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活性维生素D制剂对大鼠甲状旁腺激素分泌的抑制作用。

Inhibitory effects of active vitamin D preparations on PTH secretion in rats.

作者信息

Kugai N, Koide Y, Kimura S, Yamashita K

出版信息

Endocrinol Jpn. 1984 Apr;31(2):151-8. doi: 10.1507/endocrj1954.31.151.

Abstract

To study the effects of various vitamin D preparations on PTH secretion, serum calcium and urinary excretion of cAMP were monitored in conscious perfused rats, and the influences of a bolus iv injection of the preparations on these parameters were examined. Three hours after the administration of 0.25 microgram/kg (0.6 nmol/kg) of 1 alpha, 24(R)-dihydroxycholecalciferol [1 alpha, 24(OH)2D3], the urinary excretion of cAMP decreased to a level compatible with that of parathyroidectomized (PTX) rats (50% of initial value; p less than 0.05) with no change in the concentration of serum calcium (total and ionized). In PTX rats supplemented with bovine PTH (1 U/h), the vitamin D preparation showed no significant effects either on the urinary excretion of cAMP or on serum calcium. These effects were rather specific for active vitamin D preparations, i.e. 1 alpha, 25(OH)2D3 (0.25 micrograms/kg) and 1 alpha OHD3 (1.25-6.25 micrograms/kg). However, 24,25(OH)2D3 (up to 25 micrograms/kg) had no significant effect on these parameters. These results suggest that, in rats, active vitamin D preparations specifically inhibit PTH secretion without causing a significant increase in the serum calcium concentration, reflecting a direct feedback mechanism between active vitamin D metabolite and the parathyroid glands.

摘要

为研究各种维生素D制剂对甲状旁腺激素(PTH)分泌的影响,在清醒的灌注大鼠中监测血清钙和环磷酸腺苷(cAMP)的尿排泄情况,并检测一次性静脉注射这些制剂对这些参数的影响。给予0.25微克/千克(0.6纳摩尔/千克)的1α,24(R)-二羟基胆钙化醇[1α,24(OH)2D3]三小时后,cAMP的尿排泄量降至与甲状旁腺切除(PTX)大鼠相当的水平(初始值的50%;p<0.05),而血清钙浓度(总钙和离子钙)无变化。在补充牛PTH(1单位/小时)的PTX大鼠中,该维生素D制剂对cAMP的尿排泄或血清钙均无显著影响。这些作用对活性维生素D制剂具有相当的特异性,即1α,25(OH)2D3(0.25微克/千克)和1α-羟维生素D3(1.25 - 6.25微克/千克)。然而,24,25(OH)2D3(高达25微克/千克)对这些参数无显著影响。这些结果表明,在大鼠中,活性维生素D制剂可特异性抑制PTH分泌,而不会导致血清钙浓度显著升高,这反映了活性维生素D代谢产物与甲状旁腺之间的直接反馈机制。

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