24 research outputs found

    Electrophysiological evidence showing muscarinic agonist-antagonist activities of N-desmethylclozapine using hippocampal excitatory and inhibitory neurons

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    13301甲第4467号博士(保健学)金沢大学博士論文要旨Abstract 以下に掲載:Brain Research 1642 pp.255-262 2016. ELSEVIER. 共著者:Yuto Sugawara,Yui Kikuchi,Mitsugu Yoneda,Takako Ohno-Shosak

    Phase transformation of mesoporous calcium carbonate by mechanical stirring

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    We report a simple strategy to synthesize vaterite/calcite mesoporous calcium carbonate through collisions and organization of colloidal particles accelerated by mechanical stirring. Mechanically stirring the precursor colloidal dispersion can control the calcium carbonate polymorphs

    YM750, an ACAT Inhibitor, Acts on Adrenocortical Cells to Inhibit Aldosterone Secretion Due to Depolarization

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    Primary aldosteronism (PA) is considered the most common form of secondary hypertension, which is associated with excessive aldosterone secretion in the adrenal cortex. The cause of excessive aldosterone secretion is the induction of aldosterone synthase gene (CYP11B2) expression by depolarization of adrenocortical cells. In this study, we found that YM750, an Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor, acts on adrenocortical cells to suppress CYP11B2 gene expression and aldosterone secretion. YM750 inhibited the induction of CYP11B2 gene expression by KCl stimulation, but not by angiotensin II and forskolin stimulation. Interestingly, YM750 did not inhibit KCl-stimulated depolarization via an increase in intracellular calcium ion concentration. Moreover, ACAT1 expression was relatively abundant in the zona glomerulosa (ZG) including these CYP11B2-positive cells. Thus, YM750 suppresses CYP11B2 gene expression by suppressing intracellular signaling activated by depolarization. In addition, ACAT1 was suggested to play an important role in steroidogenesis in the ZG. YM750 suppresses CYP11B2 gene expression and aldosterone secretion in the adrenal cortex, suggesting that it may be a potential therapeutic agent for PA
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