Manley S W, Bourke J R, Huxham G J
J Endocrinol. 1987 Mar;112(3):399-405. doi: 10.1677/joe.0.1120399.
Thyrotrophin stimulated release of radioiodine from the organic iodine pool of cultured porcine thyroid cells. The response was well developed within 2-4 h of incubation. Inhibition of the Na+/K+ pump with ouabain or incubation in sodium-free medium inhibited the response to TSH. The magnesium content of cultures was reduced by ouabain, and increasing the magnesium concentration of the medium to 10 mmol/l reversed the inhibition of the TSH response by ouabain. After prolonged incubation (4-6 h), ouabain in magnesium-enriched medium stimulated release of radioiodine. Its effects were not additive with those of TSH. Incubation for 4-6 h in media of reduced sodium concentration (34 mmol/l) also stimulated release. Sodium-free medium alone did not alter basal release rates, but magnesium enrichment of sodium-free medium promoted release after 4 h of incubation. It was concluded that the previously reported inhibition of the TSH response in thyroid tissue by ouabain or sodium-free medium was due to secondary derangements of cellular function rather than to a specific blockade of the secretomotor signal. The data are consistent with the hypothesis that a reduction in the sodium ion electrochemical gradient across the cell membrane mediates the secretomotor effect of TSH.
促甲状腺激素刺激培养的猪甲状腺细胞有机碘库释放放射性碘。在孵育2 - 4小时内反应充分显现。用哇巴因抑制钠钾泵或在无钠培养基中孵育可抑制对促甲状腺激素的反应。哇巴因降低了培养物中的镁含量,将培养基中镁浓度提高到10 mmol/L可逆转哇巴因对促甲状腺激素反应的抑制。长时间孵育(4 - 6小时)后,富含镁的培养基中的哇巴因刺激放射性碘释放。其作用与促甲状腺激素的作用无相加性。在钠浓度降低(34 mmol/L)的培养基中孵育4 - 6小时也刺激释放。单独的无钠培养基不改变基础释放率,但无钠培养基中添加镁在孵育4小时后促进释放。得出的结论是,先前报道的哇巴因或无钠培养基对甲状腺组织中促甲状腺激素反应的抑制是由于细胞功能的继发性紊乱,而非对分泌运动信号的特异性阻断。这些数据与细胞膜上钠离子电化学梯度降低介导促甲状腺激素分泌运动效应的假说一致。