Effects of nitric oxide synthase inhibitor ω-Nitro-L-Arginine Methyl Ester, on silica-induced inflammatory reaction and apoptosis

被引:6
作者
Wang, He [1 ]
Leigh, James [2 ]
机构
[1] Univ Adelaide, Discipline Publ Hlth, 10 Pulteney St, Adelaide, SA 5005, Australia
[2] Univ Sydney, Sch Publ Hlth, Sydney, NSW 2006, Australia
关键词
Nitric Oxide; Intratracheal Instillation; Apoptotic Neutrophil; BALF Cell; Asbestos Fibre;
D O I
10.1186/1743-8977-3-14
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Background: Although nitric oxide is overproduced by macrophages and neutrophils after exposure to silica, its role in silica-induced inflammatory reaction and apoptosis needs further clarification. In this study, rats were intratracheally instilled with either silica suspension or saline to examine inflammatory reactions and intraperitoneally injected with.-nitro-L-arginine methyl ester ( L-NAME), an inhibitor of nitric oxide synthases, or saline to examine the possible role of nitric oxide production in the reaction. Results: Results showed that silica instillation induced a strong inflammatory reaction indicated by increased total cell number, number of neutrophils, protein concentration and lactate dehydrogenase (LDH) activity in bronchoalveolar lavage fluid (BALF). There were no significant differences in these indices between silica-instilled groups with and without L-NAME injection (p > 0.05) except LDH level. The results also showed that apoptotic leucocytes were identified in BALF cells of silica-instilled groups whereas no significant difference was found between silica-instilled groups with and without L-NAME injection in the apoptotic reaction (p > 0.05). Silica instillation significantly increased the level of BALF nitrite/nitrate and L-NAME injection reduced this increase. Conclusion: Intratracheal instillation of silica caused an obvious inflammatory reaction and leucocyte apoptosis, but these reactions were not influenced by intraperitoneal injection of L-NAME and reduced production of NO. This supports the possibility that silica-induced lung inflammation and BALF cell apoptosis are via NO-independent mechanisms.
引用
收藏
页数:9
相关论文
共 46 条
[1]   Do macrophages kill through apoptosis? [J].
Aliprantis, AO ;
DiezRoux, G ;
Mulder, LCF ;
Zychlinsky, A ;
Lang, RA .
IMMUNOLOGY TODAY, 1996, 17 (12) :573-576
[2]   INTRODUCTION OF LUMINOL-DEPENDENT CHEMILUMINESCENCE AS A METHOD TO STUDY SILICA INFLAMMATION IN THE TISSUE AND PHAGOCYTIC-CELLS OF RAT LUNG [J].
ANTONINI, JM ;
VANDYKE, K ;
YE, ZG ;
DIMATTEO, M ;
REASOR, MJ .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :37-42
[3]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[4]   INTRATRACHEAL INSTILLATION OF SILICA UP-REGULATES INDUCIBLE NITRIC-OXIDE SYNTHASE GENE-EXPRESSION AND INCREASES NITRIC-OXIDE PRODUCTION IN ALVEOLAR MACROPHAGES AND NEUTROPHILS [J].
BLACKFORD, JA ;
ANTONINI, JM ;
CASTRANOVA, V ;
DEY, RD .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 11 (04) :426-431
[5]   Mechanisms of nitric oxide-dependent apoptosis:: Involvement of mitochondrial mediators [J].
Boscá, L ;
Hortelano, S .
CELLULAR SIGNALLING, 1999, 11 (04) :239-244
[6]  
Brune B, 1996, REV PHYSIOL BIOCH P, V127, P1, DOI 10.1007/BFb0048263
[7]   Enhancement of nitric oxide production by pulmonary cells following silica exposure [J].
Castranova, V ;
Huffman, LJ ;
Judy, DJ ;
Bylander, JE ;
Lapp, LN ;
Weber, SL ;
Blackford, JA ;
Dey, RD .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1998, 106 :1165-1169
[8]   IL-10 enhances resolution of pulmonary inflammation in vivo by promoting apoptosis of neutrophils [J].
Cox, G .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1996, 271 (04) :L566-L571
[9]   Interferon-γ production by specific lung lymphocyte phenotypes in silicosis in mice [J].
Davis, GS ;
Pfeiffer, LM ;
Hemenway, DR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 22 (04) :491-501
[10]   Sensitivity of human pancreatic islets to peroxynitrite-induced cell dysfunction and death [J].
Delaney, CA ;
Tyrberg, B ;
Bouwens, L ;
Vaghef, H ;
Hellman, B ;
Eizirik, DL .
FEBS LETTERS, 1996, 394 (03) :300-306