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老年髋部骨折患者单核白细胞对糖皮质激素的敏感性,这些患者对地塞米松抑制血浆皮质醇有抵抗。

Sensitivity of mononuclear leucocytes to glucocorticoids in elderly hip-fracture patients resistant to suppression of plasma cortisol by dexamethasone.

作者信息

van Rijen E A, Harvey R A, Barton R N, Rose J G, Horan M A

机构信息

North Western Injury Research Centre, Hope Hospital, Salford, UK.

出版信息

Eur J Endocrinol. 1998 Jun;138(6):659-66. doi: 10.1530/eje.0.1380659.

Abstract

OBJECTIVE

Elderly women with proximal femur fracture show a prolonged increase in plasma cortisol, which could have undesirable catabolic effects. Suppression of cortisol by dexamethasone is impaired, suggesting resistance to glucocorticoid effects at feedback inhibitory sites. We therefore wished to find out whether peripheral glucocorticoid sensitivity is normal.

DESIGN

Peripheral blood mononuclear leucocytes were used as a model tissue. Blood samples were taken from elderly women about 2 weeks after hip fracture and from elderly control women. Each patient was then given 1 mg dexamethasone at 2300 h followed by further sampling at 0800 and 1600 h the next day.

METHODS

Glucocorticoid-receptor binding parameters were measured by incubating whole cells with [3H]dexamethasone for 2 h at 37 degrees C. Inhibition of cell proliferation by dexamethasone was assessed by addition of [3H]thymidine to cells cultured for 65 h with concanavalin A. Cortisol and dexamethasone concentrations were measured in the dexamethasone suppression test.

RESULTS

As expected, the hip-fracture patients had raised morning cortisol concentrations and impaired suppression by dexamethasone. The cells of the patients had similar numbers of glucocorticoid receptors to those of the control subjects but higher values for Kd (i.e. a lower binding affinity). The cells of the patients incorporated less [3H]thymidine than the control cells in the absence of dexamethasone. The percentage inhibition by a saturating concentration of dexamethasone was unchanged but the concentration giving half-maximal inhibition was decreased (sensitivity was increased) at the higher of the two concanavalin A concentrations used.

CONCLUSIONS

These experiments in mononuclear leucocytes give no evidence of peripheral resistance to glucocorticoids in hip-fracture patients with impaired suppression of cortisol by dexamethasone.

摘要

目的

股骨近端骨折的老年女性血浆皮质醇水平会持续升高,这可能产生不良的分解代谢作用。地塞米松对皮质醇的抑制作用受损,提示在反馈抑制位点存在糖皮质激素效应抵抗。因此,我们希望了解外周糖皮质激素敏感性是否正常。

设计

以外周血单核白细胞作为模型组织。在老年女性髋部骨折约2周后及老年对照女性中采集血样。然后于23:00给每位患者服用1mg地塞米松,次日08:00和16:00进一步采样。

方法

通过在37℃下将全细胞与[3H]地塞米松孵育2小时来测量糖皮质激素受体结合参数。通过向用伴刀豆球蛋白A培养65小时的细胞中添加[3H]胸腺嘧啶核苷来评估地塞米松对细胞增殖的抑制作用。在地塞米松抑制试验中测量皮质醇和地塞米松浓度。

结果

正如预期的那样,髋部骨折患者早晨皮质醇浓度升高,且对地塞米松的抑制作用受损。患者的细胞糖皮质激素受体数量与对照受试者相似,但解离常数(Kd)值更高(即结合亲和力更低)。在没有地塞米松的情况下,患者的细胞掺入的[3H]胸腺嘧啶核苷比对照细胞少。在使用的两种伴刀豆球蛋白A浓度中较高的浓度下,饱和浓度地塞米松的抑制百分比没有变化,但产生半数最大抑制的浓度降低(敏感性增加)。

结论

这些在单核白细胞中的实验没有证据表明地塞米松抑制皮质醇受损的髋部骨折患者存在外周糖皮质激素抵抗。

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