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在无肥胖情况下的高脂饮食不会加重小鼠手术诱导的淋巴水肿

High-Fat Diet in the Absence of Obesity Does Not Aggravate Surgically Induced Lymphoedema in Mice.

作者信息

Gousopoulos Epameinondas, Karaman Sinem, Proulx Steven T, Leu Kristin, Buschle Dorina, Detmar Michael

机构信息

Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology, ETH Zurich, Zurich, Switzerland.

出版信息

Eur Surg Res. 2017;58(3-4):180-192. doi: 10.1159/000461579. Epub 2017 Mar 17.

Abstract

BACKGROUND

Lymphoedema represents the cardinal manifestation of lymphatic dysfunction and is associated with expansion of the adipose tissue in the affected limb. In mice, high-fat diet (HFD)-induced obesity was associated with impaired collecting lymphatic vessel function, and adiposity aggravated surgery-induced lymphoedema in a mouse model. The aim of the current study was to investigate whether adiposity is necessary to impair lymphatic function or whether increased lipid exposure alone might be sufficient in a surgical lymphoedema model.

METHODS

To investigate the role of increased lipid exposure in lymphoedema development we used a well-established mouse tail lymphoedema model. Female mice were subjected to a short-term (6 weeks) HFD, without development of obesity, before surgical induction of lymphedema. Lymphoedema was followed over a period of 6 weeks measuring oedema, evaluating tissue histology and lymphatic vascular function.

RESULTS

HFD increased baseline angiogenesis and average lymphatic vessel size in comparison to the chow control group. Upon induction of lymphedema, HFD-treated mice did not exhibit aggravated oedema and no morphological differences were observed in the blood and lymphatic vasculature. Importantly, the levels of fibro-adipose tissue deposition were comparable between the 2 groups and lymphatic vessel function was not impaired as a result of the HFD. Although the net immune cell infiltration was comparable, the HFD group displayed an increased infiltration of macrophages, which exhibited an M2 polarization phenotype.

CONCLUSIONS

These results indicate that increased adiposity rather than dietary influences determines predisposition to or severity of lymphedema.

摘要

背景

淋巴水肿是淋巴功能障碍的主要表现,与患肢脂肪组织扩张有关。在小鼠中,高脂饮食(HFD)诱导的肥胖与集合淋巴管功能受损有关,在小鼠模型中,肥胖会加重手术诱导的淋巴水肿。本研究的目的是调查肥胖是否是损害淋巴功能的必要条件,或者在手术性淋巴水肿模型中,仅增加脂质暴露是否就足够了。

方法

为了研究增加脂质暴露在淋巴水肿发展中的作用,我们使用了一个成熟的小鼠尾部淋巴水肿模型。雌性小鼠在手术诱导淋巴水肿前接受短期(6周)高脂饮食,未出现肥胖。在6周的时间内跟踪淋巴水肿情况,测量水肿程度,评估组织组织学和淋巴管功能。

结果

与对照组相比,高脂饮食增加了基线血管生成和平均淋巴管大小。诱导淋巴水肿后,高脂饮食处理的小鼠未出现水肿加重,在血液和淋巴管系统中未观察到形态学差异。重要的是,两组之间纤维脂肪组织沉积水平相当,高脂饮食并未损害淋巴管功能。虽然净免疫细胞浸润相当,但高脂饮食组巨噬细胞浸润增加,表现为M2极化表型。

结论

这些结果表明,肥胖增加而非饮食影响决定了淋巴水肿的易感性或严重程度。

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