Kurose H, Sonn Y M, Jafari A, Birge S J, Avioli L V
Calcif Tissue Int. 1985 Dec;37(6):625-9. doi: 10.1007/BF02554920.
The effects of prostaglandin E2 (PGE2) (1 microM) and indomethacin (IN) (20 microM) on 1,25 dihydroxyvitamin D3 production were studied in renal cell suspensions isolated from control, streptozotocin-induced diabetic, and insulin-treated diabetic rats. Renal cortex cells were isolated by enzymatic digestion, and preincubated for 30 min at 37 degrees C with the appropriate additive(s) followed by a 1 h incubation with 8 nM 25-hydroxyvitamin D3 in serum-free medium. Radioactivity incorporated into that fraction of the cell suspension extract co-eluting with synthetic 1,25-dihydroxyvitamin D3 on high pressure liquid chromatography was determined. All animals were raised for 5 weeks on a vitamin D-deficient diet. Isolated kidney cells from vitamin D-deficient rats showed dose-dependent response of 1,25 dihydroxyvitamin D3 production to PGE2. Cells from control animals demonstrated a stimulatory effect of PGE2 (P less than 0.05) and a suppressive effect of IN (P less than 0.01) on 1,25 dihydroxyvitamin D3 production. In contrast, cells from diabetic rat kidneys failed to respond to these agents, alterations which were reversed by insulin treatment. The accumulated data suggest that depressed synthesis of 1,25 dihydroxyvitamin D3 previously observed in the experimental diabetic rat is due, at least in part, to an impaired production and response to PGE2-like prostaglandins.
研究了前列腺素E2(PGE2,1微摩尔)和吲哚美辛(IN,20微摩尔)对从对照大鼠、链脲佐菌素诱导的糖尿病大鼠以及胰岛素治疗的糖尿病大鼠分离出的肾细胞悬液中1,25-二羟维生素D3生成的影响。通过酶消化分离肾皮质细胞,在37℃下与适当的添加剂预孵育30分钟,然后在无血清培养基中与8纳摩尔25-羟维生素D3孵育1小时。测定细胞悬液提取物中与合成的1,25-二羟维生素D3在高压液相色谱上共洗脱的那部分中掺入的放射性。所有动物均在维生素D缺乏的饮食中饲养5周。来自维生素D缺乏大鼠的分离肾细胞显示1,25-二羟维生素D3生成对PGE2呈剂量依赖性反应。来自对照动物的细胞显示PGE2对1,25-二羟维生素D3生成有刺激作用(P<0.05),而IN有抑制作用(P<0.01)。相反,糖尿病大鼠肾脏的细胞对这些药物无反应,胰岛素治疗可逆转这些改变。累积的数据表明,先前在实验性糖尿病大鼠中观察到的1,25-二羟维生素D3合成降低至少部分是由于对PGE2样前列腺素的生成和反应受损。