intimal thickening in foetuses, and by the central displacement of the intima in newborn foals. It was concluded that the ductus arteriosus begins to undergo preparatory modifications during intrauterine life, when the vessel is still functional, and that the most significant starting point of change in the obliteration processes is the rearrangement of smooth muscle cells in the inner media, which occurs during pre- and post natal life.

Animals

Sensory input to cells of origin of uncrossed spinocerebellar tract located below Clarke's column in the cat.

1. Sensory inputs to and locations of uncrossed spinocerebellar tract neurones in the lower lumbar cord were studied in chloralose-anaesthetized cats. 2. Neurones with axons ascending in the ipsilateral thoracic funiculi and projecting to the cerebellum were found mainly dorsal to the central canal (laminae V and VI) in the L5-L6 segments, i.e. at levels caudal to Clarke's column. Axons considered to originate from these cells were located in the dorsal half of the lateral funiculus at the level of L2, intermingled with axons of the dorsal spinocerebellar tract originating at the levels of Clarke's column. 3. Synaptic actions of primary afferents on neurones with antidromic invasion following stimuli applied to ipsilateral thoracic funiculi or to the cerebellum were investigated using intracellular or extracellular recording in the caudal lumbar segments. 4. Monosynaptic excitatory effects were evoked by electrical stimulation of group I muscle afferents of the hindlimb ipsilateral to the cell body. The majority of neurones received monosynaptic excitation from two or more muscles, predominantly extensors. They were frequently co-excited by group Ia muscle spindle and group Ib tendon organ afferents. 5. Volleys in cutaneous afferents produced excitation with short central latencies. In addition to the monosynaptic and disynaptic excitation from low-threshold cutaneous afferents, there were indications of monosynaptic effects from slightly slower conducting fibres. The majority of these neurones also received monosynaptic excitation from group I muscle afferents. Neurones with cutaneous input tended to be located more dorsally compared with those responding only to muscle afferents. 6. Volleys in joint afferents produced monosynaptic excitatory postsynaptic potentials (EPSPs) in the neurones with EPSPs from group I or group I and cutaneous afferents. 7. Some neurones were disynaptically inhibited from group I muscle afferents. Convergence of monosynaptic group I excitation and disynaptic group I inhibition occurred in varieties of patterns. 8. Polysynaptic excitation, inhibition or mixed effects of both were evoked from ipsilateral cutaneous afferents and high-threshold muscle and joint afferents, whereas effects from the controlateral afferents were feeble.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals