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榛实酮通过激活 cAMP 信号改善高脂肪饮食喂养的小鼠的肥胖。

Filbertone Ameliorates Adiposity in Mice Fed a High-Fat Diet via Activation of cAMP Signaling.

机构信息

Department of Food and Nutrition, Brain Korea 21 PLUS Project, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.

出版信息

Nutrients. 2019 Jul 30;11(8):1749. doi: 10.3390/nu11081749.

DOI:10.3390/nu11081749
PMID:31366045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6723245/
Abstract

The aim of this research was to estimate the preventive effects of filbertone, the main flavor compound in hazelnuts, on lipid accumulation in the adipose tissue of mice fed a high-fat diet (HFD) and to reveal the underlying molecular mechanisms. Male C57BL/6N mice were fed chow, a HFD, or a 0.025% filbertone-supplemented HFD for 14 weeks. We found that filbertone supplementation resulted in significant reductions in body weight gain and lipid accumulation in adipose tissue, with parallel improvements in plasma lipid levels (triglycerides, total cholesterol, and free fatty acids) and proinflammatory cytokines (interleukin 6 (IL-6) and tumor necrosis factor alpha (TNF-α)). Molecular analysis revealed that filbertone treatment led to reprogramming of metabolic signatures in the cyclic adenosine monophosphate (cAMP) pathway. Filbertone supplementation significantly increased the cAMP level and increased downstream protein kinase A catalytic subunit (PKA) signaling in mouse adipose tissue. The mRNA level of adipogenesis-related genes was downregulated in the adipose tissue of filbertone-fed mice compared to control mice fed the HFD alone. Furthermore, filbertone treatment elevated the expression of thermogenic genes in mouse adipose tissue. Filbertone reduced intracellular lipid accumulation and increased the oxygen consumption rate in 3T3-L1 cells and these filbertone-induced changes were abrogated by the adenylate cyclases (ADCY) inhibitor. Taken together, our results suggest that the beneficial effects of filbertone on lipid accumulation may be associated with the activation of cAMP signaling.

摘要

本研究旨在评估榛果酮(榛子中的主要风味化合物)对高脂肪饮食喂养的小鼠脂肪组织脂质积累的预防作用,并揭示其潜在的分子机制。雄性 C57BL/6N 小鼠分别用标准饲料、高脂肪饮食或添加 0.025%榛果酮的高脂肪饮食喂养 14 周。结果发现,榛果酮补充显著降低了体重增加和脂肪组织中的脂质积累,同时改善了血浆脂质水平(甘油三酯、总胆固醇和游离脂肪酸)和促炎细胞因子(白细胞介素 6(IL-6)和肿瘤坏死因子α(TNF-α))。分子分析显示,榛果酮处理导致环磷酸腺苷(cAMP)通路代谢特征的重新编程。榛果酮补充显著增加了小鼠脂肪组织中 cAMP 水平和下游蛋白激酶 A 催化亚基(PKA)信号。与单独用高脂肪饮食喂养的对照组相比,榛果酮喂养的小鼠脂肪组织中脂肪生成相关基因的 mRNA 水平下调。此外,榛果酮处理还增加了小鼠脂肪组织中产热基因的表达。榛果酮减少了 3T3-L1 细胞内的脂质积累,并增加了耗氧量,而这些榛果酮诱导的变化被腺苷酸环化酶(ADCY)抑制剂所阻断。综上所述,我们的研究结果表明,榛果酮对脂质积累的有益作用可能与 cAMP 信号的激活有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd7/6723245/cb27b881d8af/nutrients-11-01749-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd7/6723245/f43fa3a327f2/nutrients-11-01749-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd7/6723245/cb27b881d8af/nutrients-11-01749-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd7/6723245/f43fa3a327f2/nutrients-11-01749-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd7/6723245/4032cb02c6f7/nutrients-11-01749-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd7/6723245/1aa013891a1d/nutrients-11-01749-g003.jpg
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