Celastrol prevents circulatory failure via induction of heme oxygenase-1 and heat shock protein 70 in endotoxemic rats

被引:18
|
作者
Wang, Yi-Li [1 ]
Lam, Kwok-Keung [2 ,3 ]
Cheng, Pao-Yun [4 ]
Lee, Yen-Mei [1 ,5 ]
机构
[1] Natl Def Med Ctr, Grad Inst Life Sci, Taipei 114, Taiwan
[2] Taipei Med Univ, Dept Pharmacol, Taipei, Taiwan
[3] Catholic Mercy Hosp, Dept Anesthesiol, Hsinchu, Taiwan
[4] Dept Physiol & Biophys, Taipei, Taiwan
[5] Natl Def Med Ctr, Dept Pharmacol, Taipei 114, Taiwan
关键词
Celastrol; Sepsis; Circulatory failure; Heme oxygenase-1; Heat shock protein 70; MYOCARDIAL ISCHEMIA/REPERFUSION INJURY; NF-KAPPA-B; NITRIC-OXIDE; PROINFLAMMATORY CYTOKINES; OXIDATIVE STRESS; SHOCK; SEPSIS; EXPRESSION; HSP70; DYSFUNCTION;
D O I
10.1016/j.jep.2014.12.062
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Celastrol, a quinone methide extracted from the root of Tripterygium wilfordii Hook, possesses anti-oxidant and anti-inflammatory effects. Tripterygium wilfordii Hook is officially listed in the Chinese Pharmacopoeia and is used traditionally against rheumatoid arthritis, ankylosing spondylitis, and cancer. Furthermore, the circulatory protective effect of celastrol on an in vivo animal model of sepsis was investigated. Aim of the study: Sepsis is a systemic inflammatory disorder that increases tissue oxidative stress and leads to multiple organ injury. We evaluated the beneficial effects of celastrol on multiple organ failure induced by lipopolysaccharide (LPS) in rats. Materials and methods: Celastrol (0.5 and 1.0 mg/kg, i.v.) was administered to anaesthetized rats 2 h before and 30 min after LPS challenge (10 mg/kg, i.v.). Eight hours later, cardiac and aortic protein expressions related to inflammatory responses, superoxide anion production, and reduced glutathione (GSH) level were measured. Results: Treatment with celastrol prevented circulatory failure (bradycardia and hypotension) 8 h after LPS challenge. The plasma levels of ALT, LDH, TNE-alpha, and nitric oxide metabolites increased markedly during sepsis, which significantly reduced after celastrol treatments. Celastrol attenuated iNOS, TNF-alpha, NF-kappa B phospho-p65 expression, superoxide anion production, and caspase 3 activity in the cardiovascular system, all of which were markedly elevated after LPS challenge. Furthermore, celastrol induced HO-1 and HSP70 expressions increase in nuclear levels of Nrf2 and HSF-1, respectively, and increase cardiac GSH level 8 h after LPS challenge. Conclusion: Anti-inflammatory and anti-oxidant effects of celastrol contribute to prevent circulatory failure in sepsis. Induction of HO-1 and HSP70 by celastrol participates in these beneficial effects. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:168 / 175
页数:8
相关论文
共 50 条
  • [1] Brain death induces renal expression of heme oxygenase-1 and heat shock protein 70
    van Dullemen, Leon F. A.
    Bos, Eelke M.
    Schuurs, Theo A.
    Kampinga, Harm H.
    Ploeg, Rutger J.
    van Goor, Harry
    Leuvenink, Henri G. D.
    JOURNAL OF TRANSLATIONAL MEDICINE, 2013, 11
  • [2] Brain death induces renal expression of heme oxygenase-1 and heat shock protein 70
    Leon FA van Dullemen
    Eelke M Bos
    Theo A Schuurs
    Harm H Kampinga
    Rutger J Ploeg
    Harry van Goor
    Henri GD Leuvenink
    Journal of Translational Medicine, 11
  • [3] Nitrotyrosine formation and heme oxygenase-1 expression in endotoxemic cirrhotic rats
    Dogru-Abbasoglu, Semra
    Parildar-Karpuzoglu, Hande
    Balkan, Jale
    Aykac-Toker, Guelcin
    Uysal, Muejdat
    ARCHIVES OF MEDICAL RESEARCH, 2007, 38 (01) : 28 - 33
  • [4] Celastrol Attenuates Hypertension-Induced Inflammation and Oxidative Stress in Vascular Smooth Muscle Cells via Induction of Heme Oxygenase-1
    Yu, Xiao
    Tao, Weiwei
    Jiang, Fengrong
    Li, Chaojun
    Lin, Jiandie
    Liu, Chang
    AMERICAN JOURNAL OF HYPERTENSION, 2010, 23 (08) : 895 - 903
  • [5] Tussilagone inhibits dendritic cell functions via induction of heme oxygenase-1
    Park, Yunsoo
    Ryu, Hwa Sun
    Lee, Hong Kyung
    Kim, Ji Sung
    Yun, Jieun
    Kang, Jong Soon
    Hwang, Bang Yeon
    Hong, Jin Tae
    Kim, Youngsoo
    Han, Sang-Bae
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2014, 22 (02) : 400 - 408
  • [6] Hepatic steatosis prevents heme oxygenase-1 induction by isoflurane in the rat liver
    Stoll, Patrick
    Schwer, Christian I.
    Goebel, Ulrich
    Buerkle, Hartmut
    Hoetzel, Alexander
    Schmidt, Rene
    WORLD JOURNAL OF GASTROENTEROLOGY, 2011, 17 (37) : 4184 - 4190
  • [7] Transduced PEP-1-Heme Oxygenase-1 Fusion Protein Attenuates Lung Injury in Septic Shock Rats
    Yan, Xue-Tao
    He, Xiang-Hu
    Wang, Yan-Lin
    Zhang, Zong-Ze
    Tang, Jun-Jiao
    OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2018, 2018
  • [8] Pharmacological Preconditioning with Vitamin C Attenuates Intestinal Injury via the Induction of Heme Oxygenase-1 after Hemorrhagic Shock in Rats
    Zhao, Bing
    Fei, Jian
    Chen, Ying
    Ying, Yi-Lin
    Ma, Li
    Song, Xiao-Qin
    Wang, Lu
    Chen, Er-Zhen
    Mao, En-Qiang
    PLOS ONE, 2014, 9 (06):
  • [9] The induction of heme oxygenase-1 suppresses heat shock protein 90 and the proliferation of human breast cancer cells through its byproduct carbon monoxide
    Lee, Wen-Ying
    Chen, Yen-Chou
    Shih, Chwen-Ming
    Lin, Chun-Mao
    Cheng, Chia-Hsiung
    Chen, Ku-Chung
    Lin, Cheng-Wei
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2014, 274 (01) : 55 - 62
  • [10] Expression pattern and regulation of heme oxygenase-1 heat shock protein 32 in human liver cells
    Bauer, I
    Rensing, H
    Florax, A
    Ulrich, C
    Pistorius, G
    Redl, H
    Bauer, M
    SHOCK, 2003, 20 (02): : 116 - 122