Enhanced adrenomedullin production by mechanical stretching in cultured rat cardiomyocytes

Citation
T. Tsuruda et al., Enhanced adrenomedullin production by mechanical stretching in cultured rat cardiomyocytes, HYPERTENSIO, 35(6), 2000, pp. 1210-1214
Citations number
28
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
HYPERTENSION
ISSN journal
0194911X → ACNP
Volume
35
Issue
6
Year of publication
2000
Pages
1210 - 1214
Database
ISI
SICI code
0194-911X(200006)35:6<1210:EAPBMS>2.0.ZU;2-P
Abstract
Adrenomedullin (AM) is secreted from cultured cardiac myocytes, In this stu dy, we examined whether mechanical stretching stimulates AM production in c ardiac myocytes, and if so, whether angiotensin II (Ang II) is involved in that mechanism. Neonatal rat cardiac myocytes cultured in serum-free medium were stretched 10% or 20% on flexible silicone rubber culture dishes, and AM mRNA expression was examined by quantitative polymerase chain reaction. The AM mRNA levels in the myocytes stretched 10% and 20% for 24 hours signi ficantly increased by 56% (P<0.05) and 88% (P<0.01), respectively, when com pared with the levels in nonstretched cells. AM secretion into the medium a fter the myocytes were stretched 10% and 20% increased by 22% (P<0.05) and 45% (P<0.01), respectively. in nonstretched myocytes incubated with 10(-6) mol/L Ang II for 24 hours, AM mRNA and secretion increased by 86% (P<0.05) and 36% (P<0.01), respectively. These effects of Ang II were abolished by 1 0(-6) mol/L CV-11974, an Ang II type I (AT(1)) receptor antagonist, but not by 10(-6) mol/L PD-123319, an Ang II type II antagonist, Stretch-induced i ncreases of AM gene expression and secretion were significantly inhibited ( P<0.05) in the presence of 10(-6) mol/L CV-11974 by 46% and 52%, respective ly; however, they were not affected by 10(-6) mol/L PD-123319, These findin gs indicate that AM production from cardiac myocytes is augmented by mechan ical stretching, partially through the AT(1) receptors, which suggests a lo cal interaction between AM and the renin-angiotensin system in stretched ca rdiac myocytes.