但晴, 赵颖, 吴志娟, 朱超, 刘丽, 徐斌, 刘昱圻, 陈琪, 李泱. 大蒜素对自发性高血压大鼠心肌 Ito重构的影响J. 药学学报, 2015,50(1): 39-44.
引用本文: 但晴, 赵颖, 吴志娟, 朱超, 刘丽, 徐斌, 刘昱圻, 陈琪, 李泱. 大蒜素对自发性高血压大鼠心肌 Ito重构的影响J. 药学学报, 2015,50(1): 39-44.
DAN Qing, ZHAO Ying, WU Zhi-juan, ZHU Chao, LIU Li, XU Bin, LIU Yu-qi, CHEN Qi, LI Yang. Effect of allitridum on remodeling of the transient outward potassium current of ventricular myocytes of spontaneously hypertensive ratsJ. Acta Pharmaceutica Sinica, 2015,50(1): 39-44.
Citation: DAN Qing, ZHAO Ying, WU Zhi-juan, ZHU Chao, LIU Li, XU Bin, LIU Yu-qi, CHEN Qi, LI Yang. Effect of allitridum on remodeling of the transient outward potassium current of ventricular myocytes of spontaneously hypertensive ratsJ. Acta Pharmaceutica Sinica, 2015,50(1): 39-44.

大蒜素对自发性高血压大鼠心肌 Ito重构的影响

Effect of allitridum on remodeling of the transient outward potassium current of ventricular myocytes of spontaneously hypertensive rats

  • 摘要: 本研究旨在探讨大蒜素 (All) 对自发性高血压大鼠 (SHR) 肥厚心肌细胞瞬时外向钾电流 (Ito) 的作用。应用All注射液 (7.5和15.0 mg·kg-1) 对SHR腹腔注射8周。双酶法分离各组大鼠心室肌细胞, 利用膜片钳技术观察All对心肌肥厚指标及 Ito的作用。结果显示, All对SHR肥厚心肌有明显的逆转作用, 使心室肌细胞的膜电容显著降低。高、低剂量组均使SHR重构的 Ito电流得以恢复, 在 +50 mV电压下, 分别使 Ito从18.23 ± 3.64升至36.47 ± 5.42 pA/pF (P < 0.01) 和25.17 ± 2.86 pA/pF (P < 0.01), 与WKY (Wistar Kyoto) 大鼠对照组接近。此效应与All减少通道稳态和关闭态失活、加速失活后恢复有关。本文发现All可降低SHR肥厚心肌心室肌细胞 Ito的重构。

     

    Abstract: We aimed to study the effect of allitridum (All) onthe transient outward potassium current (Ito) of ventricular myocytes of spontaneously hypertensive rats (SHR). Totally 30 male SHRs were randomly divided into three groups: low-dose All group (7.5 mg·kg-1), high-dose All group (15.0 mg·kg-1) and normal saline group. The other 10 sex and age matched Wistar-kyoto rats (WKY) were also taken as control group (WKY group). All animals received ip administration for 8 weeks. The dual enzymatic method was used to separate single ventricular myocyte from animals. Patch-clamp technique was used to record Ito and analyze the effect of All on the current. It was shown that the left ventricular hypertrophy of SHR was reversed significantly by All. Furthermore, the density of Ito was recovered in both high and low dose All groups. The peak current densities of Ito were enhanced from 18.23 ± 3.64 to 25.17 ± 2.86 pA/pF (P < 0.01) and 36.47 ± 5.42 pA/pF (P < 0.01) at +50 mV by All 7.5 mg·kg-1 and 15.0 mg·kg-1, respectively, which was not significantly different with WKY group. The effect was associated with positive shift of the steady-state, close-state inactivation, and shortened recovery from inactivation of Ito. It is concluded that All decreases theremodeling of Ito of ventricular hypertrophic myocytes of SHR.

     

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