Literature DB >> 15646025

Dexamethasone treatment improves sarcoplasmic reticulum function and contractile performance in aged myocardium.

Njanoor Narayanan1, Chengxin Yang, Ande Xu.   

Abstract

Corticosteroids are thought to be involved in the maintenance of normal myocardial function by mechanisms incompletely understood. This study investigated the potential therapeutic benefit of the synthetic glucocorticoid, dexamethasone, in reversing age-associated deterioration in cardiac contractile performance and Ca2+ sequestration function of the sarcoplasmic reticulum. Dexamethasone was administered to senescent (26-28-month old), male Fischer 344 rats at a rate of 4 microg/h for 5 days via subcutaneously implanted osmotic mini pumps. Control rats received vehicle solution in similar manner. Contractile performance was assessed in Langendorff-perfused, electrically paced hearts from control and dexamethasone-treated rats. The results obtained showed that dexamethasone-treatment of aged rats resulted in significant improvement in myocardial contractile performance as evidenced by (i) increase (approximately 30-60%) in developed peak tension at a wide range of beating frequencies (2-6 Hz), (ii) unaltered time to peak tension, and (iii) decrease (approximately 8-15%) in time to half-relaxation. Also, SR isolated from dexamethasone-treated rats displayed approximately 2-fold higher rates of ATP-energized Ca2+ uptake compared to SR from control rats. The deficits in contractile performance of the senescent heart (prolonged contraction duration and diminished contractile force) are reversible through a glucocorticoid-mediated improvement in SR Ca2+ pump function.

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Year:  2004        PMID: 15646025     DOI: 10.1023/b:mcbi.0000049130.58074.73

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  31 in total

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  15 in total

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Review 2.  Cardiac remodeling and subcellular defects in heart failure due to myocardial infarction and aging.

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3.  Corticosteroids and aldose reductase inhibitor Epalrestat modulates cardiac action potential via Kvβ1.1 (AKR6A8) subunit of voltage-gated potassium channel.

Authors:  Jared Tur; Sachin L Badole; Feng Cheng; Aparoop Das; Rakesh C Kukreja; Srinivas M Tipparaju
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Review 4.  Glucocorticoid signaling in the heart: A cardiomyocyte perspective.

Authors:  Robert H Oakley; John A Cidlowski
Journal:  J Steroid Biochem Mol Biol       Date:  2015-03-21       Impact factor: 4.292

Review 5.  New insights into the roles of glucocorticoid signaling dysregulation in pathological cardiac hypertrophy.

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Authors:  Jessica R Ivy; Gillian A Gray; Megan C Holmes; Martin A Denvir; Karen E Chapman
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Review 8.  Non-genomic effect of glucocorticoids on cardiovascular system.

Authors:  Sung Ryul Lee; Hyoung Kyu Kim; Jae Boum Youm; Louise Anne Dizon; In Sung Song; Seung Hun Jeong; Dae Yun Seo; Kyoung Soo Ko; Byoung Doo Rhee; Nari Kim; Jin Han
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9.  Dual role for glucocorticoids in cardiomyocyte hypertrophy and apoptosis.

Authors:  Rongqin Ren; Robert H Oakley; Diana Cruz-Topete; John A Cidlowski
Journal:  Endocrinology       Date:  2012-09-18       Impact factor: 4.736

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Authors:  Pedro E Perez; Wilson Sze; Joshua Miller
Journal:  AACE Clin Case Rep       Date:  2019-08-28
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