Kingma J G, Roy P E
Research Center, Quebec Heart Institute, Canada.
J Exp Pathol (Oxford). 1990 Apr;71(2):145-53.
The present study was undertaken to examine changes in vascular ultrastructure of rats subjected to hypervitaminosis D with or without treatment with ethane-I-hydroxy-I, I-diphosphonate (EHDP). Five groups of rats were studied. Untreated rats were given 0.9% NaCl i.p. Sham-treated rats were given vehicle (corn oil). Treated rats were given ergocalciferol (75,000 IU i.p.) dissolved in vehicle with or without EHDP (5 mM/100 g body-weight i.p.). Rats which had been given ergocalciferol without EHDP developed hypercalcemia and demonstrated significant arterial calcinosis. A similar degree of calcinosis was not observed in rats given ergocalciferol with EHDP. EHDP appeared to inhibit arterial calcinosis; however, it did not affect plasma calcium levels. This suggests that EHDP might delay calcium influx into the cell and thereby prevent calcium overload. Our findings support the suggestion that EHDP therapy can be an effective treatment for the inhibition of dystrophic arterial calcinosis.
本研究旨在检测给予或未给予乙烷-1-羟基-1,1-二膦酸盐(EHDP)治疗的维生素D过多症大鼠的血管超微结构变化。研究了五组大鼠。未治疗的大鼠腹腔注射0.9%氯化钠。假治疗的大鼠给予赋形剂(玉米油)。治疗的大鼠给予溶解于赋形剂中的麦角钙化醇(75,000 IU腹腔注射),同时给予或不给予EHDP(5 mM/100 g体重腹腔注射)。给予麦角钙化醇但未给予EHDP的大鼠出现高钙血症,并表现出明显的动脉钙化。给予麦角钙化醇并同时给予EHDP的大鼠未观察到类似程度的钙化。EHDP似乎能抑制动脉钙化;然而,它并不影响血浆钙水平。这表明EHDP可能会延迟钙流入细胞,从而防止钙超载。我们的研究结果支持EHDP治疗可作为抑制营养不良性动脉钙化的有效治疗方法这一观点。