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迷迭香酸通过减轻线粒体和内质网应激反应缓解紫外线介导的皮肤衰老。

Rosmarinic acid alleviates ultraviolet-mediated skin aging via attenuation of mitochondrial and ER stress responses.

机构信息

PK-PD and Toxicology division, CSIR-Indian Institute of Integrative Medicine, Jammu, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.

出版信息

Exp Dermatol. 2023 Jun;32(6):799-807. doi: 10.1111/exd.14773. Epub 2023 Mar 30.

Abstract

Chronic exposure to Ultraviolet B radiation (UV-B) evokes a myriad of toxic signalling events in the irradiated skin. One of such response is ER stress, which is known to exacerbate photodamage responses. Also, recent literature has highlighted the adverse impact of environmental toxicants on mitochondrial dynamics and mitophagy. Impaired mitochondrial dynamics escalates oxidative damage and causes apoptosis. There have been evidences that support crosstalk between ER stress and mitochondrial dysfunction. However, mechanistic clarification is still needed to verify the interactions between UPR responses and mitochondrial dynamics impairment in UV-B-induced photodamage models. Lastly, plant-based natural agents have garnered attention as therapeutic agents against skin photodamage. Thus, gaining mechanistic insights of plant-based natural agents is required for their application and feasibility in clinical settings. With this aim in view, this study was performed in primary human dermal fibroblasts (HDFs) and Balb/C mice. Different parameters regarding mitochondrial dynamics, ER stress, intracellular damage and histological damage were analyzed using western blot, rt-PCR and microscopy. We demonstrated that UV-B exposure leads to induction of UPR responses, upregulation of Drp-1 and inhibition of mitophagy. Further, 4-PBA treatment leads to reversal of these noxious stimuli in irradiated HDF cells, thereby, indicating an upstream role of UPR induction in mitophagy inhibition. Also, we explored the therapeutic effect of Rosmarinic acid (RA) against ER stress and impaired mitophagy in photodamage models. RA prevents intracellular damage via alleviation of ER stress and mitophagic responses in HDFs and irradiated Balb/C mice skin. The current study summarizes the mechanistic insights into UVB-mediated intracellular damage and role of natural plant-based agent (RA) in ameliorating these toxic responses.

摘要

慢性暴露于紫外线 B 辐射(UV-B)会在受照射的皮肤中引发无数种有毒信号事件。其中一种反应是内质网应激(ER stress),已知它会加剧光损伤反应。此外,最近的文献强调了环境毒物对线粒体动力学和自噬的不利影响。受损的线粒体动力学会加剧氧化损伤并导致细胞凋亡。有证据表明 ER 应激和线粒体功能障碍之间存在串扰。然而,为了验证 UPR 反应与 UV-B 诱导的光损伤模型中线粒体动力学损伤之间的相互作用,仍需要进行机制上的澄清。最后,植物源性天然药物已作为治疗皮肤光损伤的药物受到关注。因此,需要深入了解植物源性天然药物的作用机制,以评估其在临床应用中的可行性。基于此目的,本研究在原代人真皮成纤维细胞(HDF)和 Balb/C 小鼠中进行。使用 Western blot、rt-PCR 和显微镜分析了与线粒体动力学、内质网应激、细胞内损伤和组织学损伤相关的不同参数。我们证明,UV-B 暴露会导致 UPR 反应的诱导、Drp-1 的上调和自噬的抑制。此外,4-PBA 处理会导致照射的 HDF 细胞中这些有害刺激的逆转,从而表明 UPR 诱导在内质网应激诱导的自噬抑制中起上游作用。此外,我们还探索了迷迭香酸(RA)对光损伤模型中内质网应激和受损自噬的治疗作用。RA 通过减轻 HDF 和照射的 Balb/C 小鼠皮肤中的内质网应激和自噬反应来防止细胞内损伤。本研究总结了 UVB 介导的细胞内损伤的机制见解以及天然植物源性药物(RA)在改善这些毒性反应中的作用。

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