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Cardiovascular Research 1999 42(1):87-98; doi:10.1016/S0008-6363(98)00283-1
© 1999 by European Society of Cardiology
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Copyright © 1999, European Society of Cardiology

Decreased type VI adenylyl cyclase mRNA concentration and Mg2+-dependent adenylyl cyclase activities and unchanged type V adenylyl cyclase mRNA concentration and Mn2+-dependent adenylyl cyclase activities in the left ventricle of rats with myocardial infarction and longstanding heart failure

Isabelle Espinassea, Vadim Iourgenkoa, Christine Richerb, Michèle Heimburgera, Nicole Deferd, Marie-Claude Bourind, Françoise Samsonc, Eric Pussardb, Jean-François Giudicellib, Jean-Baptiste Michela, Jacques Hanouned and Jean-Jacques Mercadiera,*

aINSERM U 460, Faculté de Médecine Xavier Bichat, 16 rue Henri Huchard, F-75018 Paris, France
bDépartement de Pharmacologie, Le Krémlin-Bicêtre, France
cC.N.R.S. ERS 566, Le Plessis Robinson, France
dINSERM U 99, Hôpital Henri Mondor, Créteil, France

* Corresponding author. Tel.: +33-1-4485-6158; fax: +33-1-4485-6157; e-mail: jjmercad@pratique.fr

Objective: To address the effect of longstanding left ventricular (LV) hypertrophy and failure on LV adenylyl cyclase (AC) gene expression, mRNA concentrations of the main cardiac AC isoforms were measured in the non-infarcted area of LV from rats with myocardial infarction (MI), without (H) or with (F) LV failure, and in control (C) rats. Basal, GTP- and forskolin-stimulated Mg2+- and Mn2+-dependent AC activities were also measured in F and C rats. Methods: Two- and six months after MI, steady-state AC mRNA concentrations were assessed by Northern blot analysis and RNase protection assay with isoform-specific cDNA and cRNA probes, respectively. AC activities were assessed on LV microsomal fractions using standard procedures. Results: Types V and VI, and types IV and VII were the major and minor AC mRNA isoforms in both the LVs of F and C rats. Two months after MI, no difference in LV type V or VI mRNA to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA ratios was observed in rats with H or F compared to C. Six months after MI, no difference in LV type V mRNA concentration was observed between the three rat groups, whether this level was normalized to GAPDH, poly-(A+) or 18S RNAs. In contrast, a 35% decrease in the type VI mRNA to poly-(A+) RNA ratio and a 29% decrease in the type VI mRNA to 18S RNA ratio was observed only in rats with F compared to C (p<0.05 vs. C for the two comparisons). Two- and six months after MI, basal and forskolin-stimulated Mg2+-dependent AC activities were decreased by 30–35% in F rats compared to C (p<0.05), whereas Mn2+-dependent activities were unchanged. Conclusion: Longstanding LV hypertrophy and failure resulting from MI in rats is not associated with altered expression of the most abundant, type V, AC mRNA isoform, whereas that of type VI is decreased. The lack of change in Mn2+-dependent AC activities in the LV of F rats suggests that this decrease has no functional consequence on overall AC activity and that decreased Mg2+-dependent activities are related to alterations occurring upstream.

KEYWORDS Adenylyl cyclase; Rat heart; Ventricular hypertrophy; Heart failure


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