369 research outputs found

    BIOL 347.01: Introduction to Neuroscience

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    BMED 347.01: Introduction to Neuroscience

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    BIOL 347.01: Covering Introduction to Neuroscience

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    BMED 347.01: Covering Introduction to Neuroscience

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    Design, fabrication, and application of uniformly distributed RC networks for use in electronic circuits

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    In the design of electronic circuits, both linear and non-linear, one of the goals is the reduction of the number of elements needed to complete the design. By using distributed RC networks a reduction in the number of elements by at least 50% is usually possible. This dissertation discusses several distributed RC networks, develops detailed design procedures for each, and applies them in the design of electronic circuits. The indefinite admittance matrix (IAM) for the DRURC (double-resistive uniformly distributed RC network) and the URC (single-resistive uniformly distributed RC network) , which have been previously derived, are used as the starting points for the development of the IAM\u27s for the TURC (tapped URC) and the TDRURC (tapped DRURC) , a new distributed network. The development of the IAM for the TDRURC proceeds from the interconnection of two DRURC\u27s such that the IAM\u27s add. A similar procedure using URC\u27s yields the IAM for the TURC. These two IAM\u27s, which have not been previously published, allow the derivation of the design equations necessary to apply these networks to electronic circuits. These four distributed network elements (URC, TURC, DRURC, and TDRURC) are applied to the reduction in the numbers of elements needed for the following electronic circuits: RC-coupled amplifiers, multivibrator circuits, high-Q (10 to 150) band-pass amplifiers, and phase-shift oscillators. The application to RC-coupled amplifiers is new, while the applications to band-pass amplifiers and phase-shift oscillators are significant advances to work that has been previously suggested. A prototype of each of the four distributed networks was built by the author in 1972 using a thin-film deposition method which is described in Chapter VII. The phase-shift oscillator, band-pass amplifier, and multivibrator circuits were also built and tested. The results compared favorably with predicted results. The procedures for designing and fabricating uniformly distributed RC networks are reviewed in detail. A review of both thin-film fabrication by vacuum deposition and semiconductor fabrication by diffusion is included --Abstract, pages ii-iii

    BIOL 347.01: Introduction to Neuroscience

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    BMED 347.01: Introduction to Neuroscience

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    ASCT-1 Is a Neutral Amino Acid Exchanger with Chloride Channel Activity

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    The ubiquitous transport activity known as system ASC is characterized by a preference for small neutral amino acids including alanine, serine, and cysteine. ASCT-1 and ASCT-2, recently cloned transporters exhibiting system ASC-like selectivity, are members of a major amino acid transporter family that includes a number of glutamate transporters. Here we show that ASCT1 functions as an electroneutral exchanger that mediates negligible net amino acid flux. The electrical currents previously shown to be associated with ASCT1-mediated transport result from activation of a thermodynamically uncoupled chloride conductance with permeation properties similar to those described for the glutamate transporter subfamily. Like glutamate transporters, ASCT1 activity requires extracellular Na+. However, unlike glutamate transporters, which mediate net flux and complete a transport cycle by countertransport of K+, ASCT-1 mediates only homo- and heteroexchange of amino acids and is insensitive to K+. The properties of ASCT-1 suggest that it may function to equilibrate different pools of neutral amino acids and provide a mechanism to link amino acid concentration gradient

    BIOH 280.01: Molecules to Mind - Fundamentals of Neuroscience

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    Isolation of Current Components and Partial Reaction Cycles in the Glial Glutamate Transporter EAAT2

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    The kinetic properties of the excitatory amino acid transporter EAAT2 were studied using rapid applications of l-glutamate to outside-out patches excised from transfected human embryonic kidney 293 cells. In the presence of the highly permeant anion SCN−, pulses of glutamate rapidly activated transient anion channel currents mediated by the transporter. In the presence of the impermeant anion gluconate, glutamate pulses activated smaller currents predicted to result from stoichiometric flux of cotransported ions. Both anion and stoichiometric currents displayed similar kinetics, suggesting that anion channel gating and stoichiometric charge movements are linked to early transitions in the transport cycle. Transporter-mediated anion currents were recorded with ion and glutamate gradients favoring either unidirectional influx or exchange. Analysis of deactivation and recovery kinetics in these two conditions suggests that, after binding, translocation of substrate is more likely than unbinding under physiological conditions. The kinetic properties of EAAT2, the dominant glutamate transporter in brain astrocytes, distinguish it as an efficient sink for synaptically released glutamate
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