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基于活性的光声探针揭示肥胖症小鼠模型中肠道 MGL 和 FAAH 活性升高。

Activity-based Photoacoustic Probes Reveal Elevated Intestinal MGL and FAAH Activity in a Murine Model of Obesity.

机构信息

Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL61801, USA.

Beckman Institute for Advanced Science and Technology, Urbana, IL61801, USA.

出版信息

Angew Chem Int Ed Engl. 2022 Nov 2;61(44):e202211774. doi: 10.1002/anie.202211774. Epub 2022 Oct 5.

Abstract

Obesity is a chronic health condition characterized by the accumulation of excessive body fat which can lead to and exacerbate cardiovascular disease, type-II diabetes, high blood pressure, and cancer through systemic inflammation. Unfortunately, visualizing key mediators of the inflammatory response, such as monoacylglycerol lipase (MGL) and fatty acid amide hydrolase (FAAH), in a selective manner is a profound challenge owing to an overlapping substrate scope that involves arachidonic acid (AA). Specifically, these enzymes work in concert to generate AA, which in the context of obesity, has been implicated to control appetite and energy metabolism. In this study, we developed the first selective activity-based sensing probes to detect MGL (PA-HD-MGL) and FAAH (PA-HD-FAAH) activity via photoacoustic imaging. Activation of PA-HD-MGL and PA-HD-FAAH by their target enzymes resulted in 1.74-fold and 1.59-fold signal enhancements, respectively. Due to their exceptional selectivity profiles and deep-tissue photoacoustic imaging capabilities, these probes were employed to measure MGL and FAAH activity in a murine model of obesity. Contrary to conflicting reports suggesting levels of MGL can be attenuated or elevated, our results support the latter. Indeed, we discovered a marked increase of both targets in the gastrointestinal tract. These key findings set the stage to uncover the role of the endocannabinoid pathway in obesity-mediated inflammation.

摘要

肥胖是一种慢性健康状况,其特征是体内脂肪积累过多,这可能通过全身炎症导致并加剧心血管疾病、二型糖尿病、高血压和癌症。不幸的是,以选择性的方式可视化炎症反应的关键介质,如单酰基甘油脂肪酶(MGL)和脂肪酸酰胺水解酶(FAAH),是一个巨大的挑战,因为它们的底物范围重叠,涉及花生四烯酸(AA)。具体来说,这些酶协同作用生成 AA,在肥胖的情况下,AA 被认为可以控制食欲和能量代谢。在这项研究中,我们开发了第一个选择性基于活性的传感探针,通过光声成像来检测 MGL(PA-HD-MGL)和 FAAH(PA-HD-FAAH)的活性。其靶酶对 PA-HD-MGL 和 PA-HD-FAAH 的激活分别导致信号增强 1.74 倍和 1.59 倍。由于其出色的选择性特征和深组织光声成像能力,这些探针被用于测量肥胖小鼠模型中的 MGL 和 FAAH 活性。与表明 MGL 水平可能降低或升高的相互矛盾的报告相反,我们的结果支持后者。事实上,我们发现这两个靶点在胃肠道中都有明显增加。这些关键发现为揭示内源性大麻素途径在肥胖介导的炎症中的作用奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5339/9827994/8dc34c5f3af9/ANIE-61-0-g002.jpg

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