Menéndez-Valle Iván, Cachán-Vega Cristina, Boga José Antonio, González-Blanco Laura, Antuña Eduardo, Potes Yaiza, Caballero Beatriz, Vega-Naredo Ignacio, Saiz Pilar, Bobes Julio, García-Portilla Paz, Coto-Montes Ana
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Av. del Hospital Universitario, s/n, 33011 Oviedo, Asturias, Spain.
Instituto de Neurociencias (INEUROPA), University of Oviedo, Julián Clavería, s/n, 33006 Oviedo, Asturias, Spain.
Antioxidants (Basel). 2023 Nov 1;12(11):1948. doi: 10.3390/antiox12111948.
Schizophrenia (SCH) and bipolar disorder (BD) are two of the most important psychiatric pathologies due to their high population incidence and disabling power, but they also present, mainly in their debut, high clinical similarities that make their discrimination difficult. In this work, the differential oxidative stress, present in both disorders, is shown as a concatenator of the systemic alterations-both plasma and erythrocyte, and even at the level of peripheral blood mononuclear cells (PBMC)-in which, for the first time, the different affectations that both disorders cause at the level of the cellular interactome were observed. A marked erythrocyte antioxidant imbalance only present in SCH generalizes to oxidative damage at the plasma level and shows a clear impact on cellular involvement. From the alteration of protein synthesis to the induction of death by apoptosis, including proteasomal damage, mitochondrial imbalance, and autophagic alteration, all the data show a greater cellular affectation in SCH than in BD, which could be linked to increased oxidative stress. Thus, patients with SCH in our study show increased endoplasmic reticulum (ER)stress that induces increased proteasomal activity and a multifactorial response to misfolded proteins (UPR), which, together with altered mitochondrial activity, generating free radicals and leading to insufficient energy production, is associated with defective autophagy and ultimately leads the cell to a high apoptotic predisposition. In BD, however, oxidative damage is much milder and without significant activation of survival mechanisms or inhibition of apoptosis. These clear differences identified at the molecular and cellular level between the two disorders, resulting from progressive afflictions in which oxidative stress can be both a cause and a consequence, significantly improve the understanding of both disorders to date and are essential for the development of targeted and preventive treatments.
精神分裂症(SCH)和双相情感障碍(BD)是两种最重要的精神疾病,因其在人群中的高发病率和致残性,但它们在发病初期也表现出高度的临床相似性,这使得它们难以鉴别。在这项研究中,两种疾病中存在的差异性氧化应激被证明是全身改变(包括血浆和红细胞,甚至在外周血单核细胞(PBMC)水平)的串联因素,其中首次观察到两种疾病在细胞相互作用组水平上引起的不同影响。仅在精神分裂症中出现的明显红细胞抗氧化失衡会扩展到血浆水平的氧化损伤,并对细胞参与产生明显影响。从蛋白质合成的改变到凋亡诱导的死亡,包括蛋白酶体损伤、线粒体失衡和自噬改变,所有数据都表明精神分裂症比双相情感障碍对细胞的影响更大,这可能与氧化应激增加有关。因此,我们研究中的精神分裂症患者表现出内质网(ER)应激增加,这会诱导蛋白酶体活性增加以及对错误折叠蛋白质的多因素反应(未折叠蛋白反应),再加上线粒体活性改变,产生自由基并导致能量产生不足,这与自噬缺陷相关,最终导致细胞具有较高的凋亡倾向。然而,在双相情感障碍中,氧化损伤要轻得多,且没有明显的生存机制激活或凋亡抑制。这两种疾病在分子和细胞水平上的明显差异,源于氧化应激可能既是病因又是结果的渐进性病变,显著提高了迄今为止对这两种疾病的认识,对于开发针对性和预防性治疗至关重要。