MYCOPLASMA TRIGGERING OF NITRIC-OXIDE PRODUCTION BY CENTRAL-NERVOUS-SYSTEM GLIAL-CELLS AND ITS INHIBITION BY GLUCOCORTICOIDS

被引:34
作者
BRENNER, T [1 ]
YAMIN, A [1 ]
GALLILY, R [1 ]
机构
[1] HEBREW UNIV JERUSALEM,HADASSAH MED SCH,LAUTENBERG CTR GEN & TUMOR IMMUNOL,IL-91010 JERUSALEM,ISRAEL
关键词
MYCOPLASMA; NITRIC OXIDE; TUMOR NECROSIS FACTOR-ALPHA; PROSTAGLANDIN-E(2); GLIAL CELL; DEXAMETHASONE; MULTIPLE SCLEROSIS; AIDS DEMENTIA;
D O I
10.1016/0006-8993(94)91814-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The same cytokines that have been implicated in the pathology of central nervous system (CNS) inflammatory diseases and demyelinating diseases are also associated with the induction of nitric oxide (NO) production by macrophages and other somatic cells. Recently we have showed that mycoplasma can trigger the production of tumor necrosis factor (TNF)alpha and eicosanoids in rat astrocytes. In the present study, the effect of mycoplasma on NO production in rat glial cells was assessed. The addition of 10 mug/ml of membranes derived from M. capricolum (sheep isolate), M. fermentans (human isolate), or lipopolysaccharide (LPS) led to a 15- to 20-fold increase in NO production. The glucocorticoids dexamethasone and corticosterone, but not progesterone, markedly inhibited NO production. The addition of glucocorticoid prior or conjointly with the activator prevented large amounts of NO from being formed. Even when glucocorticoids were added 5 or 24 h after activation, effective inhibition of NO production was obtained. Thus, it is likely that glucocorticoids exert some of their ameliorating effects in neurological diseases by reducing the production of NO, cytokines and prostaglandins in the CNS.
引用
收藏
页码:51 / 56
页数:6
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