Alexander B S
Department of Pharmacology, Howard University, Washington, D.C.
Magnesium. 1988;7(4):210-8.
Male Wistar rats were injected intraperitoneally for 3 consecutive days with hydrochlorothiazide (HCTZ; 15 mg/kg), chlorothiazide (CTZ; 100 mg/kg), bendroflumethiazide (BFTZ; 1.5 mg/kg), chlorthalidone (CHLOR; 15 mg/kg), methyclothiazide (METH; 1.0 mg/kg) or metolazone (MET; 1.5 mg/kg). Magnesium content was measured in the hypothalamus, medulla oblongata, cerebral cortex, heart, skeletal muscle and serum. Although there was no consistent alteration of Mg in the serum, skeletal muscle and heart, there was a significant effect on hypothalamic and medullary Mg. Compared to a control value of 17.20 +/- 1.24 mEg/kg in the hypothamus there was a decrease by HCTZ (26%; p less than 0.01), CTZ (24%; p less than 0.01) and BFTZ (30%; p less than 0.01). Similarly, there was a decrease by HCTZ (22%; p less than 0.01), CTZ (30%; p less than 0.01) and BFTZ (25%; p less than 0.01) on Mg in medulla. In contrast MET increases Mg in hypothalamus (31%; p less than 0.01) and medulla (26%; p less than 0.01). Furthermore, digoxin infusion (0.051 ml/min) in animals pretreated with HCTZ induced arrhythmias earlier than in animals receiving digoxin alone (30 vs. 60 min; p less than 0.01). The effects of digoxin toxicity in HCTZ-pretreated animals were partially reversed by CNS administration of 50 micrograms of Mg. These findings strongly suggest that thiazide-induced depletion of Mg in the CNS predisposes to digoxin intoxication.
将雄性Wistar大鼠连续3天腹腔注射氢氯噻嗪(HCTZ;15毫克/千克)、氯噻嗪(CTZ;100毫克/千克)、苄氟噻嗪(BFTZ;1.5毫克/千克)、氯噻酮(CHLOR;15毫克/千克)、甲氯噻嗪(METH;1.0毫克/千克)或美托拉宗(MET;1.5毫克/千克)。测量下丘脑、延髓、大脑皮层、心脏、骨骼肌和血清中的镁含量。虽然血清、骨骼肌和心脏中的镁没有一致的变化,但对下丘脑和延髓中的镁有显著影响。与下丘脑对照值17.20±1.24毫当量/千克相比,氢氯噻嗪使其降低(26%;p<0.01),氯噻嗪降低(24%;p<0.01),苄氟噻嗪降低(30%;p<0.01)。同样,氢氯噻嗪使延髓中的镁降低(22%;p<0.01),氯噻嗪降低(30%;p<0.01),苄氟噻嗪降低(25%;p<0.01)。相比之下,美托拉宗使下丘脑(31%;p<0.01)和延髓(26%;p<0.01)中的镁增加。此外,在用氢氯噻嗪预处理的动物中输注地高辛(0.051毫升/分钟)比单独接受地高辛的动物更早诱发心律失常(30分钟对60分钟;p<0.01)。通过中枢神经系统给予50微克镁可部分逆转氢氯噻嗪预处理动物中地高辛毒性的影响。这些发现强烈表明,噻嗪类药物引起的中枢神经系统镁耗竭易导致地高辛中毒。