DHEAS inhibits TNF production in monocytes, astrocytes and microglial cells

被引:35
作者
DiSanto, E
Foddi, MC
RicciardiCastagnoli, P
Mennini, T
Ghezzi, P
机构
[1] MARIO NEGRI INST PHARMACOL RES,I-20157 MILAN,ITALY
[2] CNR,CTR CYTOPHARMACOL,DEPT PHARMACOL,I-20133 MILAN,ITALY
关键词
cell culture; in vitro studies; GABA; dexamethasone;
D O I
10.1159/000097282
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We previously reported that neurosteroids, including dehydroepiandrosterone sulfate (DHEAS), inhibit the production of TNF in vitro and in vivo. In this paper we evaluated the effect of DHEAS on TNF production by cultured rat astrocytes and murine glial cell clones, and compared it with the effect on monocytic THP-1 cells. We found that DHEAS at a concentration of 10(-4)-10(-7) M inhibits TNF production induced by lipopolysaccharide (LPS, 1 mu g/ml) in these cells. Since the inhibitory effect of DHEAS is not mediated by the glucocorticoid (GC) receptor and DHEAS is an allosteric antagonist of the GABA(A) receptor, we investigated the possible role of GABAA receptors in this effect. The results showed that the inhibitory effect of DHEAS (10(-6) M) on TNF production by THP-1 cells was completely reversed by addition of 10(-6) M GABA. However, a GABA(A) receptor antagonist (bicuculline) did not mimic the action of DHEAS. In conclusion, DHEAS can inhibit TNF production in astrocytic and microglial cells suggesting it could be an endogenous regulator of TNF production in the brain.
引用
收藏
页码:285 / 288
页数:4
相关论文
共 27 条
[1]  
AGGARWAL BB, 1985, J BIOL CHEM, V260, P2345
[2]   ASTROCYTES AND NEUROSTEROIDS - METABOLISM OF PREGNENOLONE AND DEHYDROEPIANDROSTERONE - REGULATION BY CELL-DENSITY [J].
AKWA, Y ;
SANANES, N ;
GOUEZOU, M ;
ROBEL, P ;
BAULIEU, EE ;
LEGOASCOGNE, C .
JOURNAL OF CELL BIOLOGY, 1993, 121 (01) :135-143
[3]   DEHYDROEPIANDROSTERONE PRETREATMENT PROTECTS RATS AGAINST THE PROOXIDANT AND NECROGENIC EFFECTS OF CARBON-TETRACHLORIDE [J].
ARAGNO, M ;
TAMAGNO, E ;
BOCCUZZI, G ;
BRIGNARDELLO, E ;
CHIARPOTTO, E ;
PIZZINI, A ;
DANNI, O .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (10) :1689-1694
[4]   PROTECTION BY DEHYDROEPIANDROSTERONE IN MICE INFECTED WITH VIRAL ENCEPHALITIS [J].
BENNATHAN, D ;
LACHMI, B ;
LUSTIG, S ;
FEUERSTEIN, G .
ARCHIVES OF VIROLOGY, 1991, 120 (3-4) :263-271
[5]   Longitudinal study of adrenal steroids in a cohort of HIV-infected patients with hemophilia [J].
Chatterton, RT ;
Green, D ;
Harris, S ;
Grossman, A ;
Hechter, O .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1996, 127 (06) :545-552
[6]  
CHAUDHRI G, 1989, J IMMUNOL, V143, P1290
[7]   CHARACTERIZATION AND MEASUREMENT OF DEHYDROEPIANDROSTERONE SULFATE IN RAT-BRAIN [J].
CORPECHOT, C ;
ROBEL, P ;
AXELSON, M ;
SJOVALL, J ;
BAULIEU, EE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (08) :4704-4707
[8]   OLIGOMERIC TUMOR-NECROSIS-FACTOR-ALPHA SLOWLY CONVERTS INTO INACTIVE FORMS AT BIOACTIVE LEVELS [J].
CORTI, A ;
FASSINA, G ;
MARCUCCI, F ;
BARBANTI, E ;
CASSANI, G .
BIOCHEMICAL JOURNAL, 1992, 284 :905-910
[9]   DEHYDROEPIANDROSTERONE PROTECTS MICE FROM ENDOTOXIN TOXICITY AND REDUCES TUMOR-NECROSIS-FACTOR PRODUCTION [J].
DANENBERG, HD ;
ALPERT, G ;
LUSTIG, S ;
BENNATHAN, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (10) :2275-2279
[10]   A glucocorticoid receptor-independent mechanism for neurosteroid inhibition of tumor necrosis factor production [J].
DiSanto, E ;
Sironi, M ;
Mennini, T ;
Zinetti, M ;
Savoldi, G ;
DiLorenzo, D ;
Ghezzi, P .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 299 (1-3) :179-186