Exercise-Stimulated Resolvin Biosynthesis in the Adipose Tissue Is Abrogated by High-Fat Diet-Induced Adrenergic Deficiency.

IF 7.4 1区 医学 Q1 HEMATOLOGY
Ernesto Pena Calderin, Jing-Juan Zheng, Nolan L Boyd, Will Lynch, Brian E Sansbury, Matthew Spite, Bradford G Hill, Jason Hellmann
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引用次数: 0

Abstract

Background: Diet-induced white adipose tissue inflammation is associated with insulin resistance and metabolic perturbations. Conversely, exercise protects against the development of diet-induced chronic inflammation and insulin resistance independent of weight loss; 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 proresolving lipid mediators. In this study, we sought to determine whether exercise stimulates proresolving pathways in adipose tissue and whether this response is modified by diet. Specifically, we hypothesized that exercise stimulates proresolving pathways by adrenergic signaling, which is inhibited by high-fat diet, priming the development of chronic inflammation in the adipose tissue.

Methods: To explore the dietary dependence of the proresolving effects of exercise, mice were fed either a control or high-fat diet for 2 weeks before, and throughout, a 4-week period of daily treadmill running. Glucose handling, body weight and composition, lipemia, and exercise performance were evaluated at the end of the feeding and exercise interventions. Likewise, changes in catecholamines and their biosynthetic enzymes were measured along with adipose tissue specialized proresolving lipid mediator levels and macrophage phenotype and abundance.

Results: When compared with sedentary controls, macrophages isolated from mice exposed to 4 weeks of exercise display elevated expression of the specialized proresolving lipid mediator biosynthetic enzyme Alox15, while adipose tissue specialized proresolving lipid mediator levels and anti-inflammatory CD301+ M2 macrophages increased. These changes were dependent upon diet as 6 weeks of feeding with high-fat diet abrogated the proresolving effect of exercise when compared with control diet-fed animals. Interestingly, exercise-induced epinephrine production was inhibited by high-fat diet, which diminished the expression of the epinephrine biosynthetic enzyme PNMT (phenylethanolamine N-methyltransferase) in adrenal glands.

Conclusions: Taken together, these results suggest that a diet high in fat diminishes the proresolving effects of exercise in the adipose tissue via decreasing the biosynthesis of catecholamines.

高脂饮食诱导的肾上腺素能缺乏会破坏脂肪组织中运动刺激的溶解素生物合成。
背景:饮食引起的白色脂肪组织炎症与胰岛素抵抗和代谢紊乱有关。相反,运动可以防止饮食引起的慢性炎症和独立于减肥的胰岛素抵抗的发展;然而,其机制在很大程度上仍然未知。我们最近的研究表明,通过巨噬细胞的肾上腺素能刺激,运动通过促进专门的促脂质介质的生物合成来促进急性腹膜炎症的解决。在这项研究中,我们试图确定运动是否会刺激脂肪组织中的促分解途径,以及这种反应是否会被饮食所改变。具体来说,我们假设运动刺激了肾上腺素能信号通路,而高脂肪饮食抑制了肾上腺素能信号通路,从而引发了脂肪组织慢性炎症的发展。方法:为了探索运动促进作用的饮食依赖性,小鼠在2周之前和4周期间每天在跑步机上跑步,分别饲喂对照组和高脂肪饮食。在喂养和运动干预结束时,对葡萄糖处理、体重和组成、血脂和运动表现进行评估。同样,儿茶酚胺及其生物合成酶的变化与脂肪组织专门的促脂质介质水平和巨噬细胞表型和丰度一起被测量。结果:与久坐对照组相比,运动4周的小鼠巨噬细胞特异性促脂介质生物合成酶Alox15表达升高,脂肪组织特异性促脂介质水平和抗炎CD301+ M2巨噬细胞水平升高。这些变化依赖于饮食,因为与对照组动物相比,6周的高脂肪饮食喂养消除了运动的促进作用。有趣的是,运动诱导的肾上腺素产生被高脂肪饮食抑制,这降低了肾上腺素生物合成酶PNMT(苯乙醇胺n -甲基转移酶)的表达。结论: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,减少了运动对脂肪组织的促进作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
337
审稿时长
2-4 weeks
期刊介绍: The journal "Arteriosclerosis, Thrombosis, and Vascular Biology" (ATVB) is a scientific publication that focuses on the fields of vascular biology, atherosclerosis, and thrombosis. It is a peer-reviewed journal that publishes original research articles, reviews, and other scholarly content related to these areas. The journal is published by the American Heart Association (AHA) and the American Stroke Association (ASA). The journal was published bi-monthly until January 1992, after which it transitioned to a monthly publication schedule. The journal is aimed at a professional audience, including academic cardiologists, vascular biologists, physiologists, pharmacologists and hematologists.
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