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生理水平的5α-双氢睾酮会抑制伤口免疫功能,并损害创伤性出血后的伤口愈合。

Physiological levels of 5 alpha-dihydrotestosterone depress wound immune function and impair wound healing following trauma-hemorrhage.

作者信息

Nitsch Stefan M, Wittmann Florian, Angele Peter, Wichmann Matthias W, Hatz Rudolf, Hernandez-Richter Thomas, Chaudry Irshad H, Jauch Karl W, Angele Martin K

机构信息

Department of Surgery, Klinikum Grosshadern, Ludwig-Maximilians University, Munich, Germany.

出版信息

Arch Surg. 2004 Feb;139(2):157-63. doi: 10.1001/archsurg.139.2.157.

Abstract

HYPOTHESIS

Studies indicate that a depressed wound immune function contributes to an increased rate of wound complications and impaired wound healing following trauma-hemorrhage (T-H). Androgen, ie, 5 alpha-dihydrotestosterone, is responsible for producing the depressed systemic cell-mediated immune responses following T-H in males. The aim of the present study was to determine whether depletion of 5 alpha-dihydrotestosterone in males before T-H has any salutary effects on wound immune cell function and wound healing in male mice following T-H.

DESIGN

Mice were castrated or sham castrated 14 days before midline laparotomy (ie, tissue trauma) and subcutaneous polyvinyl sponge implantation, followed by hemorrhage (mean +/- SEM blood pressure, 35 +/- 5 mm Hg for 90 minutes and resuscitation) or sham operation. At 24 hours thereafter, wound immune cells from the sponges were harvested and cultured with lipopolysaccharide A. Release of interleukin 1 beta (IL-1 beta) and IL-6 (in picograms per milliliter) was determined in the supernatants by enzyme-linked immunosorbent assay. In addition, IL-6 was assessed at the wound site by immunohistochemistry. Ten days after T-H, wound-breaking strength was measured.

RESULTS

Precastration prevented the significantly suppressed capacity of wound immune cells to release IL-1 beta and IL-6. In addition, precastration normalized the elevated IL-6 expression at the wound site in the T-H mice. Moreover, wound-breaking strength was improved in castrated mice 10 days after T-H.

CONCLUSIONS

Male sex steroids appear to be responsible for wound immune cell dysfunction following trauma and severe blood loss. Because decreasing androgen levels resulted in improved wound healing, our results suggest that the use of androgen receptor-blocking agents, eg, flutamide, following T-H might represent a novel adjunct for decreasing the rate of wound complications under those conditions.

摘要

假说

研究表明,伤口免疫功能低下会导致创伤性出血(T-H)后伤口并发症发生率增加及伤口愈合受损。雄激素,即5α-双氢睾酮,是导致雄性动物T-H后全身细胞介导免疫反应受抑制的原因。本研究的目的是确定雄性动物在T-H前去除5α-双氢睾酮是否对T-H后雄性小鼠的伤口免疫细胞功能和伤口愈合有任何有益影响。

设计

在中线剖腹术(即组织创伤)和皮下植入聚乙烯海绵前14天,对小鼠进行去势或假去势,随后进行出血(平均±标准误血压,35±5 mmHg,持续90分钟并复苏)或假手术。此后24小时,从海绵中收集伤口免疫细胞,并用脂多糖A进行培养。通过酶联免疫吸附测定法测定上清液中白细胞介素1β(IL-1β)和IL-6(皮克/毫升)的释放量。此外,通过免疫组织化学在伤口部位评估IL-6。T-H后10天,测量伤口抗张强度。

结果

去势预处理可防止伤口免疫细胞释放IL-1β和IL-6的能力受到显著抑制。此外,去势预处理使T-H小鼠伤口部位升高的IL-6表达恢复正常。而且,T-H后10天,去势小鼠的伤口抗张强度得到改善。

结论

雄性性激素似乎是创伤和严重失血后伤口免疫细胞功能障碍的原因。由于雄激素水平降低导致伤口愈合改善,我们的结果表明,在T-H后使用雄激素受体阻断剂,如氟他胺,可能是在这些情况下降低伤口并发症发生率的一种新辅助方法。

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