Beneficial effects of magnolol in a rodent model of endotoxin shock

被引:34
作者
Tsai, Yung-Chieh [3 ,4 ]
Cheng, Pao-Yun [5 ]
Kung, Ching-Wen [6 ]
Peng, Yi-Jen [7 ]
Ke, Tzu-Hsuan [1 ]
Wang, Jhi-Joung [2 ]
Yen, Mao-Hsiung [1 ]
机构
[1] Natl Def Med Ctr, Dept Pharmacol, Taipei 114, Taiwan
[2] Chi Mei Med Ctr, Dept Med Res, Tainan, Taiwan
[3] Chi Mei Fdn Hosp, Ctr Reprod Med, Tainan, Taiwan
[4] So Taiwan Univ Technol, Dept Biotechnol, Tainan, Taiwan
[5] China Med Univ, Grad Inst Chinese Pharmaceut Sci, Taichung, Taiwan
[6] Natl Def Med Ctr, Grad Inst Med Sci, Taipei 114, Taiwan
[7] Triserv Gen Hosp, Dept Pathol, Taipei, Taiwan
关键词
Magnolol; Reactive oxygen species; Sepsis; TNF-alpha; Nitric oxide; Circulatory failure; TUMOR-NECROSIS-FACTOR; KAPPA-B ACTIVATION; NITRIC-OXIDE; RAT MODEL; HONOKIOL; SEPSIS; INHIBITION; LIPOPOLYSACCHARIDE; MACROPHAGES; EXPRESSION;
D O I
10.1016/j.ejphar.2010.05.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Magnolol is a compound extracted from the Chinese medicinal herb Magnolia officinalis. It has multiple pharmacological effects, notably as an anti-oxidant. The aim of this study was to evaluate the effects of magnolol on sepsis induced by intravenous (i.v.) administration of lipopolysaccharide (LPS; 10 mg/kg) in anaesthetized Wistar rats. Magnolol (4 mu/kg, i.v.) was administered at 30 min after LPS injection. Post-treatment with magnolol significantly attenuated the deleterious haemodynamic changes (e.g., hypotension and bradycardia) caused by LPS. Meanwhile, magnolol significantly inhibited the elevation of plasma levels of tumor necrosis factor alpha, glutamate-oxaloacetate transaminase, glutamate-pyruvate transaminase and blood urine nitrogen caused by LPS. The induction of inducible nitrous oxide (NO) synthase and the overproduction of NO and superoxide anions by LPS were also significantly reduced by post-treatment with magnolol. Moreover, the plasma level of the thrombin antithrombin complex following administration of LPS was also reduced by post-treatment with magnolol. Thus, the beneficial effects of magnolol on LPS-induced sepsis result from its anti-inflammatory, anti-coagulatory, and anti-oxidant effects. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 73
页数:7
相关论文
共 41 条
[1]   Augmented expression of tumour necrosis factor-α induced by lipopolysaccharide in spleen of human monocyte chemoattractant protein-1 transgenic mouse enhances the lipopolysaccharide sensitivity of the marginal zone macrophages [J].
Ato, M ;
Iwabuchi, K ;
Shimada, S ;
Mukaida, N ;
Onoé, K .
IMMUNOLOGY, 2002, 106 (04) :554-563
[2]   Sepsis: A new hypothesis for pathogenesis of the disease process [J].
Bone, RC ;
Grodzin, CJ ;
Balk, RA .
CHEST, 1997, 112 (01) :235-243
[3]   Protective effect of baicalein against endotoxic shock in rats in vivo and in vitro [J].
Cheng, Pao-Yun ;
Lee, Yen-Mei ;
Wu, Yuan-Sheng ;
Chang, Tz-Wei ;
Jin, Jong-Shiaw ;
Yen, Mao-Hsiung .
BIOCHEMICAL PHARMACOLOGY, 2007, 73 (06) :793-804
[4]   Role of oxidative stress in experimental sepsis and multisystem organ dysfunction [J].
Crimi, Ettore ;
Sica, Vincenzo ;
Slutsky, Arthur S. ;
Zhang, Haibo ;
Williams-Ignarro, Sharon ;
Ignarro, Louis J. ;
Napoli, Claudio .
FREE RADICAL RESEARCH, 2006, 40 (07) :665-672
[5]   THROMBIN [J].
FENTON, JW .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1986, 485 :5-15
[6]   Magnolol and honokiol enhance HL-60 human leukemia cell differentiation induced by 1,25-dihydroxyvitamin D3 and retinoic acid [J].
Fong, WF ;
Tse, AKW ;
Poon, KH ;
Wang, C .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2005, 37 (02) :427-441
[7]   PATHOGENESIS AND POTENTIAL STRATEGIES FOR PREVENTION AND TREATMENT OF SEPTIC SHOCK - AN UPDATE [J].
GLAUSER, MP ;
HEUMANN, D ;
BAUMGARTNER, JD ;
COHEN, J .
CLINICAL INFECTIOUS DISEASES, 1994, 18 :S205-S216
[8]   Activation of the PGI2/IP system contributes to the development of circulatory failure in a rat model of endotoxic shock [J].
Hoecherl, Klaus ;
Schmidt, Christoph ;
Kurt, Birguel ;
Bucher, Michael .
HYPERTENSION, 2008, 52 (02) :330-335
[9]   Magnolol attenuates peroxidative damage and improves survival of rats with sepsis [J].
Kong, CW ;
Tsai, K ;
Chin, JH ;
Chan, WL ;
Hong, CY .
SHOCK, 2000, 13 (01) :24-28
[10]   THE OXYGEN FREE-RADICAL SYSTEM - FROM EQUATIONS THROUGH MEMBRANE-PROTEIN INTERACTIONS TO CARDIOVASCULAR INJURY AND PROTECTION [J].
KUKREJA, RC ;
HESS, ML .
CARDIOVASCULAR RESEARCH, 1992, 26 (07) :641-655