Katsumata Kyoko, Kusano Kenichiro, Hirata Michinori, Tsunemi Kunihiko, Nagano Nobuo, Burke Steven K, Fukushima Naoshi
Fuji Gotemba Research Laboratory, Chugai Pharmaceutical Co., Ltd., Shizuoka, Japan.
Kidney Int. 2003 Aug;64(2):441-50. doi: 10.1046/j.1523-1755.2003.00126.x.
Hyperphosphatemia is associated with severe complications, including ectopic calcification of soft tissues, secondary hyperparathyroidism, and renal osteodystrophy (ROD). Sevelamer hydrochloride is a nonabsorbed calcium- and metal-free phosphate binder that lowers serum phosphorus levels in hemodialysis patients. This study examined the efficacy of sevelamer in preventing ectopic calcification of soft tissues and ROD in adenine-induced renal failure rats.
Male, 12-week-old Wistar-Jcl rats were freely fed an adenine diet (0.75 g adenine in 100 g normal diet) for four weeks. After three weeks of the adenine diet, when serum phosphorus levels had significantly increased, the rats were freely fed a normal diet that contained 1% or 2% of sevelamer for another five weeks. Time course changes of serum levels of phosphorus, calcium, and parathyroid hormone (PTH) were measured. At the end of the study, calcium and phosphorus levels in the heart and aorta were measured, and the calcification of kidney, heart, aorta, and stomach were histopathologically examined. The severity of ROD was evaluated by a histopathologic and morphometric analysis of the femurs.
Compared with the adenine controls (N = 10), the sevelamer-treated (1%, N = 6; and 2%, N = 10) groups of adenine-induced renal failure rats had reduced serum phosphorus, serum calcium x phosphorus product, and serum PTH levels. Moreover, in the treatment groups, sevelamer suppressed calcification of the aorta media, and also the osteoid volume, fibrosis volume, and porosity ratio of femurs.
These results suggest that sevelamer treatment might contribute to the suppression of ectopic calcification and ROD.
高磷血症与严重并发症相关,包括软组织异位钙化、继发性甲状旁腺功能亢进和肾性骨营养不良(ROD)。盐酸司维拉姆是一种不被吸收的无钙和无金属的磷结合剂,可降低血液透析患者的血清磷水平。本研究考察了司维拉姆在预防腺嘌呤诱导的肾衰竭大鼠软组织异位钙化和ROD方面的疗效。
12周龄雄性Wistar-Jcl大鼠自由进食含腺嘌呤的饮食(100 g正常饮食中含0.75 g腺嘌呤),持续4周。在给予腺嘌呤饮食3周后,当血清磷水平显著升高时,大鼠自由进食含1%或2%司维拉姆的正常饮食,持续5周。测定血清磷、钙和甲状旁腺激素(PTH)水平的时间进程变化。在研究结束时,测量心脏和主动脉中的钙和磷水平,并对肾脏、心脏、主动脉和胃的钙化进行组织病理学检查。通过对股骨的组织病理学和形态计量学分析评估ROD的严重程度。
与腺嘌呤对照组(N = 10)相比,司维拉姆治疗组(1%,N = 6;2%,N = 10)的腺嘌呤诱导的肾衰竭大鼠血清磷、血清钙×磷乘积和血清PTH水平降低。此外,在治疗组中,司维拉姆抑制了主动脉中膜的钙化,以及股骨的类骨质体积、纤维化体积和孔隙率。
这些结果表明,司维拉姆治疗可能有助于抑制异位钙化和ROD。