Cardiac-specific knockout of ET A receptor mitigates low ambient temperature-induced cardiac hypertrophy and contractile dysfunction

Yingmei Zhang, Linlin Li, Yinan Hua, Jennifer M. Nunn, Feng Dong, Masashi Yanagisawa, Jun Ren

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

Cold exposure is associated with oxidative stress and cardiac dysfunction. The endothelin (ET) system, which plays a key role in myocardial homeostasis, may participate in cold exposure-induced cardiovascular dysfunction. This study was designed to examine the role of ET-1 in cold stress-induced cardiac geometric and contractile responses. Wild-type (WT) and ETA receptor knockout (ETAKO) mice were assigned to normal or cold exposure (4°C) environment for 2 and 5 weeks prior to evaluation of cardiac geometry, contractile, and intracellular Ca 2 properties. Levels of the temperature sensor transient receptor potential vanilloid (TRPV1), mitochondrial proteins for biogenesis and oxidative phosphorylation, including UCP2, HSP90, and PGC1α were evaluated. Cold stress triggered cardiac hypertrophy, depressed myocardial contractile capacity, including fractional shortening, peak shortening, and maximal velocity of shortening/relengthening, reduced intracellular Ca 2 release, prolonged intracellular Ca 2 decay and relengthening duration, generation of ROS and superoxide, as well as apoptosis, the effects of which were blunted by ETAKO. Western blotting revealed downregulated TRPV1 and PGC1α as well as upregulated UCP2 and activation of GSK3β, GATA4, and CREB in cold-stressed WT mouse hearts, which were obliterated by ETAKO. Levels of HSP90, an essential regulator for thermotolerance, were unchanged. The TRPV1 agonist SA13353 attenuated whereas TRPV1 antagonist capsazepine mimicked cold stress- or ET-1-induced cardiac anomalies. The GSK3β inhibitor SB216763 ablated cold stress-induced cardiac contractile (but not remodeling) changes and ET-1-induced TRPV1 downregulation. These data suggest that ETAKO protects against cold exposure-induced cardiac remodeling and dysfunction mediated through TRPV1 and mitochondrial function.

Original languageEnglish (US)
Pages (from-to)97-107
Number of pages11
JournalJournal of Molecular Cell Biology
Volume4
Issue number2
DOIs
StatePublished - Apr 2012

Fingerprint

Endothelin A Receptors
Cardiomegaly
Temperature
Endothelin-1
Down-Regulation
TRPV Cation Channels
Mitochondrial Proteins
Oxidative Phosphorylation
Endothelins
Organelle Biogenesis
Knockout Mice
Superoxides
Oxidative Stress
Homeostasis
Western Blotting
Apoptosis

Keywords

  • ET receptor
  • low ambient temperature
  • mitochondria
  • myocardial function
  • TRPV1

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology
  • Genetics

Cite this

Cardiac-specific knockout of ET A receptor mitigates low ambient temperature-induced cardiac hypertrophy and contractile dysfunction. / Zhang, Yingmei; Li, Linlin; Hua, Yinan; Nunn, Jennifer M.; Dong, Feng; Yanagisawa, Masashi; Ren, Jun.

In: Journal of Molecular Cell Biology, Vol. 4, No. 2, 04.2012, p. 97-107.

Research output: Contribution to journalArticle

Zhang, Yingmei ; Li, Linlin ; Hua, Yinan ; Nunn, Jennifer M. ; Dong, Feng ; Yanagisawa, Masashi ; Ren, Jun. / Cardiac-specific knockout of ET A receptor mitigates low ambient temperature-induced cardiac hypertrophy and contractile dysfunction. In: Journal of Molecular Cell Biology. 2012 ; Vol. 4, No. 2. pp. 97-107.
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