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甲状旁腺激素对培养的大鼠成骨细胞膜电位的早期影响:环磷酸腺苷(cAMP)和钙离子(Ca2+)的作用

Early effects of parathyroid hormone on membrane potential of rat osteoblasts in culture: role of cAMP and Ca2+.

作者信息

Fritsch J, Edelman A, Balsan S

机构信息

Laboratoire des Tissus Calcifiés, CNRS UA.583, Paris, France.

出版信息

J Bone Miner Res. 1988 Oct;3(5):547-54. doi: 10.1002/jbmr.5650030511.

DOI:10.1002/jbmr.5650030511
PMID:2461641
Abstract

Microelectrodes were used to investigate the possible involvement of cAMP and Ca2+ ions in the parathyroid hormone's, bPTH(1-34), effect on the membrane potential of rat osteoblasts in primary culture. Parathyroid hormone (10(-7) M) depolarized cell membrane by 25.0 +/- 6.1 mV (mean +/- standard deviation, SD; n = 17). Blocking Ca2+ influx with the Ca channel blocker cobalt revealed two phases in the hormone effect: a rapid and slight membrane hyperpolarization followed by sustained depolarization. In addition, cobalt significantly (p less than 0.01) decreased the magnitude of the PTH depolarizing action. The addition of dibutyryl-cAMP (10(-3) M) to the perfusion solution also resulted in a biphasic effect. At a lower concentration (10(-4) M), dibutyryl-cAMP produced only membrane hyperpolarization, suggesting a cAMP dose dependence of the opposite membrane potential changes. Forskolin (10(-5) M) and the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX) (10(-4) M) mimicked the depolarizing effect of PTH. IBMX at a low concentration (5 x 10(-6) M) potentiated the depolarizing effect of PTH. Increases in [Ca2+]i using Ca2+ ionophore A23187 and intracellular injection of CaCl2 or inositol trisphosphate decreased the PTH depolarizing action, whereas intracellular injection of EGTA enhanced this effect. These results indicate that PTH evokes a biphasic change in rat osteoblast membrane potential that seems to be mediated by an increase in cAMP and modulated by intracellular calcium.

摘要

使用微电极研究环磷酸腺苷(cAMP)和钙离子(Ca2+)是否参与甲状旁腺激素bPTH(1-34)对原代培养大鼠成骨细胞膜电位的影响。甲状旁腺激素(10(-7) M)使细胞膜去极化25.0±6.1 mV(平均值±标准差,SD;n = 17)。用钙通道阻滞剂钴阻断Ca2+内流后,激素效应呈现两个阶段:先是快速且轻微的膜超极化,随后是持续的去极化。此外,钴显著(p<0.01)降低了甲状旁腺激素去极化作用的幅度。向灌注液中添加二丁酰环磷腺苷(10(-3) M)也产生了双相效应。在较低浓度(10(-4) M)时,二丁酰环磷腺苷仅产生膜超极化,表明膜电位变化的相反方向存在cAMP剂量依赖性。福斯高林(10(-5) M)和磷酸二酯酶抑制剂异丁基甲基黄嘌呤(IBMX)(10(-4) M)模拟了甲状旁腺激素的去极化作用。低浓度(5×10(-6) M)的IBMX增强了甲状旁腺激素的去极化作用。使用钙离子载体A23187增加细胞内钙离子浓度([Ca2+]i)以及细胞内注射氯化钙或肌醇三磷酸可降低甲状旁腺激素的去极化作用,而细胞内注射乙二醇双乙胺醚四乙酸(EGTA)则增强了这种作用。这些结果表明,甲状旁腺激素引起大鼠成骨细胞膜电位的双相变化,这似乎是由cAMP增加介导,并受细胞内钙调节。

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