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非肾上腺素能、坦索罗辛不敏感的平滑肌收缩足以替代人前列腺中的α-肾上腺素能张力。

Non-Adrenergic, Tamsulosin-Insensitive Smooth Muscle Contraction is Sufficient to Replace α -Adrenergic Tension in the Human Prostate.

作者信息

Hennenberg Martin, Acevedo Alice, Wiemer Nicolas, Kan Aysenur, Tamalunas Alexander, Wang Yiming, Yu Qingfeng, Rutz Beata, Ciotkowska Anna, Herlemann Annika, Strittmatter Frank, Stief Christian G, Gratzke Christian

机构信息

Department of Urology, Ludwig-Maximilians University, Munich, Germany.

出版信息

Prostate. 2017 May;77(7):697-707. doi: 10.1002/pros.23293. Epub 2017 Jan 24.

Abstract

BACKGROUND

Lower urinary tract symptoms (LUTS) suggestive of benign prostatic hyperplasia may be caused by prostate smooth muscle contraction. Although α -blockers may improve symptoms by prostate smooth muscle relaxation, their efficacy is limited. This may be explained by non-adrenergic mediators causing contraction in parallel to α -adrenoceptors. However, little is known about the relevance and cooperative actions of non-adrenergic mediators in the prostate.

METHODS

Prostate tissues were obtained from radical prostatectomy (n = 127 patients). Contractile responses were studied in an organ bath.

RESULTS

Endothelin-1 and noradrenaline induced contractions of similar magnitude (116 ± 23 and 117 ± 18% of KCl-induced contractions). Endothelin-2- and -3-induced maximum contractions of 63 ± 8.6 and 71 ± 19% of KCl, while contractions by the thromboxane analog U46619 amounted up to 63 ± 9.4%. Dopamine-induced contractions averaged to 22 ± 4.5% of KCl, while maximum contractions by serotonin, histamine, and carbachol stayed below 10% of KCl-induced. While noradrenaline-induced contractions were inhibited by tamsulosin (300 nM), endothelin-1-, -2-, or -3-induced contraction were not. No additive effects were observed if endothelins and noradrenaline were applied consecutively to the same samples. If endothelin-1 was applied after U46619, resulting tension (172 ± 43% of KCl) significantly exceeded noradrenaline-induced contraction. Tensions following combined application of endothelin-2 or -3 with U46619 stayed below noradrenaline-induced contractions. Tension following combined application of all three endothelins with U46619 resembled maximum noradrenaline-induced tone.

CONCLUSIONS

Contractions following concomitant confrontation of human prostate tissue with noradrenaline and endothelin-1 are not additive. Endothelin-1 is sufficient to induce a smooth muscle tone resembling that of noradrenaline. This may replace lacking α -adrenergic tone under therapy with α -blockers, explaining the limited efficacy of α -blockers in LUTS treatment. Contractions by thromboxane and endothelin-1 may be additive, and may exceed α -adrenergic tone. Prostate 77:697-707, 2017. © 2017 Wiley Periodicals, Inc.

摘要

背景

提示良性前列腺增生的下尿路症状(LUTS)可能由前列腺平滑肌收缩引起。尽管α受体阻滞剂可通过松弛前列腺平滑肌改善症状,但其疗效有限。这可能是由于非肾上腺素能介质与α肾上腺素能受体同时引起收缩所致。然而,关于前列腺中非肾上腺素能介质的相关性和协同作用知之甚少。

方法

从根治性前列腺切除术患者(n = 127例)获取前列腺组织。在器官浴槽中研究收缩反应。

结果

内皮素 - 1和去甲肾上腺素引起的收缩幅度相似(分别为氯化钾诱导收缩的116±23%和117±18%)。内皮素 - 2和 - 3引起的最大收缩分别为氯化钾诱导收缩的63±8.6%和71±19%,而血栓素类似物U46619引起的收缩达63±9.4%。多巴胺引起的收缩平均为氯化钾诱导收缩的22±4.5%,而5 - 羟色胺、组胺和卡巴胆碱引起的最大收缩低于氯化钾诱导收缩的10%。虽然坦索罗辛(300 nM)可抑制去甲肾上腺素引起的收缩,但对内皮素 - 1、 - 2或 - 3引起的收缩无抑制作用。如果将内皮素和去甲肾上腺素连续应用于同一样本,未观察到相加效应。如果在U46619后应用内皮素 - 1,产生的张力(为氯化钾诱导收缩的172±43%)显著超过去甲肾上腺素引起的收缩。内皮素 - 2或 - 3与U46619联合应用后的张力低于去甲肾上腺素引起的收缩。三种内皮素与U46619联合应用后的张力类似于去甲肾上腺素引起的最大张力。

结论

人前列腺组织同时接触去甲肾上腺素和内皮素 - 1后引起的收缩无相加作用。内皮素 - 1足以诱导类似于去甲肾上腺素的平滑肌张力。这可能在α受体阻滞剂治疗期间替代缺失的α肾上腺素能张力,解释了α受体阻滞剂在治疗LUTS中疗效有限的原因。血栓素和内皮素 - 1引起的收缩可能具有相加性,且可能超过α肾上腺素能张力。《前列腺》77:697 - 707,2017年。©2017威利期刊公司

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