Uchida Atsushi, Kidokoro Kengo, Sogawa Yuji, Itano Seiji, Nagasu Hajime, Satoh Minoru, Sasaki Tamaki, Kashihara Naoki
Department of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki, Japan.
Nephrology (Carlton). 2019 Jan;24(1):28-38. doi: 10.1111/nep.13189.
Acute kidney injury (AKI) is associated with chronic kidney disease, as well as high mortality, but effective treatments for AKI are still lacking. A recent study reported the prevention of renal injury, such as ischemia-reperfusion injury, by 5-aminolevulinic acid (ALA), which induces an antioxidant effect. The current study aimed to investigate the effect of ALA in a rhabdomyolysis-induced mouse model of AKI created by intramuscular injection of 50% glycerol.
Rhabdomyolysis-induced AKI was induced by an intramuscular injection of glycerol (5 mL/kg body weight) into mice. Administration of ALA (30 mg/kg, by gavage) was started from 48 h before or 24 h after glycerol injection. The mice were sacrificed at 72 h after glycerol injection. The roles of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1), which is one of the Nrf2-related antioxidants, were further investigated through in vivo and in vitro methods.
5-aminolevulinic acid markedly reduced renal dysfunction and tubular damage in mice with rhabdomyolysis-induced AKI. ALA administration decreased oxidative stress, macrophage infiltration, and inflammatory cytokines and apoptosis. The expression of Nrf2 was upregulated by ALA administration. However, administration of Zinc protoporphyrin-9 (ZnPPIX) to inhibit HO-1 activity did not abolish these improvements by ALA. The expression of Nrf2-associated antioxidant factors other than HO-1 was also increased.
These findings indicate that ALA exerts its antioxidant activity via Nrf2-associated antioxidant factors to provide a renoprotective effect against rhabdomyolysis-induced AKI.
急性肾损伤(AKI)与慢性肾脏病相关,且死亡率高,但仍缺乏有效的AKI治疗方法。最近一项研究报道了5-氨基酮戊酸(ALA)可预防肾损伤,如缺血再灌注损伤,其可诱导抗氧化作用。本研究旨在探讨ALA在通过肌肉注射50%甘油建立的横纹肌溶解诱导的小鼠AKI模型中的作用。
通过向小鼠肌肉注射甘油(5 mL/kg体重)诱导横纹肌溶解诱导的AKI。从甘油注射前48小时或注射后24小时开始给予ALA(30 mg/kg,经口灌胃)。在甘油注射后72小时处死小鼠。通过体内和体外方法进一步研究核因子红细胞2相关因子2(Nrf2)和血红素加氧酶-1(HO-1)(Nrf2相关抗氧化剂之一)的作用。
5-氨基酮戊酸显著降低了横纹肌溶解诱导的AKI小鼠的肾功能障碍和肾小管损伤。给予ALA可降低氧化应激、巨噬细胞浸润、炎性细胞因子和细胞凋亡。给予ALA可上调Nrf2的表达。然而,给予锌原卟啉-9(ZnPPIX)抑制HO-1活性并不能消除ALA带来的这些改善。除HO-1外,Nrf2相关抗氧化因子的表达也增加。
这些发现表明,ALA通过Nrf2相关抗氧化因子发挥其抗氧化活性,从而对横纹肌溶解诱导的AKI提供肾脏保护作用。