School of Biosciences and Veterinary Medicine, University of Camerino, Via Gentile III Da Varano, 62032, Camerino, MC, Italy.
Department of Medicine, University of Leipzig, Leipzig, Germany.
Eur J Nutr. 2021 Aug;60(5):2695-2707. doi: 10.1007/s00394-020-02459-y. Epub 2021 Jan 2.
There is increasing evidence for the involvement of dietary bioactive compounds in the cross-talk modulation of endocannabinoid system and some of the key regulators of transcriptional control for adipogenesis.
We aimed to characterize the expression of cannabinoid CB1/CB2 receptors and fatty acid amide hydrolase (FAAH) along with selected adipogenesis-related genes (PPARγ, SREBP-1c and PREF-1), adipocyte-secreted factors (leptin and adiponectin), mitochondrial bioenergetic modulators (PGC-1A and UCP-2), and transient receptor potential vanilloid subtype 1 (TRPV1) and 2 (TRPV2) channels in visceral adipose tissue of rats fed with a high-fat diet (HFD) containing either tart cherry seeds alone or tart cherry seeds and juice for 17 weeks. The visceral adipose tissue was weighed and checked the expression of different markers by qRT-PCR, Western blot and immunohistochemistry.
Tart cherry supplements were able to downregulate the HFD-induced mRNA expression of CB1 receptor, SREBP-1c, PPARγ, leptin, TRPV1 and TRPV2 resulting in potential anti-adipogenic effects.
The present study points out that the intake of bioactive constituents of tart cherry may attenuate the effect of adipogenesis by acting directly on the adipose tissue and modulating the interplay between CB1, PPARγ and TRPV channel gene transcription.
越来越多的证据表明,膳食生物活性化合物参与了内源性大麻素系统的交叉对话调节,以及一些脂肪生成的关键转录调控因子。
我们旨在研究肥胖相关基因(PPARγ、SREBP-1c 和 PREF-1)、脂肪细胞分泌因子(瘦素和脂联素)、线粒体生物能量调节剂(PGC-1A 和 UCP-2)、瞬时受体电位香草醛亚型 1(TRPV1)和 2(TRPV2)通道在内脏脂肪组织中的表达,这些组织取自喂食高脂肪饮食(HFD)的大鼠,饮食中含有单独的樱桃核或樱桃核和果汁,共 17 周。测量内脏脂肪组织的重量,并通过 qRT-PCR、Western blot 和免疫组织化学检查不同标志物的表达。
樱桃补充剂能够下调 HFD 诱导的 CB1 受体、SREBP-1c、PPARγ、瘦素、TRPV1 和 TRPV2 的 mRNA 表达,从而具有潜在的抗脂肪生成作用。
本研究指出,樱桃生物活性成分的摄入可能通过直接作用于脂肪组织并调节 CB1、PPARγ 和 TRPV 通道基因转录之间的相互作用,从而减弱脂肪生成的作用。