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参松养心治疗缓慢性心律失常家兔的心率增快的基因表达谱。

Gene expression profile of increased heart rate in shensongyangxin-treated bradycardia rabbits.

机构信息

State Key Laboratory of Translational Cardiovascular Medicine, Fuwai Hospital & Cardiovascular Institute, Chinese Academy of Medical Sciences and Peking Union Medical College, 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.

Integration of Traditional and Western Medical Research Academy of Hebei Province, Shijiazhuang 050035, China.

出版信息

Evid Based Complement Alternat Med. 2014;2014:715937. doi: 10.1155/2014/715937. Epub 2014 Nov 27.

Abstract

Aims. The present study tries to investigate the gene expression profile of bradycardia rabbits' hearts after SSYX (SSYX, a traditional Chinese medicine) treatment. Methods. Eighteen adult rabbits were randomly assigned in three groups: sham, model, and SSYX treatment groups. Heart rate was recorded in rabbits and total RNA was isolated from hearts. Gene expression profiling was conducted and quantitative real-time reverse transcription-polymerase chain reaction (RT-PCR) was performed to confirm the gene expression results. Patch clamp using human induced pluripotent stem cell-derived cardiomyocytes was applied to record the calcium current in the presence of SSYX. Results. The mean RR interval reduced after six weeks due to the injury of the sinoatrial node in the model group. This effect was partially reversed by 4-week SSYX treatment. cDNA microarray demonstrated that genes related with pacemaker current, calcium ion homeostasis, and signaling were altered by SSYX treatment. Results from patch clamp demonstrated that SSYX reduced the calcium current which is consistent with gene expression results. Conclusion. The present study shows mRNA remodeling of bradycardia and demonstrates that SSYX is effective in treating bradycardia by reversing altered gene expression in bradycardia models. Reduced calcium current by SSYX also confirmed the gene expression results.

摘要

目的。本研究试图探讨稳心颗粒(SSYX,一种中药)治疗后心动过缓兔心脏的基因表达谱。方法。将 18 只成年兔随机分为三组:假手术组、模型组和 SSYX 治疗组。记录兔的心率,并从心脏中分离总 RNA。进行基因表达谱分析,并进行实时定量逆转录聚合酶链反应(RT-PCR)以验证基因表达结果。应用人诱导多能干细胞衍生的心肌细胞的膜片钳技术记录 SSYX 存在时的钙电流。结果。六周后,由于窦房结损伤,模型组的平均 RR 间期缩短。SSYX 治疗 4 周后部分逆转了这一作用。cDNA 微阵列显示,与起搏电流、钙离子稳态和信号转导相关的基因受 SSYX 治疗的影响。膜片钳结果表明,SSYX 降低了钙电流,这与基因表达结果一致。结论。本研究显示了心动过缓的 mRNA 重塑,并表明 SSYX 通过逆转心动过缓模型中改变的基因表达有效治疗心动过缓。SSYX 降低钙电流也证实了基因表达结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a19/4265696/02fc6506689d/ECAM2014-715937.001.jpg

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