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5-HT 2B 受体在去甲肾上腺素诱导的大鼠心肌病中心肌细胞凋亡中的作用。

Role of 5-HT 2B receptors in cardiomyocyte apoptosis in noradrenaline-induced cardiomyopathy in rats.

机构信息

Department of Cardiac Surgery, Xijing Hospital, Xi'an, China.

出版信息

Clin Exp Pharmacol Physiol. 2010 Jul;37(7):e145-51. doi: 10.1111/j.1440-1681.2010.05388.x. Epub 2010 Mar 30.

DOI:10.1111/j.1440-1681.2010.05388.x
PMID:20374255
Abstract
  1. Serotonin (5-hydroxytryptamine; 5-HT) plays important roles in the development of cardiac hypertrophy via activation of 5-HT receptors. The aim of the present study was to investigate the role of 5-HT(2B) receptors in the development of cardiomyocyte apoptosis and hypertrophy associated with noradrenaline (NA) overload. 2. Cardiac hypertrophy was induced in rats by intraperitoneal injection of 1.5 mg/kg NA for 4 weeks. Starting from Day 15, 5-HT2B receptor antagonist SB 204741 (i.p., 0.5 or 2 mg/kg) or SDZ SER 082 (i.p., 1 mg/kg) was injected twice daily for another 14 days. Whole-cell patch-clamp techniques were used to record ionic currents in freshly isolated ventricular cardiomyocytes. Western blot and terminal deoxyribonucleotidyl transferase-mediated dUTP-digoxigenin nick end-labelling (TUNEL) assays were used to assess myocardial apoptosis. 3. Expression of 5-HT(2B) receptors was enhanced in the hypertrophic left ventricle induced by NE overload in vivo. The 5-HT(2B) receptor antagonist SB 204741 partially reversed cardiac hypertrophy induced by NE overload (P < 0.05) and decreased L-type calcium currents in ventricular cardiomyocytes (P < 0.05). In addition, SB 204741 notably attenuated myocardial apoptosis, as evidenced by downregulation of Bax and caspase 3 (P < 0.05) and upregulation of the anti-apoptotic Bcl-2 protein (P < 0.05). 4. In conclusion, the data suggest an involvement of 5-HT(2B) receptors in the generation of apoptotic events associated with cardiac remodelling during increased adrenergic stimulation.
摘要
  1. 5-羟色胺(5-羟色胺;5-HT)通过激活 5-HT 受体在心脏肥大的发展中发挥重要作用。本研究的目的是研究 5-HT(2B)受体在与去甲肾上腺素(NA)过载相关的心肌细胞凋亡和肥大发展中的作用。

  2. 通过腹腔内注射 1.5mg/kg NA 诱导大鼠心脏肥大 4 周。从第 15 天开始,5-HT2B 受体拮抗剂 SB 204741(腹腔内,0.5 或 2mg/kg)或 SDZ SER 082(腹腔内,1mg/kg)每天两次注射,持续 14 天。使用全细胞膜片钳技术记录新鲜分离的心室肌细胞中的离子电流。Western blot 和末端脱氧核糖核苷酸转移酶介导的 dUTP-地高辛缺口末端标记(TUNEL)检测用于评估心肌细胞凋亡。

  3. 在体内 NE 过载诱导的肥厚左心室中,5-HT(2B)受体的表达增强。5-HT(2B)受体拮抗剂 SB 204741 部分逆转了 NE 过载引起的心脏肥大(P < 0.05),并降低了心室肌细胞中的 L 型钙电流(P < 0.05)。此外,SB 204741 明显减轻了心肌细胞凋亡,表现为 Bax 和 caspase 3 的下调(P < 0.05)以及抗凋亡 Bcl-2 蛋白的上调(P < 0.05)。

  4. 总之,数据表明,在肾上腺素刺激增加时,心脏重塑过程中与凋亡事件相关的 5-HT(2B)受体参与其中。

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