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Volume 151, Issue 2, Pages 106-110 (3 December 2009)


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Differential control of collagen synthesis by the sympathetic and renin–angiotensin systems in the rat left ventricle

Houcine DababCorresponding Author Informationemail address, Rafik Hachania, Wassim Hodrojb, Mohsen Saklya, Giampiero Briccab, Kamel Kacema

Received 30 April 2009; received in revised form 25 June 2009; accepted 15 July 2009.

Abstract 

In the present study, we tested the hypothesis of the indirect (via the sympathetic nervous system (SNS)) and direct (via AT1 receptors) contributions of Angiotensin II (Ang II) on the synthesis of collagen types I and III in the left ventricle (LV) in vivo. Sympathectomy and blockade of the Ang II receptor AT1 were performed alone or in combination in normotensive rats. The mRNA and protein synthesis of collagen types I and III were examined by Q-RT-PCR and immunoblotting in the LV.

Collagen types I and III mRNA were decreased respectively by 53% and 22% after sympathectomy and only collagen type I mRNA was increased by 52% after AT1 receptor blockade. mRNA was not changed for collagen type I but was decreased by 25% for collagen type III after double treatment. Only collagen protein type III was decreased after sympathectomy by 12%, but collagen proteins were increased respectively for types I and III by 145% and 52% after AT1 receptor blockade and by 45% and 60% after double treatment. Deducted interpretations from our experimental approach suggest that Ang II stimulates indirectly (via SNS) and inhibits directly (via AT1 receptors) the collagen type I at transcriptional and protein levels. For collagen type III, it stimulates indirectly the transcription and inhibited directly the protein level. Therefore, the Ang II regulates collagen synthesis differently through indirect and direct pathways.

a Unité de Physiologie Intégrée, Laboratoire de Pathologies Vasculaires, Faculté des Sciences de Bizerte, Tunisia

b EA4173, INSERM ERI-22, Agressions Vasculaires et Réponses Tissulaires, Faculté Rockefeller, Université Claude Bernard, Lyon 1, France

Corresponding Author InformationCorresponding author: Unité de Physiologie Intégrée, Laboratoire de Pathologies Vasculaires, Faculté des Sciences de Bizerte. Jarzouna 7021, Tunisia. Tel.: +216 97283876, + 216 72 590 175; fax: +216 72 590 566.

PII: S1566-0702(09)00416-0

doi:10.1016/j.autneu.2009.07.014


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