Effects of soccer matches on neutrophil and lymphocyte functions in female university soccer players.

In this study, changes in physical fatigue and biological functions of Japanese female soccer players were investigated by determining changes in neutrophil and lymphocyte functions. Study subjects included 18 female soccer players. Body composition, serum myogenic enzymes, neutrophil function, including reactive oxygen species (ROS) production capability, phagocytic activity (PA) and serum opsonic activity, as well as lymphocyte subpopulation were measured before and after a soccer match. Levels of myogenic enzymes (AST, ALT, CK and LDH) and immunoglobulins (IgG and IgA) and complements (C3) increased significantly after the match. In addition, leukocyte, neutrophils and lymphocyte counts increased whereas total PA decreased significantly. The number of T and Th1 cells (subsets of T helper cells) decreased whereas Th2 increased significantly. In addition, the number of B cells increased and NK cells decreased significantly after the match. The match was found to result in degenerative changes in and damage to athlete muscle tissues together with damage- and change-mediated stress. These data also suggest a post-match accelerated inflammatory reaction and potential immunosuppression as indicated by reductions in neutrophil PA and lymphocyte functions.

Phase advance of the light-dark cycle perturbs diurnal rhythms of brain-derived neurotrophic factor and neurotrophin-3 protein levels, which reduces synaptophysin-positive presynaptic terminals in the cortex of juvenile rats.

In adult rat brains, brain-derived neurotrophic factor (BDNF) rhythmically oscillates according to the light-dark cycle and exhibits unique functions in particular brain regions. However, little is known of this subject in juvenile rats. Here, we examined diurnal variation in BDNF and neurotrophin-3 (NT-3) levels in 14-day-old rats. BDNF levels were high in the dark phase and low in the light phase in a majority of brain regions. In contrast, NT-3 levels demonstrated an inverse phase relationship that was limited to the cerebral neocortex, including the visual cortex, and was most prominent on postnatal day 14. An 8-h phase advance of the light-dark cycle and sleep deprivation induced an increase in BDNF levels and a decrease in NT-3 levels in the neocortex, and the former treatment reduced synaptophysin expression and the numbers of synaptophysin-positive presynaptic terminals in cortical layer IV and caused abnormal BDNF and NT-3 rhythms 1 week after treatment. A similar reduction of synaptophysin expression was observed in the cortices of Bdnf gene-deficient mice and Ca(2+)-dependent activator protein for secretion 2 gene-deficient mice with abnormal free-running rhythm and autistic-like phenotypes. In the latter mice, no diurnal variation in BDNF levels was observed. These results indicate that regular rhythms of BDNF and NT-3 are essential for correct cortical network formation in juvenile rodents.

Association between Polyunsaturated Fatty Acid and Reactive Oxygen Species Production of Neutrophils in the General Population.

Little is known about the relationship between polyunsaturated fatty acids (PUFAs) and reactive oxygen species (ROS) in the general population. Therefore this study aimed to describe the association of PUFAs with ROS according to age and sex in the general population and to determine whether PUFA levels are indicators of ROS. This cross-sectional study included 895 participants recruited from a 2015 community health project. Participants were divided into 6 groups based on sex and age (less than 45 years old (young), aged 45-64 years (middle-aged), and 65 years or older (old)) as follows: male, young (n = 136); middle-aged (n = 133); old (n = 82); female, young (n = 159); middle-aged (n = 228); and old (n = 157). The PUFAs measured were arachidonic acid (AA), dihomo gamma linolenic acid (DGLA), AA/DGLA ratio, eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA). ROS considered in the analysis were basal ROS and stimulated ROS levels. Multiple linear analyses showed: (1) significant correlations between PUFA levels, especially DGLA and AA/DGLA ratio, and neutrophil function in the young and middle-aged groups; (2) no significant correlations in old age groups for either sex. Because PUFAs have associated with the ROS production, recommendation for controlled PUFA intake from a young age should be considered.

A phase advance of the light-dark cycle stimulates production of BDNF, but not of other neurotrophins, in the adult rat cerebral cortex: association with the activation of CREB.

Circadian variation in the expression of brain-derived neurotrophic factor (BDNF) indicates that BDNF is involved in the regulation of diurnal rhythms in a variety of biological processes. However, it is still unclear which brain regions alter their BDNF levels in response to external light input. Therefore, in selected brain regions of adult male rats, we investigated diurnal variation, as well as the effects of a single eight-hour phase advance of the light-dark cycle, on the levels of BDNF and of other neurotrophins. The cerebellum, hippocampus and cerebral cortex containing visual cortex (VCX) showed diurnal variation in BDNF protein levels and the VCX also in NT-3 levels. In the VCX and the region containing the entorhinal cortex and amygdala (ECX), BDNF protein levels were increased 12 h after the phase advance, while BDNF mRNA levels were increased significantly in the VCX and slightly in the ECX after 4 h. After one week, however, BDNF protein levels were reduced in eight brain regions out of 13 examined. BDNF levels in the ECX and VCX were significantly different between light rearing and dark rearing, while a hypothyroid status did not produce an effect. Cyclic AMP responsive element-binding protein (CREB), a transcription factor for BDNF, was greatly activated by the phase advance in the ECX and VCX, suggesting the existence of CREB-mediated pathways of BDNF synthesis that are responsive to external light input.

Distribution and immunohistochemical localization of GDNF protein in selected neural and non-neural tissues of rats during development and changes in unilateral 6-hydroxydopamine lesions.

The tissue distribution of glial cell line-derived neurotrophic factor (GDNF) during development and changes in GDNF levels by unilateral 6-hydroxydopamine lesions were investigated in rats using a newly established enzyme immunoassay system and by immunohistochemistry. The detection limit of the assay was 0.3 pg/0.2 ml and the system recognized glycosylated mature GDNF. Concentrations of GDNF were relatively high in the kidney and testis during the embryonic and neonatal periods, respectively, and decreased with age. In the striatum, hippocampus and brain stem, GDNF reached a maximal level at around postnatal day 14. However, brain levels were generally lower than those in non-neural tissues. In the CNS, GDNF immunoreactivity was observed in striatal neurons, pyramidal neurons in the hippocampus and the Vth layer of the cortex, large neurons in the diagonal band and brain stem, and spinal motor neurons. It was also evident in several non-neural, tissue-specific cells, such as cells in the renal collecting ducts and distal tubules, and testicular Sertoli cells. Destruction of nigral dopaminergic neurons by 6-hydroxydopamine enhanced the levels of striatal GDNF protein, with apparent involvement of astrocytes. These results suggest that GDNF is normally synthesized in neurons, but may also be produced by astroglial cells in damaged brains.

Change of Rat Embryos from a Ventrally Concave U-Shape to a Ventrally Convex C-Shape: (rat/embryo/posture/cytochalasin D/microfilaments).

In an early stage of development in murine embryos, axial rotation occurs and the body axis changes from a ventrally concave U-shape to a ventrally convex C-shape. In this study, axial rotation in Sprague-Dawley rat embryos occurred in about 5 h in vitro (from 27 h to 32 h in cultures of head-fold stage embryos). In sagittal sections, the somites in the mid-region of the body changed from a trapezoidal shape with a short dorsal side and long ventral side to the reverse trapezoidal shape with a long dorsal side and a short ventral side. The dorsal part of these somites acquired the ability to react with actin-specific antibody and developed into dermatome. On treatment with 0.1 µg/ml cytochalasin D during this 5 h period, embryos became ventrally concave with two lordosis bends. The somites in the bends had a short dorsal side, which did not show any evidence of dermatome or intense immunocytochemical staining. These results suggest that the increase in length of the dorsal side of the somites is a cause of the axial rotation and that the organization of actin filaments plays an important role in the conformational change of the somites.

Fusion of Neural Folds in the Rhombencephalic Region of Rat Embryos: (cephalic neurulation/neural folds/fusion/microfilaments/rat).

The progression of fusion of neural folds in the rhombencephalic region of rat embryos was examined using actin-specific antibody and scanning electron microscopy. In the region of unfused neural folds, actin was distributed over the entire luminal surface of the neural plate. Subsequently, the actin became localized on the luminal surface of outwardly opened, dorsolateral portions of the neural plate. Reduction in the area over which actin was distributed corresponded to the decrease in the area of the luminal surface of outwardly opened, dorsolateral portions of the neural plate. Decrease in the area of the luminal surface synchronized with elevation of the neural folds and their approach to the midline and, finally, actin became localized in areas of the apices of the neural plate that formed the bridge between the two opposing neural folds. These results suggest that formation of the bridge is orchestrated and supported by microfilaments. The procession of fusion in the rostral direction may cause approach of the neural folds to the middle, and this approach may be guaranteed by reduction in the area of the luminal surface over which actin is distributed.

The initial development of motor neurons in the neural tube of rat embryos.

The time of origin of motor neurons and their distribution in the spinal cord was studied in rat embryos by combining whole-embryo culture and the Islet-1 immunostaining technique. Cells immunostained for Islet-1 appeared in the trunk neural tube by 27 hours (corresponding to E10.625) in culture of E9.5 embryos, at which time the cell number of the neural tube in a transverse section was about 200. When the neural tube retarded developmentally by lithium treatment, the time of appearance of the motor neurons was delayed to 33 hours in culture (corresponding to E10.875), but the cell number of the neural tube was about 200. After the initial appearance of motor neurons in the ventral aspect of the neural tube, they distributed in a group in the periphery of the basal plate by 48 hours (corresponding to E11.5) in culture, although in the retarded neural tube the number of motor neurons was small and they did not form a cluster. The percentage of Islet-1-positive cells at the point of the same cell number of the trunk neural tube in the transverse section was higher in the retarded embryos than in controls. These results suggest that motor neurons begin to appear when the cell number of the neural tube in the transverse section becomes about 200 and their initial development is more stable than overall neural tube development.

Fertilization of the eggs ofCynops pyrrhogaster (japanese newt) after immersion in water.

Cynops pyrrhogaster oviducal eggs with and without jelly envelopes (jelly egg and dejellied egg respectively) were immersed in water, and then inseminated artificially. After 1 h of immersion in water, more than half the dejellied eggs were fertilized and developed, but no jelly eggs developed. The rapid decrease in the ability of jelly eggs to be fertilized after immersion in water is not due to a deficiency in the egg. Our results make it clear that hydrated jelly envelopes prevent the eggs from fertilizing. The ability of the egg to be fertilized decreases for a long time in water and this decrease proceeds more slowly in De Boer's solution or Holtfreter's balanced salt solution than in water.

Fertilization of newt coelomic eggs in the absence of jelly envelope material.

Fertilization ofCynops pyrrhogaster (Japanese newt) coelomic eggs was studied in the absence of jelly envelope material or synthetic high polymer. An undiluted sperm fluid from the vas deferens fertilized coelomic eggs in the absence of the jelly envelope material or synthetic high polymer. The fertilized eggs developed beyond gastrulae and formed tail bud embryos. These results indicate that the fertilization process does not depend upon the presence of jelly envelope material or synthetic high polymer and that the sperms within the vas deferens are already capable of fertilizing the eggs inC. pyrrhogaster. The sperm suspension in Holtfreter's balanced salt solution (H-sperm) fertilized the coelomic eggs without the jelly envelope material or synthetic high polymer. These eggs had been suspended in Holtfreter's balanced salt solution (H) or in 1/20 strength H (1/20 H) prior to insemination (H-eggs or 1/20 H-eggs). In contrast, the sperm suspension in 1/20 H (1/20 H-sperm) did not fertilize 1/20 H-eggs, but dit H-eggs. In the latter case, H surrounding the eggs may affect sperms, allowing them to be fertilized. The 1/20 H-sperms regained their ability to fertilize 1/20 H-eggs on re-exposure to H. The 1/20 H-sperm also fertilized jelly eggs. The results of the dejellied egg experiment showed the same pattern. These results indicate that the sperms within the vas deferens lose their capacity to fertilize 1/20 H-eggs on exposure to low ionic strength solution (1/20 H); this capacity is restored by exposure to high ionic strength solution (H) or to jelly envelope.

NT-4 protein is localized in neuronal cells in the brain stem as well as the dorsal root ganglion of embryonic and adult rats.

We have newly established a sensitive, two-site enzyme immunoassay system for neurotrophin-4 (NT-4) and investigated its tissue distribution in the rat nervous system. The minimal limit of detection of the assay is 0.3 pg/0.2 mL of assay mixture. Concentrations of NT-4 were found to be extremely low in all brain regions, irrespective of the animal age, the highest level being found in the brain stem of 40-day-old rats, at 0.12 ng/g wet weight. NT-4 levels in young adult rats were significantly lower in the thalamus and higher in the olfactory bulb, neocortex, hypothalamus and brain stem than respective levels in 1-week-old rats. NT-4 immunoreactivity was strong in large neurons of the red nucleus and pontine reticular nucleus as well as the locus coeruleus, and moderate in cells in the mesencephalic trigeminal nucleus and interstitial nucleus of the medial longitudinal fasciculus. In the rat embryo, stong staining of NT-4 was detected in cells of regions corresponding to the midbrain/pons from E11.5 through E15.5. The intensity was decreased after E13.5 when the cytoplasm of cells in the medulla oblongata, fibers of the cerebellar primordium, and both cells and fibers of the dorsal root ganglion were also stained. Concentrations of NT-4 were detected in regions including the hindbrain and the dorsal root ganglion. Immunoblotting of NT-4-immunoreactive proteins extracted from these two regions revealed a band corresponding to mature NT-4 with a molecular mass of approximately 14 kDa. Kainic acid and another glutamte agonist, (+/-)-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid did not affect NT-4 levels in the hippocampus. The present results show NT-4 to be localized in very limited brain cells and fibers from the embyonic period through to the young adult, suggesting specific roles in brain functions.