The catecholamine release-inhibitory "catestatin" region of chromogranin a: early decline in humans at genetic risk of hypertension.

Ann N Y Acad Sci

Department of Medicine and Center for Molecular Genetics, University of California, and VA San Diego Healthcare System, San Diego, California 92037, USA.

Published: October 2002

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http://dx.doi.org/10.1111/j.1749-6632.2002.tb04520.xDOI Listing

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Article Synopsis
  • The study examines how catestatin, a peptide linked to heart disease, predicts cardiac outcomes in patients with different types of heart failure (HF): HF with reduced ejection fraction (HFrEF), mildly reduced ejection fraction (HFmrEF), and preserved ejection fraction (HFpEF).
  • Researchers measured plasma catestatin levels in 228 HF patients and found that its association with cardiac death varied across the different ejection fraction groups during an average follow-up of 52.5 months.
  • Elevated plasma catestatin levels were identified as a stronger predictor of cardiac death in patients with HFmrEF/HFpEF than in those with HFrEF, with a significant risk identified at a cut-off level of
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Catestatin (CST) is a catecholamine release-inhibitory peptide secreted from the adrenergic neurons and the adrenal glands. It regulates the cardiovascular functions and it is associated with cardiovascular diseases. Though its mechanisms of actions are not known, there are evidences of cross-talk between the adrenergic and CST signaling.

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Catestatin (CTS), a catecholamine-release inhibitory peptide, exerts pleiotropic cardiac protective effects. Pulmonary embolism caused by deep vein thrombosis involving vascular dysfunction. The present study aims to investigate the effects of CTS on thrombus formation that may inhibit the development of pulmonary embolism and its potential pathway.

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Catestatin, a catecholamine-release inhibitory peptide, has multiple cardiovascular activities. Conflicting results have been recently reported by increased or decreased plasma levels of catestatin in patients with coronary artery disease (CAD). However, there have been no previous reports regarding the effects of catestatin on arteriosclerosis.

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Chromogranins: from discovery to current times.

Pflugers Arch

January 2018

Department of Biology, Ecology and Earth Sciences, University of Calabria, Arcavata de Rende, Italy.

The discovery in 1953 of the chromaffin granules as co-storage of catecholamines and ATP was soon followed by identification of a range of uniquely acidic proteins making up the isotonic vesicular storage complex within elements of the diffuse sympathoadrenal system. In the mid-1960s, the enzymatically inactive, major core protein, chromogranin A was shown to be exocytotically discharged from the stimulated adrenal gland in parallel with the co-stored catecholamines and ATP. A prohormone concept was introduced when one of the main storage proteins collectively named granins was identified as the insulin release inhibitory polypeptide pancreastatin.

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