Shankar R, Crowden S, Sallis J D
Atherosclerosis. 1984 Aug;52(2):191-8. doi: 10.1016/0021-9150(84)90117-5.
This study reports the ability of phosphocitrate and its enzyme-resistant analogue N-sulpho-2-amino tricarballylate to inhibit aortic calcification. Dystrophic calcification of aorta was induced by transplanting fresh aortic segments in Millipore chambers to the peritoneal walls of recipient rats. Daily intraperitoneal injection of the new inhibitors remarkably reduced calcium accumulation by the aortae and prevented the appearance of hydroxyapatite-like crystalline structures. Phosphocitrate was the most effective of the anti-calcifying agents tested, preventing aortic calcification at 1 mumole/day/rat. N-sulpho-2-amino tricarballylate was less effective, reducing aortic calcification by 60% at 10 mumoles/day/rat. The new inhibitors might prove therapeutically useful in man to arrest soft tissue calcification.
本研究报告了磷酸柠檬酸及其酶抗性类似物N-磺基-2-氨基三羧基丙烷抑制主动脉钙化的能力。通过将新鲜主动脉段移植到Millipore腔室中并植入受体大鼠的腹膜壁来诱导主动脉营养不良性钙化。每天腹腔注射新型抑制剂可显著减少主动脉的钙积累,并防止类似羟基磷灰石晶体结构的出现。在所测试的抗钙化剂中,磷酸柠檬酸最为有效,以1微摩尔/天/大鼠的剂量可预防主动脉钙化。N-磺基-2-氨基三羧基丙烷效果稍差,以10微摩尔/天/大鼠的剂量可使主动脉钙化减少60%。新型抑制剂可能在治疗人类软组织钙化方面具有治疗作用。