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虾青素调节自噬对肠缺血再灌注损伤大鼠认知功能的影响OA北大核心CSTPCD

Effect of astaxanthin regulating autophagy on cognitive function of rats with intestinal ischemia/reperfusion injury

中文摘要英文摘要

目的:评价虾青素(AST)对肠缺血再灌注(I/R)损伤大鼠认知功能的影响及自噬在其中的作用.方法:8周龄SPF级雄性Sprague-Dawley(SD)大鼠随机分为假手术(sham)组、I/R组、AST组和AST+3-甲基腺嘌呤(3-MA)组,每组12只.其中,sham组大鼠仅暴露肠系膜上动脉(SMA)而不夹闭,其余3组夹闭SMA 90 min后开夹再灌注建立肠I/R模型.AST组大鼠造模前3 d给予AST(45 mg·kg-1·d-1)腹腔注射,AST+3-MA组大鼠造模前3 d给予AST(45 mg·kg-1·d-1)+3-MA(1.5 mg·kg-1·d-1)腹腔注射.术后48 h采用Morris水迷宫评估大鼠认知功能;苏木精-伊红(HE)染色评估肠组织损伤;额叶皮质尼氏染色评估神经元损伤;ELISA试剂盒测定额叶皮质和海马组织内白细胞介素6(IL-6)、IL-1β和肿瘤坏死因子α(TNF-α)水平;Western blot检测额叶皮质和海马组织内beclin-1、微管相关蛋白1轻链3(LC3)和P62的表达水平.结果:与sham组相比,I/R组大鼠游泳距离增加,潜伏期延长,Chiu's评分升高,额叶皮质神经元数量减少(P<0.01),额叶皮质和海马组织IL-6、IL-1β和TNF-α含量升高(P<0.01),额叶皮质和海马组织beclin-1表达水平和LC3-II/LC3-I比值均升高(P<0.05或P<0.01);与I/R组对比,AST组大鼠游泳距离和潜伏期缩短,Chiu's评分降低,额叶皮质神经元数量增加(P<0.01),额叶皮质和海马组织IL-6、IL-1β和TNF-α含量降低(P<0.01),额叶皮质和海马组织beclin-1表达水平升高而P62表达水平降低(P<0.05或P<0.01);与AST组相比,AST+3-MA组大鼠游泳距离增加,潜伏期延长,Chiu's评分升高,额叶皮质神经元数量减少(P<0.05),额叶皮质和海马组织IL-6、IL-1β和TNF-α含量升高,额叶皮质和海马beclin-1表达水平和LC3-II/LC3-I比值降低,P62表达水平升高(P<0.01).结论:AST可通过促进自噬抑制神经炎症,从而缓解大鼠肠I/R引起的认知障碍.

AIM:To evaluate the effect of astaxanthin(AST)on cognitive function of intestinal ischemia/re-perfusion(I/R)injury in rats and the role of autophagy.METHODS:Eight-week-old SPF-grade male Sprague-Dawley(SD)rats were randomly divided into sham group,I/R group,AST group and AST+3-methyladenine(3-MA)group,with 12 animals in each group.The superior mesenteric artery(SMA)of the rats in sham group was only exposed without clamping.The SMA in other 3 groups was clamped for 90 min,and then the arterial clamp was released to restore blood supply and perform reperfusion,thus establishing the intestinal I/R model.The rats in AST group were intraperitoneally in-jected with AST(45 mg·kg-1·d-1)3 d before modeling,and those in AST+3-MA group were intraperitoneally injected with AST(45 mg·kg-1·d-1)+3-MA(1.5 mg·kg-1·d-1)3 d before modeling.Morris water maze was used to evaluate the cogni-tive function of rats 48 h after surgery.Hematoxylin-eosin(HE)staining was used to evaluate intestinal tissue damage.Nissl staining of the frontal cortex was used to evaluate neuronal damage.The levels of interleukin-6(IL-6),IL-1β and tu-mor necrosis factor-α(TNF-α)in the frontal cortex and hippocampus were measured by ELISA kits.The protein levels of beclin-1,microtubule-associated protein 1 light chain 3(LC3)and P62 in the frontal cortex and hippocampus were detected by Western blot.RESULTS:Compared with sham group,the swimming distance of rats in I/R group was increased,with prolonged latency,elevated Chiu's score and decreased number of neurons(P<0.01),while the levels of IL-6,IL-1β and TNF-α in the frontal cortex and hippocampus were increased(P<0.01).Beclin-1 expression and LC3-II/LC3-I ratio in the frontal cortex and hippocampus were increased(P<0.05 or P<0.01).Compared with I/R group,the swimming distance and latency of rats in AST group were shortened,with decreased Chiu's score,increased neuronal number(P<0.01),de-creased IL-6,IL-1β and TNF-α levels in the frontal cortex and hippocampus(P<0.01),and increased beclin-1 expres-sion and decreased of P62 expression in the frontal cortex and hippocampus(P<0.05 or P<0.01).Compared with AST group,the swimming distance of rats in AST+3-MA group was increased,with prolonged latency,elevated Chiu's score,decreased number of neurons(P<0.05),increased levels of IL-6,IL-1β and TNF-α in the frontal cortex and hippocam-pus,and decreased beclin-1 expression and LC3-II/LC3-I ratio and increased P62 expression in the frontal cortex and hip-pocampus(P<0.01).CONCLUSION:Astaxanthin alleviates intestinal I/R-induced cognitive impairment in rats by pro-moting autophagy and inhibiting neuroinflammation.

张伟;王迎斌;张晶玉;曹璐;刘艳;张丽

兰州大学第二医院麻醉科,甘肃 兰州 730030兰州大学第二临床医学院,甘肃 兰州 730030

临床医学

虾青素;肠缺血再灌注损伤;认知;自噬;神经炎症

astaxanthin;intestinal ischemia/reperfusion injury;cognition;autophagy;neuroinflammation

《中国病理生理杂志》 2024 (005)

836-843 / 8

甘肃省自然科学基金资助项目(No.23JRRA0988)

10.3969/j.issn.1000-4718.2024.00.016

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