Effects of L-carnitine and Ginkgo biloba extract (EGb 761) in experimental bleomycin-induced lung fibrosis

被引:57
作者
Daba, MH
Abdel-Aziz, AA
Moustafa, AM
Al-Majed, AA
Al-Shabanah, OA
El-Kashef, HA
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacol, Riyadh 11451, Saudi Arabia
[2] King Saud Univ, Coll Pharm, Dept Clin Pharm, Riyadh 11451, Saudi Arabia
关键词
bleomycin; L-carnitine; TNF-alpha; Ginkgo biloba; lung fibrosis;
D O I
10.1006/phrs.2002.0985
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of Ginkgo biloba extract (EGb 761) and L-carnitine on bleomycin (BLM)-induced lung fibrosis were studied in rats. BLM (cumulative dose of 180 mg kg(-1)) was given intraperitoneally (i.p.) three times weekly for 4 consecutive weeks. Treatment with BLM enhanced the responsiveness of isolated pulmonary arterial rings to serotonin (5-HT), significantly increased the normal serum level of tumour necrosis factor (TNF-alpha) by similar to105% and markedly elevated the level of lipid peroxide (LPO) and collagen content in the lung homogenates by 34 and 83%, respectively. EGb 761 (100 mg kg(-1)), given in drinking water for the whole study period, totally abolished the BLM-induced alterations in the measured biochemical and pharmacological parameters. Meanwhile, L-carnitine (500 mg kg(-1)), administered in drinking water, significantly decreased the BLM-induced elevations of serum TNF-alpha, LPO level in lung tissues and the enhanced responsiveness of pulmonary arterial rings to 5-HT. However, L-carnitine did not reduce the increase in the collagen content produced by BLM. The results of the present study indicate the beneficial effects of EGb 761 and L-carnitine against lung toxicity induced by BLM treatment. Furthermore, the present data shows the advantageous use of EGb 761 as a protective agent in BLM-induced lung fibrosis under the experimental circumstances. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:461 / 467
页数:7
相关论文
共 51 条
[1]   Acute and chronic effects of adriamycin on fatty acid oxidation in isolated cardiac myocytes [J].
AbdelAleem, S ;
ElMerzabani, MM ;
SayedAhmed, M ;
Taylor, DA ;
Lowe, JE .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (02) :789-797
[2]  
Agha AM, 2001, J EXP CLIN CANC RES, V20, P39
[3]   Platelet-activating factor is an important mediator in hypoxic ischemic brain injury in the newborn rat [J].
Akisü, M ;
Kültürsay, N ;
Coker, I ;
Hüseyinov, A .
BIOLOGY OF THE NEONATE, 1998, 74 (06) :439-444
[4]   Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[5]  
BLOCK ER, 1989, VASCULAR ENDOTHELIUM, P29
[6]   PULMONARY TOXICITY AFTER TREATMENT WITH BLEOMYCIN ALONE OR IN COMBINATION WITH HYPEROXIA - STUDIES IN THE RAT [J].
BLOMMUILWIJK, MC ;
VRIESENDORP, R ;
VENINGA, TS ;
HOFSTRA, W ;
SLEYFER, DT ;
WIERINGA, RA ;
KONINGS, AWT .
BRITISH JOURNAL OF ANAESTHESIA, 1988, 60 (01) :91-97
[7]  
CHANDLER DB, 1990, CLIN CHEST MED, V11, P21
[8]  
CLOSTRE F, 1999, ANN PHARM FR, V57, pS8, DOI DOI 10.1093/ECAM/NEM096
[9]  
CROSS CE, 1985, J LAB CLIN MED, V106, P433
[10]  
DEFEUDIS FV, 1991, GINKGO BILOBA EXTRAC, P25