Zhou X, Chen L
Cardiovascular Institute, CAMS, Beijing.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1997 Feb;19(1):35-40.
In this study, the role of angiotensin II (Ang II) receptor, Ca2+ in the Ang II-stimulated neoeatal myocytes protein synthesis were investigated and the effect of Ang II on expression of c-fos gene was observed. The results showed that the stimulatory effect of Ang II on protein synthesis was blocked by the Ang II antagonist-[Sar1 Ile8] Ang II. When verapamil, EG-TA, dantrolene, and Fura-2/AM, were added to the medium, the 3H-leucine incorporations stimulated by Ang II were reduced by 17%, 19%, 22%, and 27%. Using calcium ionophore-A23187 did not stimulate protein synthesis, but enhanced Ang II-induced 3H-leucine incorporation. In addition, Ang II could induce expression of c-fos gene. These results indicated that the hypertrophic effect of Ang II on the myocytes was mediated by Ang II receptor and depended on increase in [Ca2+]i and may be associated with enhanced expression of c-fos.
本研究探讨了血管紧张素II(Ang II)受体、Ca2+在Ang II刺激新生心肌细胞蛋白质合成中的作用,并观察了Ang II对c-fos基因表达的影响。结果显示,Ang II拮抗剂-[Sar1 Ile8] Ang II可阻断Ang II对蛋白质合成的刺激作用。当向培养基中添加维拉帕米、乙二醇双四乙酸(EG-TA)、丹曲林和Fura-2/AM时,Ang II刺激的3H-亮氨酸掺入量分别降低了17%、19%、22%和27%。使用钙离子载体A23187不会刺激蛋白质合成,但会增强Ang II诱导的3H-亮氨酸掺入。此外,Ang II可诱导c-fos基因表达。这些结果表明,Ang II对心肌细胞的肥大作用是由Ang II受体介导的,依赖于细胞内钙离子浓度([Ca2+]i)的升高,且可能与c-fos表达增强有关。