RESUMO
Whether mammalian scent-tracking is aided by inter-nostril comparisons is unknown. We assessed this in humans and found that (i) humans can scent-track, (ii) they improve with practice, (iii) the human nostrils sample spatially distinct regions separated by approximately 3.5 cm and, critically, (iv) scent-tracking is aided by inter-nostril comparisons. These findings reveal fundamental mechanisms of scent-tracking and suggest that the poor reputation of human olfaction may reflect, in part, behavioral demands rather than ultimate abilities.
Assuntos
Aprendizagem/fisiologia , Odorantes , Reconhecimento Psicológico , Olfato/fisiologia , Adolescente , Adulto , Análise Discriminante , Feminino , Lateralidade Funcional , Humanos , Masculino , Transtornos do Olfato/fisiopatologia , Desempenho Psicomotor , Análise Espectral , Fatores de TempoRESUMO
Forty years ago, von Békésy demonstrated that the spatial source of an odorant is determined by comparing input across nostrils, but it is unknown how this comparison is effected in the brain. To address this, we delivered odorants to the left or right of the nose, and contrasted olfactory left versus right localization with olfactory identification during brain imaging. We found nostril-specific responses in primary olfactory cortex that were predictive of the accuracy of left versus right localization, thus providing a neural substrate for the behavior described by von Békésy. Additionally, left versus right localization preferentially engaged a portion of the superior temporal gyrus previously implicated in visual and auditory localization, suggesting that localization information extracted from smell was then processed in a convergent brain system for spatial representation of multisensory inputs.
Assuntos
Córtex Cerebral/fisiologia , Condutos Olfatórios/fisiologia , Orientação/fisiologia , Olfato/fisiologia , Percepção Espacial/fisiologia , Adulto , Mapeamento Encefálico , Córtex Cerebral/anatomia & histologia , Feminino , Lateralidade Funcional/fisiologia , Humanos , Imageamento por Ressonância Magnética , Masculino , Cavidade Nasal/fisiologia , Rede Nervosa/anatomia & histologia , Rede Nervosa/fisiologia , Odorantes , Mucosa Olfatória/fisiologia , Condutos Olfatórios/anatomia & histologia , Estimulação Física , Córtex Somatossensorial/anatomia & histologia , Córtex Somatossensorial/fisiologia , Lobo Temporal/anatomia & histologia , Lobo Temporal/fisiologia , Córtex Visual/anatomia & histologia , Córtex Visual/fisiologiaRESUMO
The genetic basis of pancreatic ductal adenocarcinoma, which constitutes the most common type of pancreatic malignancy, involves the sequential activation of oncogenes and inactivation of tumor suppressor genes. Among the pivotal genetic alterations are Ki-RAS oncogene activation and p53 tumor suppressor gene inactivation. We explain that the combination of these genetic events facilitates pancreatic carcinogenesis as revealed in novel three-dimensional cell (spheroid cyst) culture and in vivo subcutaneous and orthotopic xenotransplantation models. N-cadherin, a member of the classic cadherins important in the regulation of cell-cell adhesion, is induced in the presence of Ki-RAS mutation but subsequently downregulated with the acquisition of p53 mutation as revealed by gene microarrays and corroborated by reverse transcription-PCR and Western blotting. N-cadherin modulates the capacity of pancreatic ductal cells to migrate and invade, in part via complex formation with keratinocyte growth factor receptor and neural cell adhesion molecule and in part via interaction with p120-catenin. However, modulation of these complexes by Ki-RAS and p53 leads to enhanced cell migration and invasion. This preferentially induces the downstream effector AKT over mitogen-activated protein kinase to execute changes in cellular behavior. Thus, we are able to define molecules that in part are directly affected by Ki-RAS and p53 during pancreatic ductal carcinogenesis, and this provides a platform for potential new molecularly based therapeutic interventions.
Assuntos
Caderinas/metabolismo , Movimento Celular , Proteína Oncogênica p21(ras)/metabolismo , Ductos Pancreáticos/citologia , Ductos Pancreáticos/patologia , Receptor Tipo 2 de Fator de Crescimento de Fibroblastos/metabolismo , Proteína Supressora de Tumor p53/metabolismo , Junções Aderentes/patologia , Animais , Carcinoma Ductal Pancreático/patologia , Técnicas de Cultura de Células , Transformação Celular Neoplásica , Cistos/patologia , Ativação Enzimática , Regulação Neoplásica da Expressão Gênica , Camundongos , Mutação/genética , Invasividade Neoplásica/patologia , Moléculas de Adesão de Célula Nervosa/metabolismo , Proteína Oncogênica p21(ras)/genética , Ligação Proteica , Proteínas Proto-Oncogênicas c-akt/metabolismo , Proteína Supressora de Tumor p53/genéticaRESUMO
Central to the concept of attention is the fact that identical stimuli can be processed in different ways. In olfaction, attention may designate the identical flow of air through the nose as either respiration or olfactory exploration. Here we have used functional magnetic resonance imaging (fMRI) to probe this attentional mechanism in primary olfactory cortex (POC). We report a dissociation in POC that revealed attention-dependent and attention-independent subregions. Whereas a temporal subregion comprising temporal piriform cortex (PirT) responded equally across conditions, a frontal subregion comprising frontal piriform cortex (PirF) and the olfactory tubercle responded preferentially to attended sniffs as opposed to unattended sniffs. In addition, a task-specific anticipatory response occurred in the attention-dependent region only. This dissociation was consistent across two experimental designs: one focusing on sniffs of clean air, the other focusing on odor-laden sniffs. Our findings highlight the role of attention at the earliest cortical levels of olfactory processing.