Department I of Internal Medicine, University of Kiel, Kiel, Germany.
PLoS One. 2012;7(2):e32437. doi: 10.1371/journal.pone.0032437. Epub 2012 Feb 23.
Obesity is associated with macrophage infiltration of adipose tissue. These inflammatory cells affect adipocytes not only by classical cytokines but also by the secreted glycopeptide wnt5a. Healthy adipocytes are able to release the wnt5a inhibitor sFRP5. This protective effect, however, was found to be diminished in obesity. The aim of the present study was to examine (1) whether obese human subjects exhibit increased serum concentrations of wnt5a and (2) whether wnt5a and/or sFRP5 serum concentrations in obese subjects can be influenced by caloric restriction.
23 obese human subjects (BMI 44.1 ± 1.1 kg/m(2)) and 12 age- and sex-matched lean controls (BMI 22.3 ± 0.4 kg/m(2)) were included in the study. Obese subjects were treated with a very low-calorie diet (approximately 800 kcal/d) for 12 weeks. Body composition was assessed by impedance analysis, insulin sensitivity was estimated by HOMA-IR and the leptin-to-adiponectin ratio and wnt5a and sFRP5 serum concentrations were measured by ELISA. sFRP5 expression in human adipose tissue biopsies was further determined on protein level by immunohistology.
Pro-inflammatory wnt5a was not measurable in any serum sample of lean control subjects. In patients with obesity, however, wnt5a became significantly detectable consistent with low grade inflammation in such subjects. Caloric restriction resulted in a weight loss from 131.9 ± 4.0 to 112.3 ± 3.2 kg in the obese patients group. This was accompanied by a significant decrease of HOMA-IR and leptin-to-adiponectin ratio, indicating improved insulin sensitivity. Interestingly, these metabolic improvements were associated with a significant increase in serum concentrations of the anti-inflammatory factor and wnt5a-inhibitor sFRP5.
CONCLUSIONS/SIGNIFICANCE: Obesity is associated with elevated serum levels of pro-inflammatory wnt5a in humans. Furthermore, caloric restriction beneficially affects serum concentrations of anti-inflammatory sFRP5 in such subjects. These findings suggest a novel regulatory system in low grade inflammation in obesity, which can be influenced by nutritional therapy.
肥胖与脂肪组织中巨噬细胞浸润有关。这些炎性细胞不仅通过经典细胞因子,还通过分泌的糖肽 wnt5a 影响脂肪细胞。健康的脂肪细胞能够释放 wnt5a 抑制剂 sFRP5。然而,在肥胖中发现这种保护作用减弱了。本研究的目的是检查(1)肥胖的人体是否表现出增加的 wnt5a 血清浓度,以及(2)肥胖患者的 wnt5a 和/或 sFRP5 血清浓度是否可以通过热量限制来影响。
23 名肥胖的人体受试者(BMI 44.1 ± 1.1 kg/m2)和 12 名年龄和性别匹配的瘦对照组(BMI 22.3 ± 0.4 kg/m2)被纳入研究。肥胖受试者接受极低热量饮食(约 800 kcal/d)治疗 12 周。通过阻抗分析评估身体成分,通过 HOMA-IR 估计胰岛素敏感性,通过 ELISA 测量瘦素与脂联素的比值和 wnt5a 和 sFRP5 血清浓度。进一步通过免疫组织化学法在蛋白质水平上确定人脂肪组织活检中的 sFRP5 表达。
瘦对照组的任何血清样本中均未检测到促炎 wnt5a。然而,在肥胖患者中,wnt5a 变得可检测到,与这些患者的低度炎症一致。热量限制导致肥胖患者体重从 131.9 ± 4.0 降至 112.3 ± 3.2 kg。这伴随着 HOMA-IR 和瘦素与脂联素比值的显著降低,表明胰岛素敏感性提高。有趣的是,这些代谢改善与抗炎因子和 wnt5a 抑制剂 sFRP5 的血清浓度显著增加有关。
结论/意义:肥胖与人类血清中促炎 wnt5a 水平升高有关。此外,热量限制对肥胖患者血清中抗炎 sFRP5 浓度有有益影响。这些发现表明,肥胖低度炎症中存在一种新的调节系统,可通过营养治疗来影响。