期刊文献+

雷公藤红素治疗变应性鼻炎大鼠的机制研究 被引量:6

Protective effect of celastrol on allergic rhinitis in rats
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摘要 目的:研究雷公藤红素对大鼠变应性鼻炎(AR)的治疗作用并初步探讨相关作用机制。方法:构建大鼠AR模型,测定大鼠第1天、第4天和第7天的行为学特征改变、鼻黏膜呼吸区组织超氧化物歧化酶(SOD)、丙二醛(MDA)、还原型谷胱甘肽(GSH)和谷胱甘肽过氧化物酶(GSH-PX)的水平;测定鼻黏膜呼吸区组织核因子E2p45相关因子2(NRF2)的核内蛋白表达及谷氨酸半胱氨酸连接酶催化亚基(GCLC)的浆蛋白表达。结果:AR大鼠第1、4、7天的行为学特征改变显著(P<0.01),鼻黏膜呼吸区组织SOD、GSH、GSH-PX降低,MDA升高;NRF2的核内蛋白表达降低,GCLC的浆蛋白表达降低。雷公藤红素低剂量治疗组和高剂量治疗组能不同程度改善上述指标的变化,同时提高了鼻黏膜呼吸区组织NRF2的核蛋白表达和GCLC的浆蛋白表达。结论:雷公藤红素能改善AR大鼠的症状,其机制可能与提高鼻黏膜呼吸区组织NRF2的核蛋白表达和GCLC的浆蛋白表达相关。 Objective:To investigate the protective effect of celastrol on allergic rhinitis rats and its possible mechanism. Method:Allergic rhinitis (AR) model of rats was established by OVA. The behavioural characteris- tics were observed at the 1st, 4th and 7th dayafter stimulation treatment. The levels of superoxide dismutase (SOD), malondialdehyde (MDA), glutathione (GSH) and glutathione peroxidase (GSH-PX) in the nasal mucosa breathing zone were measured. The expression of the nuclear factor erythroid 2 related factor 2 (NRF2) nuclear protein and the catalytic submit of glutamylcysteine ligase (GCLC) cytoplasmic protein in the nasal mucosa breath- ing zone were determined. Result:We observed obvious behaviour changes related with allergic rhinitis in AR rats, together with decrease of SOD, GSH and GSH-PX and increase of MDA in the nasal mucosa breathing zone. Mo- reover, NRF2 nuclear protein expression and GCLC cytoplasmic expression were suppressed in the nasal muucosa. The changes above were alleviated in celastrol pretreatment group. The potential mechanism may be related to the upregulation of NRF2 nuclear protein expression and GCLC cytoplasmic expression after celastrol pretreatment. Conclusion:Celastrol can significantly relieve the allergic symptoms in AR rats. The mechanism of this protective effects may relate to the upregulation of NRF2 nuclear protein expression and GCLC cytoplasmic expression in the nasal mucosa breathing zone.
出处 《临床耳鼻咽喉头颈外科杂志》 CAS 北大核心 2014年第8期550-553,共4页 Journal of Clinical Otorhinolaryngology Head And Neck Surgery
关键词 雷公藤红素 鼻炎 变应性 核因子E2 p45相关因子2 谷氨酸半胱氨酸连接酶催化亚基 氧化应激 celastrol rhinitis, allergic NRF2 GCLC oxidative stress
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参考文献15

  • 1STEWART M G. Identification and management of un- diagnosed and undertreated allergic rhinitis in adults and children[J]. Clin Exp Allergy, 2008,38 :751 - 760.
  • 2KNIPPING S, HOLZHAUSEN H J, RIEDERER A, et al. [Immunoelectron microscopic findings in patients with allergic rhinitis ] [J]. Laryngorhinootologie, 2002,81: 86 1- 865.
  • 3LI X L, ZHOU A G, ZHANG L, et al. Antioxidant status and immune activity of glycyrrhizin in allergic rhinitis mice[J]. Int J MolSci,2011,12:905-916.
  • 4MA Q. Role of nff2 in oxidative stress and toxicity[J]. Annu Rev Pharmacol Toxicol, 2013,53:401-426.
  • 5YU X, TAO W, JIANG F,et al. Celastrol attenuates hypertension-induced inflammation and oxidative stress in vascular smooth muscle cells viainduction of heme oxygenase-1 [J]. Am J Hypertens, 2010, 23.. 895-903.
  • 6HANSEN J, PALMFELDT J, VANG S,et al. Quan- titative proteomics reveals cellular targets of celastrol [J]. PLoS One, 2011,6 : e26634.
  • 7李颖,陈向东.雷公藤红素对变应性鼻炎大鼠鼻黏膜组织中NF-κB和Eotaxin表达的影响[J].临床耳鼻咽喉头颈外科杂志,2012,26(20):943-945. 被引量:5
  • 8刘建国,杨政,刘月辉.变应性鼻炎大鼠模型建造[J].江西医学院学报,2008,48(5):33-34. 被引量:24
  • 9PETALAS K, DURHAM S R. Allergen immunotherapy for allergic rhinitis[J]. Rhinology, 2013,51 : 99- 110.
  • 10DI LORENZO G, MINCIULLO P L, LETO-BAR- ONE M S, et al. Differences in the behavior of ad- vanced glycation end products and advanced oxidation protein products in patients with allergic rhinitis[J]. J Investig Allergol Clin Immunol, 2013,23 : 101 - 106.

二级参考文献14

  • 1赵秀杰,赵德荣.鼻超敏反应实验模型的建立[J].中华耳鼻咽喉科杂志,1993,28(1):17-18. 被引量:207
  • 2赵宇,C.Andrew vanHasselt,吴港生,黄约爱,梁传余,梁秉中.卵白蛋白经鼻致敏建立变应性鼻炎动物模型[J].中华耳鼻咽喉头颈外科杂志,2005,40(3):176-180. 被引量:52
  • 3佘文煜,董震.实验性变应性鼻炎鼻黏膜组织重塑的特点[J].中华耳鼻咽喉头颈外科杂志,2006,41(1):48-53. 被引量:46
  • 4CHEN F, CASTRANOVA V, SHI X, et al. New insights into the role of nuclear factor-κappaB, a ubiquitous transcription factor in the initiation of diseases [J]. Clin Chem, 1999,45:7-17.
  • 5LI D,WANG D,GRIFFITHS-JOHNSON D A,et al.Eotaxin protein and gene expression in guinea-pig lungs:constitutive expression and upregulation after allergen challenge[J].Eur Respir J,1997,10:1946-1954.
  • 6ZIMMERMANN N. DAUGHERTY B L, STARK J M, et al. Molecular analysis of CCR-3 events in eosinophilic cells [J].J Immunol, 2000, 164: 1055- 1061.
  • 7FUJISAWA T, KATO Y, NAGASE H, et at. Chemokines induce eosinophil degranulation through CCR-3[J]. J Allergy Clin Immunol, 2000, 106: 507-513.
  • 8J ASTHMA. Eosinophil chemokines and chemokine receptors:their role in eosinophil accumulation and activation in asthma and potential as therapeutic targets[J]. J Asthma, 2001, 38 : 605 - 613.
  • 9YING S, MENG Q, ZEIBECOGLOU K, et al. Eosinophil chemotactic chemokines (eotaxin, eotaxin-2,RANTES, monocyte chemoattractant protein-3 ( MCP-3), and MCP-4), and C C chemokine receptor 3 expression in bronchial biopsies from atopic and nonatopic(Intrinsic) asthmatics [J]. J Immunol, 1999,163:6321 -6329.
  • 10MATTOLI S, STACEY M A, SUN G, et al. Eotaxin expression and eosinophilic inflammation in asthma[J]. Biochem Biophys Res Commun, 1997, 236: 299-301.

共引文献27

同被引文献83

  • 1赵建东,王世振,马凤梅.Th1和Th2细胞及相关细胞因子在变应性鼻炎发病中的变化[J].临床耳鼻咽喉科杂志,2005,19(17):794-796. 被引量:31
  • 2徐慧贤,阮岩,王士贞,刘晔.豚鼠肾阳虚变应性鼻炎模型的建立[J].中药新药与临床药理,2005,16(6):427-429. 被引量:18
  • 3周鋆,吴叔明,陈晓宇,彭延申.雷公藤红素对三硝基苯磺酸诱导的大鼠结肠炎的保护作用[J].胃肠病学,2007,12(3):144-147. 被引量:13
  • 4王峻霞,唐炜,左建平.青蒿素类衍生物抗炎免疫抑制活性研究进展[J].国际药学研究杂志,2007,34(5):336-340. 被引量:19
  • 5Zhang XW, Zhang TP, Zhou XT, et al. Enhancement of Oral Bioavail- ability of Tripterine Through Lipid Nanospheres : Preparation, Character- ization, and Absorption Evaluation [ J ]. Journal of Pharmaceutical Sci- ences ,2014,103 (6) : 1711 - 1719.
  • 6Xu XH,Zhong J,Wu ZL,et al. Effects of tripterine on mRNA expression of TGF-beta 1 and collagen IV expression in BWF1 mice[ J ]. Cell Bio- chemistry and Function,2007,25 (5) :501 - 507.
  • 7Li H,Zhang YY,Tan HW,et al. Therapeutic effect of tripterine on adju- rant arthritis in rats [ J ]. Journal of Ethnopharmacology ,2008,118 (3) : 479 - 484.
  • 8Lu CH,Zhang XP,Zhang DH, et al. Short Time Tripterine Treatment En- hances Endothelial Progenitor Cell Function via Heat Shock Protein 32 [ J ]. Journal of Cellular Physiology ,2015,230 (5) :1139 - 1147.
  • 9Quan S,Xu YH,Xia XP,et al. Tripterine induces apoptosis of human a- cute myelocytic leukemic cells via up - regulating Fas/FasL and down- regulating NF-κB [ J ]. African Journal of Pharmacy and Pharmacology, 2010,4(7 ) :431 -435.
  • 10Wu F, Han M, Wilson JX. Tripterine prevents endothelial barrier dys- function by inhibiting endogenous peroxynitfite formation [ J ]. British Joumal of Pharmacology,2009,157 (6) : 1014 - 1023.

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