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1
L-carnitine reduces doxorubicin-induced apoptosis through a prostacyclin-mediated pathway in neonatal rat cardiomyocytes.左旋肉碱通过前列环素介导的途径减少阿霉素诱导的新生大鼠心肌细胞凋亡。
Int J Cardiol. 2011 Jan 21;146(2):145-52. doi: 10.1016/j.ijcard.2009.06.010. Epub 2009 Jun 23.
2
Cardioprotective effects of tanshinone IIA on myocardial ischemia injury in rats.丹参酮IIA对大鼠心肌缺血损伤的心脏保护作用。
Pharmazie. 2009 May;64(5):332-6.
3
Involvement of reactive oxygen species in urotensin II-induced proliferation of cardiac fibroblasts.活性氧在尾加压素II诱导的心脏成纤维细胞增殖中的作用
Eur J Pharmacol. 2008 Sep 28;593(1-3):24-9. doi: 10.1016/j.ejphar.2008.07.025. Epub 2008 Jul 17.
4
Tanshinone IIA: a new activator of human cardiac KCNQ1/KCNE1 (I(Ks)) potassium channels.丹参酮IIA:一种新型的人心脏KCNQ1/KCNE1(I(Ks))钾通道激活剂。
Eur J Pharmacol. 2008 Aug 20;590(1-3):317-21. doi: 10.1016/j.ejphar.2008.06.005. Epub 2008 Jun 7.
5
Apoptosis: a potentially reversible, meta-stable state of the heart.细胞凋亡:心脏一种潜在可逆的亚稳态。
Heart Fail Rev. 2008 Jun;13(2):175-9. doi: 10.1007/s10741-007-9069-3.
6
Tanshinone IIA protects neonatal rat cardiomyocytes from adriamycin-induced apoptosis.丹参酮IIA保护新生大鼠心肌细胞免受阿霉素诱导的凋亡。
Transl Res. 2008 Feb;151(2):79-87. doi: 10.1016/j.trsl.2007.11.005. Epub 2007 Dec 28.
7
Tanshinone IIA from Salvia miltiorrhiza BUNGE inhibits human aortic smooth muscle cell migration and MMP-9 activity through AKT signaling pathway.丹参中的丹参酮IIA通过AKT信号通路抑制人主动脉平滑肌细胞迁移和MMP-9活性。
J Cell Biochem. 2008 May 1;104(1):15-26. doi: 10.1002/jcb.21599.
8
Inhibition of apoptosis-regulated signaling kinase-1 and prevention of congestive heart failure by estrogen.雌激素对凋亡调节信号激酶-1的抑制作用及对充血性心力衰竭的预防作用
Circulation. 2007 Jun 26;115(25):3197-204. doi: 10.1161/CIRCULATIONAHA.106.657981. Epub 2007 Jun 11.
9
Tanshinone IIA protects cardiac myocytes against oxidative stress-triggered damage and apoptosis.丹参酮IIA可保护心肌细胞免受氧化应激引发的损伤和凋亡。
Eur J Pharmacol. 2007 Jul 30;568(1-3):213-21. doi: 10.1016/j.ejphar.2007.04.031. Epub 2007 Apr 27.
10
Angiotensin II stimulates apoptosis via TGF-beta1 signaling in ventricular cardiomyocytes of rat.血管紧张素II通过转化生长因子-β1信号通路刺激大鼠心室心肌细胞凋亡。
J Mol Med (Berl). 2006 Nov;84(11):975-83. doi: 10.1007/s00109-006-0090-0. Epub 2006 Aug 19.

丹参酮 IIA 通过 Akt 通路减轻血管紧张素 II 诱导的乳鼠心肌细胞凋亡。

Tanshinone IIA attenuates angiotensin II-induced apoptosis via Akt pathway in neonatal rat cardiomyocytes.

机构信息

School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan, China.

出版信息

Acta Pharmacol Sin. 2010 Dec;31(12):1569-75. doi: 10.1038/aps.2010.176. Epub 2010 Nov 22.

DOI:10.1038/aps.2010.176
PMID:21102479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4002950/
Abstract

AIM

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.

METHODS

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.

RESULTS

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.

CONCLUSION

tanshinone IIA prevents Ang II-induced apoptosis, thereby suggesting that tanshinone IIA may be used for the prevention of the cardiac remodeling process.

摘要

目的

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。

方法

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。

结果

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。

结论

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。