基础医学与临床 ›› 2018, Vol. 38 ›› Issue (1): 80-86.

• 研究论文 • 上一篇    下一篇

氨氯地平减轻腹主动脉缩窄性高血压大鼠心肌内质网应激

刘静1,赵连友2,李雪3,郭丽3,张志敏3,丁璐3,李晓莉3   

  1. 1. 第四军医大学附属唐都医院
    2. 第四军医大学唐都医院心脏内科 西安
    3. 第四军医大学唐都医院
  • 收稿日期:2016-11-29 修回日期:2017-03-28 出版日期:2018-01-05 发布日期:2017-12-26
  • 通讯作者: 刘静 E-mail:liujing1314aiwojia@163.com

Amlodipine decreases myocardial endoplasmic reticulum stress in rats with abdominal aortic banding hypertension

  • Received:2016-11-29 Revised:2017-03-28 Online:2018-01-05 Published:2017-12-26
  • Contact: LIU Jing E-mail:liujing1314aiwojia@163.com

摘要: 目的 观察高血压大鼠心肌组织葡萄糖调节蛋白94(GRP94)和CAAT/增强子结合蛋白同源蛋白(CHOP)的表达,探讨氨氯地平与内质网应激高血压大鼠心室肥厚的关系。方法 将SD大鼠随机分为假手术组、腹主动脉缩窄术(AAB)组和氨氯地平干预(AAB+Aml)组,每组40只。给予氨氯地平10 mg/(kg?d)。随机分为2、4和8周3个亚组,测定平均动脉压(MAP);计算左心室质量/体质量(LVM/BW);HE染色观察心肌细胞的形态;免疫组化及Western blot检测心肌组织GRP94和CHOP的表达。结果 随着术后时间的延长,AAB组MAP逐渐升高,明显高于假手术组〔2周(144±10)比(118±9)、4周(163±8)比(120±7)、8周(177±10)比(120±6) mmHg〕(P<0.05);AAB组LVM/BW显著高于假手术组〔2周(2.21±0.17)比(1.91±0.12)、4周( 2.45±0.16)比(2.01±0.14)、8周 (2.68±0.15)比(2.05±0.09) mg/g〕(P<0.05); AAB组心肌细胞较假手术组明显肥大;术后2周 AAB组心肌组织GRP94明显表达,4周达最高值,8周减低;AAB组GRP94表达量高于假手术组(P<0.05);随术后时间的延长,CHOP蛋白含量逐渐增加,8周达最高值。使用氨氯地平后,AAB+Aml组较AAB组MAP降低〔2 周(126±6)比(144±10)、4 周(125±8)比(163±8)、8 周(128±5)比(177±10) mmHg〕(P<0.05);使用氨氯地平后,AAB+Aml组较AAB组LVM/BW降低〔2周(2.21±0.17)比(1.94±0.15)、4周(2.45±0.16)比(2.13±0.08)、8周(2.68±0.15)比(2.18±0.10) mg/g〕(P<0.05);使用氨氯地平后AAB+Aml组较AAB组心肌细胞肥大程度减低。AAB+Aml组心肌组织GRP94及CHOP表达量低于AAB组(均P<0.05)。结论:氨氯地平可能通过减弱高血压触发的内质网应激而保护心肌细胞及减弱心室肥厚。

关键词: 氨氯地平, 内质网应激, 葡萄糖调节蛋白94, CAAT/增强子结合蛋白同源蛋白, 心室肥厚

Abstract: Objective To study the expression of protein 94 (GRP94) and C/EBP-homologous protein (CHOP) in myocardial tissue of hypertensive rats, and investigate the effects of amlodipine on endoplasm retieulum stress(ERS) and ventricular hypertrophy in abdominal aortic banded rats. Methods 120 adult male SD rats with criteria were divided randomly into three groups:sham-operated group, abdominal aortic banding(AAB) and AAB treated with amlodipine (AAB+Aml)groups(n=40). In sham-operated rats, the abdominal aorta was isolated but not constricted, while the abdominal aorta were constricted in AAB rats. The AAB+Aml group were underwent abdominal aortic constriction and treated with amlodipine (10 mg/(kg?d)). According to the time of surgery,each group was further divided into 2, 4 and 8-week postoperative subgroups (n=6). Mean arterial pressure (MAP), the 1eft ventricular mass (LVM) and body mass (BM) were measured and (LVM/BM) was calculated. The morphology of cardiomyocytes was observed by HE staining. The protein levels of GRP94 and CHOP were analyzed by immunohistochemistry and western blot. Results 1)With time after surgery, MAP and LVM/BW of AAB group increased gradually, and they were obviously higher than the sham operation group〔MAP: 2 weeks (144 ± 10)vs(118 ± 9), 4 weeks (163 ± 8)vs(120 ± 7), 8周(177 ± 10)vs(120 ± 6) mmHg; LVW/BW: 2 weeks (2.21±0.17) vs (1.91±0.12), 4 weeks (2.45±0.16) vs (2.01±0.14), 8 weeks (2.68±0.15) vs (2.05±0.09) mm Hg;(P<0.05)〕.The cardiomyocytes in AAB group were hypertrophic compared to the sham group. The expression of GRP94 in AAB group increased significantly at 2 weeks post-operation, and reached peak level at 4 weeks after the surgery and was on the decline thereafter. The expression of CHOP and GRP94 in AAB rats were significantly higher than sham group, and reached the peak at the 8 weeks after surgery. 2)Treatment with amlodipine significantly reduced MAP and LVM/BW in AAB rats〔(MAP: 2 weeks (126±6) vs (144±10), 4 weeks (125±8) vs (163±8), 8 weeks (128±5) vs (177±10)mmHg;LVM/BW: 2 weeks (1.94±0.15) vs (2.21±0.17), 4 weeks (2.13±0.08) vs (2.45±0.16), 8 weeks (2.18±0.10) vs (2.68±0.15)mg/g; (P<0.05)〕.The myocardial hypertrophic was alleviated in AAB+Aml group. The levels of GRP94 and CHOP in AAB+Aml group were lower than those in AAB rats(all P<0.05). Conclusion Our results suggested that endoplasmic reticulum stress is involved in the ventricular remodeling caused by hypertension, and use of amlodipine can reduce ventricular hypertrophy in hypertension models possibly by inhibiting endoplasmic reticulum stress via down-regulation of GRP94 and CHOP.

Key words: Amlodipine, Endoplasmic reticulum stress, Glucose-regulated protein 94, CAAT/enhancer-binding protein homologous protein, Ventricular hypertrophy