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    contractility

    Explore "contractility" with insightful episodes like "Inotrope therapy: Which one and when?", "biosights: March 5, 2018", "biosights: July 3, 2017" and "biosights: January 2, 2017" from podcasts like ""Neuro Resus", "biosights", "biosights" and "biosights"" and more!

    Episodes (4)

    Inotrope therapy: Which one and when?

    Inotrope therapy: Which one and when?

    Inotropic agents are commonly used in critically ill patients to support myocardia contractility either in the setting of cardiac surgery or ischemia or in the setting of sepsis associated myocardial dysfunction. The most commonly used agents are beta-agonist drugs (dobutamine), mixed beta and alpha agents (adrenaline and dopamine), phosphodiesterase inhibitors (inodilators) such as milrinone or enoximone or calcium sensitizers (levosimendan). Such agents are currently used according to clinician and/or unit preference based on tradition, mentorship, belief, inductive physiological reasoning, familiarity, understanding of pharmacokinetic and pharmacodynamics properties, side effects, and cost. No randomized controlled trials exist to support the notion that treatment targeted to similar physiological outcomes (ie cardiac index or MVO2) with one drug versus another would yield a different clinical outcome. More recently, however, two double-blind RCTs have compared adjunctive inotropic therapy with levosimendan in patients with post-operative low-cardiac output syndrome or low pre-operative ejection fraction. Both found that the addition of levosimendan was not superior to the edition of placebo.  

    biosights: March 5, 2018

    biosights: March 5, 2018

    The nucleus comes through in the clutch

    In addition to its roles in DNA replication and gene expression, the nucleus has an important physical impact on cellular behavior. Graham et al. reveal that, although the nucleus is dispensable for cell polarization and migration on 2D surfaces, it is crucial for regulating the cell's responses to mechanical cues. This biosights episode presents the paper by Graham et al. from the March 5th, 2018, issue of the Journal of Cell Biology and includes an interview with the paper's first author, David Graham, and its two senior authors, Jim Bear and Keith Burridge (University of North Carolina at Chapel Hill). Produced by Caitlin Sedwick and Ben Short. See the associated paper in JCB for details on the funding provided to support this original research.

    biosights

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    The Rockefeller University Press
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    biosights: July 3, 2017

    biosights: July 3, 2017

    Myosins team up to help secretory granules integrate

    Actomyosin contractility drives a variety of membrane remodeling events, including the integration of secretory granules into the apical plasma membrane after exocytosis. By visualizing granule integration in the salivary glands of live mice, Milberg et al. reveal that myosin IIA and myosin IIB act at different stages of the process and that the activation and assembly of these myosin isoforms into contractile filaments is regulated by the F-actin scaffold, which assembles on secretory granules and recruits myosin light chain kinase. This biosights episode presents the paper by Milberg et al. from the July 3rd, 2017, issue of The Journal of Cell Biology and includes an interview with the paper's senior author, Roberto Weigert (National Institutes of Health, Bethesda, MD). Produced by Caitlin Sedwick and Ben Short. See the associated paper in JCB for details on the funding provided to support this original research.

    biosights

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    The Rockefeller University Press
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    biosights: January 2, 2017

    biosights: January 2, 2017

    Tumor cells feel the pressure after protease inhibition

    Primary fibroblasts use a high pressure, “nuclear piston” mode of migration to move through highly cross-linked 3D extracellular matrices. Petrie et al. reveal that tumor cells with high levels of matrix metalloproteinase activity generally migrate by forming lamellipodia but, when their protease activity is inhibited, they can switch to the nuclear piston mechanism to force their nuclei through small gaps in the extracellular matrix. This biosights episode presents the paper by Petrie et al. from the January 2nd, 2017, issue of The Journal of Cell Biology and includes an interview with the paper’s senior author, Ryan Petrie (Drexel University, Philadelphia, PA). Produced by Caitlin Sedwick and Ben Short. See the associated paper in JCB for details on the funding provided to support this original research.

    biosights

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    The Rockefeller University Press
    biosights@rockefeller.edu