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We are analyzing https://link.springer.com/article/10.1007/s00395-012-0323-z.

Title:
Activation of Liver X receptors in the heart leads to accumulation of intracellular lipids and attenuation of ischemia–reperfusion injury | Basic Research in Cardiology
Description:
Liver X receptor (LXR)-α and -β play a major role in lipid and glucose homeostasis. Their expression and function in the heart is not well characterized. Our aim was to describe the expression of LXRs in the murine heart, and to determine effects of cardiac LXR activation on target gene expression, lipid homeostasis and ischemia. Both LXRα and -β were expressed in heart tissues, HL-1 cells and isolated cardiomyocytes as determined by qRT-PCR. Elevated cardiac expression of LXR target genes and LXRβ was observed 24 h after in vivo permanent coronary artery ligation. The synthetic LXR agonist GW3965 induced mRNA expression of the LXR target genes in HL-1 cells and isolated cardiomyocytes. This was associated with a buildup of intracellular triglycerides and expanding lipid droplets as quantified by confocal microscopy. Mice injected with GW3965 had cardiac LXR activation as judged by increased target gene expression and lipid droplet accumulation. GW3965 in vivo and in vitro increased expression of genes inducing triglyceride synthesis, and altered expression of lipid droplet-binding protein genes. GW3965 protected HL-1 cells against hypoxia-reoxygenation induced apoptosis. LXR activation by GW3965 in vivo prior to heart isolation and perfusion with induced global ischemia and reperfusion improved left ventricular contractile function and decreased infarct size. In conclusion, LXRs are expressed in the murine heart in the basal state, and are activated by myocardial infarction. Activation of LXR by the synthetic agonist GW3965 is associated with intracardiac accumulation of lipid droplets and protection against myocardial ischemia–reperfusion injury.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,643,078 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We can't tell how the site generates income.

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Keywords {🔍}

article, pubmed, google, scholar, cas, lipid, lxr, heart, liver, res, mol, cell, receptor, expression, cardiac, myocardial, basic, biol, metabolism, fatty, oslo, activation, accumulation, physiol, acid, receptors, lei, nebb, haugen, cells, cardiol, research, peng, gene, endocrinol, cholesterol, university, privacy, cookies, content, injury, valen, role, target, genes, agonist, protein, signalling, lipotoxicity, dois,

Topics {✒️}

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Schema {🗺️}

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         headline:Activation of Liver X receptors in the heart leads to accumulation of intracellular lipids and attenuation of ischemia–reperfusion injury
         description:Liver X receptor (LXR)-α and -β play a major role in lipid and glucose homeostasis. Their expression and function in the heart is not well characterized. Our aim was to describe the expression of LXRs in the murine heart, and to determine effects of cardiac LXR activation on target gene expression, lipid homeostasis and ischemia. Both LXRα and -β were expressed in heart tissues, HL-1 cells and isolated cardiomyocytes as determined by qRT-PCR. Elevated cardiac expression of LXR target genes and LXRβ was observed 24 h after in vivo permanent coronary artery ligation. The synthetic LXR agonist GW3965 induced mRNA expression of the LXR target genes in HL-1 cells and isolated cardiomyocytes. This was associated with a buildup of intracellular triglycerides and expanding lipid droplets as quantified by confocal microscopy. Mice injected with GW3965 had cardiac LXR activation as judged by increased target gene expression and lipid droplet accumulation. GW3965 in vivo and in vitro increased expression of genes inducing triglyceride synthesis, and altered expression of lipid droplet-binding protein genes. GW3965 protected HL-1 cells against hypoxia-reoxygenation induced apoptosis. LXR activation by GW3965 in vivo prior to heart isolation and perfusion with induced global ischemia and reperfusion improved left ventricular contractile function and decreased infarct size. In conclusion, LXRs are expressed in the murine heart in the basal state, and are activated by myocardial infarction. Activation of LXR by the synthetic agonist GW3965 is associated with intracardiac accumulation of lipid droplets and protection against myocardial ischemia–reperfusion injury.
         datePublished:2012-12-25T00:00:00Z
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      headline:Activation of Liver X receptors in the heart leads to accumulation of intracellular lipids and attenuation of ischemia–reperfusion injury
      description:Liver X receptor (LXR)-α and -β play a major role in lipid and glucose homeostasis. Their expression and function in the heart is not well characterized. Our aim was to describe the expression of LXRs in the murine heart, and to determine effects of cardiac LXR activation on target gene expression, lipid homeostasis and ischemia. Both LXRα and -β were expressed in heart tissues, HL-1 cells and isolated cardiomyocytes as determined by qRT-PCR. Elevated cardiac expression of LXR target genes and LXRβ was observed 24 h after in vivo permanent coronary artery ligation. The synthetic LXR agonist GW3965 induced mRNA expression of the LXR target genes in HL-1 cells and isolated cardiomyocytes. This was associated with a buildup of intracellular triglycerides and expanding lipid droplets as quantified by confocal microscopy. Mice injected with GW3965 had cardiac LXR activation as judged by increased target gene expression and lipid droplet accumulation. GW3965 in vivo and in vitro increased expression of genes inducing triglyceride synthesis, and altered expression of lipid droplet-binding protein genes. GW3965 protected HL-1 cells against hypoxia-reoxygenation induced apoptosis. LXR activation by GW3965 in vivo prior to heart isolation and perfusion with induced global ischemia and reperfusion improved left ventricular contractile function and decreased infarct size. In conclusion, LXRs are expressed in the murine heart in the basal state, and are activated by myocardial infarction. Activation of LXR by the synthetic agonist GW3965 is associated with intracardiac accumulation of lipid droplets and protection against myocardial ischemia–reperfusion injury.
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         Myocardial infarction
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                     type:PostalAddress
                  type:Organization
                  name:University of Oslo
                  address:
                     name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
                     type:PostalAddress
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                  name:University of Oslo
                  address:
                     name:Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
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                     name:Center for Heart Failure Research, Oslo, Norway
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            name:Anton Baysa
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                  name:University of Oslo
                  address:
                     name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
                     type:PostalAddress
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                     name:Center for Heart Failure Research, Oslo, Norway
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                     name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
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                  address:
                     name:Center for Heart Failure Research, Oslo, Norway
                     type:PostalAddress
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            name:Tor Skomedal
            affiliation:
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                  address:
                     name:Department of Pharmacology, Oslo University Hospital, University of Oslo, Oslo, Norway
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                  address:
                     name:Center for Heart Failure Research, Oslo, Norway
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      name:Huazhong Agricultural University
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         name:College of Life Science and Technology, Huazhong Agricultural University, Wuhan, People’s Republic of China
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      address:
         name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
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      name:Tor Skomedal
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            name:Oslo University Hospital, University of Oslo
            address:
               name:Department of Pharmacology, Oslo University Hospital, University of Oslo, Oslo, Norway
               type:PostalAddress
            type:Organization
            name:Center for Heart Failure Research
            address:
               name:Center for Heart Failure Research, Oslo, Norway
               type:PostalAddress
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      name:Jan Bjørn Osnes
      affiliation:
            name:Oslo University Hospital, University of Oslo
            address:
               name:Department of Pharmacology, Oslo University Hospital, University of Oslo, Oslo, Norway
               type:PostalAddress
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            name:Center for Heart Failure Research
            address:
               name:Center for Heart Failure Research, Oslo, Norway
               type:PostalAddress
            type:Organization
      name:Zaiqing Yang
      affiliation:
            name:Huazhong Agricultural University
            address:
               name:College of Life Science and Technology, Huazhong Agricultural University, Wuhan, People’s Republic of China
               type:PostalAddress
            type:Organization
      name:Fred Haugen
      affiliation:
            name:University of Oslo
            address:
               name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
               type:PostalAddress
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            name:Center for Heart Failure Research
            address:
               name:Center for Heart Failure Research, Oslo, Norway
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:College of Life Science and Technology, Huazhong Agricultural University, Wuhan, People’s Republic of China
      name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
      name:Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
      name:Center for Heart Failure Research, Oslo, Norway
      name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
      name:Center for Heart Failure Research, Oslo, Norway
      name:Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
      name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
      name:Center for Heart Failure Research, Oslo, Norway
      name:Department of Pharmacology, Oslo University Hospital, University of Oslo, Oslo, Norway
      name:Center for Heart Failure Research, Oslo, Norway
      name:Department of Pharmacology, Oslo University Hospital, University of Oslo, Oslo, Norway
      name:Center for Heart Failure Research, Oslo, Norway
      name:College of Life Science and Technology, Huazhong Agricultural University, Wuhan, People’s Republic of China
      name:Department of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway
      name:Center for Heart Failure Research, Oslo, Norway
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