Bruun Jens M, Stallknecht Bente, Helge Jørn W, Richelsen Bjørn
Department of Endocrinology and Metabolism C, Aarhus University Hospital, Aarhus Sygehus, DK-8000 Aarhus C, Denmark.
Eur J Endocrinol. 2007 Oct;157(4):465-71. doi: 10.1530/EJE-07-0206.
Interleukin (IL)-18 is associated with obesity, insulin resistance, and cardiovascular disease. The present study compared 1) IL-18 in adipocytes versus stromal vascular (SV) cells, 2) IL-18 in plasma and adipose tissue (AT) in obese versus lean subjects, and 3) IL-18 in plasma, AT, and skeletal muscle (SM) in obese subjects after weight loss.
At baseline, plasma and AT IL-18 in 23 obese subjects were compared with that in 12 lean subjects. The obese subjects were submitted to a 15-week life-style intervention (hypocaloric diet and daily exercise) after which plasma samples, AT, and SM biopsies were obtained. Analyses were performed by ELISA and RT-PCR respectively.
IL-18 expression in isolated adipocytes was approximately 2% of that in SV cells. Plasma IL-18 was higher in obese subjects (P < 0.001) and associated with insulin resistance (HOMA; P < 0.001). AT expression of IL-18, CD14, and CD68 was higher in obese (P < 0.01). The intervention reduced body weight (P < 0.001), plasma IL-18 (P < 0.001), and increased insulin sensitivity (HOMA; P < 0.05). AT and SM expression of IL-18 remained unchanged after the intervention. Changes in plasma IL-18 were associated with changes in insulin sensitivity (P < 0.05) but not with BMI or AT expression of IL-18.
Plasma IL-18 is associated with changes in insulin resistance and reduced after weight loss. AT expression of IL-18 is increased in obesity but not affected by weight loss, indicating that changes in plasma IL-18 are related to insulin resistance rather than changes in obesity per se.
白细胞介素(IL)-18与肥胖、胰岛素抵抗及心血管疾病相关。本研究比较了:1)脂肪细胞与基质血管(SV)细胞中的IL-18;2)肥胖与瘦受试者血浆及脂肪组织(AT)中的IL-18;3)肥胖受试者体重减轻后血浆、AT及骨骼肌(SM)中的IL-18。
在基线时,将23名肥胖受试者的血浆及AT中的IL-18与12名瘦受试者的进行比较。肥胖受试者接受为期15周的生活方式干预(低热量饮食及每日锻炼),之后采集血浆样本、AT及SM活检样本。分别通过酶联免疫吸附测定(ELISA)和逆转录-聚合酶链反应(RT-PCR)进行分析。
分离的脂肪细胞中IL-18的表达约为SV细胞中的2%。肥胖受试者血浆中的IL-18较高(P<0.001),且与胰岛素抵抗相关(稳态模型评估法;P<0.001)。肥胖者AT中IL-18、CD14及CD68的表达较高(P<0.01)。干预使体重减轻(P<0.001)、血浆IL-18降低(P<0.001),并提高了胰岛素敏感性(稳态模型评估法;P<0.05)。干预后AT及SM中IL-18的表达未发生变化。血浆IL-18的变化与胰岛素敏感性的变化相关(P<0.05),但与体重指数或AT中IL-18的表达无关。
血浆IL-18与胰岛素抵抗的变化相关,且体重减轻后降低。肥胖时AT中IL-18的表达增加,但不受体重减轻的影响,这表明血浆IL-18的变化与胰岛素抵抗相关,而非肥胖本身的变化。