School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan, China.
Acta Pharmacol Sin. 2010 Dec;31(12):1569-75. doi: 10.1038/aps.2010.176. Epub 2010 Nov 22.
to examine the effects of tanshinone IIA, the main effective component of Salvia miltiorrhiza (known as 'Danshen' in traditional Chinese medicine) on angiotensin II (Ang II)-mediated cardiomyocyte apoptosis.
rat neonatal cardiomyocytes were primarily cultured with Ang II or Ang II plus tanshinone IIA. Myocyte apoptosis was evaluated by caspase-3 activity and DNA strand break level with TdT-mediated dUTP nick-end labeling (TUNEL) staining. Western blot analysis was employed to determine the related protein expression and flow cytometry assay was used to determine the TUNEL positive cells and the intracellular reactive oxygen species (ROS) production. SiRNA targeted to Akt was used.
ang II (0.1 micromol/L) remarkably increased caspase-3 activity, TUNEL positive cells, and cleaved caspase-3 and cytochrome c expression, but reduced Bcl-X(L) expression. These effects were effectively antagonized by pretreatment with tanshione IIA (1-3 micromol/L). Tanshinone IIA had no effect on basal ROS level, while attenuated the ROS production by Ang II. Interestingly, tanshione IIA significantly increased the phosphorylated Akt level, which was countered by the PI3K antagonist wortmannin or LY294002. Knockdown of Akt with Akt siRNA significantly reduced Akt protein levels and tanshinone IIA protective effect.
tanshinone IIA prevents Ang II-induced apoptosis, thereby suggesting that tanshinone IIA may be used for the prevention of the cardiac remodeling process.
观察丹参酮Ⅱ A(丹参的主要有效成分,中药名为“丹参”)对血管紧张素Ⅱ(AngⅡ)介导的心肌细胞凋亡的影响。
原代培养新生大鼠心肌细胞,用 AngⅡ或 AngⅡ加丹参酮Ⅱ A 处理。用 caspase-3 活性和 TdT 介导的 dUTP 缺口末端标记(TUNEL)染色评估心肌细胞凋亡。Western blot 分析用于确定相关蛋白表达,流式细胞术用于确定 TUNEL 阳性细胞和细胞内活性氧(ROS)的产生。使用 Akt 的 siRNA。
AngⅡ(0.1μmol/L)显著增加 caspase-3 活性、TUNEL 阳性细胞和裂解的 caspase-3 和细胞色素 c 的表达,但降低 Bcl-X(L)的表达。丹参酮Ⅱ A(1-3μmol/L)预处理可有效拮抗这些作用。丹参酮Ⅱ A 对基础 ROS 水平无影响,但可减弱 AngⅡ引起的 ROS 产生。有趣的是,丹参酮Ⅱ A 显著增加磷酸化 Akt 水平,而 PI3K 拮抗剂wortmannin 或 LY294002 可拮抗其作用。用 Akt siRNA 敲低 Akt 可显著降低 Akt 蛋白水平和丹参酮Ⅱ A 的保护作用。
丹参酮Ⅱ A 可预防 AngⅡ诱导的细胞凋亡,提示丹参酮Ⅱ A 可能用于预防心脏重构过程。