Brown A J, Zhong M, Finch J, Ritter C, Slatopolsky E
Department of Medicine, Washington University, St. Louis, Missouri 63110.
Endocrinology. 1995 Apr;136(4):1419-25. doi: 10.1210/endo.136.4.7895652.
Expression of the vitamin D receptor (VDR) in the parathyroid glands is decreased in secondary hyperparathyroidism associated with chronic renal failure by undefined mechanisms. In the present study, we examined the effects of hyperparathyroidism and dietary calcium and 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] on the expression of VDR in rat parathyroid glands. Vitamin D-deficient rats were maintained on diets containing 0.02% Ca (-D, LCD), 0.4% Ca (-D, NCD), or 2.0% Ca (-D, HCD) for 6 weeks. Serum ionized Ca (ICa) in the rats on the three diets ranged from 2.5-5.2 mg/dl. Serum PTH ranged from 22-590 pg/ml and correlated inversely with ICa (r = -0.835; P < 0.001). Rats with the highest ICa had normal PTH values, suggesting that vitamin D deficiency per se does not lead to hyperparathyroidism. VDR messenger RNA (mRNA) levels in the parathyroid glands correlated positively with ICa (r = 0.845; P < 0.001) and negatively with PTH (r = -0.716; P < 0.001). VDR mRNA levels in the rats fed the -D, HCD were 6 times higher than those receiving -D, LCD and the same as those in rats fed a normal (Purina) diet. Thus, prevention of hyperparathyroidism with high dietary calcium prevented the drop in VDR expression. Treatment of the rats on all three diets with 0, 25, or 100 ng 1,25-(OH)2D3, ip, 48 and 12 h before death dose dependently increased ICa and decreased PTH, as expected, and also increased parathyroid gland VDR mRNA. This coordinate regulation of VDR mRNA by calcium and 1,25-(OH)2D3 was also observed in the kidney, but intestinal VDR mRNA was not stimulated by dietary calcium or 1,25-(OH)2D3. Analysis of covariance for parathyroid gland VDR mRNA and ICa for the three doses of 1,25-(OH)2D3 revealed no significant independent effect of 1,25-(OH)2D3 on VDR mRNA, suggesting that the up-regulation of VDR expression by 1,25-(OH)2D3 in the parathyroid glands may be mediated primarily by increasing serum calcium.
在与慢性肾衰竭相关的继发性甲状旁腺功能亢进中,甲状旁腺中维生素D受体(VDR)的表达因不明机制而降低。在本研究中,我们检测了甲状旁腺功能亢进、饮食钙和1,25 - 二羟基维生素D3 [1,25-(OH)2D3]对大鼠甲状旁腺中VDR表达的影响。将维生素D缺乏的大鼠分别维持在含0.02%钙(-D,低钙饮食)、0.4%钙(-D,正常钙饮食)或2.0%钙(-D,高钙饮食)的饲料中6周。三种饮食组大鼠的血清离子钙(ICa)范围为2.5 - 5.2mg/dl。血清甲状旁腺激素(PTH)范围为22 - 590pg/ml,且与ICa呈负相关(r = -0.835;P < 0.001)。ICa最高的大鼠PTH值正常,这表明维生素D缺乏本身并不导致甲状旁腺功能亢进。甲状旁腺中VDR信使核糖核酸(mRNA)水平与ICa呈正相关(r = 0.845;P < 0.001),与PTH呈负相关(r = -0.716;P < 0.001)。喂食-D,高钙饮食的大鼠VDR mRNA水平比喂食-D,低钙饮食的大鼠高6倍,与喂食正常(普瑞纳)饲料的大鼠相同。因此,高钙饮食预防甲状旁腺功能亢进可防止VDR表达下降。在处死前48小时和12小时,对所有三种饮食组的大鼠腹腔注射0、25或100ng 1,25-(OH)2D3,如预期的那样,剂量依赖性地增加了ICa并降低了PTH,同时也增加了甲状旁腺VDR mRNA。在肾脏中也观察到钙和1,25-(OH)2D3对VDR mRNA的这种协同调节,但饮食钙或1,25-(OH)2D3未刺激肠道VDR mRNA。对三种剂量的1,25-(OH)2D3的甲状旁腺VDR mRNA和ICa进行协方差分析,结果显示1,25-(OH)2D3对VDR mRNA无显著独立影响,这表明1,25-(OH)2D3在甲状旁腺中对VDR表达的上调可能主要是通过增加血清钙来介导的。