Valeeva I Kh, Ziganshina L E, Burnashova Z A, Ziganshin A U
Kazan State Medical University, Butlerova Str., 49, Kazan, Tatarstan, 420012 Russia.
Eksp Klin Farmakol. 2003 Jan-Feb;66(1):46-9.
The parameters of mineral metabolism, a lipid peroxidation (LPO) process, and the efficacy of antioxidant enzyme preparations were studied in rats with an osteoporosis model induced by the administration of prednisolone in a daily dose of 100 mg/kg (i.p.) over 3 days, which is analogous to a pulsed therapy schedule in clinics. The treatment with glucocorticosteroid enhanced the excretion of hydroxyproline and inorganic phosphates with urine, increased the LPO rate and antioxidant activity of the blood serum, and decreases the level of ceruloplasmin and the catalase activity in the blood. A prophylactic treatment with dimephosphon (208 mg/kg, p.o.) and xydiphone (45 mg/kg, p.o.) prevents from the prednisolone-induced LPO activation. Dimephosphon, in contrast to xydiphone, also prevents from a prednisolone-induced increase in the excretion of hydroxyproline and inorganic phosphates with urine.
在通过每天腹腔注射100mg/kg泼尼松龙,连续注射3天诱导建立骨质疏松模型的大鼠中,研究了矿物质代谢参数、脂质过氧化(LPO)过程以及抗氧化酶制剂的功效,这类似于临床中的脉冲治疗方案。糖皮质激素治疗增加了尿中羟脯氨酸和无机磷酸盐的排泄,提高了血清脂质过氧化速率和抗氧化活性,并降低了血清铜蓝蛋白水平和血液中的过氧化氢酶活性。用二膦酸盐(208mg/kg,口服)和羟乙膦酸钠(45mg/kg,口服)进行预防性治疗可防止泼尼松龙诱导的脂质过氧化激活。与羟乙膦酸钠不同,二膦酸盐还可防止泼尼松龙诱导的尿中羟脯氨酸和无机磷酸盐排泄增加。