Khatua Biswajit, El-Kurdi Bara, Patel Krutika, Rood Christopher, Noel Pawan, Crowell Michael, Yaron Jordan R, Kostenko Sergiy, Guerra Andre, Faigel Douglas O, Lowe Mark, Singh Vijay P
Department of Medicine, Mayo Clinic, Scottsdale, AZ, USA.
Saint Louis University School of Medicine, Saint Louis, MO, USA.
Sci Adv. 2021 Jan 29;7(5). doi: 10.1126/sciadv.abd6449. Print 2021 Jan.
Obesity sometimes seems protective in disease. This obesity paradox is predominantly described in reports from the Western Hemisphere during acute illnesses. Since adipose triglyceride composition corresponds to long-term dietary patterns, we performed a meta-analysis modeling the effect of obesity on severity of acute pancreatitis, in the context of dietary patterns of the countries from which the studies originated. Increased severity was noted in leaner populations with a higher proportion of unsaturated fat intake. In mice, greater hydrolysis of unsaturated visceral triglyceride caused worse organ failure during pancreatitis, even when the mice were leaner than those having saturated triglyceride. Saturation interfered with triglyceride's interaction and lipolysis by pancreatic triglyceride lipase, which mediates organ failure. Unsaturation increased fatty acid monomers in vivo and aqueous media, resulting in greater lipotoxic cellular responses and organ failure. Therefore, visceral triglyceride saturation reduces the ensuing lipotoxicity despite higher adiposity, thus explaining the obesity paradox.
肥胖有时在疾病中似乎具有保护作用。这种肥胖悖论主要在西半球关于急性疾病的报告中有所描述。由于脂肪甘油三酯组成与长期饮食模式相对应,我们在研究来源国饮食模式的背景下,进行了一项荟萃分析,以模拟肥胖对急性胰腺炎严重程度的影响。在不饱和脂肪摄入量比例较高的较瘦人群中,观察到疾病严重程度增加。在小鼠中,不饱和内脏甘油三酯的更大程度水解在胰腺炎期间导致更严重的器官衰竭,即使这些小鼠比摄入饱和甘油三酯的小鼠更瘦。饱和度干扰了甘油三酯与胰腺甘油三酯脂肪酶的相互作用及脂肪分解,而胰腺甘油三酯脂肪酶介导器官衰竭。不饱和状态在体内和水性介质中增加了脂肪酸单体,导致更大的脂毒性细胞反应和器官衰竭。因此,尽管肥胖程度较高,但内脏甘油三酯饱和度降低了随之而来的脂毒性,从而解释了肥胖悖论。