Pena Calderin Ernesto H, Zheng Jing-Juan, Boyd Nolan L, Lynch Will, Sansbury Brian E, Spite Matthew, Hill Bradford G, Hellmann Jason
bioRxiv. 2024 Aug 19:2024.08.14.608014. doi: 10.1101/2024.08.14.608014.
Diet-induced white adipose tissue inflammation is associated with insulin resistance and metabolic perturbations. Conversely, exercise (Exe) protects against the development of chronic inflammation and insulin resistance independent of changes in weight; however, the mechanisms remain largely unknown. We have recently shown that, through adrenergic stimulation of macrophages, exercise promotes resolution of acute peritoneal inflammation by enhancing the biosynthesis of specialized pro-resolving lipid mediators (SPMs). In this study, we sought to determine if exercise stimulates pro-resolving pathways in adipose tissue and whether this response is modified by diet. Specifically, we hypothesized that high fat diet feeding disrupts exercise-stimulated resolution by inhibiting adrenergic signaling, priming the development of chronic inflammation in adipose tissue (AT).
To explore the dietary dependence of the pro-resolving effects of Exe, mice were fed either a control or high-fat diet (HFD) for 2 weeks prior to, and throughout, a 4 wk period of daily treadmill running. Glucose handling, body weight and composition, and exercise performance were evaluated at the end of the feeding and exercise interventions. Likewise, catecholamines and their biosynthetic enzymes were measured along with AT SPM biosynthesis and macrophage phenotype and abundance. When compared with sedentary controls (Sed), macrophages isolated from mice exposed to 4 wk of exercise display elevated expression of the SPM biosynthetic enzyme Alox15, while whole AT SPM levels and anti-inflammatory CD301+ M2 macrophages increased. These changes were dependent upon diet as 6 wk of feeding with HFD abrogated the pro-resolving effect of exercise when compared with control diet-fed animals. Interestingly, exercise-induced epinephrine production was inhibited by HFD, which diminished expression of the epinephrine biosynthetic enzyme phenylethanolamine N-methyltransferase (PNMT) in adrenal glands.
Taken together, these results suggest that a diet high in fat diminishes the pro-resolving effects of exercise in adipose tissue via decreasing the biosynthesis of catecholamines.
饮食诱导的白色脂肪组织炎症与胰岛素抵抗和代谢紊乱有关。相反,运动可预防慢性炎症和胰岛素抵抗的发生,且与体重变化无关;然而,其机制仍 largely 未知。我们最近发现,通过巨噬细胞的肾上腺素能刺激,运动可通过增强特异性促解决脂质介质(SPMs)的生物合成来促进急性腹膜炎的消退。在本研究中,我们试图确定运动是否刺激脂肪组织中的促解决途径,以及这种反应是否会因饮食而改变。具体而言,我们假设高脂饮食喂养通过抑制肾上腺素能信号传导来破坏运动刺激的消退,引发脂肪组织(AT)中慢性炎症的发展。
为了探究运动促解决作用的饮食依赖性,在为期 4 周的每日跑步机跑步期间及之前 2 周,给小鼠喂食对照饮食或高脂饮食(HFD)。在喂养和运动干预结束时评估葡萄糖处理、体重和组成以及运动表现。同样,测量儿茶酚胺及其生物合成酶以及 AT SPM 生物合成、巨噬细胞表型和丰度。与久坐对照(Sed)相比,从接受 4 周运动的小鼠中分离出的巨噬细胞显示 SPM 生物合成酶 Alox15 的表达升高,而整个 AT SPM 水平和抗炎性 CD301 + M2 巨噬细胞增加。与对照饮食喂养的动物相比,这些变化取决于饮食,因为 6 周的 HFD 喂养消除了运动的促解决作用。有趣的是,HFD 抑制了运动诱导的肾上腺素产生,这降低了肾上腺中肾上腺素生物合成酶苯乙醇胺 N - 甲基转移酶(PNMT)的表达。
综上所述,这些结果表明高脂肪饮食通过减少儿茶酚胺的生物合成来降低运动对脂肪组织的促解决作用。