Neuroprotective effect of 6-hydroxy-2,2,4-trimethyl-1,2-dihydroquinoline mediated via regulation of antioxidant system and inhibition of inflammation and apoptosis in a rat model of cerebral ischemia/reperfusion

被引:9
作者
Kryl'skii, E. D. [1 ]
Chupandina, E. E. [2 ]
Popova, T. N. [1 ]
Shikhaliev, Kh. S. [3 ]
Mittova, V. O. [4 ]
Popov, S. S. [5 ]
Verevkin, A. N. [1 ]
Filin, A. A. [2 ]
机构
[1] Voronezh State Univ, Dept Med Biochem & Microbiol, Voronezh, Russia
[2] Voronezh State Med Univ, Dept Pathol Anat, Voronezh, Russia
[3] Voronezh State Univ, Dept Organ Chem, Voronezh, Russia
[4] Voronezh State Med Univ, Dept Biochem, Voronezh, Russia
[5] Voronezh State Med Univ, Dept Org Pharmaceut Business Clin Pharm & Pharmac, Voronezh, Russia
关键词
Cerebral ischemia; reperfusion; Oxidative stress; Dihydroquinoline derivatives; Inflammation; Apoptosis; Antioxidants; ISCHEMIA-REPERFUSION-INJURY; OXIDATIVE STRESS; BRAIN ISCHEMIA; DAMAGE; MYELOPEROXIDASE; ETHOXYQUIN; PROTEINS; PROTECTS; EXPOSURE; CATALASE;
D O I
10.1016/j.biochi.2021.04.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of the study was the assessment of the neuroprotective potential of 6-hydroxy-2,2,4-trimethyl-1,2-dihydroquinoline (DHQ) and its effect on inflammation, apoptosis, and transcriptional regulation of the antioxidant system in cerebral ischemia/reperfusion (CIR) in rats. The CIR rat model was constructed using the bilateral common carotid artery occlusion followed by reoxygenation. DHQ was administered at a dose of 50 mg/kg for three days. Histological staining was performed using hematoxylin and eosin. The level of S100B protein, 8-hydroxy-2-deoxyguanosine, and 8-isoprostane was assessed using an enzyme immunoassay. The intensity of apoptosis was assessed based on the activity of caspases and DNA fragmentation. The activity of enzymes was measured spectrophotometrically, the level of gene transcripts was assessed by real-time PCR. DHQ reduced the histopathological changes and normalized levels of S100B, lactate, pyruvate, and HIF-1 mRNA in the CIR rat model. In addition, DHQ decreased the oxidative stress markers in animals with a pathology. The tested compound also inhibited inflammation by decreasing the activity of myeloper-oxidase, expression of interleukins and Nfkb2. DHQ-treated rats with CIR showed decreased caspase activity, DNA fragmentation, and AIF expression. DHQ changed activity of antioxidant enzymes to the control values, decreased the expression of Cat, Gsr, and Nfe2l2, which was overexpressed in CIR, and activated the expression of Sod1, Gpx1, Gsta2, and Foxo1. DHQ showed a neuroprotective effect on CIR in rats. The neuroprotective effect involve mechanisms such as the inhibition of oxidative stress, leading to a reduction in the inflammatory response and apoptosis and the modulation of the antioxidant defense components. (c) 2021 Elsevier B.V. and Soci & eacute;t & eacute; Fran & ccedil;aise de Biochimie et Biologie Mol & eacute;culaire (SFBBM). All rights reserved.
引用
收藏
页码:130 / 146
页数:17
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