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1.
J Strength Cond Res ; 24(8): 2249-54, 2010 Aug.
Article in English | MEDLINE | ID: mdl-19918193

ABSTRACT

We aimed to determine the responses of salivary secretory immunoglobulin A (SIgA) and the incidence of upper respiratory tract infections (URTI) symptoms among elite speed skaters during an actual competition period. The subjects were 8 international-class elite speed skaters. Saliva samples were obtained 3, 2, and 1 days before the race, the day of the race, and 1 day after the race. Salivary secretory immunoglobulin A concentration was measured by enzyme immunoassay, and SIgA secretion rate was calculated. A visual analogue scale was used to subjectively assess fatigue and tension. Daily URTI symptoms were recorded by using a questionnaire. There was no statistically significant difference in the saliva flow rate (p = 0.69), SIgA concentration (p = 0.07), and subjective fatigue (p = 0.07) during the competition period. The SIgA secretion rate recorded for the day of the race was significantly high compared with that of 3 and 2 days before and 1 day after the race (p < 0.05). The subjective tension recorded on the race day was significantly high compared with that for 3, 2, and 1 days before the race (p < 0.05). Two subjects exhibited URTI symptoms after the race. These findings suggest that salivary SIgA in elite speed skaters increased after a tapering period and that an actual high-intensity speed skating race decreased salivary SIgA in elite speed skaters. These data also suggest that the incidence of URTI symptoms might be related to the SIgA level. Coaches may need to take precautions after competitions to minimize their athletes' contact with cold viruses and adjust training load for a few days after competition to improve the decreased mucosal immune function.


Subject(s)
Immunoglobulin A, Secretory/analysis , Saliva/immunology , Skating/physiology , Adult , Female , Humans , Male , Muscle Fatigue/immunology , Muscle Fatigue/physiology , Respiratory Tract Infections/immunology , Respiratory Tract Infections/physiopathology , Salivation/immunology , Salivation/physiology , Time Factors
2.
Arch Histol Cytol ; 71(5): 317-32, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19556693

ABSTRACT

Continuously growing rodent incisors have a special epithelial structure for maintaining adult stem cells that shows a bulbous epithelial protrusion at the apical end and is referred to as an "apical bud". Guinea pig cheek teeth (premolars and molars), also continuously growing teeth, have a complex crown shape consisting of plural cusps. The present study clarifies the existence of apical buds in guinea pig premolars/molars as it examines the relationship between the crown shape and the orientation of the apical buds by micro-computed tomography (micro-CT) and immunohistochemistry for 5-bromo-2'-deoxyuridine (BrdU). One premolar and three molar teeth in each side of the maxillae and mandibles assumed characteristic features: each horizontally-sectioned tooth showing a complex zigzag shape was composed of a core of dentin covered by a layer of enamel on all axial surfaces except the buccal of the uppers and the lingual of the lowers. Furthermore, four bulbous epithelial protrusions--including the stellate reticulum--were recognized in the apical end of each tooth, where slow-cycling long-term label-retaining cells resided 20 days after a peritoneal injection of BrdU. These data indicate that guinea pig premolars/molars have four apical buds where the epithelial adult stem cells reside. In contrast, rodent incisors, which show a single cone appearance, are covered by enamel on the labial side and possess only one apical bud. The results of this study suggest that plural apical buds, being arranged bucco-lingually and mesio-distally, produce the crown mold in a zigzag fashion.


Subject(s)
Bromodeoxyuridine/metabolism , Cheek/anatomy & histology , Cuspid/cytology , Staining and Labeling , Stem Cells/cytology , Animals , Cuspid/anatomy & histology , Cuspid/diagnostic imaging , Cuspid/growth & development , Epithelial Cells/cytology , Guinea Pigs , Kinetics , X-Ray Microtomography , X-Rays
3.
Arch Oral Biol ; 50(2): 153-7, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15721143

ABSTRACT

Rodent incisors are known to be continuously growing teeth that are maintained by both the cell-proliferation at the apical end and the attrition of the incisal edge. This type of tooth had a special epithelial structure for the maintenance of stem cells, showing the bulbous epithelial protrusion at the apical end. The morphological transition of the epithelial-mesenchymal compartment by serial transverse sections of the apical end toward the incisal direction is likely to reflect the development of the tooth germ in the prenatal stage. Based on the present histological and previous molecular biological studies, the special structure at the apical end is obviously different from the cervical loop giving rise to Hertwig's epithelial root sheath (HERS), in human, mouse and rat molar tooth germs. Hence, we propose a new concept that the eternal tooth bud producing various dental progeny is formed at the apical end of continuously growing teeth, and a new term "apical bud" for indicating this specialized epithelial structure. Furthermore, BrdU labelling analysis suggested that the guinea-pig molars, which were continuously growing teeth, also possessed plural specific proliferative regions and "apical bud" at the apical end.


Subject(s)
Regeneration/physiology , Rodentia/embryology , Stem Cells/cytology , Tooth Apex/cytology , Tooth Germ/physiology , Animals , Guinea Pigs , Incisor/cytology , Incisor/growth & development , Mice , Molar/cytology , Molar/growth & development
4.
Gan To Kagaku Ryoho ; 30(7): 977-80, 2003 Jul.
Article in Japanese | MEDLINE | ID: mdl-12894713

ABSTRACT

We experienced a case in which severe alveolar hemorrhage occurred in the course of gefitinib therapy. A 56-year-old man with non-small cell lung cancer had been treated with CDDP + CPT-11, CDDP + GEM + VNR, CDDP + TXT. After the chemotherapy with these regimens was found to be ineffective, daily oral gefitinib was started. Four weeks later, the patient complained of cough, bloody sputum and dyspnea. Chest X-ray and CT showed bilateral infiltrations with air bronchogram. Fiberoptic bronchoscopy revealed alveolar hemorrhage with an increase of lymphocytes in the BALF. After the cessation of gefitinib therapy and the administration of steroid, he gradually recovered.


Subject(s)
Adenocarcinoma/drug therapy , Antineoplastic Agents/adverse effects , Hemorrhage/etiology , Lung Diseases/etiology , Lung Neoplasms/drug therapy , Quinazolines/adverse effects , Gefitinib , Humans , Male , Middle Aged , Pulmonary Alveoli , Respiratory Insufficiency/etiology
5.
Nihon Kokyuki Gakkai Zasshi ; 41(1): 48-53, 2003 Jan.
Article in Japanese | MEDLINE | ID: mdl-12693006

ABSTRACT

A 59-year-old woman whose first clinical manifestations were polyuria and polydipsia was admitted to our hospital. Brain MRI showed multiple mass lesions and a thickened pituitary stalk. Chest CT showed hilar and mediastinal lymphadenopathy and a small nodule measuring about 1.5 cm in the apex of the right lung. Histopathological examination revealed adenocarcinoma of the lung, and primary lung cancer with diabetes insipidus secondary to pituitary stalk metastasis was diagnosed. She received systemic chemotherapy and whole-brain irradiation concurrent with intranasal desmopressin (DDAVP) treatment. Although the size of the tumor was reduced, her symptoms did not improve and the same dose of hormone replacement therapy was required. We present this rare case and review the twenty cases of metastatic pituitary lesions arising from lung cancer reported in the literature.


Subject(s)
Adenocarcinoma/secondary , Diabetes Insipidus, Neurogenic/etiology , Lung Neoplasms/pathology , Pituitary Neoplasms/secondary , Adenocarcinoma/diagnosis , Adenocarcinoma/pathology , Adenocarcinoma/therapy , Combined Modality Therapy , Diabetes Insipidus, Neurogenic/diagnosis , Female , Humans , Lung Neoplasms/diagnosis , Lung Neoplasms/therapy , Middle Aged , Pituitary Neoplasms/diagnosis , Pituitary Neoplasms/therapy
6.
Protein Eng ; 15(2): 123-30, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11917148

ABSTRACT

PACE4, furin and PC6 are Ca2+-dependent serine endoproteases that belong to the subtilisin-like proprotein convertase (SPC) family. Recent reports have supported the involvement of these enzymes in processing of growth/differentiation factors, viral replication, activation of bacterial toxins and tumorigenesis, indicating that these enzymes are a fascinating target for therapeutic agents. In this work, we evaluated the sensitivity and selectivity of three rat alpha1-antitrypsin variants which contained RVPR352, AVRR352 and RVRR352, respectively, within their reactive site loop using both inhibition of enzyme activity toward a fluorogenic substrate in vitro and formation of a SDS-stable protease/inhibitor complex ex vivo. The RVPR variant showed relatively broad selectivity, whereas the AVRR and RVRR variants were more selective than the RVPR variant. The AVRR variant inhibited furin and PC6 but not PACE4. This selectivity was further confirmed by complex formation and inhibition of pro-complement C3 processing. On the other hand, although the RVRR variant inhibited both PACE4 and furin effectively, it needed a 600-fold higher concentration than the RVPR variant to inhibit PC6 in vitro. These inhibitors will be useful tools in helping us to understand the roles of PACE4, furin and PC6.


Subject(s)
Arginine/metabolism , Serine Endopeptidases/drug effects , Serine Proteinase Inhibitors/pharmacology , Subtilisins/antagonists & inhibitors , alpha 1-Antitrypsin/pharmacology , Animals , Cadherins/metabolism , DNA Primers/chemistry , Furin , Humans , Mutagenesis, Site-Directed , Polymerase Chain Reaction , Precipitin Tests , Proprotein Convertase 5 , Proprotein Convertases , Rats , Recombinant Proteins/pharmacology , Subtilisins/metabolism , Transfection , Tumor Cells, Cultured/drug effects , Tumor Cells, Cultured/metabolism , alpha 1-Antitrypsin/genetics
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