Dupuis Y, Tardivel S, Lacour B, Fournier P
Métabolisme Minéral des Mammifères (E.P.H.E.), Physiologie, Faculté de Pharmacie, Châtenay-Malabry, Paris, France.
Miner Electrolyte Metab. 1992;18(1):61-8.
Calcium transport in the ileal-ligated loop was studied in the adult rat in the presence of either phosphate alone or phosphate-binding compounds, namely either hydroxylated or aminated substances. Sorbitol or creatine (50 mM) added to a 10-mM CaCl2 solution, which was instilled into ileal loop, markedly enhanced calcium transport, as determined by 45Ca radioactivity appearing in plasma and from 45Ca radioactivity disappearing from the loop. The presence of both compounds maintained Ca soluble in an instilled solution at a constant concentration, whereas with a control solution the Ca concentration progressively decreased towards zero after an incubation period of 60 min. Phosphate, which was either simultaneously added with sorbitol or creatine or which was present as sorbitol or creatine phosphate, led to an equally marked decrease in calcium transport. Calcium transfer was even more reduced when phosphate alone was present with calcium in the ileal loop, in the absence of sorbitol. Similar to the above phosphate-binding compounds, adenosine and its constitutive component, ribose, increased calcium transfer, whereas adenine, the other constitutive component of adenosine, was ineffective. Guanosine was twice more active than adenosine in stimulating ileal calcium transport. Interestingly, the structure of guanosine allows the binding of two phosphates, with one binding site being on the ribose and the other on the guanine base moiety. Thus guanosine is capable of binding a greater amount of phosphate than the two other aminated compounds examined, namely adenosine and alanine, when transphosphorylation from ATP is studied with intestinal microvilli preparations.(ABSTRACT TRUNCATED AT 250 WORDS)
在成年大鼠中,研究了在单独存在磷酸盐或磷酸盐结合化合物(即羟基化或胺化物质)的情况下,回肠结扎肠袢中的钙转运。将山梨醇或肌酸(50 mM)添加到注入回肠肠袢的10 mM氯化钙溶液中,通过血浆中出现的45Ca放射性以及肠袢中45Ca放射性的消失来确定,显著增强了钙转运。两种化合物的存在使注入溶液中的钙保持在恒定浓度,而对照溶液在孵育60分钟后钙浓度逐渐降至零。与山梨醇或肌酸同时添加的磷酸盐,或以山梨醇磷酸或肌酸磷酸形式存在的磷酸盐,导致钙转运同样显著降低。当回肠肠袢中仅存在磷酸盐与钙,而没有山梨醇时,钙转运甚至更低。与上述磷酸盐结合化合物类似,腺苷及其组成成分核糖增加了钙转运,而腺苷的另一种组成成分腺嘌呤则无效。鸟苷在刺激回肠钙转运方面的活性是腺苷的两倍。有趣的是,鸟苷的结构允许结合两个磷酸盐,一个结合位点在核糖上,另一个在鸟嘌呤碱基部分。因此,在用肠微绒毛制剂研究从ATP的转磷酸作用时,鸟苷能够比所研究的另外两种胺化化合物(即腺苷和丙氨酸)结合更多的磷酸盐。(摘要截短于250字)