311 research outputs found

    The Money Market Mutual Fund Liquidity Facility

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    Preferences for descriptiveness and co-explanation in evaluating explanations

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    Good explanations can be distinguished from bad ones in different ways, for instance by how much of the available information they can explain (i.e., maximise the likelihood of) the available data. Here, we consider two different components of likelihood: descriptiveness (the likelihood of the individual data points) and co-explanation (the likelihood of the specific subset of data under consideration). We consider whether people prefer explanations that are high in descriptiveness vs. coexplanation. Moreover, we consider whether people who endorse conspiracy theories prefer explanations for either quality. In a medical diagnosis task, participants make binary choices between two fictional disease variants: one higher in descriptiveness versus another higher in co-explanation. Overall, participants displayed a weak preference for descriptiveness. This preference, however, did not vary across increasing levels of descriptiveness. Moreover, such preferences were unrelated to conspiracy mentality. Thus, both explanatory virtues may play a role in the appeal of likely explanations

    Mineralocorticoid receptors are indispensable for nongenomic modulation of hippocampal glutamate transmission by corticosterone

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    The adrenal hormone corticosterone transcriptionally regulates responsive genes in the rodent hippocampus through nuclear mineralocorticoid and glucocorticoid receptors. Via this genomic pathway the hormone alters properties of hippocampal cells slowly and for a prolonged period. Here we report that corticosterone also rapidly and reversibly changes hippocampal signaling. Stress levels of the hormone enhance the frequency of miniature excitatory postsynaptic potentials in CA1 pyramidal neurons and reduce paired-pulse facilitation, pointing to a hormone-dependent enhancement of glutamate-release probability. The rapid effect by corticosterone is accomplished through a nongenomic pathway involving membrane-located receptors. Unexpectedly, the rapid effect critically depends on the classical mineralocorticoid receptor, as evidenced by the effectiveness of agonists, antagonists, and brain-specific inactivation of the mineralocorticoid but not the glucocorticoid receptor gene. Rapid actions by corticosterone would allow the brain to change its function within minutes after stress-induced elevations of corticosteroid levels, in addition to responding later through gene-mediated signaling pathways

    Mineralocorticoid and glucocorticoid receptors in the brain. Implications for ion permeability and transmitter systems

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