Differential expression of the angiotensin-(1-12)/chymase axis in human atrial tissue. (August 2015)

• Record Type: Journal Article
• Authors: Nagata, Sayaka; Varagic, Jasmina; Kon, Neal D.; Wang, Hao; Groban, Leanne; Simington, Stephen W.; Ahmad, Sarfaraz; Dell'Italia, Louis J.; VonCannon, Jessica L.; Deal, Dwight; Ferrario, Carlos M.
• Is Part Of: Therapeutic advances in cardiovascular disease. Volume 9:Number 4(2015:Aug.)
• Page Start: 168
• Page End: 180
• Publication Date: 2015-08
• Subjects: angiotensin II -- angiotensin converting enzyme inhibitors -- antihypertensive therapy -- aortic valve disease -- arrhythmia -- cardiac chymase -- coronary heart disease -- enzymes -- heart surgery; Cardiovascular system -- Diseases -- Periodicals; Cardiovascular system -- Diseases -- Treatment -- Periodicals; Cardiovascular pharmacology -- Periodicals; Cardiovascular Diseases -- diagnosis -- Periodicals; Cardiovascular Diseases -- therapy -- Periodicals; Cardiovascular Agents -- therapeutic use -- Periodicals; Cardiovascular Diseases -- drug therapy -- Periodicals; Cardiovascular System -- drug effects -- Periodicals; Cardiologie; Hart- en vaatziekten; Appareil cardiovasculaire -- Maladies -- Périodiques; Appareil cardiovasculaire -- Maladies -- Traitement -- Périodiques; Pharmacologie cardiovasculaire -- Périodiques; 616.10605
• DOI: 10.1177/1753944715589717
• Languages: English
• ISSNs: 1753-9447

Abstract

Objective: Heart chymase rather than angiotensin converting enzyme has higher specificity for angiotensin (Ang) I conversion into Ang II in humans. A new pathway for direct cardiac Ang II generation has been revealed through the demonstration that Ang-(1-12) is cleaved by chymase to generate Ang II directly. We address here whether Ang-(1-12) and chymase gene expression and activity are detected in the atrial appendages of 44 patients (10 females) undergoing heart surgery for the correction of valvular heart disease, resistant atrial fibrillation or ischemic heart disease. Methods and results: Immunoreactive Ang-(1-12) expression was 54% higher in left atrial compared with right atrial appendages. This was associated with higher abundance of left atrial appendage chymase gene transcripts and chymase activity, but no differences in angiotensinogen mRNA. Atrial chymase enzymatic activity was highly correlated with left atrial but not right atrial enlargement as determined by echocardiography, while both tyrosine hydroxylase and neuropeptide Y atrial appendage mRNAs correlated with atrial angiotensinogen mRNAs. Conclusions: Higher Ang-(1-12) expression and upregulation of chymase gene transcripts and enzymatic activity from the atrial appendages connected to the enlarged left versus right atrial chambers of subjects with left heart disease defines a role of this alternate Ang II forming pathway in the processes accompanying adverse atrial and ventricular remodeling.