This short review deals with the role of a recently found signalling m
olecule, nitric oxide (NO), in inflammatory and immune responses. NO r
egulates inflammatory erythema and oedema and has cytotoxic action aga
inst micro-organisms. In some instances (such as reperfusion injury) N
O has cytoprotective properties. Production of large amounts of NO by
activated macrophages accounts for their ability to suppress lymphocyt
e proliferation. NO synthesis in lymphocytes is questionable but cytok
ines secreted by activated lymphocytes regulate NO synthesis by macrop
hages. Constitutive NO synthase is activated in neutrophils in respons
e to inflammatory stimuli and NO has diverse, often biphasic effects o
n neutrophil functions. Increased concentrations of nitrite and nitrat
e (metabolites of NO) are present in arthritic joints. NO is synthesiz
ed not only by migrated inflammatory cells but also by articular chond
rocytes and inflamed synovial membrane. In the inflamed joint, NO regu
lated the synthesis of several inflammatory mediators and functions of
inflammatory cells. In addition, NO seems to mediate some destructive
effects of proinflammatory cytokines such as interleukin-1. In conclu
sion, NO regulates several humoral and cellular responses in inflammat
ion, having both anti-inflammatory and proinflammatory properties depe
nding on the type and phase of the inflammatory reaction.