Effect of ligustrazine on Ca2+ uptake by inside-out red cell membrane vesicles from renal hypertensive rats.

H Luo, Y Y Wen, M Q Chen
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Abstract

The effect of ligustrazine (Lig) on blood pressure and Ca2+ uptake by inside-out red cell membrane vesicles (IOV) was investigated in renal hypertensive rats (RHR). After oral administration of Lig (30 mg/kg body weight/day) for 10 days, the blood pressure of RHR was not significantly changed (before vs after experiment: 147.50 +/- 2.50 vs 150.00 +/- 13.42 mmHg). The active Ca2+ uptake rate of IOVs from RHR was 5.03 +/- 1.15 nmol/ng IOV protein/min, and this was lower than that of IOVs from normotensive Wistar rats (8.95 +/- 1.08 nmol/ng IOV protein/min, P less than 0.01). In RHR, no change in IOV Ca2+ uptake capacity was observed after administration of Lig in vivo. Experiments in vitro showed that Lig markedly reduced Ca2+ uptake by IOVs from both RHR and control rats. The results indicate that the active Ca2+ transport capacity of red cell membranes is decreased in RHR and not significantly affected by oral administration of Lig; this drug, however, exerts an inhibitory effect on the transport process in vitro.

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川芎嗪对肾性高血压大鼠内外红细胞膜囊泡Ca2+摄取的影响。
研究了川芎嗪(Lig)对肾性高血压大鼠(RHR)血压和内外向红细胞膜囊泡(IOV) Ca2+摄取的影响。口服Lig (30 mg/kg体重/天)10天后,RHR血压无明显变化(实验前vs实验后:147.50 +/- 2.50 vs 150.00 +/- 13.42 mmHg)。RHR细胞对Ca2+的活性吸收速率为5.03 +/- 1.15 nmol/ng IOV蛋白/min,低于正常血压Wistar大鼠(8.95 +/- 1.08 nmol/ng IOV蛋白/min, P < 0.01)。在RHR中,体内给药Lig后,未观察到IOV Ca2+摄取能力的变化。体外实验表明,Lig显著降低了RHR和对照大鼠IOVs对Ca2+的摄取。结果表明,口服Lig对RHR红细胞膜活性Ca2+转运能力的影响不显著;然而,该药物在体外对转运过程有抑制作用。
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