Effect of 2-Week Naringin Supplementation on Neurogenesis and BDNF Levels in Ischemia-Reperfusion Model of Rats.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-03-08 DOI:10.1007/s12017-023-08771-0
Esen Yilmaz, Gozde Acar, Ummugulsum Onal, Ender Erdogan, Abdulkerim Kasim Baltaci, Rasim Mogulkoc
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Abstract

Background: Ischemic stroke is the leading cause of mortality and disability worldwide with more than half of survivors living with serious neurological sequelae; thus, it has recently attracted a lot of attention in the field of medical study.

Purpose: The aim of this study was to determine the effect of naringin supplementation on neurogenesis and brain-derived neurotrophic factor (BDNF) levels in the brain in experimental brain ischemia-reperfusion.

Study design: The research was carried out on 40 male Wistar-type rats (10-12 weeks old) obtained from the Experimental Animals Research and Application Center of Selçuk University. Experimental groups were as follows: (1) Control group, (2) Sham group, (3) Brain ischemia-reperfusion group, (4) Brain ischemia-reperfusion + vehicle group (administered for 14 days), and (5) Brain ischemia-reperfusion + Naringin group (100 mg/kg/day administered for 14 days).

Methods: In the ischemia-reperfusion groups, global ischemia was performed in the brain by ligation of the right and left carotid arteries for 30 min. Naringin was administered to experimental animals by intragastric route for 14 days following reperfusion. The training phase of the rotarod test was started 4 days before ischemia-reperfusion, and the test phase together with neurological scoring was performed the day before and 1, 7, and 14 days after the operation. At the end of the experiment, animals were sacrificed, and then hippocampus and frontal cortex tissues were taken from the brain. Double cortin marker (DCX), neuronal nuclear antigen marker (NeuN), and BDNF were evaluated in hippocampus and frontal cortex tissues by Real-Time qPCR analysis and immunohistochemistry methods.

Results: While ischemia-reperfusion increased the neurological score values, DCX, NeuN, and BDNF levels decreased significantly after ischemia in the hippocampus and frontal cortex tissues. However, naringin supplementation restored the deterioration to a certain extent.

Conclusion: The results of the study show that 2 weeks of naringin supplementation may have protective effects on impaired neurogenesis and BDNF levels after brain ischemia and reperfusion in rats.

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补充两周柚皮苷对缺血再灌注模型大鼠神经发生和 BDNF 水平的影响
背景:目的:本研究旨在确定补充柚皮苷对实验性脑缺血再灌注中脑神经发生和脑源性神经营养因子(BDNF)水平的影响:研究对象是从塞尔丘克大学实验动物研究与应用中心获得的 40 只雄性 Wistar 型大鼠(10-12 周龄)。实验组如下(1) 对照组;(2) Sham 组;(3) 脑缺血再灌注组;(4) 脑缺血再灌注+载体组(给药 14 天);(5) 脑缺血再灌注+柚皮苷组(100 毫克/千克/天,给药 14 天):方法:在缺血再灌注组中,通过结扎左右颈动脉进行大脑缺血 30 分钟。再灌注后通过胃内途径给实验动物注射柚皮苷14天。在缺血再灌注前4天开始训练阶段,在手术前一天、手术后1天、7天和14天进行测试阶段和神经系统评分。实验结束后,动物被处死,然后从大脑中提取海马和额叶皮层组织。通过实时 qPCR 分析和免疫组化方法对海马和额叶皮层组织中的双皮质素标记(DCX)、神经元核抗原标记(NeuN)和 BDNF 进行了评估:结果:缺血再灌注会增加神经系统评分值,但缺血后海马和额叶皮层组织中的DCX、NeuN和BDNF水平显著下降。然而,补充柚皮苷可在一定程度上恢复这种恶化:研究结果表明,大鼠脑缺血和再灌注后,补充 2 周的柚皮苷可能对受损的神经发生和 BDNF 水平有保护作用。
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CiteScore
7.20
自引率
4.30%
发文量
567
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