基础医学与临床 ›› 2024, Vol. 44 ›› Issue (5): 626-629.doi: 10.16352/j.issn.1001-6325.2024.05.0626

• 研究论文 • 上一篇    下一篇

Na+/Ca2+交换体抑制剂SN-6和维拉帕米降低肾上腺皮质癌细胞系NCI-H295R醛固酮合成酶表达

王宇1,2, 高寅洁2, 任卫东1,3*, 童安莉2*   

  1. 1.河北北方学院 研究生院,河北 张家口 075000;
    2.中国医学科学院 北京协和医学院 北京协和医院 内分泌科 国家卫生健康委员会内分泌重点实验室,北京 100730;
    3.河北北方学院附属第一医院 内分泌科,河北 张家口 075000
  • 收稿日期:2024-02-20 修回日期:2024-03-19 出版日期:2024-05-05 发布日期:2024-04-23
  • 通讯作者: *tonganli@hotmail.com;15530396532@126.com
  • 基金资助:
    国家重点研发计划(2021YFC2501600,2021YFC2501603);国家自然科学基金(82070822);中央高水平医院临床科研业务费(2022-PUMCH-C-028)

Na+/Ca2+ exchanger inhibitor SN-6 and verapamil reduce aldosterone synthase expression in adrenocortical carcinoma cell line NCI-H295R

WANG Yu1,2, GAO Yinjie2, REN Weidong1,3*, TONG Anli2*   

  1. 1. Graduate School, Hebei North University, Zhangjiakou 075000;
    2. Department of Endocrinology, Key Laboratory of Endocrinology of National Health Commission,Peking Union Medical College Hospital, CAMS & PUMC, Beijing 100730;
    3. Department of Endocrinology,the First Hospital Affiliated to Hebei North University,Zhangjiakou 075000,China
  • Received:2024-02-20 Revised:2024-03-19 Online:2024-05-05 Published:2024-04-23
  • Contact: *tonganli@hotmail.com;15530396532@126.com

摘要: 目的 研究Na+/Ca2+交换体(NCX)抑制剂SN-6和钙通道阻滞剂(CCB)维拉帕米对钾离子(K+)刺激的肾上腺皮质癌细胞系NCI-H295R(H295R)醛固酮合成酶表达的影响。方法 H295R细胞分为对照组、K+(15 mmol/L)处理组、钙通道阻滞剂维拉帕米(verapamil)(10 μmol/L)处理组、SN-6(10 μmol/L)处理组、K++维拉帕米处理组、K++SN-6处理组、维拉帕米+SN-6处理组和K++维拉帕米+SN-6处理组,用实时荧光定量PCR检测醛固酮合成酶(CYP11B2)的mRNA表达,用FLIPR Calcium6检测细胞内钙离子水平。结果 与对照组相比,K+刺激醛固酮合成酶CYP11B2的mRNA表达(P<0.001);SN-6和维拉帕米均抑制K+刺激的CYP11B2的mRNA表达(P<0.01); 与K++SN-6组相比,K++SN-6+维拉帕米组更能显著抑制CYP11B2的mRNA表达(P<0.001)。SN-6和维拉帕米显著降低K+刺激的细胞内钙离子水平(P<0.0001)。结论 SN-6和维拉帕米均抑制K+诱导的H295R细胞的醛固酮合成酶的表达;SN-6联合维拉帕米处理,抑制作用更显著。

关键词: SN-6, 维拉帕米, NCI-H295R细胞, 细胞内钙离子, CYP11B2

Abstract: Objective To investigate the effect of Na+/Ca2+ exchanger inhibitors SN-6 and calcium channel blocker verapamil on potassium-stimulated expression of aldosterone synthase in adrenocortical carcinoma cell line NCI-H295R(H295R). Methods H295R cells were treated in different groups, including control group, K+ (15 mmol/L) treated group, verapamil (10 μmol/L) group, SN-6 (10 μmol/L) group, combination of K+/verapamil treated group, combination of K+/SN-6 treated group, combination of K+/verapamil and SN-6 treated group. Real-time PCR was used to detect the mRNA expression of aldosterone synthetase (CYP11B2), and FLIPR Calcium 6 was used to detect the intracellular calcium ion level. Results Compared with the control group, K+ stimulated CYP11B2 mRNA expression. Both SN-6 and verapamil decreased K+ induced CYP11B2 mRNA expression(P<0.01). Compared with the K++SN-6 treated group, the K+,SN-6 and verapamil treated group all significantly inhibited CYP11B2 mRNA expression (P<0.001). Both of SN-6 and verapamil significantly reduced the intracellular calcium level stimulated by K+ (P<0.0001). Conclusions Both SN-6 and verapamil inhibit K+-induced expression of aldosterone synthase in adrenocortical carcinoma H295R cells. The inhibitory effect is more significant when treated by the combination of verapamil and SN6.

Key words: SN-6, verapamil, NCI-H295R cell, intracellular calcium, CYP11B2

中图分类号: