Dipartimento di Medicina Sperimentale, Università di Genoa, Via De Toni 14, 16132, Genova, Italy.
Centro di Biologia Integrata (CIBIO), Università di Trento, Via Sommarive, 9, Povo, 38123, Trento, Italy.
Free Radic Biol Med. 2020 Nov 20;160:368-375. doi: 10.1016/j.freeradbiomed.2020.08.014. Epub 2020 Aug 24.
We have previously shown that the retinal rod outer segments (OS) produce reactive oxygen species in the function of illumination in vitro, establishing a relationship among the extra-mitochondrial oxidative phosphorylation and phototransduction. This source of oxidative stress in the OS can be modulated by polyphenols, acting as inhibitors of FF-ATP synthase. The present study aimed at exploring whether sclareol, a diterpene, interacts with FF-ATP synthase mitigating the light-induced free radical production in the rod OS. Characterization of bovine retinal sections was conducted by immunogold analysis. Reactive oxygen intermediates production, oxygen consumption, the activity of the four respiratory complexes and ATP synthesis were evaluated in purified bovine rod OS. Molecular docking analyses were also conducted. Sclareol reduced free radical production by light-exposed rod OS. Such antioxidant effect was associated with an inhibition of the respiratory complexes and oxygen consumption (OCR), in coupled conditions. Sclareol also inhibited the rod OS ATP synthetic ability. Since the inhibitor effect on respiratory complexes and OCR is not observed in uncoupled conditions, it is supposed that the modulating effect of sclareol on the ectopic oxidative phosphorylation in the rod OS targets specifically the FF-ATP synthase. This hypothesis is confirmed by the in silico molecular docking analyses, which shows that sclareol binds the F moiety of ATP synthase with high affinity. In conclusion, a beneficial effect of sclareol can be envisaged as a modulator of oxidative stress in the photoreceptor, a risk factor for the degenerative retinal diseases, suggestive of its potential beneficial action also in vivo.
我们之前已经证明,在体外光照的作用下,视网膜杆状细胞外段(OS)会产生活性氧,这建立了细胞外线粒体氧化磷酸化和光转导之间的关系。OS 中的这种氧化应激源可以被多酚调节,多酚可以作为 FF-ATP 合酶的抑制剂。本研究旨在探索二萜类化合物雪松醇是否与 FF-ATP 合酶相互作用,从而减轻 OS 中光诱导的自由基产生。通过免疫金分析对牛视网膜切片进行了特征描述。在纯化的牛杆 OS 中评估了活性氧中间体的产生、耗氧量、四个呼吸复合物的活性和 ATP 合成。还进行了分子对接分析。雪松醇减少了光暴露的 OS 中的自由基产生。这种抗氧化作用与呼吸复合物和耗氧量(OCR)的抑制有关,在偶联条件下。雪松醇还抑制了 OS 的 ATP 合成能力。由于在非偶联条件下未观察到对呼吸复合物和 OCR 的抑制作用,因此推测雪松醇对 OS 异位氧化磷酸化的调节作用专门针对 FF-ATP 合酶。这一假设通过计算机分子对接分析得到了证实,该分析表明雪松醇与 ATP 合酶的 F 部分具有高亲和力。总之,雪松醇的有益作用可以被设想为光感受器中氧化应激的调节剂,这是退行性视网膜疾病的一个风险因素,这表明它在体内也可能具有潜在的有益作用。