ABSTRACT
The temporomandibular joint (TMJ) functions as a load-bearing diarthrodial joint during mastication, and its continuous use and stress can lead to degeneration over age. Using senescence-accelerated (SAMP8) mice that develop early osteoarthritis-like changes in synovial joints at high frequency, we analyzed possible molecular mechanisms of TMJ degeneration and tested whether and how malocclusion may accelerate it. Condylar articular cartilage in young SAMP8 mice displayed early-onset osteoarthritic changes that included reductions in superficial/chondroprogenitor cell number, proteoglycan/collagen content, and Indian hedgehog (Ihh)-expressing chondrocytes. Following malocclusion induced by tooth milling, the SAMP8 condyles became morphologically defective, displayed even lower proteoglycan levels, and underwent abnormal chondrocyte maturation compared with malocclusion-treated condyles in wild-type mice. Malocclusion also induced faster progression of pathologic changes with increasing age in SAMP8 condyles as indicated by decreased PCNA-positive proliferating chondroprogenitors and increased TUNEL-positive apoptotic cells. These changes were accompanied by steeper reductions in Ihh signaling and by expression of matrix metalloproteinase 13 at the chondro-osseous junction in SAMP8 articular cartilage. In sum, we show for the first time that precocious TMJ degeneration in SAMP8 mice is accompanied by--and possibly attributable to--altered Ihh signaling and that occlusal dysfunction accelerates progression toward degenerative TMJ disease in this model.
Subject(s)
Hedgehog Proteins/analysis , Osteoarthritis/metabolism , Signal Transduction/physiology , Temporomandibular Joint Disorders/metabolism , Age Factors , Animals , Apoptosis/genetics , Carrier Proteins/analysis , Cartilage, Articular/pathology , Chondrocytes/pathology , Collagen/analysis , Collagen Type I/analysis , Collagen Type II/analysis , Collagen Type X/analysis , Disease Models, Animal , Disease Progression , Kruppel-Like Transcription Factors/analysis , Malocclusion/complications , Mandibular Condyle/pathology , Matrix Metalloproteinase 13/analysis , Membrane Glycoproteins/analysis , Mice , Mice, Inbred Strains , Patched Receptors , Proliferating Cell Nuclear Antigen/analysis , Proteoglycans/analysis , Receptors, Cell Surface/analysis , Stem Cells/pathology , Zinc Finger Protein GLI1 , Zinc Finger Protein Gli2ABSTRACT
BACKGROUND AND OBJECTIVE: Electric current is used to promote wound healing. However, it is unclear whether electrical stimulation contributes to gingival tissue remodeling. This study examined the effects of electrical stimulation on gingival tissue remodeling in a rat periodontitis model. MATERIAL AND METHODS: Male Wistar rats (n = 28, 8 wks of age) were divided into four groups of seven rats each. The control group did not receive any treatment for 6 wks. In the other groups, periodontitis was ligature-induced for 4 wks. After 4 wks, the rats with periodontitis were given daily electrical stimulation of 0, 50 or 100 µA for 2 wks. RESULTS: The periodontitis group stimulated with 0 µA showed a higher density of polymorphonuclear leukocytes and a lower density of collagen in gingival tissue compared with the control group (p < 0.05). The two remaining groups treated with 50 or 100 µA of electrical stimulation exhibited a lower density of polymorphonuclear leukocytes (p < 0.05) and a higher density of collagen than the group stimulated with 0 µA (p < 0.05). They also showed higher expression of fibroblast growth factor-2 than the group treated with 0 µA of electrical stimulation (p < 0.05). CONCLUSION: Electric stimulation may offer a novel approach to promote gingival tissue remodeling in periodontal lesions.
Subject(s)
Electric Stimulation Therapy/methods , Gingiva/physiopathology , Periodontitis/therapy , Alveolar Bone Loss/pathology , Animals , Collagen/ultrastructure , Connective Tissue/pathology , Epithelial Attachment/pathology , Fibroblast Growth Factor 2/analysis , Fibroblasts/pathology , Gingiva/pathology , Leukocyte Count , Male , Matrix Metalloproteinase 3/analysis , Matrix Metalloproteinase 8/analysis , Matrix Metalloproteinase 9/analysis , Matrix Metalloproteinase Inhibitors/analysis , Neutrophils/pathology , Osteoblasts/pathology , Periodontitis/pathology , Random Allocation , Rats , Rats, Wistar , Tissue Inhibitor of Metalloproteinase-1/analysis , Tissue Inhibitor of Metalloproteinase-2/analysis , Tissue Inhibitor of Metalloproteinase-3/analysis , Tooth Cervix/pathology , Wound Healing/physiologyABSTRACT
Xenon (Xe) and other inert gases produce anesthesia via an inhibitory mechanism in neuronal networks. To better understand this mechanism, we measured the electrical signals from cultured rat cortical neuronal networks in a multi-electrode array (MEA) under an applied Xe pressure. We used the MEA to measure the firing of the neuronal network with and without Xe gas pressurized to 0.3MPa. The MEA system monitored neuronal spikes on 16 electrodes (each 50×50µm(2)) at a sampling rate of 20kHz. The embryo rat cortical cells were first cultured on MEAs without Xe for approximately 3weeks, at which time they produced synchronized bursts that indicate maturity. Then, with an applied Xe pressure, the synchronized bursts quickly ceased, whereas single spikes continued. The Xe-induced inhibition-recovery of neuronal network firing was reversible: after purging Xe from the system, the synchronized bursts gradually resumed. Thus, Xe did not inhibit single neuron firing, yet reversibly inhibited the synaptic transmission. This finding agrees with the channel-blocker and a modified-hydrate hypothesis of anesthesia, but not the lipid-solubility hypothesis.
Subject(s)
Anesthetics, Inhalation/pharmacology , Cerebral Cortex/drug effects , Nerve Net/drug effects , Neural Inhibition/drug effects , Neurons/drug effects , Xenon/pharmacology , Action Potentials/drug effects , Action Potentials/physiology , Animals , Cells, Cultured , Cerebral Cortex/physiology , Nerve Net/physiology , Neural Inhibition/physiology , Neurons/physiology , Rats , Rats, WistarABSTRACT
Primary cilia regulate limb and axial skeletal formation and hedgehog signaling, but their roles in temporomandibular joint (TMJ) development are unknown. Thus, we created conditional mouse mutants deficient in ciliary transport protein Kif3a in cartilage. In post-natal wild-type mice, primary cilia were occasionally observed on the superior, inferior, or lateral side of condylar cells. Cilia were barely detectable in mutant chondrocytes but were evident in surrounding tissues, attesting to the specificity of chondrocyte Kif3a ablation. Mutant condyles from 3-month-old mice were narrow and flat along their antero-posterior and medio-lateral axes, were often fused with the articular disc, and displayed an irregular bony surface. The polymorphic layer in P15 mutants contained fewer Sox9-expressing chondroprogenitor cells because of reduced mitotic activity, and newly differentiated chondrocytes underwent precocious hypertrophic enlargement accompanied by early activation of Indian hedgehog (Ihh). Interestingly, there was excessive intramembranous ossification along the perichondrium, accompanied by local expression of the hedgehog receptor Patched-1 and up-regulation of Osterix and Collagen I. In summary, Kif3a and primary cilia are required for coordination of chondrocyte maturation, intramembranous bone formation, and chondrogenic condylar growth. Defects in these processes in Kif3a condylar cartilage are likely to reflect abnormal hedgehog signaling topography and dysfunction.
Subject(s)
Cilia/physiology , Hedgehog Proteins/physiology , Kinesins/physiology , Mandibular Condyle/growth & development , Temporomandibular Joint/growth & development , Animals , Cartilage, Articular/metabolism , Cells, Cultured , Chondrocytes/cytology , Chondrogenesis/genetics , Collagen Type I/genetics , Collagen Type I/metabolism , Gene Expression Regulation, Developmental , Growth Plate/metabolism , Hedgehog Proteins/genetics , Kinesins/genetics , Mice , Mice, Knockout , Mitosis , Ossification, Heterotopic/genetics , Osteogenesis/genetics , Patched Receptors , Patched-1 Receptor , Receptors, Cell Surface/genetics , Receptors, Cell Surface/physiology , SOX9 Transcription Factor/genetics , SOX9 Transcription Factor/physiology , Signal Transduction , Sp7 Transcription Factor , Transcription Factors/genetics , Transcription Factors/physiologyABSTRACT
Symphyseal secondary cartilage is important for mandibular development, but the molecular mechanisms underlying its formation remain largely unknown. Here we asked whether Indian hedgehog (Ihh) regulates symphyseal cartilage development and growth. By embryonic days 16.5 to 18.5, Sox9-expressing chondrocytes formed within condensed Tgfß-1/Runx2-expressing mesenchymal cells at the prospective symphyseal joint site, and established a growth-plate-like structure with distinct Ihh, collagen X, and osteopontin expression patterns. In post-natal life, mesenchymal cells expressing the Ihh receptor Patched1 were present anterior to the Ihh-expressing secondary cartilage, proliferated, differentiated into chondrocytes, and contributed to anterior growth of alveolar bone. In Ihh-null mice, however, symphyseal development was defective, mainly because of enhanced chondrocyte maturation and reduced proliferation of chondroprogenitor cells. Proliferation was partially restored in dual Ihh;Gli3 mutants, suggesting that Gli3 is normally a negative regulator of symphyseal development. Thus, Ihh signaling is essential for symphyseal cartilage development and anterior mandibular growth.
Subject(s)
Chin/growth & development , Chondrogenesis/genetics , Gene Expression Regulation, Developmental , Hedgehog Proteins/physiology , Mandible/growth & development , Animals , Cartilage/embryology , Cartilage/growth & development , Cartilage/metabolism , Cell Proliferation , Chin/embryology , Chondrocytes/cytology , Chondrocytes/metabolism , Collagen Type X/biosynthesis , Gene Expression , Growth Plate/embryology , Heparitin Sulfate/metabolism , Kruppel-Like Transcription Factors/physiology , Mandible/embryology , Mesoderm/metabolism , Mice , Mice, Knockout , Morphogenesis , Nerve Tissue Proteins/physiology , Osteopontin/biosynthesis , Patched Receptors , Patched-1 Receptor , Receptors, Cell Surface/biosynthesis , Signal Transduction/genetics , Zinc Finger Protein Gli3ABSTRACT
To investigate the minimum neuron and neurite densities required for synchronized bursts, we cultured rat cortical neurons on planar multi-electrode arrays (MEAs) at five plating densities (2500, 1000, 500, 250, and 100 cells/mm(2)) using two culture media: Neuron Culture Medium and Dulbecco's Modified Eagle Medium supplemented with serum (DMEM/serum). Long-term recording of spontaneous electrical activity clarified that the cultures exhibiting synchronized bursts required an initial plating density of at least 250 cells/mm(2) for Neuron Culture Medium and 500 cells/mm(2) for DMEM/serum. Immediately after electrical recording, immunocytochemistry of microtubule-associated protein 2 (MAP2) and Neurofilament 200 kD (NF200) was performed directly on MEAs to investigate the actual densities of neurons and neurites forming the networks. Immunofluorescence observation revealed that the construction of complicated neuronal networks required the same initial plating density as for synchronized bursts, and that overly sparse cultures showed significant decreases of neurons and neurites. We also found that the final densities of surviving neurons at 1 month decreased greatly compared with the initial plating densities and became saturated in denser cultures. In addition, the area of neurites and the number of nuclei were saturated in denser cultures. By comparing both the results of electrophysiological recording and immunocytochemical observation, we revealed that there is a minimum threshold of neuron densities that must be met for the exhibition of synchronized bursts. Interestingly, these minimum densities of MAP2-positive final neurons did not differ between the two culture media; the density was approximately 50 neurons/mm(2). This value was obtained in the cultures with the initial plating densities of 250 cells/mm(2) for Neuron Culture Medium and 500 cells/mm(2) for DMEM/serum.
Subject(s)
Action Potentials/physiology , Cerebral Cortex/cytology , Neurons/physiology , Animals , Benzimidazoles/metabolism , Cell Count/methods , Cells, Cultured , Culture Media, Conditioned/pharmacology , Electrodes , Embryo, Mammalian , Microtubule-Associated Proteins/metabolism , Neurites/physiology , Neurofilament Proteins/metabolism , Neurons/cytology , Rats , Rats, WistarABSTRACT
In clinical practice, self-efficacy refers to how certain a patient feels about his or her ability to take the necessary action to improve the indicators and maintenance of health. It is assumed that the prognosis for patient behaviour can be improved by assessing the proficiency of their self-efficacy through providing psychoeducational instructions adapted for individual patients, and promoting behavioural change for self-care. Therefore, accurate assessment of self-efficacy is an important key in daily clinical preventive care. The previous research showed that the self-efficacy scale scores predicted patient behaviour in periodontal patients and mother's behaviour in paediatric dental practice. Self-efficacy belief is constructed from four principal sources of information: enactive mastery experience, vicarious experience, verbal persuasion, and physiological and affective states. Thus, self-efficacy can be enhanced by the intervention exploiting these sources. The previous studies revealed that behavioural interventions to enhance self-efficacy improved oral-care behaviour of patients. Therefore, assessment and enhancement of oral-care specific self-efficacy is important to promote behaviour modification in clinical dental practice. However, more researches are needed to evaluate the suitability of the intervention method.
Subject(s)
Health Behavior , Oral Health , Self Efficacy , Affect , Attitude to Health , Dentist-Patient Relations , Humans , Learning , Oral Hygiene , Patient Education as Topic , Persuasive Communication , Self CareABSTRACT
Indian hedgehog (Ihh) is essential for embryonic mandibular condylar growth and disc primordium formation. To determine whether it regulates those processes during post-natal life, we ablated Ihh in cartilage of neonatal mice and assessed the consequences on temporomandibular joint (TMJ) growth and organization over age. Ihh deficiency caused condylar disorganization and growth retardation and reduced polymorphic cell layer proliferation. Expression of Sox9, Runx2, and Osterix was low, as was that of collagen II, collagen I, and aggrecan, thus altering the fibrocartilaginous nature of the condyle. Though a disc formed, it exhibited morphological defects, partial fusion with the glenoid bone surface, reduced synovial cavity space, and, unexpectedly, higher lubricin expression. Analysis of the data shows, for the first time, that continuous Ihh action is required for completion of post-natal TMJ growth and organization. Lubricin overexpression in mutants may represent a compensatory response to sustain TMJ movement and function.
Subject(s)
Cartilage, Articular/growth & development , Hedgehog Proteins/physiology , Mandibular Condyle/growth & development , Temporomandibular Joint/anatomy & histology , Temporomandibular Joint/growth & development , Aggrecans/biosynthesis , Aggrecans/genetics , Animals , Ankylosis/genetics , Ankylosis/metabolism , Cartilage, Articular/anatomy & histology , Chondrocytes/pathology , Collagen Type II/biosynthesis , Collagen Type II/genetics , Core Binding Factor Alpha 1 Subunit/biosynthesis , Core Binding Factor Alpha 1 Subunit/genetics , Down-Regulation , Fibrocartilage/anatomy & histology , Fibrocartilage/growth & development , Growth Plate/abnormalities , Hedgehog Proteins/genetics , Mandibular Condyle/anatomy & histology , Mice , Mice, Knockout , Proteoglycans/biosynthesis , SOX9 Transcription Factor/biosynthesis , SOX9 Transcription Factor/genetics , Sp7 Transcription Factor , Temporomandibular Joint Disc/anatomy & histology , Temporomandibular Joint Disc/growth & development , Temporomandibular Joint Disorders/genetics , Temporomandibular Joint Disorders/metabolism , Transcription Factors/biosynthesis , Transcription Factors/geneticsABSTRACT
Primary cilia regulate several developmental processes and mediate hedgehog signaling. To study their roles in cranial base development, we created conditional mouse mutants deficient in Polaris, a critical primary cilium component, in cartilage. Mutant post-natal cranial bases were deformed, and their synchondrosis growth plates were disorganized. Expression of Indian hedgehog, Patched-1, collagen X, and MMP-13 was reduced and accompanied by decreases in endochondral bone. Interestingly, there was excessive intramembranous ossification along the perichondrium, accompanied by excessive Patched-1 expression, suggesting that Ihh distribution was wider and responsible for such excessive response. Indeed, expression of heparan sulfate proteoglycans (HS-PGs), normally involved in restricting hedgehog distribution, was barely detectable in mutant synchondroses. Analyses of the data provides further evidence for the essential roles of primary cilia and hedgehog signaling in cranial base development and chondrocyte maturation, and point to a close interdependence between cilia and HS-PGs to delimit targets of hedgehog action in synchondroses.
Subject(s)
Chondrocytes/cytology , Growth Plate/metabolism , Osteogenesis/genetics , Skull Base/growth & development , Tumor Suppressor Proteins/physiology , Animals , Animals, Newborn , Cell Proliferation , Chondrocytes/chemistry , Chondrocytes/physiology , Cilia/chemistry , Collagen Type X/biosynthesis , Gene Expression Regulation, Developmental , Hedgehog Proteins/biosynthesis , Hedgehog Proteins/physiology , Heparan Sulfate Proteoglycans/biosynthesis , Immunoenzyme Techniques , Matrix Metalloproteinase 13/biosynthesis , Mice , Mice, Mutant Strains , Mice, Transgenic , Patched Receptors , Patched-1 Receptor , Receptors, Cell Surface/biosynthesis , Signal Transduction , Skull Base/cytology , Tumor Suppressor Proteins/deficiency , X-Ray MicrotomographyABSTRACT
BACKGROUND AND OBJECTIVE: The effects of laser irradiation on Porphyromonas gingivalis have been reported, but the results are still controversial regarding the efficiency because of the differences of the light sources and irradiation conditions. The aim of this study was to determine the wavelength and irradiation conditions under which the most effective inhibitory effect on P. gingivalis growth was seen without any photosensitizers. MATERIAL AND METHODS: Using an Okazaki large spectrograph, monochromatic light spectra ranging from 400 to 700 nm were evaluated to determine which spectra effectively inhibited bacterial growth. Moreover, using a monochromatic 405-nm irradiating device, the effects of various irradiating conditions on P. gingivalis growth were examined. RESULTS: Growth of bacteria irradiated at 400 nm and 410 nm was significantly suppressed compared with a nonirradiated control, whereas wavelengths of 430 nm and longer produced no significant inhibition. A constant energy density of 15 J/cm2 was found to be enough to show an inhibitory effect. Significant inhibition of bacterial growth was found after only 1 min at 50 mW/cm2 irradiation. CONCLUSION: These results indicate that P. gingivalis growth is specifically suppressed by 405-nm light irradiation, suggesting that visible blue light irradiation is a promising means for eradicating periodontopathogenic bacteria from periodontal lesions.
Subject(s)
Light , Porphyromonas gingivalis/radiation effects , Colony Count, Microbial , Microbial Viability/radiation effects , Porphyromonas gingivalis/growth & development , SpectrophotometryABSTRACT
BACKGROUND AND PURPOSE: In the treatment of carotid atherosclerosis, the rate of stenosis and characteristics of plaque should be assessed to diagnose vulnerable plaques that increase the risk for cerebral infarction. We performed carotid black-blood (BB) MR imaging to diagnose plaque components and assess plaque hardness based on MR signals. MATERIALS AND METHODS: Three images of BB-MR imaging per plaque were obtained from 70 consecutive patients who underwent carotid endarterectomy (CEA) to generate T1- and T2-weighted images. To evaluate the relative signal intensity (rSI) of plaque components and the relationship between histologic findings and symptoms, we prepared sections at 2-mm intervals from 34 intact plaques. We then calculated the relative overall signal intensity (roSI) of 70 plaques to assess the relationship between MR signal intensity and plaque hardness and symptoms. RESULTS: The characteristics of rSI values on T1- and T2-weighted images of fibrous cap (FC), fibrosis, calcification, myxomatous tissue, lipid core (LC) with intraplaque hemorrhage (IPH), and LC without IPH differed. Symptomatic plaques were associated with FC disruption (P < .001) and LC with IPH (P < .05). The roSI on T1-weighted images was significantly higher for soft than nonsoft plaques. When the roSI cutoff value was set at 1.25 (mean of the roSI), soft plaques were diagnosed with 79.4% sensitivity and 84.4% specificity. The roSI was also significantly higher for symptomatic than for asymptomatic plaques. Soft and nonsoft plaques as well as symptomatic and asymptomatic plaques did not significantly differ on T2-weighted images. CONCLUSION: BB-MR imaging can diagnose plaque components and predict plaque hardness. This procedure provides useful information for planning therapeutic strategies of carotid atherosclerosis.
Subject(s)
Blood Cells/pathology , Carotid Stenosis/pathology , Image Interpretation, Computer-Assisted/methods , Information Storage and Retrieval/methods , Magnetic Resonance Imaging/methods , Aged , Aged, 80 and over , Female , Humans , Image Enhancement/methods , Male , Middle Aged , Reproducibility of Results , Sensitivity and SpecificityABSTRACT
Wnt proteins and beta-catenin signaling regulate major processes during embryonic development, and we hypothesized that they regulate cranial base synchondrosis development and growth. To address this issue, we analyzed cartilage-specific beta-catenin-deficient mice. Mutant synchondroses lacked typical growth plate zones, and endochondral ossification was delayed. In reciprocal transgenic experiments, cartilage overexpression of a constitutive active Lef1, a transcriptional mediator of Wnt/beta-catenin signaling, caused precocious chondrocyte hypertrophy and intermingling of immature and mature chondrocytes. The developmental changes seen in beta-catenin-deficient synchondroses were accompanied by marked reductions in Ihh and PTHrP as well as sFRP-1, an endogenous Wnt signaling antagonist and a potential Ihh signaling target. Thus, Wnt/beta-catenin signaling is essential for cranial base development and synchondrosis growth plate function. This pathway promotes chondrocyte maturation and ossification events, and may exert this important role by dampening the effects of Ihh-PTHrP together with sFRP-1.
Subject(s)
Cranial Sutures/growth & development , Signal Transduction/physiology , Skull Base/growth & development , Wnt Proteins/physiology , beta Catenin/physiology , Animals , Cartilage/growth & development , Chondrocytes/pathology , Collagen Type I/analysis , Collagen Type II/analysis , Collagen Type X/analysis , Growth Plate/growth & development , Hedgehog Proteins/analysis , Hypertrophy , Intercellular Signaling Peptides and Proteins/analysis , Lymphoid Enhancer-Binding Factor 1/genetics , Membrane Proteins/analysis , Mice , Mice, Transgenic , Mutation/genetics , Osteogenesis/genetics , Parathyroid Hormone-Related Protein/analysis , Sp7 Transcription Factor , Transcription Factors/analysis , Transcription, Genetic/genetics , Zinc Fingers , beta Catenin/geneticsABSTRACT
Empyema caused by methicillin-resistant Staphylococcus aureus (MRSA) remains an intractable infection producing high mortality. The authers report a case of MRSA empyema following video-assisted thoracic surgery (VATS) for lung cancer. The case was 73-year-old male with some risks such as pulmonary emphysema, decreased renal function, and previous history of brain infarction. He received wedge resection and the staple lines were wrapped with polyglycolic acid (PGA) felt. Ten days after the operation, he was complicated MRSA pyothorax. By thoracoscopic procedures under local anesthesia, fibrinopurulent tissues were cleaned and 3 of chest tubes were replaced. Intrathoracic infected space was cleaned with physiological saline solution. The patient made favorable progress and recovered. Further empyema has not been developed for 24 months. VATS under local anesthesia and irrigation technique was safe and so useful. Nowadays, PGA felt is often used to reinforce the staple lines of lung. PGA felt is an absorbable but artificial material. We have to care about infectious problems. However, we could control the MRSA pyothrax without removing the PGA felt.
Subject(s)
Empyema, Pleural/surgery , Lung Neoplasms/surgery , Postoperative Complications/surgery , Thoracic Surgery, Video-Assisted , Aged , Anesthesia, Local , Empyema, Pleural/microbiology , Humans , Male , Methicillin Resistance , Perioperative Care , Pneumonectomy/methods , Polyglycolic Acid , Postoperative Complications/microbiology , Staphylococcal Infections , Suture Techniques , Sutures , Therapeutic Irrigation , Treatment OutcomeABSTRACT
The case was 54-year-old male with some risks such as chronic heart failure, atrial fibrillation, and liver chirrhosis. He was admitted because of severe back pain and diagnosed as empyema by preoperative thoracentesis. By thoracoscopic procedures under local anesthesia, fibrinopurulent tissues were cleaned as much as possible and 3 of chest tubes were replaced. The final diagnosis was Bacillus cereus pyothorax by bacterial cultures of pleural effusion. Intrathoracic cavity was cleaned with physiological saline solution. The patient made favorable progress and recovered. Thoracoscopic surgery under local anesthesia with thoracic irrigation was so effective and safe methods to control the infection.
Subject(s)
Anesthesia, Local , Bacillus cereus , Empyema, Pleural/surgery , Gram-Positive Bacterial Infections , Thoracoscopy , Anti-Bacterial Agents/therapeutic use , Cardiomyopathy, Dilated/complications , Clarithromycin/therapeutic use , Empyema, Pleural/microbiology , Humans , Liver Cirrhosis/complications , Male , Middle Aged , Therapeutic Irrigation , Thoracic CavityABSTRACT
A case of a 53-year-old Japanese man with osteopetrosis complicated by osteomyelitis of the mandible is presented. The patient experienced frequent exacerbations and remissions of osteomyelitis of the mandible, despite undergoing several surgical debridements and sequesterectomies with appropriate antimicrobial therapy, for 3 years. Finally, the patient underwent mandibular segmental resection followed by reconstruction with a titanium reconstruction plate. Fifty-one months after surgery there is no evidence of recurrent osteomyelitis of the mandible, suggesting that a more radical surgical approach is preferable for patients with severe complications resulting from osteopetrosis. Also presented here are the histopathological and biochemical features of the osteopetrotic bone. The osteopetrotic cortical bone was morbidly sclerotic with compact and irregular laminations. Degradation of osteocytes in the osteopetrotic bone was due to hypoxia and lack of nutrition resulting from osteosclerosis. There were no significant differences between osteopetrotic and normal bone according to X-ray diffraction, Fourier transform infrared spectroscopy, collagen content or mineral content. Micro-Vickers hardness measurements showed that osteopetrotic bone was significantly harder than normal bone, and the standard deviation of hardness was greater in osteopetrotic bone. Such a loss of integrity in osteopetrotic bone is considered to be a primary reason for the greater risk of a variety of complications such as pathological fracture and refractory osteomyelitis.
Subject(s)
Mandibular Diseases/pathology , Osteomyelitis/etiology , Osteopetrosis/complications , Bone Plates , Fatal Outcome , Hardness , Humans , Male , Mandibular Diseases/surgery , Mandibular Prosthesis , Microscopy, Electron, Transmission , Middle Aged , Osteocytes/pathology , Osteomyelitis/pathology , Osteomyelitis/surgery , Osteopetrosis/pathology , Osteopetrosis/surgery , Spectroscopy, Fourier Transform Infrared , X-Ray DiffractionABSTRACT
We report a case of a previously healthy 76-year-old male with cavitating pleomorphic carcinoma of the lung. He was admitted because of an abnormal lung shadow on chest X-ray. Computed tomography (CT) showed a well-demarcated nodular shadow within thin-walled cavity in the right upper lobe. Because the lesion was revealed as adenocarcinoma by transbronchial lung biopsy, right upper lobectomy was performed. By histopathologic examination of the resected specimen, the nodule contained a component of spindle cell features and the cavity wall was composed of adenocarcinoma. The final diagnosis was pleomorphic carcinoma. Postoperative course has been uneventful for 12 months after surgery.
Subject(s)
Carcinoma/diagnostic imaging , Lung Neoplasms/diagnostic imaging , Adenocarcinoma/diagnosis , Aged , Carcinoma/pathology , Carcinoma/surgery , Diagnosis, Differential , Humans , Lung Neoplasms/pathology , Lung Neoplasms/surgery , Male , Pneumonectomy , Radiography, Thoracic , Tomography, X-Ray ComputedABSTRACT
AIMS: To screen six isoflavones isolated from Erythrina poeppigiana (Leguminosae) for their antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). METHODS AND RESULTS: Stem bark of E. poeppigiana was macerated with acetone and the methylene chloride-soluble fraction of the residue was applied to repeated silica gel column chromatography and eluted. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined by a broth dilution method. Inactive compounds that failed inhibiting bacterial growth at 25 microg ml(-1) were further investigated for their combination effects with methicillin and oxacillin. Of the isolated isoflavones, 5,7,4'-trihydroxy-8,3'-di(gamma,gamma-dimethylallyl)isoflavone (isolupalbigenin) exhibited the highest anti-MRSA activity (MICs: 1.56-3.13 microg ml(-1); MBCs: 6.25-12.5 microg ml(-1)), followed by 5,7,4'-trihydroxy-6-gamma,gamma-dimethylallylisoflavone (erythrinin B). Inactive compounds were combined with methicillin or oxacillin, 5,4'-dihydroxy-(3'',4''-dihydro-3''-hydroxy)-2'',2''-dimethylpyrano[5'',6'':6,7]isoflavone (M-Wi-2) intensifying the susceptibility of MRSA strains to these antibiotics. In all but one strain, the MIC values of methicillin were reduced from > or =100 to 6.25-12.5 microg ml(-1) in the presence of M-Wi-2 (25 microg ml(-1)). CONCLUSIONS: Isoflavones from E. poeppigiana showed two different antibacterial activities against MRSA: direct growth inhibition and intensification of methicillin sensitivity. SIGNIFICANCE AND IMPACT OF THE STUDY: Isolupalbigenin and M-Wi-2 could lead to the development of compounds for new approaches against MRSA infection.