西北药学杂志
西北藥學雜誌
서북약학잡지
2014年
3期
261-264
,共4页
汪耀%王养正%Changqing Lee%肖湘华%杨华%刘先宁%安娜%朱娟莉%朱秀萍
汪耀%王養正%Changqing Lee%肖湘華%楊華%劉先寧%安娜%硃娟莉%硃秀萍
왕요%왕양정%Changqing Lee%초상화%양화%류선저%안나%주연리%주수평
17α-己酸羟孕酮%地塞米松%糖皮质激素抵抗%外周血单个核细胞
17α-己痠羥孕酮%地塞米鬆%糖皮質激素牴抗%外週血單箇覈細胞
17α-기산간잉동%지새미송%당피질격소저항%외주혈단개핵세포
17α-hydroxyprogesterone caproate%dexamethasone%glucocorticoid resistant%peripheral blood mononuclear cells
目的:探讨17α-己酸羟孕酮对外周血单个核细胞抵抗地塞米松的逆转作用。方法分离健康男性外周血单个核细胞,利用白介素2(IL-2)和IL-4以及植物血凝素刺激外周血单个核细胞,建立地塞米松抵抗的炎症细胞实验模型;单用地塞米松和地塞米松与17α-己酸羟孕酮联合应用于该模型,酶联免疫吸附法检测细胞的IL-2值的改变。结果地塞米松对植物血凝素诱导人外周血产生的IL-2呈现显著的浓度依赖性的抑制作用;用IL-2(13 ng · mL -1)和IL-4(6.5 ng · mL -1)刺激,再用植物血凝素(15μg · mL -1)刺激外周血单个核细胞可以作为评价地塞米松抵抗的细胞实验模型;在17α-己酸羟孕酮的浓度为10-11,10-10,10-7和10-5 mol · L -1时,可显著提高地塞米松对人外周血产生的IL-2的抑制率,降低地塞米松的IC50(半数抑制浓度)值至少100倍以上。结论17α-己酸羟孕酮逆转外周血单个核细胞对地塞米松的抵抗,可作为地塞米松等糖皮质激素的增敏剂。
目的:探討17α-己痠羥孕酮對外週血單箇覈細胞牴抗地塞米鬆的逆轉作用。方法分離健康男性外週血單箇覈細胞,利用白介素2(IL-2)和IL-4以及植物血凝素刺激外週血單箇覈細胞,建立地塞米鬆牴抗的炎癥細胞實驗模型;單用地塞米鬆和地塞米鬆與17α-己痠羥孕酮聯閤應用于該模型,酶聯免疫吸附法檢測細胞的IL-2值的改變。結果地塞米鬆對植物血凝素誘導人外週血產生的IL-2呈現顯著的濃度依賴性的抑製作用;用IL-2(13 ng · mL -1)和IL-4(6.5 ng · mL -1)刺激,再用植物血凝素(15μg · mL -1)刺激外週血單箇覈細胞可以作為評價地塞米鬆牴抗的細胞實驗模型;在17α-己痠羥孕酮的濃度為10-11,10-10,10-7和10-5 mol · L -1時,可顯著提高地塞米鬆對人外週血產生的IL-2的抑製率,降低地塞米鬆的IC50(半數抑製濃度)值至少100倍以上。結論17α-己痠羥孕酮逆轉外週血單箇覈細胞對地塞米鬆的牴抗,可作為地塞米鬆等糖皮質激素的增敏劑。
목적:탐토17α-기산간잉동대외주혈단개핵세포저항지새미송적역전작용。방법분리건강남성외주혈단개핵세포,이용백개소2(IL-2)화IL-4이급식물혈응소자격외주혈단개핵세포,건입지새미송저항적염증세포실험모형;단용지새미송화지새미송여17α-기산간잉동연합응용우해모형,매련면역흡부법검측세포적IL-2치적개변。결과지새미송대식물혈응소유도인외주혈산생적IL-2정현현저적농도의뢰성적억제작용;용IL-2(13 ng · mL -1)화IL-4(6.5 ng · mL -1)자격,재용식물혈응소(15μg · mL -1)자격외주혈단개핵세포가이작위평개지새미송저항적세포실험모형;재17α-기산간잉동적농도위10-11,10-10,10-7화10-5 mol · L -1시,가현저제고지새미송대인외주혈산생적IL-2적억제솔,강저지새미송적IC50(반수억제농도)치지소100배이상。결론17α-기산간잉동역전외주혈단개핵세포대지새미송적저항,가작위지새미송등당피질격소적증민제。
Objective To investigate the reversal effect of 17α-hydroxyprogesterone caproate on dexamethasone resistant in human peripheral blood mononuclear cells .Methods Peripheral blood mononuclear cells (PBMCs) were isolated from healthy volunteers and were stimulated with interleukin-2(IL-2) IL-2 ,IL-4 and phytohemagglutinin to establish a cell study model of dexamethasone (DEX) resistance .By using the model ,PBMCs were stimulated with DEX alone or in combination with 17α-hydroxyprogesterone caproate(17HPC) ,and the IL-2 levels were quantified by enzyme linked immunosorbent assay (ELISA) .Results The production of IL-2 was inhibited by DEX in a significant ,dose-dependent manner .Following the pretreatment with IL-2(13 ng · mL -1 ) and IL-4(6 .5 ng · mL -1 ) ,PBMCs were stimulated with phytohemagglutinin and the experimental model of DEX resistance was estab-lished .The inhibition effects of DEX on the production of IL-2 were enhanced significantly by 17HPC .The IC50 values(50% in-hibitory concentrations) of DEX were decreased at least 100-fold compared to the control (without 17HPC) caused by 10-11 , 10-10 ,10-7 and 10-5 mol · L -1 17HPC .Conclusion 17α-hydroxyprogesterone caproate can reverse dexamethasone resistance in human peripheral blood mononuclear cells and it may be used as a glucocorticoid sensitizer .