Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P50583 (asymmetrical)
 12,197 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A non-disintegrating polymeric capsule system, in which asymmetric membrane offers an improved osmotic effect, was used to deliver poorly water-soluble drugs in a control manner. The capsule wall membrane was made by a phase inversion process, in which asymmetric membrane was formed on stainless-steel mold pins by dipping the mold pins into a coating solution containing a polymeric material followed by dipping into a quench solution. This study evaluates the influence of coating formulation that was cellulose acetate (CA), ethylcellulose (EC), and plasticizer (glycerin and triethyl citrate). Results show capsule that made by CA with glycerin (formulation A), which appear in asymmetric structure and are able to release chlorpheniramine maleate (CM) in significant percentage. Two poorly water-soluble drugs of felodipine (FL) and nifedipine (NF) were selected as the model drug to demonstrate how the controlled release characteristics can be manipulated by the design of polymeric capsules with an asymmetric membrane and core formulations. Results show that sodium lauryl sulfate (SLS) is able to promote the release of FL from polymeric capsules prepared with CA with asymmetrical membrane. The addition of solubilizer, including RH40, PVP K-17, and PEG 4000 could enhance the release of FL but with an extent not being related to its solubility. Based on these results, influence of core formulation variables, including the viscosity and added amount of hydroxypropyl methylcellulose (HPMC), the added amount of SLS, and drug loading were examined on the release of NF. It was found that HPMC of 50 cps was suitable to be a thickening agent and both added amount of HPMC and SLS showed a comparable and profoundly positive effect, whereas NF loading had no influence on the drug release percent and rate. There existed a synergistic interaction between HPMC and SLS on the release percent and rate.
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PMID:Asymmetric membrane capsules for delivery of poorly water-soluble drugs by osmotic effects. 1588 36

Spike timing dependent plasticity (STDP) is a synaptic learning rule where the relative timing between the presynaptic and postsynaptic action potentials determines the sign and strength of synaptic plasticity. In its basic form STDP has an asymmetric form which incorporates both persistent increases and persistent decreases in synaptic strength. The basic form of STDP, however, is not a fixed property and depends on the dendritic location. An asymmetric curve is observed in the distal dendrites, whereas a symmetrical one is observed in the proximal ones. A recent computational study has shown that the transition from the asymmetry to symmetry is due to inhibition under certain conditions. Synapses have also been observed to be unreliable at generating plasticity when excitatory postsynaptic potentials and single spikes are paired at low frequencies. Bursts of spikes, however, are reliably signaled because transmitter release is facilitated. This article presents a two-compartment model of the CA1 pyramidal cell. The model is neurophysiologically plausible with its dynamics resulting from the interplay of many ionic and synaptic currents. Plasticity is measured by a deterministic Ca(2+) dynamics model which measures the instantaneous calcium level and its time course in the dendrite and change the strength of the synapse accordingly. The model is validated to match the asymmetrical form of STDP from the pairing of a presynaptic (dendritic) and postsynaptic (somatic) spikes as observed experimentally. With the parameter set unchanged the model investigates how pairing of bursts with single spikes and bursts in the presence or absence of inhibition shapes the STDP curve. The model predicts that inhibition strength and frequency are not the only factors of the asymmetry-to-symmetry switch of the STDP curve. Burst interspike interval is another factor. This study is an important first step towards understanding how STDP is affected under natural firing patterns in vivo.
Cogn Neurodyn 2012 Oct
PMID:Bursts shape the NMDA-R mediated spike timing dependent plasticity curve: role of burst interspike interval and GABAergic inhibition. 2408 63

According with a featural organization of semantic memory, this work is aimed at investigating, through an attractor network, the role of different kinds of features in the representation of concepts, both in normal and neurodegenerative conditions. We implemented new synaptic learning rules in order to take into account the role of partially shared features and of distinctive features with different saliency. The model includes semantic and lexical layers, coding, respectively for object features and word-forms. Connections among nodes are strongly asymmetrical. To account for the feature saliency, asymmetrical synapses were created using Hebbian rules of potentiation and depotentiation, setting different pre-synaptic and post-synaptic thresholds. A variable post-synaptic threshold, which automatically changed to reflect the feature frequency in different concepts (i.e., how many concepts share a feature), was used to account for partially shared features. The trained network solved naming tasks and word recognition tasks very well, exploiting the different role of salient versus marginal features in concept identification. In the case of damage, superordinate concepts were preserved better than the subordinate ones. Interestingly, the degradation of salient features, but not of marginal ones, prevented object identification. The model suggests that Hebbian rules, with adjustable post-synaptic thresholds, can provide a reliable semantic representation of objects exploiting the statistics of input features.
Cogn Neurodyn 2018 Dec
PMID:A feature-based neurocomputational model of semantic memory. 3048 62