[1]杨雪,左中夫.桦褐孔菌多糖经Nrf2信号通路对糖尿病大鼠视网膜组织氧化应激和炎症反应的抑制作用[J].眼科新进展,2020,40(8):717-721.[doi:10.13389/j.cnki.rao.2020.0163]
 YANG Xue,ZUO Zhongfu.Inhibition of oxidative stress and inflammation in retinal tissue of diabetic rats by inonotus obliquus polysaccharides via Nrf2 signaling pathway[J].Recent Advances in Ophthalmology,2020,40(8):717-721.[doi:10.13389/j.cnki.rao.2020.0163]
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桦褐孔菌多糖经Nrf2信号通路对糖尿病大鼠视网膜组织氧化应激和炎症反应的抑制作用/HTML
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《眼科新进展》[ISSN:1003-5141/CN:41-1105/R]

卷:
40卷
期数:
2020年8期
页码:
717-721
栏目:
实验研究
出版日期:
2020-08-05

文章信息/Info

Title:
Inhibition of oxidative stress and inflammation in retinal tissue of diabetic rats by inonotus obliquus polysaccharides via Nrf2 signaling pathway
作者:
杨雪左中夫
121000 辽宁省锦州市,锦州医科大学基础医学院(杨雪,左中夫);121000 辽宁省锦州市,锦州医科大学附属第一医院消化科(杨雪);530021 广西壮族自治区南宁市,广西医科大学基础医学博士后科研流动站(左中夫)
Author(s):
YANG Xue12ZUO Zhongfu13
1.Basic Medical College,Jinzhou Medical University,Jinzhou 121000,Liaoning Province,China
2.Department of Gastroenterology,the First Affiliated Hospital of Jinzhou Medical University,Jinzhou 121000,Liaoning Province,China
3.Postdoctoral Research Station,Guangxi Medical University,Nanning 530021,Guangxi Zhuang Autonomous Region, China
关键词:
糖尿病视网膜病变桦褐孔菌多糖氧化应激Nrf2信号通路
Keywords:
diabetic retinopathyinonotus obliquus polysaccharidesoxidative stressNrf2 signaling pathway
分类号:
R774.1
DOI:
10.13389/j.cnki.rao.2020.0163
文献标志码:
A
摘要:
目的 探讨桦褐孔菌多糖经Nrf2信号通路对糖尿病大鼠视网膜组织氧化应激和炎症反应的抑制作用。方法 选取12周龄雄性SD大鼠40只,随机分为4组:正常对照组10只、糖尿病组10只、IOP组(给予大鼠桦褐孔菌多糖300 mg·kg-1)10只和抑制剂组(给予大鼠桦褐孔菌多糖300 mg·kg-1+锌原卟啉20 mg·kg-1)10只。除正常对照组外,其余大鼠均采用一次性腹腔注射10 g·L-1链脲佐菌素(60 mg·kg-1)制作糖尿病大鼠模型,桦褐孔菌多糖采用灌胃法给药;抑制剂组在桦褐孔菌多糖灌胃前24 h将锌原卟啉经腹腔注射给大鼠。正常对照组和糖尿病组灌胃相同体积的生理盐水,并于12周后禁食不禁水12 h后进行实验。将分离到的新鲜视网膜,石蜡包埋,切片,用于HE染色和免疫组织化学染色。检测视网膜样品组织中丙二醛(MDA)、谷胱甘肽(GSH)、超氧化物歧化酶(SOD)含量;采用HE染色观察视网膜形态并检测视网膜神经节细胞密度;免疫组织化学染色观察细胞HO-1阳性染色情况;采用Western blot法检测视网膜HO-1、Nrf2和COX-2蛋白的表达。结果 造模后12周,糖尿病组、IOP组、抑制剂组大鼠体质量均低于正常对照组,血糖浓度均高于正常对照组,差异均有统计学意义(均为P<0.01)。造模后,糖尿病组大鼠视网膜组织中SOD、GSH的含量均明显低于正常对照组(均为P<0.01);MDA含量明显高于正常对照组,差异有统计学意义(P<0.01)。IOP组视网膜组织中SOD、GSH含量高于糖尿病组及抑制剂组,MDA含量显著低于糖尿病组及抑制剂组,差异均有统计学意义(均为P<0.05)。正常对照组、糖尿病组、抑制剂组和IOP组视网膜神经节细胞密度分别为(2300±100)个·mm-2、(1400±100)个·mm-2 、(1505±95)个·mm-2、(2250±95)个·mm-2。Western blot结果显示:糖尿病组HO-1、Nrf2及COX-2蛋白的表达均高于正常对照组(均为P<0.01)。IOP组大鼠视网膜组织中HO-1、Nrf2蛋白表达高于糖尿病组,COX-2蛋白的表达低于糖尿病组(均为P<0.01);抑制剂组大鼠视网膜组织中HO-1、Nrf2蛋白表达低于IOP组,COX-2蛋白的表达高于IOP组,差异均有统计学意义(均为P<0.01)。结论 桦褐孔菌多糖能够通过激活Nrf2通路降低糖尿病大鼠视网膜氧化应激及炎症反应。
Abstract:
Objective To explore the inhibition of oxidative stress and inflammation in retinal tissue of diabetic rats by inonotus obliquus polysaccharides (IOP) via Nrf2 signaling pathway.Methods All of 40 male SD rats aged 12 weeks were selected and randomly divided into 4 groups (10 rats in each group): control group, diabetic group, IOP group (300 mg·kg-1 IOP was given to the rats) and inhibitor group (300 mg·kg-1 IOP+20 mg·kg-1 zinc protoporphyrin was given to the rats). Except for the control group, all the other groups were given 10 g·L-1 streptozotocin (60 mg·kg-1) once intraperitoneal injection to make the diabetic rat model.IOP was given by gavage. Zinc protoporphyrin was intraperitoneally injected to the rats in the inhibitor group 24 h before the IOP gavage. The control group and the diabetic group were given the same amount of saline, and the experiment was carried out after 12 weeks of fasting and uninhibited water for 12 h. The fresh retina was embedded in paraffin and sliced for HE staining and immunohistochemical staining. MDA, GSH and SOD contents in retinal samples were detected. The morphology of the retina was observed by HE staining and the density of retinal ganglion cells was detected; HO-1 positive staining was observed by immunohistochemical staining; Western blot was used to detect the expression of retinal HO-1, Nrf2 and COX-2 proteins.Results Twelve weeks after modeling, the body mass of rats in diabetes group, IOP group and inhibitor group were all lower than those in the control group, the blood glucose levels of rats were all higher than those in the control group, and the differences were statistically significant(all P<0.01). After modeling, the contents of SOD and GSH in retinal tissue of diabetic rats was significantly lower than those of the control group (all P<0.01), MDA content was significantly higher than that of the control group, and the difference was statistically significant (all P<0.01). The contents of SOD and GSH in retinal tissue of the IOP group was higher than those of the diabetic group and inhibitor group, and the content of MDA was significantly lower than that of diabetic group and inhibitor group, and the difference was statistically significant (all P<0.05). The retinal ganglion cell densities of the control group, diabetes group, inhibitor group and IOP group were (2300±100) cells·mm-2, (1400±100) cells·mm-2, (1505±95) cells·mm-2, (2250±95) cells·mm-2. Western blot results showed that HO-1, Nrf2 and COX-2 proteins in the diabetic group were all higher than those in the control group (all P<0.01). The protein expression levels of HO-1 and Nrf2 in the retinal tissues of rats in the IOP group was higher than those in the diabetic group, while the protein expression of COX-2 was lower than that in the diabetic group (all P<0.01). The protein expression levels of HO-1 and Nrf2 in retinal tissues of the inhibitor group was lower than those of the IOP group, and the protein expression of COX-2 was higher than that of the IOP group, and the differences were statistically significant (all P<0.01).Conclusion IOP can reduce retinal oxidative stress and inflammatory response in diabetic rats, and the mechanism is related to the activation of Nrf2 pathway.

参考文献/References:

[1] KANSANEN E,KUOSMANEN S M,LEVONEN A L.The Keap1-Nrf2 pathway:mechani-sms of activation and dysregulation in cancer[J].Redox Biol,2013,1(1):45-49.
[2] RUSHNORE T H,MORTON M R,PICKETT C B.The antioxidant responsive element.Activation by oxidative stress and identification of the DNA consensus sequence required for functional activity[J].J Biol Chem,1991,266(18):11632-11639.
[3] 吕金玲,顾德辉.桦褐孔菌中多糖的提取及对糖尿病的病理研究[J].中国伤残医学,2010,18(6):114-116.
LYU J L,GU D H.Extraction of polysaccharides from Inonotus obliquus and pathological study on diabetes mellitus[J].Chin J Trau Disa Med,2010,18(6):114-116.
[4] WHITING D R,GUARIGUATA L,WEIL C.IDF diabetes atlas:global estimates of the prevalence of diabetes for 2011 and 2030[J].Diabetes Res Clin Pract,2011,94(3):311-321.
[5] 赵进喜,王世东,黄为钧.中医药防治糖尿病及其并发症研究述评[J].世界中医药,2017,12(1):10-15.
ZHAO J X,WANG S D,HUANG W J.Review of TCM treatment for diabetes and its complications[J].World Chin Med,2017,12(1):10-15.
[6] GUARIGUATA L,WHITING D R,HAMBLETON I.Global estimates of diabetes prevalence for 2013 and projections for 2035[J].Diabetes Res Clin Pract,2014,103(2):137-149.
[7] XU Z,WEI Y,GONG J,CHO H,PARK J K,SUNF E R,et al.Nrf2 plays a protective role in diabetic retinopathy in mice[J].Diabetologia,2014,57(1):204-213.
[8] RENE C,LOPEZ E,CLAUSTRES M.NF-E2-related factor2,a key inducer of anioxidant defenses,negatively regulates the CFTR transcription[J].Cell Mol Life Sci,2010,67(13):2297-2309.
[9] HIRAI S,HORII S,MATSUZALI Y.Anti-inflammatory effect of pyroglutamyl-leucine on lipopolysaccharide-stimulated RAW 264.7 macrophages[J].Life Sci,2014,117(1):1-6.
[10] 潘桂萍,刘光辉,谢勇军.环氧合酶-2抑制剂塞来昔布对早期糖尿病大鼠视网膜组织促红细胞生成素的影响[J].临床眼科杂志,2014,22(2):176-179.
PAN G P,LIU G H,XIE Y J.Effect of celecoxib,a cyclooxygenase-2 inhibitor,on the expression of erythropoietin in retina of diabetic rats[J].J Clin Ophthalmol,2014,22(2):176-179.
[11] 孙国玲,李筱荣,孙靖.环氧化酶2在早期糖尿病大鼠视网膜中表达的研究[J] 天津医科大学学报,2008,14(3):335-338.
SUN G L,LI X R,SUN J.Expression of cyclooxygenase- 2 in the retina of early stage diabetic rats[J].J Tianjin Med Univ,2008,14(3):335-338.
[12] SANO T,OZAKI K,KODAMA Y.Assessment of alloxan-induced diabetic rats as a periodontal disease model using a selective cyclooxygenase (COX)-2 inhibitor[J].J Toxicol Pathol,2014,27(2):123-129.
[13] KIM J H,SUN W,HAN D W.INSC suppress macrophage-induced inflammation by repressing COX-2 [J].In Vitro Cell Dev Biol Anim,2015,51(2):157-164.
[14] 戴玉成,李玉.中国六种重要药用真菌名称的说明[J].菌物学报,2011,30(4):515-518.
DAI Y C,LI Y.Notes on the nomenclature of six important medicinal fungi in China[J].Mycosystema,2011,30(4):515-518.
[15] LIU C,ZHAO C,PAN H H,KANG J,YU X T,WANG H Q,et al.Chemical constituents from Inonotus obliquus and their biological activities[J].J Nat Prod,2014,77(1):35-41.
[16] 常晨,包怡红.桦褐孔菌多糖的研究进展[J].食品与机械,2017,33(1):199-202.
CHANG C,BAO Y H.Research progress of inonotus obliquus polysaccharides[J].Food Machin,2017,33(1):199-202.
[17] ZHANG N,CHEN H X,MA L S.Physical modifications of polysaccharide from Inonotus obliquus and theantioxidant properties[J].Int J Biol Macromol,2013,54(8):209-215.

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备注/Memo

备注/Memo:
辽宁省自然科学基金(编号:2019-ZD-0807);博士后科学基金第61批面上项目(编号:2017M612870)
更新日期/Last Update: 2020-08-05