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Akiko Mano

Researcher at Kyoto Prefectural University of Medicine

Publications -  20
Citations -  718

Akiko Mano is an academic researcher from Kyoto Prefectural University of Medicine. The author has contributed to research in topics: Apoptosis & Mitochondrial permeability transition pore. The author has an hindex of 13, co-authored 19 publications receiving 690 citations. Previous affiliations of Akiko Mano include Kyoto Prefectural University.

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Intracellular ATP is required for mitochondrial apoptotic pathways in isolated hypoxic rat cardiac myocytes

TL;DR: It is demonstrated that ATP, generated through glycolysis, is a critical determinant of the form of cell death in hypoxic myocytes, independently of cellular acidification.
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Aldosterone Directly Induces Myocyte Apoptosis Through Calcineurin-Dependent Pathways

TL;DR: It is demonstrated for the first time that the specific plasma membrane receptor (coupled with phospholipase C) for aldosterone is present on cardiac myocytes and that a Aldosterone accelerates the mitochondrial apoptotic pathway through activation of calcineurin and dephosphorylation of Bad, suggesting that the proapoptotic action of ald testosterone may directly contribute to the progression of heart failure.
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Amlodipine inhibits doxorubicin-induced apoptosis in neonatal rat cardiac myocytes

TL;DR: Amlodipine significantly inhibits doxorubicin-induced myocyte apoptosis by suppressing the mitochondrial apoptotic pathway, and this antiapoptotic action was more effective than that seen with other antioxidants, including probucol, ascorbic acid, and alpha-tocopherol.
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Important role of energy-dependent mitochondrial pathways in cultured rat cardiac myocyte apoptosis.

TL;DR: The data suggest that staurosporine induces cell demise through a mitochondrial death signaling pathway and that the presence of intracellular ATP favors a shift from necrosis to apoptosis through caspase activation.
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Nicorandil regulates Bcl-2 family proteins and protects cardiac myocytes against hypoxia-induced apoptosis.

TL;DR: It is demonstrated that nicorandil regulates Bcl-2 family proteins via opening of mitoK(ATP) channels and nitric oxide-cGMP signaling and inhibits hypoxia-induced mitochondrial death pathway.