Hydrogen Sulfide and Substance P in Inflammation

被引:35
作者
Bhatia, Madhav [1 ,2 ,3 ]
机构
[1] Univ Otago, Dept Pathol, Christchurch 8140, New Zealand
[2] Natl Univ Singapore, Inst Life Sci, Cardiovasc Biol Res Programme, Singapore 117548, Singapore
[3] Natl Univ Singapore, Dept Pharmacol, Singapore 117548, Singapore
基金
英国医学研究理事会;
关键词
INDUCED CHEMOKINE SYNTHESIS; PANCREATIC ACINAR-CELLS; PUNCTURE-INDUCED SEPSIS; CECAL LIGATION; PROTECTS MICE; NEUROKININ-1; RECEPTOR; MURINE MACROPHAGES; GENE-PRODUCTS; NITRIC-OXIDE; LUNG INJURY;
D O I
10.1089/ars.2009.2927
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydrogen sulfide (H2S) plays an important role in cardiovascular, central nervous, and gastrointestinal systems. Being the third gaseous mediator, H2S has been shown to act as a vasodilator. In recent times, more and more attention has been paid to the biological functions of H2S in inflammation. Substance P is an 11 amino acid neuropeptide that is released from nerve endings in many tissues. Subsequent to its release, substance P binds to neurokinin-1 (NK-1) receptors on the surface of effector cells and, in addition to being a mediator of pain, it plays an important role in many inflammatory states including asthma, immune-complex-mediated lung injury, experimental arthritis, and inflammatory bowel disease. Substance P has been shown to increase microvascular permeability and promote plasma extravasation. Using animalmodels of inflammation of different etiologies such as acute pancreatitis, sepsis, and burns, studies in our laboratory have recently shown an important role of the pro-inflammatory action of H2S and substance P. Antioxid. Redox Signal. 12, 1191-1202.
引用
收藏
页码:1191 / 1202
页数:12
相关论文
共 57 条
[1]  
ARP AJ, 1987, J EXP BIOL, V128, P139
[2]   A CRITICAL-REVIEW OF THE LITERATURE ON HYDROGEN-SULFIDE TOXICITY [J].
BEAUCHAMP, RO ;
BUS, JS ;
POPP, JA ;
BOREIKO, CJ ;
ANDJELKOVICH, DA .
CRC CRITICAL REVIEWS IN TOXICOLOGY, 1984, 13 (01) :25-97
[3]   Hydrogen sulfide as a vasodilator [J].
Bhatia, M .
IUBMB LIFE, 2005, 57 (09) :603-606
[4]   Role of hydrogen sulfide in acute pancreatitis and associated lung injury [J].
Bhatia, M ;
Wong, FL ;
Fu, D ;
Lau, HY ;
Moochhala, SM ;
Moore, PK .
FASEB JOURNAL, 2005, 19 (01) :623-+
[5]   Hydrogen sulphide is a mediator of carrageenan-induced hindpaw oedema in the rat [J].
Bhatia, M ;
Sidhapuriwala, J ;
Moochhala, SM ;
Moore, PK .
BRITISH JOURNAL OF PHARMACOLOGY, 2005, 145 (02) :141-144
[6]   Pathophysiology of acute pancreatitis [J].
Bhatia, M ;
Wong, FL ;
Cao, Y ;
Lau, HY ;
Huang, J ;
Puneet, P ;
Chevali, L .
PANCREATOLOGY, 2005, 5 (2-3) :132-144
[7]  
Bhatia M., 2003, Current Medicinal Chemistry - Anti-Inflammatory & Anti-Allergy Agents, V2, P19, DOI 10.2174/1568014033355862
[8]   Role of substance P and the neurokinin 1 receptor in acute pancreatitis and pancreatitis-associated lung injury [J].
Bhatia, M ;
Saluja, AK ;
Hofbauer, B ;
Frossard, JL ;
Lee, HS ;
Castagliuolo, I ;
Wang, CC ;
Gerard, N ;
Pothoulakis, C ;
Steer, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (08) :4760-4765
[9]   Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome [J].
Bhatia, M ;
Moochhala, S .
JOURNAL OF PATHOLOGY, 2004, 202 (02) :145-156
[10]   Preprotachykinin-A gene deletion protects mice against acute pancreatitis and associated lung injury [J].
Bhatia, M ;
Slavin, J ;
Cao, YQ ;
Basbaum, AI ;
Neoptolemos, JP .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 284 (05) :G830-G836