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合成大麻素XLR-11通过损害内源性大麻素介导的线粒体功能稳态调节和触发细胞凋亡来诱导体外肾毒性。

The synthetic cannabinoid XLR-11 induces in vitro nephrotoxicity by impairment of endocannabinoid-mediated regulation of mitochondrial function homeostasis and triggering of apoptosis.

作者信息

Silva João P, Carmo Helena, Carvalho Félix

机构信息

UCIBIO, REQUIMTE, Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, 4050-313, Porto, Portugal.

UCIBIO, REQUIMTE, Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, 4050-313, Porto, Portugal.

出版信息

Toxicol Lett. 2018 May 1;287:59-69. doi: 10.1016/j.toxlet.2018.01.023. Epub 2018 Feb 3.

Abstract

Synthetic cannabinoids (SCBs)-related intoxications and deaths have been increasingly reported, turning its widespread recreational use into a major public health concern. Specifically, a direct link between SCBs and acute kidney injury (AKI) has been established. XLR-11 is an SCB commonly found in the toxicological analysis of patients with SCB-associated AKI. However, the pathophysiology of AKI among SCB consumers remains unknown. This work thus represents the first in vitro assessment of SCB nephrotoxicity, as a first approach to identify its cellular targets. We demonstrate that XLR-11, at biologically relevant concentrations (in the nanomolar range), primarily targets mitochondrial function in human proximal tubule (HK-2) cells, inducing a transient hyperpolarization of the mitochondrial membrane and increasing ATP production, accompanied by Bax translocation from cytosol into mitochondria. These phenomena further triggered energy-dependent apoptotic cell death pathways, indicated by increased caspase-3 activity and chromatin condensation. Experiments using SR141716A and SR144258, specific antagonists for CB1 and CB2 receptors, respectively, as well as HEK293T cells (which do not express CBRs) highlighted these processes' dependence on CBR activation. Nevertheless, ATP formation seemed to follow a CBR-independent pathway. Our findings using specific inhibitors of endogenous cannabinoids biosynthesis (i.e. MAFP and THL) further evidenced the involvement of the endocannabinoid system in the regulation of these processes, as XLR-11 binding to CBRs seemed to compromise endocannabinoid-mediated preservation of mitochondrial function. Nevertheless, the exact mechanisms involved require further clarification.

摘要

与合成大麻素(SCBs)相关的中毒和死亡报告日益增多,其广泛的娱乐性使用已成为一个主要的公共卫生问题。具体而言,SCBs与急性肾损伤(AKI)之间已建立直接联系。XLR-11是在SCB相关AKI患者毒理学分析中常见的一种SCB。然而,SCB使用者中AKI的病理生理学仍不清楚。因此,这项工作代表了对SCB肾毒性的首次体外评估,作为确定其细胞靶点的第一步。我们证明,在生物学相关浓度(纳摩尔范围)下,XLR-11主要靶向人近端小管(HK-2)细胞中的线粒体功能,诱导线粒体膜的短暂超极化并增加ATP生成,同时伴有Bax从细胞质转位到线粒体。这些现象进一步触发了能量依赖性凋亡细胞死亡途径,表现为caspase-3活性增加和染色质凝聚。分别使用CB1和CB2受体的特异性拮抗剂SR141716A和SR144258以及不表达大麻素受体(CBRs)的HEK293T细胞进行的实验突出了这些过程对CBR激活的依赖性。然而,ATP形成似乎遵循一条不依赖CBR的途径。我们使用内源性大麻素生物合成特异性抑制剂(即MAFP和THL)的研究结果进一步证明了内源性大麻素系统参与这些过程的调节,因为XLR-11与CBRs的结合似乎损害了内源性大麻素介导的线粒体功能保护。然而,其中的确切机制仍需进一步阐明。

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