盐酸克仑特罗通过激活CREB1抑制SREBP-1c的表达。

Lei Zhou, Yixing Li, Tao Nie, Shengqiu Feng, Jihong Yuan, Huaping Chen, Zaiqing Yang
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引用次数: 22

摘要

作为一种β(2)-肾上腺素能激动剂,瘦肉精可以减少体脂,但这一过程的分子机制尚不清楚。在本研究中,我们用盐酸克仑特罗处理293T和L-02细胞,发现盐酸克仑特罗下调SREBP-1c表达,上调CREB1表达。考虑到SREBP-1c具有调节多种脂质酶转录的功能,我们认为下调SREBP-1c是克仑特罗降低体脂的原因。许多先前的研究发现克伦特罗显著增加细胞内cAMP水平,因此,我们也研究了CREB1是否参与这一过程。我们的实验数据表明,CREB1过表达会抑制SREBP-1c的转录,并且这种作用会被CREB1的竞争性抑制剂CREB2拮抗。此外,由于PPAR能够抑制SREBP-1c的转录,我们研究了克伦特罗和CREB1是否通过一个涉及PPAR激活的途径发挥作用。然而,我们的研究结果显示,克伦特罗或CREB1过表达抑制了293T和L-02细胞中PPARs的转录,这表明它们以其他方式损害SREBP-1c的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clenbuterol inhibits SREBP-1c expression by activating CREB1.

As a beta(2)-adrenergic agonist, clenbuterol decreases body fat, but the molecular mechanism underlying this process is unclear. In the present study, we treated 293T and L-02 cells with clenbuterol and found that clenbuterol downregulates SREBP-1c expression and upregulates CREB1 expression. Considering SREBP-1c has the function of regulating the transcription of several lipogenic enzymes, we considered that the downregulation of SREBP-1c is responsible for body fat reduction by clenbuterol. Many previous studies have found that clenbuterol markedly increases intracellular cAMP levels, therefore, we also investigated whether CREB1 is involved in this process. The data from our experiments indicate that CREB1 overexpression inhibits SREBP-1c transcription, and that this action is antagonized by CREB2, a competitive inhibitor of CREB1. Furthermore, since PPARs are able to repress SREBP-1c transcription, we investigated whether clenbuterol and CREB1 function via a pathway involving PPAR activation. However, our results showed that clenbuterol or CREB1 overexpression suppressed PPARs transcription in 293T and L-02 cells, which suggested that they impair SREBP-1c expression in other ways.

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