Impairment of immunological functions in generically epilepsy-prone rats

被引:5
作者
DeSarro, G
Liberto, MC
Berlinghieri, MC
Foca, A
Aragona, M
Cavaliere, R
Gulletta, E
机构
[1] UNIV REGGIO CALABRIA,FAC MED,CHAIR PHARMACOL,CALABRIA,ITALY
[2] UNIV REGGIO CALABRIA,FAC MED,CHAIR MICROBIOL,CALABRIA,ITALY
[3] UNIV REGGIO CALABRIA,FAC MED,CHAIR IMMUNOHEMATOL,CALABRIA,ITALY
[4] UNIV MESSINA,FAC MED,INST ONCOL,I-98100 MESSINA,ITALY
来源
GENERAL PHARMACOLOGY | 1996年 / 27卷 / 04期
关键词
genetically epilepsy-prone rats; macrophages; lymphocytes; phagocytosis; epilepsy; immune system;
D O I
10.1016/0306-3623(95)02090-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. In genetically epilepsy-prone rats (GEPR-9s), which represent a natural genetic model of epilepsy, we observed that the number of peritoneal macrophages was significantly lower with respect to normal rats, and that some functional parameters (i.e. phagocytosis and intracellular killing) of these macrophages were impaired. 2. The count of lymphocyte populations showed a predominance of T-helper over T-cytotoxic/suppressor both in the spleen and lymph nodes. Moreover, an increased T-cell/B-cell ratio was observed in GEPR-9s. Flow cytometry revealed that GEPR-9s spleens possessed a large percentage of T-helper cells in comparison to normal rats. 3. By using concanavalin A induced proliferation of GEPR-9s cultured lymphocytes, we have shown increased functional activation. 4. We suggest that the alterations in T cell functions in GEPR-9s could be due to the involvement of the neuroendocrine system in the modulation of immunity, in the shift between Th1 and Th2, and in the activation of stress response.
引用
收藏
页码:643 / 646
页数:4
相关论文
共 17 条
[1]   REVERSAL OF THE IMMUNOSENESCENT PHENOTYPE BY DEHYDROEPIANDROSTERONE - HORMONE-TREATMENT PROVIDES AN ADJUVANT EFFECT ON THE IMMUNIZATION OF AGED MICE WITH RECOMBINANT HEPATITIS-B SURFACE-ANTIGEN [J].
ARANEO, BA ;
WOODS, ML ;
DAYNES, RA .
JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (04) :830-840
[2]   INDEXES OF NORADRENERGIC FUNCTION IN THE CENTRAL-NERVOUS-SYSTEM OF SEIZURE-NAIVE GENETICALLY EPILEPSY-PRONE RATS [J].
DAILEY, JW ;
JOBE, PC .
EPILEPSIA, 1986, 27 (06) :665-670
[3]  
Fisher D A, 1985, PEDIATRIC ADOLESCENT, V14, P75
[4]  
FORD DH, 1977, THYROID HORMONES BRA, P1
[5]   ABNORMALITIES IN MONOAMINE LEVELS IN THE CENTRAL NERVOUS-SYSTEM OF THE GENETICALLY EPILEPSY-PRONE RAT [J].
JOBE, PC ;
LAIRD, HE ;
KO, KH ;
RAY, T ;
DAILEY, JW .
EPILEPSIA, 1982, 23 (04) :359-366
[6]  
JOBE PC, 1973, J PHARMACOL EXP THER, V184, P1
[7]  
JOHNSTON RB, 1978, J EXP MED, V148, P115
[8]   EVIDENCE OF HYPOTHYROIDISM IN THE GENETICALLY EPILEPSY-PRONE RAT [J].
MILLS, SA ;
SAVAGE, DD .
EPILEPSY RESEARCH, 1988, 2 (02) :102-110
[9]   THYROID-HORMONE AND DEVELOPMENT OF THE RAT HIPPOCAMPUS - MORPHOLOGICAL ALTERATIONS IN GRANULE AND PYRAMIDAL CELLS [J].
RAMI, A ;
PATEL, AJ ;
RABIE, A .
NEUROSCIENCE, 1986, 19 (04) :1217-1226
[10]   EVIDENCE OF ALTERED LYMPHOCYTE-T NUMBER AND PROLIFERATIVE RESPONSES IN GENETICALLY EPILEPSY-PRONE RATS [J].
RAZANIBOROUJERDI, S ;
ROWLAND, RRR ;
ORTIZ, KA ;
SAVAGE, DD ;
TOKUDA, S .
JOURNAL OF NEUROIMMUNOLOGY, 1992, 37 (1-2) :93-97