Stage-specific Differential Activation of Mitogen-activated Protein Kinases in Hypertrophied and Failing Rat Hearts

• Published in: Journal of molecular and cellular cardiology 2001-04, Vol.33 (4), p.733-744
• Main Authors: Hayashida, Wataru, Kihara, Yasuki, Yasaka, Asuka, Inagaki, Koichi, Iwanaga, Yoshitaka, Sasayama, Shigetake
• Format: Article
• Language: English
• Subjects: Angiotensin; Angiotensin II - metabolism; Angiotensin-Converting Enzyme Inhibitors - pharmacology; Animals; Enzyme Activation; Gene Expression; Heart - drug effects; Heart - physiopathology; Heart failure; Heart Failure - enzymology; Heart Failure - physiopathology; Heart Ventricles - enzymology; Hemodynamics; Hypertrophy; Hypertrophy, Left Ventricular - enzymology; Hypertrophy, Left Ventricular - physiopathology; In Vitro Techniques; JNK Mitogen-Activated Protein Kinases; Male; Mitogen-Activated Protein Kinases - metabolism; Myocardium - enzymology; p38 Mitogen-Activated Protein Kinases; Peptidyl-Dipeptidase A - genetics; Rats; RNA, Messenger; Signal transduction
• ISSN: 0022-2828; 1095-8584
• DOI: 10.1006/jmcc.2001.1341

Mitogen-activated protein kinases (MAPKs) are involved in the early development of cardiac hypertrophy, but their roles in chronic left ventricular hypertrophy (LVH) are unclear. We studied the angiotensin (Ang) II-induced cardiac MAPK activation of the hypertensive Dahl salt-sensitive (DS) rats in the subacute developing LVH stage, the chronic compensated LVH stage, and the congestive heart failure (CHF) stage. In the isolated, coronary-perfused heart preparation, Ang II infusion (1×10−6mol/l) activated extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK) and p38-MAPK in the LV myocardium. No substantial differences were observed in the Ang II-induced ERK activation between the normotensive control DS rats and the hypertensive DS rats in either stage. In contrast, the Ang II-induced activation of JNK and p38-MAPK was augmented in the subacute LVH stage of the hypertensive DS rats, but then progressively attenuated in the chronic LVH and CHF stages. Chronic treatment with an angiotensin converting enzyme inhibitor, temocapril (20 mg/kg/day), ameliorated the responsiveness of the JNK/p38-MAPK activation, suggesting that the decreased JNK/p38-MAPK activation is a consequence of negative feedback regulation for the activated cardiac renin–angiotensin system in chronic LVH and CHF. Thus, the Ang II-induced activation of multiple cardiac MAPK pathways are differentially regulated, depending on the stages of chronic hypertrophic process. The JNK and p38-MAPK activation may be involved in the early development of adaptive LVH. However, the responsiveness of the cardiac JNK/p38-MAPK pathways progressively decreased in chronic LVH and CHF under the chronic activation of tissue renin-angiotensin system.