Biomedical subjects

Catherine R Dermon

Publications and source records attributed to Catherine R Dermon.

4 recordsLinked to original sources

PubMed2006

Early post-hatching sex differences in cell proliferation and survival in the quail telencephalic ventricular zone and intermediate medial mesopallium.

Previous studies indicated that avian telencephalic areas related to learned behavior, such as song perception and production, are sexually dimorphic. Our study focused on the eventual occurrence of dimorphism in the intermediate medial mesopallium, an area associated with learning in non-singing birds. During early post-hatching life (days 1 and 5) cell proliferation and survival of newborn cells were studied by means of 5-bromo-2-deoxy-uridine immunocytochemistry. Programmed cell death (apoptosis) was investigated at post-hatching day 10. The ventricular zone, intermediate medial part of mesopallium and lateral septal area was analyzed using stereological methods for cell counts. Short-term experiments revealed significantly higher numbers of newborn cells in male ventricular zone of mesopallium compared to female at post-hatching day 1. Long-term survival until post-hatching day 20 showed significantly higher numbers of labeled cells in the male compared to female intermediate medial part of mesopallium, which is the final destination of migrating cells born in the overlying ventricular zone. The vast majority of these early post-hatching newborn cells residing in the intermediate medial part of mesopallium expressed a neuronal phenotype. In addition to neurogenesis, higher numbers of apoptotic figures were found in the male intermediate medial part of mesopallium at post-hatching day 10, suggesting that cell death plays a role in the control of telencephalic regional cell density in males. Our findings indicate that sex-specific mechanisms possibly stimulate increased cell genesis and survival, as well as the counteracting event of increased apoptotic cell death that characterized the male intermediate medial part of mesopallium.

Animals↗

PubMed2005

Comparative anatomy of alpha(2) and beta adrenoceptors in the adult and developing brain of the marine teleost the red porgy (Pagrus pagrus, Sparidae): [(3)H]clonidine and [(3)H]dihydroalprenolol quantitative autoradiography and receptor subtypes immunohistochemistry.

The present study aimed to determine the anatomic distribution and developmental profile of alpha(2) and beta adrenoceptors (AR) in marine teleost brain. Alpha 2 and beta adrenoceptors were studied at different developmental stages by using [(3)H]clonidine and [(3)H]dihydroalprenolol, respectively, by means of in vitro quantitative autoradiography. Furthermore, immunohistochemical localization of the receptor subtypes was performed to determine their cellular distribution. Saturation studies determined a high-affinity component of [(3)H]clonidine and [(3)H]dihydroalprenolol binding sites. High levels of both receptors were found in preglomerular complex, ventral hypothalamus, and lateral torus. Dorsal hypothalamus and isthmus included high levels of alpha(2) AR, whereas pretectum and molecular and proliferative zone of cerebellum were specifically characterized by high densities of beta AR. From the first year of life, adult levels of both AR were found in most medial telencephalic, hypothalamic, and posterior tegmental areas. Decreases in both receptors densities with age were prominent in ventral and posterior telencephalic, pretectal, ventral thalamic, hypothalamic, and tegmental brain regions. Immunohistochemical data were well correlated with autoradiography and demonstrated the presence of alpha(2A), alpha(2C), beta(1), and beta(2) AR subtype-like immunoreactivity. Both the neuronal (perikaryal or dendritic) and the glial localization of receptors was revealed. The localization and age-dependent alterations in alpha(2) and beta AR were parallel to plasticity mechanisms, such as cell proliferation in periventricular thalamus, hypothalamus, and cerebellum. In addition, the biochemical characteristics, distribution pattern, and neuronal or glial specificity of the receptors in teleost brain support a similar profile of noradrenergic transmission in vertebrate brain evolution.

Adrenergic alpha-Agonists↗

PubMed2004

Late granule cell genesis in quail cerebellum.

Proliferation of avian cerebellar neurons, including granule cells, is thought to be completed during embryonic life, and aspects of cell addition in cerebellar lobules in posthatching life are unknown. The present study tested the hypothesis that cell genesis in late embryonic and posthatching stages of quail cerebellum occurs in parallel with the performance of motor programs. After exposure to bromodeoxyuridine, short (20 hours) and long survival time points were selected to investigate survival and migration of labeled cells. Quantitative analysis of the lobular distribution of labeled cells was performed with the stereological disector method. External granular layer (EGL) proliferation did not cease after hatching, indicating that there is an extended posthatching period, lasting until P20, when cells can be added into the internal granular layer, modifying the cerebellar circuitry and function. Indeed, long survival experiments suggested that EGL-labeled cells migrated into the internal granular layer and survived for a prolonged time, although many of the progenitor cells remained in the EGL for days. Double-labeling experiments revealed that most of the late-generated granule cells were NeuN positive, but only few expressed nitric oxide synthase. In addition to granule cells, the white matter and a glutamic acid decarboxylase (GAD)-positive cell population in the molecular layer around Purkinje somata showed bromodeoxyuridine labeling. Although all lobules showed significant posthatching proliferation, an anteroposterior gradient was evident. The index of granule cell production and survival supports a spatiotemporal pattern, in correlation with the functional division of cerebellum into anterior and posterior domains.

Animals↗

PubMed2004

Protein synthesis profiling in the developing brain: a graph theoretic clustering approach.

Mapping regional brain development in terms of protein synthesis (PS) activity yields insight on specific spatio-temporal ontogenetic patterns. The biosynthetic activity of an individual brain nucleus is represented as a time-series object, and clustering of time-series contributes to the problem of inducing indicative patterns of brain developmental events and forming respective PS chronological maps. Clustering analysis of PS chronological maps, in comparison with epigenetic influences of alpha2 adrenoceptors treatment, reveals relationships between distantly located brain structures. Clustering is performed with a novel graph theoretic clustering approach (GTC). The approach is based on the weighted graph arrangement of the input objects and the iterative partitioning of the corresponding minimum spanning tree. The final result is a hierarchical clustering-tree organization of the input objects. Application of GTC on the PS patterns in developing brain revealed five main clusters that correspond to respective brain development indicative profiles. The induced profiles confirm experimental findings, and provide evidence for further experimental studies.

Animals↗