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糖皮质激素对嗜酸性粒细胞集落生长的影响。

Effects of glucocorticoids on eosinophil colony growth.

作者信息

Butterfield J H, Ackerman S J, Weiler D, Eisenbrey A B, Gleich G J

出版信息

J Allergy Clin Immunol. 1986 Sep;78(3 Pt 1):450-7. doi: 10.1016/0091-6749(86)90032-1.

Abstract

The in vivo and in vitro effects of glucocorticoids on eosinophilopoiesis were examined with soft agar cultures of bone marrow and peripheral blood cells. Prednisone, 10 mg four times daily for three days, administered to normal volunteers, caused a significant drop in circulating eosinophil numbers (p less than 0.005) but did not decrease eosinophil colony numbers in cultures of bone marrow or peripheral blood. A patient with peripheral blood eosinophilia demonstrated a larger percentage decrease in mean eosinophil colony numbers (50%) after prednisone than did any normal volunteer. Incubation of bone marrow cells for 1 hour with either high concentrations of hydrocortisone, up to 3.3 X 10(-4) mol/L, or with postinfusion plasma from volunteers administered intravenous hydrocortisone, plasma levels to 1.6 X 10(-5) mol/L, did not decrease the numbers of eosinophil colonies. At a concentration of 3.3 X 10(-6) mol/L of hydrocortisone, there was a slight but statistically significant stimulation of eosinophil colony numbers. In contrast, incubation with high concentrations of dexamethasone, 3.3 X 10(-4) mol/L or 3.3 X 10(-6) mol/L, significantly reduced eosinophil colony numbers. Prednisone caused a significant reduction in plasma levels of Charcot-Leyden crystal protein but not of eosinophil granule major basic protein. The results indicate that soft agar assay of eosinophil colony growth by blood or bone marrow cells cannot be used to model the in vivo eosinopenic effect of glucocorticoids, levels of dexamethasone in excess of levels commonly administered in clinical practice are required to inhibit eosinophilopoiesis in vitro, and patients with peripheral blood eosinophilia may be more susceptible to the eosinopenic effects of glucocorticoids than normal subjects.

摘要

采用骨髓和外周血细胞软琼脂培养法,研究了糖皮质激素对嗜酸性粒细胞生成的体内和体外效应。给正常志愿者每日4次、每次10mg泼尼松,连用3天,可使循环嗜酸性粒细胞数量显著下降(p<0.005),但并未减少骨髓或外周血培养物中嗜酸性粒细胞集落数量。1例外周血嗜酸性粒细胞增多患者,服用泼尼松后平均嗜酸性粒细胞集落数量下降百分比(50%)比任何正常志愿者都大。用高达3.3×10⁻⁴mol/L的高浓度氢化可的松或静脉注射氢化可的松的志愿者输注后血浆(血浆水平达1.6×10⁻⁵mol/L)孵育骨髓细胞1小时,并未减少嗜酸性粒细胞集落数量。在氢化可的松浓度为3.3×10⁻⁶mol/L时,嗜酸性粒细胞集落数量有轻微但具有统计学意义的增加。相比之下,用3.3×10⁻⁴mol/L或3.3×10⁻⁶mol/L的高浓度地塞米松孵育,可显著减少嗜酸性粒细胞集落数量。泼尼松可使夏科-莱登结晶蛋白的血浆水平显著降低,但对嗜酸性粒细胞颗粒主要碱性蛋白则无此作用。结果表明,血液或骨髓细胞嗜酸性粒细胞集落生长的软琼脂试验不能用于模拟糖皮质激素的体内嗜酸性粒细胞减少效应,体外抑制嗜酸性粒细胞生成需要地塞米松水平超过临床常用水平,外周血嗜酸性粒细胞增多的患者可能比正常受试者对糖皮质激素的嗜酸性粒细胞减少效应更敏感。

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