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1.
Arq. neuropsiquiatr ; 74(4): 329-336, Apr. 2016. tab, graf
Article in English | LILACS | ID: lil-779808

ABSTRACT

ABSTRACT Pathology of the rhinencephalon has been a subject of interest in the fields of neurodegenerative diseases, trauma, epilepsy and other neurological conditions. Most of what is known about the human rhinencephalon comes from comparative anatomy studies in other mammals and histological studies in primates. Functional imaging studies can provide new and important insight into the function of the rhinencephalon in humans but have limited spatial resolution, limiting its contribution to the study of the anatomy of the human rhinencephalon. In this study we aim to provide a brief and objective review of the anatomy of this important and often overlooked area of the nervous system.


RESUMO As patologias do rinencéfalo tem sido assunto de interesse para os estudiosos das doenças neurodegenerativas, do traumatismo cranio-encefálico, epilepsia e outras doenças neurológicas. A maior parte do conhecimento sobre a anatomia do rinencéfalo vem de estudos de anatomia comparativa com outros mamíferos e estudos histológicos em primatas. Estudos de imagem funcional, apesar de proporcionarem informações úteis e interessantes a respeito do funcionamento do rinencéfalo em humanos, sofrem de resolução espacial limitada, e portanto contribuem de maneira restrita ao estudo dos limites das áreas anatômicas. Neste artigo buscamos proporcionar ao neurologista e neurocientista interessado uma revisão prática e objetiva da anatomia desta área importante e muitas vezes esquecida do sistema nervoso.


Subject(s)
Humans , Olfactory Cortex/anatomy & histology , Medical Illustration , Olfactory Receptor Neurons , Olfactory Bulb/anatomy & histology , Olfactory Mucosa/anatomy & histology
2.
Armaghane-danesh. 2010; 15 (4): 345-355
in Persian | IMEMR | ID: emr-125818

ABSTRACT

Nowadays, cellular and tissues transplant has become the focus of attention for spinal cord injury. It has been shown olfactory nerve cells or olfactory mucosa whi have more efficient on nervous tissue repair and they have been more studied in experimental study. Furthermore, they were used in a few clinical centers for spinal defect. But mucosa tissue and spinal tissue have different structure and there is doubt about the integration of mucosa tissue in nervous tissue. Thus, in this research the morphology and the effect of the fetal olfactory mucosa [FOM] on spinal tissue sparing were studied after transplanted into the spinal cord hemisection in rats. This experimental study was conducted at Iran university of Medical Sciences in 2008. Of thirty eight female Sprague-Dawley [200-250g] rats twenty- eight were spinally hemisected at the L1 spinal level and were randomized into two groups of 14 animals. Treatment group received FOM graft and the control received fetal respiratory mucosa graft [FRM]. The other animals received surgical procedure without spinal cord injury as a sham group. The morphology of the transplant region and spinal tissue sparing was examined histological eight weeks after transplantation. The collected data was analyzed by the SPSS software using ANOVA and the morphology of the transplant region were studied by light microscope. Histological study showed that the both mucosa tissues could not integrate with the parenchyma of the spinal tissue. Although the FOM were fused more then the FRM with the host tissue but clear boundary was seen at the graft-host interface. The mean spinal tissue sparing of the treatment group increased a little compare to the control but a significant difference was not apparent whereas, the spinal tissue sparing in treatment and control groups compare to the sham group decreased significantly [P <0.05]. Transplantation of the mucosa tissue directly, into the spinal cord injury was created different cytoarchitecture with spinal tissue and FOM partially preserving tissue sparing


Subject(s)
Female , Animals, Laboratory , Spinal Cord Injuries , Olfactory Mucosa/anatomy & histology , Rats, Sprague-Dawley , Respiratory Mucosa
3.
São Paulo; s.n; 2008. [143] p. ilus, tab, graf.
Thesis in Portuguese | LILACS | ID: lil-540834

ABSTRACT

INTRODUÇÃO: A biópsia do neuroepitélio olfatório (NeuO) oferece perspectivas para aplicações terapêuticas tanto em doenças do olfato como doenças neurodegenerativas. Uma coleta bem sucedida desse tecido in vivo ainda não é rotina, devido á carência de estudos sobre a distribuição do NeuO em conchas superior (CS) e média (CM). Neste trabalho, descrevemos a distribuição do NeuO na CS e CM em cadáveres a partir da retirada integral dessas estruturas e posterior análise histológica por coloração de hematoxilina e eosina (HE) e imunoistoquímica. Além disso, também analisamos a influência do sexo, idade e lateralidade no grau de presença do NeuO nas CS e CM. CASUÍSTICA E MÉTODOS: Estudo anatômico prospectivo realizado de março de 2006 a janeiro de 2008. A CS e a CM foram endoscopicamente retiradas de um total de 25 cadáveres frescos com menos de 12 horas de óbito. Cada concha foi seccionada na metade de seu comprimento ântero-posterior. Assim, cada um dos 25 cadáveres deu origem a oito fragmentos de mucosa de regiões anatômicas distintas, totalizando 200 lâminas para análise tanto por coloração de HE como por reação de imunoistoquímica. Nas lâminas coradas por HE, classificamos a distribuição do NeuO em graus 0, 1, 2, 3, 4, sendo que a análise foi realizada por 3 patologistas de forma cega. Para imunoistoquímica, só obtivemos positividade com a proteína S-100. A concordância entre os três patologistas foi avaliada aos pares utilizando-se o coeficiente de Kappa. A distribuição do NeuO foi analisada de acordo com a idade, sexo, tempo de óbito, simetria entre as fossas nasais e acurácia da imunoistoquímica. RESULTADOS: Pela HE na CS, o NeuO esteve presente em 82,9% das vezes e, na CM, em 17,1%. Na CS, o NeuO foi detectado em 82,9 % das lâminas, 4,9 vezes a prevalência na CM, que foi de 17,1 % das lâminas (p < 0,001). Pela imunoistoquímica, foi possível encontrar NeuO em um total de 15 fragmentos. Desses, 10 (20%) eram da metade posterior da CS e cinco (7,6%)...


INTRODUCTION: Olfactory neuroepithelium (ON) biopsy provides perspectives for several therapeutic applications, both in disorders of olfaction and in neurodegenerative diseases. Successful in vivo collection of ON is still not routine, due to a dearth of studies on ON distribution in the superior and middle turbinate (ST and MT respectively). This study describes the distribution of ON in cadaver ST and MT as determined by complete endoscopic removal of turbinates and histological analysis with hematoxylin and eosin (H&E) and immunohistochemical staining. We also analyzed the influence of gender, age, and naris side on the extent to which ON is present in the superior and middle turbinate. CASE SELECTION AND METHODS: We conducted a prospective anatomical study from March 2006 to January 2008. The superior and middle turbinates of 25 fresh cadavers (less than 12 hours post-mortem) were removed endoscopically. Each turbinate was halved into anterior and posterior fragments. Eight anatomically distinct fragments were therefore obtained from each of the 25 cadavers for a total of 200 specimens, which were analyzed through H&E staining and immunohistochemistry. Hematoxylin and eosin-stained slides were subjected to blind examination by three independent pathologists; ON distribution was graded on a fivepoint numeric scale (grade 0, 1, 2, 3, or 4). Immunohistochemistry was only positive through S-100 staining. Pairwise agreement between pathologists was assessed by means of the Kappa coefficient. The distribution of ON was analyzed regarding age, gender, time elapsed between death and specimen harvesting, symmetry between nares, and accuracy of immunohistochemistry results. RESULTS: In H&E-stained slides, olfactory neuroepithelium was present in 82.9% of ST and 17.1% of MT specimens; prevalence in the superior turbinate was therefore 4.9-fold greater (p < 0.001). Immunohistochemical analysis was able to identify ON in 15 fragments, 10 of which (20%)...


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged, 80 and over , Cadaver , Eosine Yellowish-(YS) , Endoscopy/methods , Hematoxylin , Immunohistochemistry , Olfactory Mucosa/anatomy & histology
4.
Pesqui. vet. bras ; 27(9): 388-392, set. 2007. ilus
Article in Portuguese | LILACS | ID: lil-471008

ABSTRACT

O epitélio olfatório apresenta um mecanismo de diferenciação em que células-tronco dão origem a células progenitoras amplificadoras, as quais expressam um gene pró-neural denominado Mammalian Achaete Scute Homolog 1 (Mash1). Estas células podem se diferenciar em receptores olfatórios. O epitélio olfatório de cães sem raça definida (3 machos de um ano e 2 fêmeas de três de idade) foi analisado por imunolocalização do antígeno nuclear de proliferação celular (PCNA) e por microscopia eletrônica de transmissão. Verificou-se marcação positiva para PCNA em células do epitélio olfatório, particularmente acima da linha da membrana basal. A ultra-estrutura do epitélio olfatório revelou células adjacentes à lâmina basal, cuja eletrodensidade assemelha-se àquelas presentes no epitélio de sustentação, reforçando a idéia da renovação das células de sustentação e dos neurônios olfatórios locais. O epitélio olfatório é composto células basais, comprometidas com sua renovação, caracterizadas através da intensa atividade mitótica, identificada pela reação positiva ao PCNA. Estes resultados sugerem que há reposição das células sustentaculares locais e do sistema através de mecanismos semelhantes.


Olfactory epithelium presents a mechanism of differentiation where stem cells give arise to amplifying progenitor cell which express Mammalian Achaete Scute Homolog 1 (Mash1). These cells can be differentiated into olfactory receptors. An immunolocalization study and ultrastructural analysis by transmission electron microscopy of olfactory epithelium of mongrel dogs were made using 3 males (one year old) and 2 females (three years old). Labeled cells with positive staining by Proliferating cell nuclear antigen (PCNA) were observed in specific areas of the olfactory epithelium, especially above the basal membrane. The ultrastructure revealed cells adjacent to the basal membrane with morphology resembling sustentacular cells, supporting the idea of renewal of sustentacular and olfactory sensorial cells. Olfactory epithelium contains basal cells committed to self-renewal, characterized by high metabolic activity, identified by positive reaction to PCNA. These results suggested the renewal of sustentacular and sensorial olfactory cells through the same pathway.


Subject(s)
Animals , Male , Female , Proliferating Cell Nuclear Antigen/analysis , Dogs , Microscopy, Electron/methods , Olfactory Mucosa/anatomy & histology , Olfactory Mucosa/cytology , Olfactory Mucosa/ultrastructure
5.
J Biosci ; 2000 Jun; 25(2): 181-90
Article in English | IMSEAR | ID: sea-111320

ABSTRACT

The vomeronasal organ is a poorly understood accessory olfactory organ, present in many tetrapods. In mammals, amphibians and lepidosaurian reptiles, it is an encapsulated structure with a central, fluid-filled lumen. The morphology of the lubricatory system of the vomeronasal organ (the source of this fluid) varies among classes, being either intrinsic (mammalian and caecilian amphibian vomeronasal glands) or extrinsic (anuran and urodele nasal glands). In the few squamate reptiles thus far examined, there are no submucosal vomeronasal glands. In this study, we examined the vomeronasal organs of several species of Australian squamates using histological, histochemical and ultrastructural techniques, with the goal of determining the morphology of the lubricatory system in the vomeronasal organ. Histochemically, the fluid within the vomeronasal organ of all squamates is mucoserous, though it is uncertain whether mucous and serous constituents constitute separate components. The vomeronasal organ produces few secretory granules intrinsically, implying an extrinsic source for the luminal fluid. Of three possible candidates, the Harderian gland is the most likely extrinsic source of this secretion.


Subject(s)
Animals , Elapidae/anatomy & histology , Female , Harderian Gland/anatomy & histology , Histological Techniques , Lizards/anatomy & histology , Male , Nasal Cavity/anatomy & histology , Olfactory Mucosa/anatomy & histology , Smell , Vomeronasal Organ/anatomy & histology
6.
J Biosci ; 2000 Jun; 25(2): 173-9
Article in English | IMSEAR | ID: sea-111262

ABSTRACT

The luminal surface of the chemosensory epithelia of the main olfactory organ of terrestrial vertebrates is covered by a layer of fluid. The source of this fluid layer varies among vertebrates. Little is known regarding the relative development of the sources of fluid (sustentacular cells and Bowman's glands) in reptiles, especially in gekkotan lizards (despite recent assertions of olfactory speciality). This study examined the extent and morphology of the main olfactory organ in several Australian squamate reptiles, including three species of gekkotans, two species of skinks and one snake species. The olfactory mucosa of two gekkotan species (Christinus marmoratus and Strophurus intermedius) is spread over a large area of the nasal cavity. Additionally, the sustentacular cells of all three gekkotan species contained a comparatively reduced number of secretory granules, in relation to the skinks or snake examined. These observations imply that the gekkotan olfactory system may function differently from that of either skinks or snakes. Similar variation in secretory granule abundance was previously noted between mammalian and non-mammalian olfactory sustentacular cells. The observations in gekkotans suggests that the secretory capacity of the non-mammalian olfactory sustentacular cells show far more variation than initially thought.


Subject(s)
Animals , Cytoplasmic Granules/ultrastructure , Elapidae/anatomy & histology , Female , Histological Techniques , Lizards/anatomy & histology , Male , Nasal Cavity/anatomy & histology , Olfactory Mucosa/anatomy & histology , Smell
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