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A concise discussion of the regulatory role of cGMP kinase I in cardiac physiology and pathology

  • Franz Hofmann
Review

Abstract

The underlying cause of cardiac hypertrophy, fibrosis, and heart failure has been investigated in great detail using different mouse models. These studies indicated that cGMP and cGMP-dependent protein kinase type I (cGKI) may ameliorate these negative phenotypes in the adult heart. Recently, evidence has been published that cardiac mitochondrial BKCa channels are a target for cGKI and that activation of mitoBKCa channels may cause some of the positive effects of conditioning in ischemia/reperfusion injury. It will be pointed out that most studies could not present convincing evidence that it is the cGMP level and the activity cGKI in specific cardiac cells that reduces hypertrophy or heart failure. However, anti-fibrotic compounds stimulating nitric oxide-sensitive guanylyl cyclase may be an upcoming therapy for abnormal cardiac remodeling.

Keywords

NO Guanylyl cyclase cGMP cGMP-dependent protein kinase I Heart failure Cardiac hypertrophy Fibrosis PKG ANP BNP CNP 

Notes

Compliance with ethical standards

Conflict of interest

The author has no conflict of interest.

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© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Institut für Pharmakologie und ToxikologieTU MünchenMunichGermany

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