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在大鼠模型中,甲基泼尼松龙可增强去甲肾上腺素对股动脉的收缩作用。

Femoral artery constriction by norepinephrine is enhanced by methylprednisolone in a rat model.

作者信息

Drescher Wolf, Varoga Deike, Liebs Thoralf R, Lohse Janne, Herdegen Thomas, Hassenpflug Joachim, Pufe Thomas

机构信息

Department of Orthopaedic Surgery, University Hospital Schleswig-Holstein, Campus Kiel, D-24105 Kiel, Germany.

出版信息

J Bone Joint Surg Am. 2006 Nov;88 Suppl 3:162-6. doi: 10.2106/JBJS.F.00452.

Abstract

BACKGROUND

Corticosteroids are associated with femoral head osteonecrosis and arterial hypertension. The patho-mechanism of femoral head osteonecrosis is often attributed to ischemia. The aim of this study was to investigate if corticosteroids directly constrict the femoral artery or if they have a permissive effect on norepinephrine and endothelin-1-induced vasoconstriction.

METHODS

Femoral artery segments were harvested from twenty Wistar rats and mounted as ring preparations on a small-vessel myograph for the purpose of making isometric force measurements. For the norepinephrine study, twenty femoral artery segments from ten rats were stimulated cumulatively with norepinephrine before and after incubation with methylprednisolone (5 mug/mL). For the endothelin-1 study, forty femoral artery segments from ten rats were used. The four artery segments from each animal were randomized by pairs to either a corticosteroid treatment group (5 mug/mL methylprednisolone incubation, n = 20) or a control group (placebo incubation, n = 18, as two of the twenty control-group vessels did not meet protocol requirements). Isometric wall tension was plotted and quantified by the EC(50) (the plasma concentration of endothelin-1 required for obtaining 50% of maximal constriction in vivo).

RESULTS

In the norepinephrine-stimulated group, incubation with methylprednisolone did not directly induce any vasoconstriction but did enhance norepinephrine-elicited vasoconstriction. The norepinephrine dose-response curve displayed a shift to the left after incubation with methylprednisolone. This shift was reflected by a significantly lower mean EC50 of 9.5 x 10(-7) M +/- 5.1 x 10(-7) M after methylprednisolone incubation compared with a mean of 2.5 x 10(-6) M +/- 1.1 x 10(-6) M before incubation (p < 0.005). In the endothelin-1-stimulated group, the endothelin-1 dose-response curve displayed a tendency toward stronger contraction in the vessels that were incubated with methylprednisolone, but this tendency did not reach significance.

CONCLUSIONS

Incubation with methylprednisolone enhances norepinephrine-mediated contraction of the femoral artery in a rat model.

CLINICAL RELEVANCE

Vasoconstriction of the vascular bed supplying the femoral head can diminish femoral head blood flow, and this may be a factor in the early pathogenesis of corticosteroid-associated femoral head osteonecrosis.

摘要

背景

皮质类固醇与股骨头坏死和动脉高血压有关。股骨头坏死的发病机制通常归因于缺血。本研究的目的是调查皮质类固醇是否直接收缩股动脉,或者它们是否对去甲肾上腺素和内皮素 -1 诱导的血管收缩有允许作用。

方法

从 20 只 Wistar 大鼠身上获取股动脉段,并将其制成环形标本安装在小型血管肌动描记器上,以进行等长力测量。在去甲肾上腺素研究中,来自 10 只大鼠的 20 个股动脉段在与甲泼尼龙(5μg/mL)孵育前后,用去甲肾上腺素进行累积刺激。在内皮素 -1 研究中,使用来自 10 只大鼠的 40 个股动脉段。将每只动物的四个动脉段随机配对分为皮质类固醇治疗组(5μg/mL 甲泼尼龙孵育,n = 20)或对照组(安慰剂孵育,n = 18,因为 20 个对照组血管中有两个不符合实验方案要求)。绘制等长壁张力曲线,并通过 EC50(体内获得最大收缩 50%所需的内皮素 -1 血浆浓度)进行量化。

结果

在去甲肾上腺素刺激组中,与甲泼尼龙孵育并未直接诱导任何血管收缩,但确实增强了去甲肾上腺素引起的血管收缩。与孵育前平均 2.5×10⁻⁶ M±1.1×10⁻⁶ M 相比,甲泼尼龙孵育后去甲肾上腺素剂量 - 反应曲线向左移动。这种移动表现为甲泼尼龙孵育后平均 EC50 显著降低,为 9.5×10⁻⁷ M±5.1×10⁻⁷ M(p < 0.005)。在内皮素 -1 刺激组中,内皮素 -1 剂量 - 反应曲线显示,与甲泼尼龙孵育的血管有更强收缩的趋势,但这种趋势未达到显著水平。

结论

在大鼠模型中,与甲泼尼龙孵育可增强去甲肾上腺素介导的股动脉收缩。

临床意义

供应股骨头的血管床血管收缩可减少股骨头血流,这可能是皮质类固醇相关股骨头坏死早期发病机制中的一个因素。

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