Karaboğa İhsan, Okuyan Hamza Malik, Doğan Serdar, Ayçiçek Şeyda Öznur, Çakıroğlu Hüseyin
Department of Histology and Embryology, Faculty of Medicine, Kırklareli University, Kırklareli, Türkiye.
Department of Physiotherapy and Rehabilitation-Faculty of Health Sciences, Biomedical Technologies Application and Research Center, Physiotherapy and Rehabilitation Application and Research Center, Sakarya University of Applied Sciences, Sakarya, Türkiye.
Vet Med Sci. 2025 Mar;11(2):e70318. doi: 10.1002/vms3.70318.
Acute kidney injury (AKI) is one of the most serious complications of sepsis, with substantial morbidity and mortality, and no effective treatment exists. Ebselen is of pharmacological significance in the treatment and prevention of a variety of human diseases, such as cancer and cardiovascular disorders. Nevertheless, the role of Ebselen in the pathogenesis of sepsis-induced AKI remains unknown. Therefore, we aimed to elucidate the impact of Ebselen, an active seleno-organic compound, on AKI induced by lipopolysaccharide (LPS) and the associated molecular mechanisms, including endoplasmic reticulum (ER) stress, apoptosis, and oxidative stress. We established the sepsis-induced AKI rat model by injecting 5 mg/kg of LPS intraperitoneally. The rats were given Ebselen (5 and 10 mg/kg, orally) before receiving the LPS injection. Ebselen treatment alleviated renal tubular injury and reduced the levels of blood urea nitrogen (BUN) and creatinine (CREA) in LPS-induced sepsis model. Immunohistochemical and terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL) analyses revealed that Ebselen reduced caspase-3 expressions and apoptotic cells triggered by LPS in kidney tissues. LPS-induced sepsis caused ER stress, and Ebselen treatment alleviated the ER stress by regulating eukaryotic translation initiation factor 2-alpha kinase 3 (EIF2AK3) and GRP78 in kidney tissue, as well as activating transcription factor 4 (ATF4) and activating transcription factor 6 (ATF6) in serum. Ebselen decreased malondialdehyde (MDA) levels induced by LPS. Ebselen alleviated LPS-induced oxidative stress by modulating MDA and superoxide dismutase (SOD) levels in kidney tissues and SOD, glutathione peroxidase (GPx) and serum total antioxidant status (TAS) levels in serum. In conclusion, we report for the time that Ebselen might alleviate sepsis-induced AKI through the regulation of ER stress apoptosis and oxidative stress.
急性肾损伤(AKI)是脓毒症最严重的并发症之一,具有较高的发病率和死亡率,且尚无有效治疗方法。依布硒啉在治疗和预防多种人类疾病(如癌症和心血管疾病)方面具有药理学意义。然而,依布硒啉在脓毒症诱导的急性肾损伤发病机制中的作用仍不清楚。因此,我们旨在阐明活性有机硒化合物依布硒啉对脂多糖(LPS)诱导的急性肾损伤的影响及其相关分子机制,包括内质网(ER)应激、细胞凋亡和氧化应激。我们通过腹腔注射5mg/kg LPS建立了脓毒症诱导的急性肾损伤大鼠模型。在注射LPS前,给大鼠口服依布硒啉(5mg/kg和10mg/kg)。依布硒啉治疗可减轻LPS诱导的脓毒症模型中的肾小管损伤,并降低血尿素氮(BUN)和肌酐(CREA)水平。免疫组织化学和末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)分析显示,依布硒啉可降低LPS诱导的肾组织中caspase-3表达和凋亡细胞。LPS诱导的脓毒症会引起内质网应激,依布硒啉治疗可通过调节肾组织中的真核翻译起始因子2α激酶3(EIF2AK3)和GRP78,以及激活血清中的转录因子4(ATF4)和转录因子6(ATF6)来减轻内质网应激。依布硒啉可降低LPS诱导的丙二醛(MDA)水平。依布硒啉通过调节肾组织中的MDA和超氧化物歧化酶(SOD)水平以及血清中的SOD、谷胱甘肽过氧化物酶(GPx)和血清总抗氧化状态(TAS)水平,减轻LPS诱导的氧化应激。总之,我们首次报道依布硒啉可能通过调节内质网应激、细胞凋亡和氧化应激来减轻脓毒症诱导的急性肾损伤。