Targeting the PANoptosome with 3,4-Methylenedioxy-β-Nitrostyrene, Reduces PANoptosis and Protects the Kidney against Renal İschemia-Reperfusion Injury

医学 谷胱甘肽过氧化物酶 丙二醛 超氧化物歧化酶 细胞凋亡 过氧化氢酶 再灌注损伤 坏死性下垂 二甲基亚砜 上睑下垂 肾切除术 药理学 内分泌学 缺血 氧化应激 炎症体 生物化学 内科学 程序性细胞死亡 受体 化学 有机化学
作者
Erdal Uysal,Mehmet Dokur,Faruk Küçükdurmaz,Serdar Altınay,Sait Polat,Kadir Batçıoğlu,Efe Sezgın,Tuğçe Sapmaz Erçakallı,Asli Yaylalı,Yakup Yılmaztekin,Zafer Çetin,Eyüp İlker Saygılı,Osman Barut,Hatem Kazımoğlu,Göktürk Maralcan,Suna Koç,Türkan Güney,Nadire Eser,Mehmet Sökücü,Sema Nur Dokur
出处
期刊:Journal of Investigative Surgery [Taylor & Francis]
卷期号:35 (11-12): 1824-1835 被引量:20
标识
DOI:10.1080/08941939.2022.2128117
摘要

The objectives of this study were a) to investigate the effect of targeting the PANoptosome with 3,4-methylenedioxy-β-nitrostyrene (MNS) on PANoptosis in the Renal ischemia-reperfussion (RIR) model b) to investigate the kidney protective effect of MNS toward RIR injury.Thirty-two rats were divided into four groups randomly. The groups were assigned as Control, Sham, DMSO (dimethyl sulfoxide) and MNS groups. The rats in the MNS group were intraperitoneally given 20 mg/kg of MNS 30 minutes before reperfusion. 2% DMSO solvent that dissolves MNS were given to the rats in DMSO group. Left nephrectomy was performed on the rats under anesthesia at the 6th hour after reperfusion. Glutathione peroxidase (GPx), malondialdehyde (MDA), catalase (CAT), superoxide dismutase (SOD) and 8-Okso-2'-deoksiguanozin (8-OHdG) levels were measured. Immunohistochemical analysis, electron microscopic and histological examinations were carried out in the tissues.Total tubular injury score was lower in the MNS group (p < 0.001). Caspase-3, Gasdermin D and MLK (Mixed Lineage Kinase Domain Like Pseudokinase) expressions were considerably decreased in the MNS group (p < 0.001). Apoptotic index (AI) was found to be low in the MNS group (p < 0.001). CAT and SOD levels were higher in the MNS Group (p = 0.006, p = 0.0004, respectively). GPx, MDA, and 8-OH-dG levels were similar (p > 0.05) in all groups. MNS considerably improved the tissue structure, based on the electron microscopic analysis.Our results suggested that MNS administrated before the reperfusion reduces pyroptosis, apoptosis and necroptosis. These findings suggest that MNS significantly protects the kidney against RIR injury by reducing PANoptosis as a result of specific inhibition of Nod-like receptor pyrin domain-containing 3 (NLRP 3), one of the PANoptosome proteins.
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