Department of Medicine, Nephrology, University of Padua, Padua Italy.
Department of Medicine, Hypertension, University of Padua, Padua Italy.
PLoS One. 2018 Sep 27;13(9):e0204618. doi: 10.1371/journal.pone.0204618. eCollection 2018.
Fabry disease is characterized by deficient expression/activity of α-GalA with consequent lysosomal accumulation in various organs of its substrate Gb3. Despite enzyme replacement therapy, Fabry disease progresses with serious myocardial, cerebral and renal manifestations. Gb3 accumulation may induce oxidative stress (OxSt), production of inflammatory cytokines and reduction of nitric oxide, which may impact on Fabry disease's clinical manifestations.
OxSt status was characterized in 10 patients compared with 10 healthy subjects via protein expression of p22phox, subunit of NADH/NADPH oxidase, (Western blot), Heme oxygenase (HO)-1 levels (ELISA), antioxidant/anti-inflammatory, lipid peroxidation as malondialdehyde (MDA) production (colorimetric assay), phosphorylation state of Extracellular Signal Regulated Kinase (ERK)1/2 and Myosin Phosphatase Target Protein (MYPT)-1 (Western blot), marker of Rho kinase activation, both involved in OxSt signaling. Cardiac left ventricular (LV) mass was also evaluated (M-mode echocardiography).
LV mass was higher in Fabry's males (123.72±2.03SEM g/m2) and females (132.09±6.72g/m2). p22phox expression was also higher in patients (1.04±0.09 d.u. vs 0.54±0.05 d.u. p<0.01) as well as MDA levels (54.51±3.97 vs 30.05±7.11 nmol/mL p = 0.01) while HO-1 was reduced (8.84±0.79 vs 14.03±1.23 ng/mL, p<0.02). MYPT-1's phosphorylation was increased in patients (0.52±0.11 d.u. vs 0.03±0.08 d.u., p<0.01) while phosphorylation of ERK1/2 was reduced (0.91±0.08 d.u. vs 1.53±0.17 d.u., p = 0.004).
This study documents OxSt activation and the altered reaction to it in Fabry patients. Cardiac remodeling, Rho kinase signaling activation and reduction of protective HO-1 might suggest that, in addition to enzyme replacement therapy, OxSt inhibition by either pharmacological or nutritional measures, is likely to prove useful for the prevention/treatment of Fabry patients' cardiovascular-renal remodeling.
法布里病的特征是α-半乳糖苷酶 A 的表达/活性不足,导致其底物 Gb3 在各种器官中的溶酶体积累。尽管进行了酶替代治疗,但法布里病仍会进展,并伴有严重的心肌、大脑和肾脏表现。Gb3 的积累可能会诱导氧化应激(OxSt)、炎性细胞因子的产生和一氧化氮的减少,这可能会影响法布里病的临床表现。
通过 NADH/NADPH 氧化酶亚基 p22phox 的蛋白表达(Western blot)、血红素加氧酶(HO)-1 水平(ELISA)、抗氧化/抗炎、丙二醛(MDA)产生的脂质过氧化(比色法测定),比较 10 名法布里病患者和 10 名健康对照者的 OxSt 状态,评估 10 名法布里病患者的心脏左心室(LV)质量。
法布里病男性(123.72±2.03SEM g/m2)和女性(132.09±6.72g/m2)的 LV 质量均较高。患者的 p22phox 表达也较高(1.04±0.09 d.u. 比 0.54±0.05 d.u.,p<0.01),MDA 水平也较高(54.51±3.97 比 30.05±7.11 nmol/mL,p = 0.01),而 HO-1 水平较低(8.84±0.79 比 14.03±1.23 ng/mL,p<0.02)。患者的 MYPT-1 磷酸化增加(0.52±0.11 d.u. 比 0.03±0.08 d.u.,p<0.01),而 ERK1/2 的磷酸化减少(0.91±0.08 d.u. 比 1.53±0.17 d.u.,p = 0.004)。
本研究记录了法布里病患者 OxSt 的激活及其对 OxSt 的反应改变。心脏重构、Rho 激酶信号转导的激活和保护性 HO-1 的减少表明,除了酶替代治疗外,通过药理学或营养措施抑制 OxSt,可能有助于预防/治疗法布里病患者的心血管-肾脏重构。