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Anxinil (Buspirone)
+ BONUS
 
Buspirone

Anxinil is a novel anxiolytic agent unrelated to the benzodiazepines in structure or pharmacologic properties. Extensive clinical studies have shown Anxinil to be effective in the treatment of anxiety, with efficacy comparable to diazepam or clorazepate. Anxinil exhibits a unique pharmacologic profile in that it alleviates anxiety without causing sedation or functional impairment and does not promote abuse or physical dependence. Furthermore, pre-clinical studies have shown that Anxinil does not possess anti-convulsant or muscle relaxant properties and does not interact significantly with central nervous system depressants. Biochemical and electrophysiologic studies indicate that Anxinil alters monoaminergic and GABAergic systems in a manner different from that of the benzodiazepines. The uniform depressant action of the benzodiazepines upon serotonergic, noradrenergic, and dopaminergic cell firing may result from their facilitatory effect on gamma-aminobutyric acid and its known inhibitory influence in these monoaminergic areas. Unlike the benzodiazepines, Anxinil exerts a differential influence upon monoaminergic neuronal activity, suppressing serotonergic activity while enhancing dopaminergic and noradrenergic cell firing. The mechanism of action of Anxinil challenges the notion that only one neurotransmitter mediates anxiety. The interaction with multiple neurotransmitters at multiple brain sites suggests that Anxinil may alter diverse activities within a “neural matrix of anxiety.” In contrast to the benzodiazepines, Anxinil orchestrates activity within this neural matrix to achieve effective treatment of anxiety while preserving arousal and attentional processes.

Other names for this medication:
Buspirone, Buspar, Ansial, Ansitec, Ansiten, Anxinil, Anxiron, Bespar, Busansil, Busirone, Buspin, Buspiron, Buspirona, Ledion, Narol, Neurosine, Paxon, Sorbon, Spamilan, Spitomin,

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Such polymers are expected to show not only good intrinsic conductivity but also possibly a good transparency in the visible spectrum for their use as infrared sensors/detectors. However, the sex chromosome complement (XX versus XY) is also a determinant of sex differences and may regulate miRNA expression in adipocytes. Fas/CD95 prevents autoimmunity independently of lipid raft localization and efficient apoptosis induction. It does not significantly change death review panel determinations.

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The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of ichthyosis vulgaris-the most common disorder of keratinization-and also a strong genetic risk factor for atopic eczema, marked a significant breakthrough in the understanding of eczema pathogenesis. Smoking cessation should be promoted among other professional groups. Non-invasive brain tissue characterization using qMRI or hMRI has significant implications for both research and clinics.

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The measurement of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in biological samples may provide a useful biomarker of intake. Multi-Biomarkers for Early Detection of Type 2 Diabetes, Including 10- and 12-(Z,E)-Hydroxyoctadecadienoic Acids, Insulin, Leptin, and Adiponectin. These strains possess a normal complement of high-affinity binding sites for diphtheria toxin, but these receptors are unable to deliver active toxin fragment A to the cytosol.

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Professional support for family caregivers of people with serious and persistent mental illnesses. A comparison of three methods of glycogen measurement in tissues.

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