Department of Endocrinology and Nutrition, Diabetes and Obesity Research Laboratory, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Spain; CIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Spain.
Obesity (Silver Spring). 2014 Mar;22(3):698-704. doi: 10.1002/oby.20541. Epub 2013 Sep 18.
This study compares the patterns of visceral (VIS) and subcutaneous (SC) adipose tissue (AT)-derived metabolites from non-obese (BMI 24-26 kg/m2) and obese subjects (BMI > 40 kg/m2) with no major metabolic risk factors other than BMI.
SC- and VIS- AT obtained from obese (Ob) and non-obese (NOb) subjects during surgery were incubated to obtain their metabolites. Differences related to obesity or anatomical provenances of AT were assessed using an untargeted metabolomics approach based on gas chromatography-mass spectrometry.
The overall effect of obesity on the metabolite profile resulted more remarkable than the effect of regional AT. Only the depletion of 2-ketoisocaproic (2-KIC) acid reached statistical significance for the SC-AT alone, although it was observed in both depots. Obesity induced more significant changes in several amino acids levels of the VIS-AT metabolites. On the one hand, higher released levels of glutamine and alanine were detected in the VIS- obese AT, whereas on the other, the VIS- obese AT presented a diminished uptake of essential amino acids (methionine, threonine, lysine), BCAAs, leucine, and serine.
This study shows that obesity markedly affects the amino acid metabolic signature of the AT before the clinical onset of other significant metabolic alterations aside from BMI.
本研究比较了非肥胖(BMI 24-26 kg/m2)和肥胖(BMI>40 kg/m2)受试者内脏(VIS)和皮下(SC)脂肪组织(AT)来源代谢产物的模式,这些受试者除 BMI 外没有其他主要代谢危险因素。
在手术过程中从肥胖(Ob)和非肥胖(NOb)受试者中获取 SC- 和 VIS-AT,并进行孵育以获得其代谢产物。使用基于气相色谱-质谱的非靶向代谢组学方法评估与肥胖或 AT 解剖来源相关的差异。
肥胖对代谢物谱的整体影响比 AT 区域的影响更为显著。尽管在两个脂肪库中都观察到 2-酮异己酸(2-KIC)酸的消耗,但仅 SC-AT 的单独消耗达到了统计学意义。肥胖症在 VIS-AT 代谢物的几种氨基酸水平上引起了更显著的变化。一方面,在 VIS-肥胖 AT 中检测到谷氨酰胺和丙氨酸的释放水平更高,而另一方面,VIS-肥胖 AT 对必需氨基酸(蛋氨酸、苏氨酸、赖氨酸)、支链氨基酸(BCAAs)、亮氨酸和丝氨酸的摄取减少。
这项研究表明,肥胖症在 BMI 以外的其他重要代谢改变出现之前,就显著影响了 AT 的氨基酸代谢特征。