KEY ROLE FOR PREGNENOLONE IN COMBINATION THERAPY THAT PROMOTES RECOVERY AFTER SPINAL-CORD INJURY

被引:90
作者
GUTH, L [1 ]
ZHANG, ZY [1 ]
ROBERTS, E [1 ]
机构
[1] CITY HOPE NATL MED CTR, BECKMAN RES INST, DEPT NEUROBIOCHEM, DUARTE, CA 91010 USA
关键词
ATTENUATION; DEHYDROEPIANDROSTERONE; BACTERIAL LIPOPOLYSACCHARIDE; INDOMETHACIN; AXONAL REGENERATION;
D O I
10.1073/pnas.91.25.12308
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Controlled compressive injury to rat spinal cord was chosen to test therapies that might attenuate the progression of tissue destruction and locomotor deficits that characteristically occur after spinal injury. A highly significant reduction of damage was achieved by immediate postinjury treatment with a combination of the following: an antiinflammatory substance, indomethacin; a stimulator of cytokine secretion, bacterial lipopolysaccharide; and the parent steroid, from which all other steroids arise, pregnenolone. This treatment reduced histopathological changes, spared tissue from secondary injury, and increased restoration of motor function. Remarkably, 11 of 16 of the animals treated with the above combination were able to stand and walk at 21 days after injury, 4 of them almost normally. The results were far superior to those obtained in controls or in animals to which the substances were given separately or in combinations of two. This approach may prove to be applicable to nervous system injury, in general, and to injury in other tissues.
引用
收藏
页码:12308 / 12312
页数:5
相关论文
共 36 条
[1]  
Abelson R.P., 1970, QUANTITATIVE ANAL SO, P407
[2]   NEUROSTEROIDS - BIOSYNTHESIS, METABOLISM AND FUNCTION OF PREGNENOLONE AND DEHYDROEPIANDROSTERONE IN THE BRAIN [J].
AKWA, Y ;
YOUNG, J ;
KABBADJ, K ;
SANCHO, MJ ;
ZUCMAN, D ;
VOURCH, C ;
JUNGTESTAS, I ;
HU, ZY ;
LEGOASCOGNE, C ;
JO, DH ;
CORPECHO, C ;
SIMON, P ;
BAULIEU, EE ;
ROBEL, P .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 40 (1-3) :71-81
[3]   SPINAL-CORD INJURY AND PROTECTION [J].
ANDERSON, DK ;
DEMEDIUK, P ;
SAUNDERS, RD ;
DUGAN, LL ;
MEANS, ED ;
HORROCKS, LA .
ANNALS OF EMERGENCY MEDICINE, 1985, 14 (08) :816-821
[4]   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
[5]  
ARANEO BA, 1993, ARCH SURG-CHICAGO, V128, P318
[6]  
BALENTINE JD, 1978, LAB INVEST, V39, P236
[7]   PROLIFERATION OF OLIGODENDROCYTE PRECURSOR CELLS DEPENDS ON ELECTRICAL-ACTIVITY IN AXONS [J].
BARRES, BA ;
RAFF, MC .
NATURE, 1993, 361 (6409) :258-260
[8]   INFLAMMATORY CYTOKINES WITHIN THE CENTRAL-NERVOUS-SYSTEM - SOURCES, FUNCTION, AND MECHANISM OF ACTION [J].
BENVENISTE, EN .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :C1-C16
[9]  
BOWLBY MR, 1993, MOL PHARMACOL, V43, P813
[10]   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