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1.
Neuroscience ; 316: 344-66, 2016 Mar 01.
Article in English | MEDLINE | ID: mdl-26746357

ABSTRACT

Neuronal persistent activity has been primarily assessed in terms of electrical mechanisms, without attention to the complex array of molecular events that also control cell excitability. We developed a multiscale neocortical model proceeding from the molecular to the network level to assess the contributions of calcium (Ca(2+)) regulation of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels in providing additional and complementary support of continuing activation in the network. The network contained 776 compartmental neurons arranged in the cortical layers, connected using synapses containing AMPA/NMDA/GABAA/GABAB receptors. Metabotropic glutamate receptors (mGluR) produced inositol triphosphate (IP3) which caused the release of Ca(2+) from endoplasmic reticulum (ER) stores, with reuptake by sarco/ER Ca(2+)-ATP-ase pumps (SERCA), and influence on HCN channels. Stimulus-induced depolarization led to Ca(2+) influx via NMDA and voltage-gated Ca(2+) channels (VGCCs). After a delay, mGluR activation led to ER Ca(2+) release via IP3 receptors. These factors increased HCN channel conductance and produced firing lasting for ∼1min. The model displayed inter-scale synergies among synaptic weights, excitation/inhibition balance, firing rates, membrane depolarization, Ca(2+) levels, regulation of HCN channels, and induction of persistent activity. The interaction between inhibition and Ca(2+) at the HCN channel nexus determined a limited range of inhibition strengths for which intracellular Ca(2+) could prepare population-specific persistent activity. Interactions between metabotropic and ionotropic inputs to the neuron demonstrated how multiple pathways could contribute in a complementary manner to persistent activity. Such redundancy and complementarity via multiple pathways is a critical feature of biological systems. Mediation of activation at different time scales, and through different pathways, would be expected to protect against disruption, in this case providing stability for persistent activity.


Subject(s)
Calcium/metabolism , Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels/metabolism , Models, Neurological , Neocortex/cytology , Neurons/metabolism , Action Potentials/physiology , Animals , Computer Simulation , Humans , Receptors, AMPA/metabolism , Receptors, N-Methyl-D-Aspartate/metabolism , Synapses/metabolism
2.
J Dent ; 28(5): 367-73, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10785304

ABSTRACT

PURPOSE: The purpose of this study was to evaluate the effects of wet and dry finishing/polishing procedures on the microleakage and surface texture of resin-modified glass ionomer (RMGI) restorative materials. MATERIALS AND METHODS: Class V cavity preparations were made at the cemento-enamel junction (CEJ) on the buccal and lingual surface of 30 extracted human molars. The teeth were restored in three groups of 10 (20 preparations in each group) using Fuji II LC and Vitremer, both RMGIs, and Fuji II, a capsulated conventional glass ionomer cement (control). One restoration per tooth was finished/polished with copious applications of water and the other was finished/polished without water. All restorations were finished/polished using a sequence of four abrasive disks. Finishing/polishing was initiated according to manufacturers' instructions-immediately after light-curing Fuji II LC and Vitremer, and 15min after placement for Fuji II. The specimens were thermocycled and subjected to a silver nitrate leakage test. Each tooth was sectioned buccolingually and examined with an optical microscope at 40x to determine the extent of microleakage at enamel and dentin margins. The data were subjected to a non-parametric statistical analysis. To evaluate surface roughness after polishing, three disks each of Vitremer and Fuji II LC were fabricated in Teflon molds. One disk of each material was not finished/polished (control). The others were finished/polished using Sof-Lex abrasive disks. One specimen of each material was kept wet during all finishing/polishing procedures, while the other was kept dry. Atomic force microscopy was used to determine the average roughness (R(a)) of the specimens. RESULTS: For each material, microleakage at the enamel margin was very slight. Leakage of the conventional glass ionomer Fuji II was severe at dentin margins. Statistical analysis indicated that both Vitremer and Fuji II LC had significantly less leakage than Fuji II, and that Vitremer had significantly less leakage than Fuji II LC (p<0.05). Leakage at enamel margins was significantly less than at dentin margins. Differences related to wet and dry polishing were not statistically significant. Profilometry data indicated that polished specimens were rougher than those cured against a Mylar strip. Wet polishing created greater surface roughness than dry polishing. CONCLUSIONS: RMGIs rather than conventional glass ionomers should be used in Class V cavity sites to allow immediate finishing and to reduce the incidence of microleakage. Dry finishing of RMGIs with abrasive disks is recommended because it produces a smoother surface and does not contribute to microleakage. However, wet finishing of conventional glass ionomers is still recommended to avoid desiccation.


Subject(s)
Dental Leakage/diagnosis , Dental Polishing , Dental Restoration, Permanent , Glass Ionomer Cements/chemistry , Resin Cements/chemistry , Composite Resins/chemistry , Dental Cavity Preparation/classification , Dental Enamel/ultrastructure , Dentin/ultrastructure , Humans , Materials Testing , Microscopy, Atomic Force , Molar/ultrastructure , Resins, Synthetic/chemistry , Silver Staining , Statistics, Nonparametric , Surface Properties , Thermodynamics , Tooth Cervix/ultrastructure , Water
4.
South Med J ; 79(5): 640-2, 1986 May.
Article in English | MEDLINE | ID: mdl-3704739

ABSTRACT

An adenomyoma was found in an endometriotic cyst of the right ovary of a 36-year-old woman. We have not seen a previous report of this entity. The most likely source of the smooth muscle component of this tumor is from within endometrial tissue lining the cyst.


Subject(s)
Endometriosis/pathology , Ovarian Cysts/pathology , Ovarian Neoplasms/pathology , Adult , Endometriosis/complications , Female , Humans , Ovarian Cysts/complications , Ovarian Neoplasms/complications
9.
W V Med J ; 62(1): 18-9, 1966 Jan.
Article in English | MEDLINE | ID: mdl-5216665
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