Törnquist K, Lamberg-Allardt C
Acta Endocrinol (Copenh). 1987 Jan;114(1):55-9. doi: 10.1530/acta.0.1140055.
The effect of 1,25-dihydroxy-vitamin D3 (1,25-(OH)2-D3) on the TRH induced TSH release was investigated. Wistar rats were injected with 1,25-(OH)2-D3 (0.05 microgram/kg/day) for three days, and TRH was injected iv on the third day. Blood was drawn every 10 min during the following 40 min, and TSH was determined. The TSH release was significantly higher in rats treated with 1,25-(OH)2-D3 than in controls. The rats treated with 1,25-(OH)2-D3 were hypercalcaemic and thus, in order to find out if the effect was mediated through hypercalcaemia rats treated as above, were infused with EDTA (30 mg/kg/100 min) starting 60 min before the TRH test. This treatment made the rats normocalcaemic, and the significant increase in the TSH release was still seen in the 1,25-(OH)2-D3 treated rats as compared to controls. The results thus indicate that 1,25-(OH)2-D3 enhances the TRH induced TSH release and that the effect is not mediated through an increase in the serum calcium concentration at the time of the TRH test. In order to find out if the effect could be mediated by changes in intracellular calcium the rats were treated with the calcium antagonist verapamil (25 mg/kg/day) and the adrenergic blocker propranolol (5 mg/kg/day) alone or together with 1,25-(OH)2-D3. In rats treated with verapamil or propranolol alone or 1,25-(OH)2-D3 + propranolol, no effect was observed on the TRH induced TSH release. Verapamil + 1,25-(OH)2-D3 significantly increased the TSH release as compared to both controls and rats treated with 1,25-(OH)2-D3 alone.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了1,25 - 二羟基维生素D3(1,25-(OH)2-D3)对促甲状腺激素释放激素(TRH)诱导的促甲状腺激素(TSH)释放的影响。给Wistar大鼠连续三天注射1,25-(OH)2-D3(0.05微克/千克/天),并在第三天静脉注射TRH。在随后的40分钟内每隔10分钟取血一次,测定TSH。用1,25-(OH)2-D3处理的大鼠TSH释放明显高于对照组。用1,25-(OH)2-D3处理的大鼠出现高钙血症,因此,为了确定该作用是否通过高钙血症介导,对上述处理的大鼠在TRH试验前60分钟开始输注乙二胺四乙酸(EDTA,30毫克/千克/100分钟)。这种处理使大鼠血钙正常,与对照组相比,用1,25-(OH)2-D3处理的大鼠TSH释放仍显著增加。因此,结果表明1,25-(OH)2-D3增强了TRH诱导的TSH释放,且该作用在TRH试验时并非通过血清钙浓度升高介导。为了确定该作用是否可由细胞内钙的变化介导,大鼠单独或与1,25-(OH)2-D3一起用钙拮抗剂维拉帕米(25毫克/千克/天)和肾上腺素能阻滞剂普萘洛尔(5毫克/千克/天)处理。单独用维拉帕米或普萘洛尔或1,25-(OH)2-D3 + 普萘洛尔处理的大鼠,对TRH诱导的TSH释放未观察到影响。与对照组和单独用1,25-(OH)2-D3处理的大鼠相比,维拉帕米 + 1,25-(OH)2-D3显著增加了TSH释放。(摘要截选至250字)