cGMP-dependent protein kinase (PKG) mediates the anticontractile capacity of perivascular adipose tissue.

Abstract

AIM:

The aim of this study was to investigate the role of cGMP-dependent protein kinase (PKG) in mediating the anticontractile function of perivascular adipose tissue (PVAT) and whether its activation can rescue PVAT activity which is lost in an experimental model of inflammation.

METHODS AND RESULTS:

Contractile responses to norepinephrine were assessed using wire myography from small arterial segments obtained from PKG(-/-), PKG(+/+), adipo(-/-), and C57Bl6/J mice with and without PVAT during normal oxygenation and hypoxia. An anticontractile effect of PVAT was observed in control blood vessels. This was not present in arteries from PKG(-/-) or PKG(+/+) with inhibition of PKG signalling using DT-2/ODQ. Hypoxia-induced loss of PVAT function was rescued by ANP activation of PKG as there was no effect in blood vessels from PKG(-/-) mice or in the presence of DT-2. Solution transfer studies demonstrated that PKG was necessary for the normal paracrine effects of PVAT on smooth muscle and endothelium. PKG activation by atrial natriuretic peptide (ANP) did not restore the absent PVAT anticontractile capacity in arteries from adiponectin(-/-) mice; however, inhibition of PKG did not further abrogate this effect suggesting dysregulation of PKG signalling pathways in this model. The absence of PKG was associated with reduced adipocyte adiponectin expression.

CONCLUSION:

PKG plays a key role in regulating normal PVAT function both in modulating anticontractile factor release from adipocytes as well as being essential for its downstream dilator function in arterial smooth muscle.

• Authors: Sarah B Withers, Laura Simpson, Sharif Fattah, Matthias E Werner, Anthony M Heagerty
• Journal: Cardiovascular research (Cardiovasc Res) Vol. 101 Issue 1 Pg. 130-7 (Jan 01 2014) ISSN: 1755-3245 [Electronic] England
• PMID: 24095868 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Adiponectin
• Atrial Natriuretic Factor
• Superoxide Dismutase
• Cyclic GMP-Dependent Protein Kinases

Topics

• Adiponectin (metabolism)
• Adipose Tissue (physiology)
• Animals
• Atrial Natriuretic Factor (metabolism)
• Cyclic GMP-Dependent Protein Kinases (metabolism)
• Hypoxia (physiopathology)
• In Vitro Techniques
• Male
• Mesenteric Arteries (physiology)
• Mice
• Mice, Inbred C57BL
• Mice, Knockout
• Myography
• Superoxide Dismutase (metabolism)
• Vasoconstriction