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Loose Connective Tissue (loose + connective_tissue)
Selected AbstractsGentamicin used as an adjunct to GTRJOURNAL OF CLINICAL PERIODONTOLOGY, Issue 5 2003An experimental study in rats Abstract Objectives: To evaluate in a discriminating "capsule" model whether local application of gentamicin may have an added effect on bone formation produced by Bio-Oss® and guide tissue regeneration (GTR). Material and Methods: Thirty male 3-month-old Wistar rats were used. After elevation of muscle-periosteal flaps, a rigid hemispherical Teflon capsule, loosely packed with 0.025 g of Bio-Oss® impregnated with 2 mg/ml gentamicin sulfate (Garamycin®), was placed with its open part facing the lateral bone surface of the mandibular ramus (test) in one side of the jaw. A capsule filled only with Bio-Oss® (control) was placed on the contralateral side of the jaw. After healing periods of 1, 2 and 4 months, groups of 10 animals were sacrificed and the specimens were processed for histological examination. The volumes of (1) the space created by the capsule, (2) newly formed bone, (3) Bio-Oss® particles, (4) loose connective tissue, and (5) acellular space in the capsule were estimated by a point-counting technique in three to four histological sections of each specimen, taken by uniformly random sampling. Results: The histological evaluation showed limited but increasing bone fill in the capsules from 1 to 4 months in both the test and control sides. After 4 months, the newly formed bone occupied 11.9% (CV: 0.39) of the space created by the capsules at the test sides versus 13.2% (CV: 0.41) at the control sides. There was no statistical significant difference between test and control specimens at any observation time (p>0.05). Conclusion: It is concluded that local application of gentamicin has no added effect on bone formation when combined with Bio-Oss® and GTR. Zussamenfassung Gentamycin als Adjunktiv zur GTR genutzt. Eine experimentelle Studie bei Ratten Ziele:Überprüfung in einem "unterscheidenden" Kapselmodell, ob die lokale Applikation von Gentamycin einen zusätzlichen Effekt bei der Knochenbildung, die durch Bio-Oss® bei der GTR hervorgerufen wurde, hat. Material und Methoden: 30 männliche 3monatige Wistar-Ratten wurden genutzt. Nach der Elevation von Muskel-Periost-Lappen wurde eine rigide halbsphärische Teflonkapsel, die locker mit 0,025 g von Bio-Oss®, was mit Gentamycinsulfat 2mg/ml (Garamycin®) imprägniert war, auf einer Seite des Unterkieferramus (Test) so platziert, dass der offene Teil zur lateralen Knochenoberfläche gerichtet war. Eine Kapsel, die nur mit Bio-Oss gefüllt war (Kontrolle), wurde auf der kontralateralen Seite des Kiefers platziert. Nach der Heilungsperiode von 1, 2 und 4 Monaten wurden Gruppen von 10 Tieren getötet und die Proben für die histologische Überprüfung aufbereitet. Das Volumen von 1) dem Spalt, der durch die Kapsel geschaffen wurde, 2) dem neu gebildeten Knochen, 3) den Bio-Oss Partikeln, 4) dem lockeren Bindegewebe und 5) dem azellulären Spalt in der Kapsel wurden mit einer Punktzähltechnik in 3 bis 4 histologischen Schnitten von jeder Probe unter Nutzung einer allgemeinen Zufallsauswahl bestimmt. Ergebnisse: Die histologische Überprüfung zeigte eine limitierte aber zunehmende Knochenfüllung in der Kapsel vom 1. zum 4. Monat sowohl in der Test- als auch der Kontrollseite. Nach 4 Monaten besetzte der neu gebildete Knochen 11,9% (cv: 0,39) des von der Kapsel geschaffenen Spaltes bei den Testseiten verglichen mit 13,2% (cv: 0,41) bei den Kontrollseiten. Es gab keine statistisch signifikante Differenz zwischen Test- und Kontrollproben zu irgendeiner Beobachtungszeit (p>0,05). Schlussfolgerung: Es wird geschlossen, dass die lokale Applikation von Gentamycin keinen zusätzlichen Effekt auf die Knochenbildung hat, wenn eine Kombination mit Bio-Oss und der GTR erfolgt. Résumé La gentamycine utilisée en association à la GTR. Une étude expérimentale chez le rat Le but de cette étude a été d'évaluer si l'application locale de gentamycine dans un modèle de capsule discriminatoire pouvait avoir un effet additionnel bénéfique sur la formation osseuse produite par le Bio-Oss® et la GTR. Cette étude a eu recours à trente rats Wistar mâles de trois mois. Après l'élévation de lambeaux muscle-périoste, une capsule en téflon hémisphérique rigide, remplie de manière lâche avec 0,025 g de Bio-Oss® imprégnée avec 2mg/ml de sulfate de gentamycine (Garamycin®) a été placée avec sa face ouverte en regard de la surface osseuse latérale de la branche mandibulaire (test) d'un côté de la mâchoire. Une capsule remplie uniquement de Bio-Oss® (contrôle) a été placée dans le site contralatéral. Après des périodes de guérison de un, deux et quatre mois, des groupes de dix animaux ont été tués et les spécimens analysés histologiquement. Les volumes de 1) l'espace créé par la capsule, 2) l'os néoformé, 3) les particules de Bio-Oss®, 4) le tissu conjonctif lâche et 5) l'espace acellulaire dans la capsule ont été estimés par la technique de comptage par points dans trois à quatre coupes histologiques de chaque échantillon, pris de manière uniformément et randomisée. L'évaluation histologique a montré une augmentation limitée d'os dans les caspsules de un à quatre mois tant dans les sites tests que contrôles. Après quatre mois l'os néoformé occupait 11,9% (cv : 0,39) de l'espace créé par les capsules au niveau des sites tests vs 13,2% (cv : 0,41) au niveau des contrôles. Il n'y avait aucune différence statistique entre les échantillons tests et contrôles à aucun des temps d'observation (p>0,05). L'application locale de gentamycine n'aurait donc aucun effet sur la formation osseuse lorsqu'elle est placée avec le Bio-Oss® en association avec la GTR. [source] Osteogenesis by guided tissue regeneration and demineralized bone matrixJOURNAL OF CLINICAL PERIODONTOLOGY, Issue 3 2003N. Mardas Abstract Aim:, To evaluate in a discriminating capsule model whether bone formation by guided tissue regeneration (GTR) may be influenced by concomitant implantation of demineralized bone matrix (DBM). Materials and Methods:, Thirty 4-month-old male albino rats of the Wistar strain were used in the study. Following surgical exposure of the mandibular ramus, a hemispherical, Teflon capsule (5.0 mm in diameter), loosely packed with a standardized amount of DBM, was placed with its open part facing the lateral bone surface of the ramus. At the contralateral side, an empty capsule was placed, serving as control. After healing periods of 15, 30, and 120 days, groups of 10 animals were sacrificed and 40,70 ,m thick undecalcified sections of the capsules were produced. In the sections, the cross-sectional areas of (1) the space created by the capsule, (2) newly formed bone, (3) DBM particles, (4) loose connective tissue as well as the (5) height of the capsules, and (6) that of the newly formed bone were measured. Results:, Increasing bone fill was observed in both test and control sites from 30 to 120 days. After 30 days of healing, the mean amount of bone was approx. 3% of the cross-sectional area of the capsules at the test sites while it was 8% in the control sites (p<0.05). However, no statistically significant differences were observed between the test (46%) and control (64%) sites after 120 days regarding any of the measured parameters (p>0.05). The newly formed bone in the DBM group at 120 days, on the other hand, appeared more dense than that in the control capsules. Conclusion:, DBM used as an adjunct to GTR did not provide any added effect on bone formation but increased the density of the newly formed bone. Zusammenfassung Ziel: Die Untersuchung in einem Kapselmodell, welches differenzieren kann, ob die Knochenbildung durch GTR durch die gleichzeitige Implantation von demineralisierter Knochenmatrix (DBM) beeinflusst werden könnte Material und Methoden: Dreißig männliche 4-Monate-alte Albinoratten des Wistar Stammes wurden in der Studie verwendet. Nach der chirurgischen Freilegung des Unterkieferastes wurde eine halbkugelförmige Teflonkapsel (5,0 mm Durchmesser), welche locker mit einer standardisierten Menge von DBM versehen war, wurde mit ihrer offenen Fläche auf die seitlichen Knochenfläche des Ramus gelegt. Auf der kontralateralen Seite diente eine leere Kapsel als Kontrolle. Nach Heilungsintervallen von 15, 30 und 120 Tagen wurden Gruppen von 10 Tieren geopfert und 40-70 ,m dicke nicht-entkalkte Schnitte der Kapseln wurden hergestellt. An den Schnitten wurde die Querschnittsfläche von: 1) der Fläche, die von der Kapsel geschaffen wurde, 2) dem neu gebildeten Knochen, 3) den DBM-Partikeln, 4) dem lockeren Bindegewebe gemessen, als auch 5) die Höhe der Kapseln und 6) des neu gebildeten Knochens bestimmt. Ergebnisse: Von Tag 30 zu Tag 120 wurde sowohl bei den Test- als auch bei den Kontrollstellen eine erhöhte Knochenauffüllung beobachtet. Nach 30 Tagen der Heilung betrug an den Teststellen die mittlere Knochenmenge ungefähr 3% der Querschnittsfläche der Kapseln, während sie an den Kontrollstellen 8% (p<0,05) betrug. Jedoch wurde nach 120 Tagen bei keinem der gemessenen Parameter eine statistisch signifikante Differenz zwischen den Test- (46%) und den Kontrollstellen (64%) beobachtet. Auf der anderen Seite erschien nach 120 Tagen in der DBM-Gruppe der neu gebildete Knochen dichter als in den Kontrollkapseln Schlussfolgerung: DBM welches als Zusatz bei der GTR verwendet wurde, lieferte keinen zusätzlichen Effekt bei der Knochenbildung, aber erhöhte die Dichte des neu gebildeten Knochens. Résumé Le but de cette étude a été d'évaluer dans un modèle de capsule discriminatoire si la formation osseuse par regénération tissulaire guidée (GTR) pouvait être influencée par l'implantation concomitante de matrice osseuse déminéralisée (DBM). Trente rats albinos mâles âgés de quatre mois de la souche Wistar ont été utilisés pour cette étude. A la suite de l'exposition chirurgicale de la branche montante mandibulaire, une capsule en téflon hémisphérique de 0,5 mm de diamètre remplie sans tassement avec une quantité standardisée de DBM a été placée avec sa partie ouverte contre la surface osseuse latérale de la branche. Du côté contralatéral, une capsule vide était placée servant de contrôle. Après des périodes de guérison de 15, 30 et 120 jours, des groupes de dix animaux ont été tués et des coupes non-décalcifiées de 40 à 70 ,m d'épaisseur des capsules ont été effectuées. Dans ces coupes, une aire sur coupe transversale contenant 1) l'espace créé par la capsule, 2) l'os néoformé, 3) des particules DBM, 4) du tissu conjonctif lâche; 5) la hauteur des capsules et 6) et celle de l'os néoformé ont été mesurés. Un comblement osseux de plus en plus important tant dans les sites contrôles que les sites tests a été constaté entre les jours 30 et 120. Après 30 jours de guérison, la quantité moyenne d'os formait approximativement 3% de l'aire de la coupe des capsules dans les sites tests tandis qu'elle était de 8% dans les sites contrôles (p<0,05). Cependant, aucune différence statistique n'a été observée entre les sites tests (46%) et les sites contrôles (64%) après 120 jours pour les paramètres mesurés (p>0,05). L'os néoformé dans le groupe DBM à 120 jours semblait plus dense que dans les capsules contrôles. Le DBM utilisé durant la GTR n'apportait aucun effet additionnel sur la formation osseuse mais augmentait cependant la densité du nouvel os formé. [source] The musculotendinous system of an anguilliform swimmer: Muscles, myosepta, dermis, and their interconnections in Anguilla rostrataJOURNAL OF MORPHOLOGY, Issue 1 2008Nicole Danos Abstract Eel locomotion is considered typical of the anguilliform swimming mode of elongate fishes and has received substantial attention from various perspectives such as swimming kinematics, hydrodynamics, muscle physiology, and computational modeling. In contrast to the extensive knowledge of swimming mechanics, there is limited knowledge of the internal body morphology, including the body components that contribute to this function. In this study, we conduct a morphological analysis of the collagenous connective tissue system, i.e., the myosepta and skin, and of the red muscle fibers that sustain steady swimming, focusing on the interconnections between these systems, such as the muscle-tendon and myosepta-skin connections. Our aim is twofold: (1) to identify the morphological features that distinguish this anguilliform swimmer from subcarangiform and carangiform swimmers, and (2) to reveal possible pathways of muscular force transmission by the connective tissue in eels. To detect gradual morphological changes along the trunk we investigated anterior (0.4L), midbody (0.6L), and posterior body positions (0.75L) using microdissections, histology, and three-dimensional reconstructions. We find that eel myosepta have a mediolaterally oriented tendon in each the epaxial and hypaxial regions (epineural or epipleural tendon) and two longitudinally oriented tendons (myorhabdoid and lateral). The latter two are relatively short (4.5,5% of body length) and remain uniform along a rostrocaudal gradient. The skin and its connections were additionally analyzed using scanning electron microscopy (SEM). The stratum compactum of the dermis consists of ,30 layers of highly ordered collagen fibers of alternating caudodorsal and caudoventral direction, with fiber angles of 60.51 ± 7.05° (n = 30) and 57.58 ± 6.92° (n = 30), respectively. Myosepta insert into the collagenous dermis via fiber bundles that pass through the loose connective tissue of the stratum spongiosum of the dermis and either weave into the layers of the stratum compactum (weaving fiber bundles) or traverse the stratum compactum (transverse fiber bundles). These fiber bundles are evenly distributed along the insertion line of the myoseptum. Red muscles insert into lateral and myorhabdoid myoseptal tendons but not into the horizontal septum or dermis. Thus, red muscle forces might be distributed along these tendons but will only be delivered indirectly into the dermis and horizontal septum. The myosepta-dermis connections, however, appear to be too slack for efficient force transmission and collagenous connections between the myosepta and the horizontal septum are at obtuse angles, a morphology that appears inadequate for efficient force transmission. Though the main modes of undulatory locomotion (anguilliform, subcarangiform, and carangiform) have recently been shown to be very similar with respect to their midline kinematics, we are able to distinguish two morphological classes with respect to the shape and tendon architecture of myosepta. Eels are similar to subcarangiform swimmers (e.g., trout) but are substantially different from carangiform swimmers (e.g., mackerel). This information, in addition to data from kinematic and hydrodynamic studies of swimming, shows that features other than midline kinematics (e.g., wake patterns, muscle activation patterns, and morphology) might be better for describing the different swimming modes of fishes. J. Morphol., 2008. © 2007 Wiley-Liss, Inc. [source] Neuropathological analysis of an asymptomatic adult case with Dandy,Walker variantNEUROPATHOLOGY & APPLIED NEUROBIOLOGY, Issue 3 2006G. Notaridis The Dandy-Walker (DW) complex is a rare posterior fossa malformation, usually observed during the prenatal period or the early infancy. Clinically, it is characterized by mental retardation, seizures, cerebellar ataxia as well as symptoms of hydrocephalus. Structural imaging reveal a hypoplasia or agenesis of the cerebellar vermis, enlargement of the fourth ventricle with a posterior fossa cyst. Additional neurodevelopmental changes such as agenesis of the corpus callosum, lissencephaly and cortical dysplasia are also present. We report the first neuropathological analysis of an adult asymptomatic DW case. Brain computerized tomography showed a massive posterior fossa cyst and hypoplasia of the cerebellum. An Ehlers-Danlos syndrome type IV characterized by repetitive intestinal perforations and a saccular aneurysm on the left posterior communicating artery was also present. Macroscopic brain examination revealed hypoplasia of both cerebellar hemispheres and posterior part of the vermis, as well as dilatation of the fourth ventricle without hydrocephalus. The posterior fossa cyst wall was formed by an external arachnoid layer, middle layer with loose connective tissue and an internal layer of ependymal cells. There were two foci of cerebellar cortical dysplasia but no ectopic neurons, neuronal loss or gliosis in both cerebellum and cerebral cortex. No vascular or significant neurodegenerative lesions were observed. In comparison with previous reports in DW infants, this adult case displayed milder brain abnormalities compatible with a diagnosis of DW variant. The preservation of the cortical cytoarchitecture as well as the paucity of additional neurodevelopmental changes may explain the absence of clinical expression. [source] Access of autonomic nerves through the optic canal, and their orbital distribution in manTHE ANATOMICAL RECORD : ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY, Issue 1 2003Gordon L. Ruskell Abstract The notion that autonomic nerves from the internal carotid plexus are transmitted to the orbit with the ophthalmic artery through the optic canal has been variously assumed, disregarded, or denied, but never demonstrated. The objective of this study was to examine the contents of the canal, identify any autonomic nerves, and follow their passage within the orbit. The soft tissues of the optic canal, and the apical tissues of the orbit were removed and examined histologically using 10 cadaver preparations. Additionally, tissues from an orbital exenteration and 10 ocular enucleation or donor specimens were prepared. Some of the latter material was examined with an electron microscope. Numerous autonomic nerves (four to 25, ranging in diameter from 23 to 130 ,m) entered the orbit from the internal carotid plexus in the periosteum of the optic canal, the optic nerve dura mater, or the adventitia of the ophthalmic artery. In the orbit they advanced in the loose connective tissue covering the optic nerve dura and joined ciliary nerves close to the eye or entered the eye directly. None were observed to penetrate the dura, apart from a nerve accompanying the central retinal artery. Others were distributed with the ophthalmic artery and its branches. It is concluded that the optic canal is a regular, and often major, route for autonomic nerve distribution to the eye and orbit. Anat Rec Part A 275A:973,978, 2003. © 2003 Wiley-Liss, Inc. [source] Light and Electron Microscopic Studies of the Trachea in the One-Humped Camel (Camelus dromedarius)ANATOMIA, HISTOLOGIA, EMBRYOLOGIA, Issue 1 2007A. R. Raji Summary Histology of trachea of camel (Camelus dromedarius) was studied using light, scanning (SEM) and transmission electron microscopy (TEM). Tissue samples taken from the trachea (proximal, middle and distal part) were routinely prepared for histology (LM, EM) and stained with haematoxylin and eosin, Van Giesson (VG), Alcian blue, Periodic acid schiff (PAS), Masson's trichrome (MT), Verhof, PAS,VG and PAS,MT. The trachea of camel consists of 66,75 incomplete cartilaginous rings of hyaline. The lamina epithelium is composed of pseudostratified-ciliated columnar epithelium with many goblet cells. Submucosal layers were loose connective tissue with many elastic fibres. The mucosal and submucosal layers were 517.2 ± 61.6 ,m (n = 20) thick. Submucosal glands were tubuloalveolar with mucous (acidic and neutral) secretions. Trachealis muscle was attached to the inside sheet of tracheal cartilage. Ultrastructural studies showed that surface epithelium is pseudostratified with mucus-producing goblet cells, ciliated and basal cells, similar to other mammals. The ciliated cells contained many mitochondria, oval nucleus and many big granules. In scanning electron microscopy (SEM) studies, viscoelastic layers were observed on the epithelial surface of trachea, and there were highly condensed cilia under this layer. [source] Angiogenesis and Interstitial Pressure in a Rat Tumour ModelANATOMIA, HISTOLOGIA, EMBRYOLOGIA, Issue 2005H. Hünigen Introduction and Aim:, Angiogenesis, the formation of new blood vessels, is a crucial process in physiological and pathological growth. Pathological angiogenesis is responsible for growth and metastasis of solid tumours, and, when blocked, improves prognosis. As a result of the angiogenic cascade in solid tumours an irregular, leaky capillary network develops. The aim of the present study was to define malignant tumours' vascular characteristics and reveal functional anatomy by quantification of the microvasculature and interstitial pressure (IP) in relation to tumour fluid dynamics as visualized by contrast enhanced magnetic resonance imaging (MRI). Material and Methods:, Dynamic MRI and measurement of the IP was performed in 21 rats implanted with colon carcinomas subcutaneously. Angiogenesis was studied by morphometry of the capillaries, and immunolocalization of the angiogenic factor VEGF and VEGF-Receptor 2. Results and Conclusions:, Histology, immunohistochemistry and MRI confirmed concentric arrangement of 4 tumour zones. The tumour margin included loose connective tissue with abundant mononuclear cells. Many large microvessels were seen in this most intensely vascularized zone. IP measurement in this zone was adjusted to the zero level. Diameter of the peripheral zone of vital cells measured 1.3 mm. Capillaries were smaller and sparse. Dynamic MRI revealed peripheral washout of the contrast agent in this zone. After an initial increase of the signal intensity a hypo-intense rim was formed within a few minutes. The intermediate region was characterized by islands of vital tumour cells containing 3% capillaries (hot spots). The innermost area, the necrotic zone, took 35% of the total tumour area with less than 0.5% vessels. The IP increased from the periphery to the centre. VEGF and VEGF-receptor 2 was found in the vessels of the tumour margin and vital tumour cells of the peripheral zone. From this can be concluded that the peripheral washout phenomenon seems to be correlated with elevated interstitial pressure and increased capillary density and therefore may be a reliable sign of malignancy. [source] 2431: The eyelid margin: an underestimated contributor to ocular surface health and diseaseACTA OPHTHALMOLOGICA, Issue 2010E KNOP Purpose The eyelid margin is frequently underestimated in the consideration of factors in ocular surface health and disease. Clinically the whole free end of the lid margin is often addressed simply as "margin" without further differentiation. It is attempted to review the structure, embryology and function of the lid margin as well as its involvement in ocular surface pathology. Methods A review based on the available literature on the lid margin is prepared together with own findings on the histology of normal and pathological tissues. Results The human lid margin is divided into distinct zones that consist, coming from the skin side, of a rounded outer lid border, a free lid margin (between the eye lashes and the opening of the meibomian glands), the muco-cutaneous junction and a sharp inner lid border. The embryological development of the eye lids and their tissue components (loose connective tissue, lid muscles, ciliary hairs, Meibomian glands and vascular and neural components) takes place during the period of sealed lids. During this time the development of the Meibomian glands shows considerable similarity to that of the ciliary hairs. The sealing of the mesodermal lid folds and their eventual separation is dependent on several factors that may be involved in pathology. Various disease states, as well as the aging process, can lead to destruction of the lid margin and, conversely, this can lead to deterioration of the cornea and conjunctiva. Conclusion The eyelid margin is an underestimated contributor to ocular surface health and disease. Increased awareness of the anatomy, embryology, physiology and pathophysiology of the lid margin and it tissue components appears important for the preservation of ocular surface integrity. Support DFG KN317/11 [source] Histopathology of a functioning mitomycin-C trabeculectomyCLINICAL & EXPERIMENTAL OPHTHALMOLOGY, Issue 3 2009Steve Y-W Liang MBBS Abstract The ideal trabeculectomy bleb is diffuse, normally vascularized and characterized by microcystic change in the overlying conjunctiva. We compare and contrast the histopathology of a normally functioning mitomycin-C trabeculectomy site obtained from an eye enucleated for iris melanoma with abnormal blebs discussed in the literature. Representative sections of the normally functioning bleb were examined under the light microscope. The conjunctiva is composed of a uniform three-layered non-keratinizing stratified squamous epithelium overlying a single layer of oedematous basal cells. The conjunctival stroma consisted of loose connective tissue, traversed by capillaries and scattered small cystic spaces lined by endothelial cells. There were no goblet cells and few inflammatory cells and fibroblasts. The scleral trapdoor was evident as a cleft in the scleral wall in communication with the anterior chamber at the surgically created sclerostomy. Because the histopathological findings in our case correlate well with this clinical appearance, we conclude that whereas augmentation with anti-metabolites, such as mitomycin-C, can be associated with significantly altered conjunctival histopathology and consequent hypotony, but, if used carefully, normal architecture is conserved. [source] Histologic Analysis of Clinical Biopsies Taken 6 Months and 3 Years after Maxillary Sinus Floor Augmentation with 80% Bovine Hydroxyapatite and 20% Autogenous Bone Mixed with Fibrin GlueCLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH, Issue 2 2001Mats Hallman DDS Abstract: Background: Bovine hydroxyapatite (Bio-Oss®, Geistlich Pharmaceutical, Wollhausen, Switzerland) has been suggested to be used in maxillary sinus floor augmentation procedures prior to or in conjunction with implant placement. However, the long-term histologic fate of this material is not well understood. Purpose: The aim with this study was to histologically evaluate the tissue response in patients to a mixture of bovine hydroxyapatite (BH), autogenous bone, and fibrin glue 6 months and 3 years after a maxillary sinus floor augmentation procedure. Materials and Method: Biopsies were taken from a group of 20 consecutive patients 6 months (n = 16) and 3 years (n = 12) after maxillary sinus floor augmentation with a mixture of BH (80%), autogenous bone (20%), and fibrin glue and prepared for histologic analysis. Results: Light microscopy and morphometry from biopsies taken after 6 months showed various amounts of mineralized bone tissue. The specimen area was occupied by 54.1 ± 12.6% nonmineralized tissue, followed by 21.2 ± 24.5% lamellar bone, 14.5 ± 10.3% BH particles, and 10.2 ± 13.4% woven bone. The nonmineralized tissue seen in bone-forming areas consisted of a loose connective tissue, rich with vessels and cells. There were no signs of resorption of the BH particles. The lamellar bone appeared to have originated from the recipient site and was seldom in contact with the BH particles. After 3 years, the nonmineralized tissue area had decreased to 36.0 ± 19.0% (p > .05) and consisted mainly of bone marrow tissue. The surface area of lamellar bone had increased to 50.7 ± 22.8% (p > .05), and there was almost no immature bone. The mean specimen area occupied by BH particles, was 12.4 ± 8.7% and had not changed from 6 months (not significant). Moreover, the sizes of the particles were similar after 6 months and 3 years. The degree of BH particle,bone contact had increased from 28.8%± 19.9% after 6 months to 54.5 ± 28.8% after 3 years (p > .05). Conclusion: Histology of specimens from maxillary sinuses augmented with 80% BH particles, 20% autogenous bone, and fibrin glue showed a positive bone tissue response after 6 months and 3 years after augmentation of the maxillary sinus floor prior to implant placement in a group fo 20 patients. The bone surrounding and in contact with the BH particles after 6 months was mainly immature woven bone, which with time was replaced by mature lamellar bone filling the interparticle space as observed in the 3-year specimens. Moreover, bone-integrated BH particles seem to be resistant to resorption. The results indicate that the procedure may be considered when only small amounts of intraoral autogenous bone graft are available. [source] The expression of cyclooxygenase-2 in human temporomandibular joint samples: an immunohistochemical studyJOURNAL OF ORAL REHABILITATION, Issue 12 2002H. Yoshida summary, The aim of this investigation was to evaluate the immunohistochemical expression of cyclooxygenase-2 (COX-2) in the temporomandibular joint (TMJ) and to compare it with that control specimens. Expression of COX-2 in the TMJ disc and the synovial membrane in 26 human TMJ samples (internal derangement of TMJ; n=16, and control; n=10) was measured by an immunohistological technique using paraffin-embedded tissue and specific antihuman COX-2 polyclonal antibody. There were obvious distinction of COX-2 immunoreactivity between the control specimens and internal derangement cases, in the region of posterior and/or anterior loose connective tissues. In particular, intensive COX-2 expression was detected in the synovial membrane of internal derangement cases. The findings of the present study suggest that COX-2 might be an important mechanism regulating inflammation in the synovial membrane with internal derangement of TMJ. [source] The distribution of cyclooxygenase-1 in human temporomandibular joint samples: an immunohistochemical studyJOURNAL OF ORAL REHABILITATION, Issue 6 2001H. Yoshida Cyclooxygenase-1,2 (COX-1,2) or prostaglandin (PG) H synthase, is the first enzyme of the pathway in which arachidonic acid is oxidized to PGs. Thus, we examined the expression of COX-1 in 16 human temporomandibular joint (TMJ) samples with internal derangement and in 10 control specimens by an immunohistological technique using paraffin-embedded tissue and specific antihuman COX-1 polyclonal antibody. There was obvious distinction of COX-1 immunoreactivity between the control specimens and internal derangement cases, at the endothelial cells and fibroblasts, in the region of posterior and/or anterior loose connective tissues and synovial membrane. The findings of the present study suggest that COX-1 might be an important mechanism for maintaining normal homeostasis at the endothelial cells and fibroblasts with internal derangement of TMJ. [source] |