Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Russia.
Biochemistry Department, Institute of Chemistry, University of São Paulo (IQUSP), AV. Professor Lineu Prestes avenue, 748, USP, CEP: 05508-000 São Paulo, Brazil.
J Photochem Photobiol B. 2022 Apr;229:112425. doi: 10.1016/j.jphotobiol.2022.112425. Epub 2022 Mar 4.
Lipid peroxidation (LPO) plays a key role in many age-related neurodegenerative conditions and other disorders. Light irradiation can initiate LPO through various mechanisms and is of importance in retinal and dermatological pathologies. The introduction of deuterated polyunsaturated fatty acids (D-PUFA) into membrane lipids is a promising approach for protection against LPO. Here, we report the protective effects of D-PUFA against the photodynamically induced LPO, using illumination in the presence of the photosensitizer trisulfonated aluminum phthalocyanine (AlPcS) in liposomes and giant unilamellar vesicles (GUV), as assessed in four experimental models: 1) sulforhodamine B leakage from liposomes, detected with fluorescence correlation spectroscopy (FCS); 2) formation of diene conjugates in liposomal membranes, measured by absorbance at 234 nm; 3) membrane leakage in GUV assessed by optical phase-contrast intensity observations; 4) UPLC-MS/MS method to detect oxidized linoleic acid (Lin)-derived metabolites. Specifically, in liposomes or GUV containing H-PUFA (dilinoleyl-sn-glycero-3-phosphatidylcholine), light irradiation led to an extensive oxidative damage to bilayers. By contrast, no damage was observed in lipid bilayers containing 20% or more D-PUFA (D2-Lin or D10-docosahexanenoic acid). Remarkably, addition of tocopherol increased the dye leakage from liposomes in H-PUFA bilayers compared to photoirradiation alone, signifying tocopherol's pro-oxidant properties. However, in the presence of D-PUFA the opposite effect was observed, whereby adding tocopherol increased the resistance to LPO. These findings suggest a method to augment the protective effects of D-PUFA, which are currently undergoing clinical trials in several neurological and retinal diseases that involve LPO.
脂质过氧化 (LPO) 在许多与年龄相关的神经退行性疾病和其他疾病中起着关键作用。光照可以通过多种机制引发 LPO,并且在视网膜和皮肤病理学中具有重要意义。将氘代多不饱和脂肪酸 (D-PUFA) 引入膜脂质是一种有前途的防止 LPO 的方法。在这里,我们报告了 D-PUFA 对光动力诱导的 LPO 的保护作用,方法是在存在光敏剂三磺化铝酞菁 (AlPcS) 的脂质体和巨大单层囊泡 (GUV) 中进行光照,使用了四种实验模型:1) 通过荧光相关光谱法 (FCS) 检测从脂质体中漏出的 sulforhodamine B;2) 通过在 234nm 处的吸光度测量测定脂质体膜中二烯轭合物的形成;3) 通过光学相差强度观察评估 GUV 中的膜泄漏;4) 通过 UPLC-MS/MS 方法检测氧化的亚油酸 (Lin) 衍生代谢物。具体而言,在含有 H-PUFA (二亚油酰基-sn-甘油-3-磷酸胆碱) 的脂质体或 GUV 中,光照会导致双层膜发生广泛的氧化损伤。相比之下,在含有 20%或更多 D-PUFA (D2-亚油烯酸或 D10-二十二碳六烯酸) 的脂质双层中未观察到损伤。值得注意的是,与单独光照射相比,向含有 H-PUFA 的双层中添加生育酚会增加染料从脂质体中的漏出,表明生育酚具有促氧化剂特性。然而,在存在 D-PUFA 的情况下,观察到相反的效果,即添加生育酚会增加对 LPO 的抵抗力。这些发现为增强目前正在几种涉及 LPO 的神经和视网膜疾病的临床试验中的 D-PUFA 的保护作用提供了一种方法。