Hector J, Schwarzloh B, Goehring J, Strate T G, Hess U F, Deuretzbacher G, Hansen-Algenstaedt N, Beil F-U, Algenstaedt P
Department of Internal Medicine III, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Horm Metab Res. 2007 Apr;39(4):250-5. doi: 10.1055/s-2007-973075.
Adiponectin and visfatin are newly discovered adipokines that are strongly expressed in human visceral adipose tissue. To identify new regulatory mechanisms in fat, the effect of TNF-alpha (TNF) on adiponectin, on its two receptors, and on visfatin was investigated by incubating human visceral adipose tissue from patients without diabetes mellitus with TNF for 24, 48 and 72 hours. The mRNA expression of visfatin, adiponectin, and its two receptors, as well as the protein expression of adiponectin were determined. A decrease of adiponectin mRNA expression of 97% after incubation with TNF (5.75 nmol/l) for 24 hours, a decrease of 91% after 48 hours, and a decrease of 96% after 72 hours were measured. The reduction of protein expression was measured to be 42% after 24 hours, 28% after 48 hours, and 39% after 72 hours of incubation with TNF (5.75 nmol/l). The mRNA level of adiponectin receptor 1 (AdipoR1) was elevated about 72% after 48 hours of incubation and 67% after 72 hours of incubation, whereas the mRNA expression of adiponectin receptor 2 (AdipoR2) was not altered significantly. The visfatin mRNA level was found to be highly increased by 255% after 24 hours and 335% after 48 hours and 341% after 72 hours of incubation with TNF (5.75 nmol/l). Our results support the concept of visceral adipose tissue as an endocrine organ. We demonstrate that TNF has regulatory functions on adiponectin, AdipoR1 and on visfatin in human visceral adipose tissue. TNF levels are elevated in states of obesity and insulin resistance. Due to this fact TNF could be the reason that there is a decrease in the level of adiponectin, whereas there is an increase in the level of visfatin in states of obesity and insulin resistance.
脂联素和内脂素是新发现的脂肪因子,在人体内脏脂肪组织中大量表达。为了确定脂肪中的新调节机制,通过将无糖尿病患者的人体内脏脂肪组织与肿瘤坏死因子-α(TNF)孵育24、48和72小时,研究了TNF对脂联素、其两种受体以及内脂素的影响。测定了内脂素、脂联素及其两种受体的mRNA表达,以及脂联素的蛋白表达。与TNF(5.75 nmol/l)孵育24小时后,脂联素mRNA表达下降97%,48小时后下降91%,72小时后下降96%。与TNF(5.75 nmol/l)孵育24小时后,蛋白表达下降42%,48小时后下降28%,72小时后下降39%。脂联素受体1(AdipoR1)的mRNA水平在孵育48小时后升高约72%,72小时后升高67%,而脂联素受体2(AdipoR2)的mRNA表达无明显改变。与TNF(5.75 nmol/l)孵育24小时后,内脂素mRNA水平显著升高255%,48小时后升高335%,72小时后升高341%。我们的结果支持内脏脂肪组织作为内分泌器官的概念。我们证明TNF对人体内脏脂肪组织中的脂联素、AdipoR1和内脂素具有调节功能。肥胖和胰岛素抵抗状态下TNF水平升高。基于这一事实,TNF可能是肥胖和胰岛素抵抗状态下脂联素水平降低而内脂素水平升高的原因。