The effects of dantrolene alone or in combination with nimodipine in glutamate-induced neurotoxicity in cerebellar granular cell cultures of rat pups

被引:21
作者
Gepdiremen, A [1 ]
Düzenli, S
Hacimüftüoglu, A
Süleyman, H
Öztas, S
机构
[1] Ataturk Univ, Fac Med, Dept Pharmacol, TR-25240 Erzurum, Turkey
[2] Ataturk Univ, Fac Med, Dept Med Genet, TR-25240 Erzurum, Turkey
关键词
dantrolene; nimodipine; glutamate; neurotoxicity; calcium; neurone; rat;
D O I
10.1006/phrs.2000.0770
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the existence of some positive and negative reports on dantrolene in ischemic states, combined application of an endoplasmic reticulum Ca2+ release inhibitor and a calcium channel blocker has not yet been elucidated. In the present study, we have investigated the role of dantrolene in subsequent doses alone or in coexistence with the dihydropyridine calcium antagonist nimodipine (10(-4) M concentration) in glutamate-induced (10(-7) M) neurotoxicity in cerebellar granular cell cultures of rat pups, Glutamate induced neuronal cell death at a concentration of 10(-7) M. Despite the fact that none of the groups tested were able to reverse cell death to control values, dantrolene was found to be effective in preventing glutamate toxicity in cerebellar cultures of rat pups. The protective effect of dantrolene potentialized in combination with nimodipine at all doses tested. The most effective dose of dantrolene was found to be 10(-4) M in combination with nimodipine. As a result, both extracellular and internal calcium stores play important roles in the genesis of neuronal cell death induced by glutamate. (C) 2001 Academic Press.
引用
收藏
页码:241 / 244
页数:4
相关论文
共 29 条
[11]   OXIDIZED GLUTATHIONE DECREASES LUMINAL CA2+ CONTENT OF THE ENDOTHELIAL-CELL INS(1,4,5)P-3-SENSITIVE CA2+ STORE [J].
HENSCHKE, PN ;
ELLIOTT, SJ .
BIOCHEMICAL JOURNAL, 1995, 312 :485-489
[12]   STROKE - EARLY PATHOPHYSIOLOGY AND TREATMENT - SUMMARY OF THE FIFTH ANNUAL DECADE OF THE BRAIN SYMPOSIUM [J].
HEROS, RC ;
GRADY, PA ;
WALKER, MD ;
CHOI, DW ;
PULSINELLI, WA ;
BROTT, T ;
CAPLAN, LR ;
LATCHAW, RE ;
GINSBERG, MD ;
GROTTA, JC ;
HALL, ED ;
ROBERTSON, JT .
STROKE, 1994, 25 (09) :1877-1881
[13]  
LIPTON P, 1988, J NEUROSCI METH, V28, P147
[14]   Endoplasmic reticulum stress proteins block oxidant-induced Ca2+ increases and cell death [J].
Liu, H ;
Miller, E ;
van de Water, B ;
Stevens, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :12858-12862
[15]  
Malcolm CS, 1996, J NEUROCHEM, V66, P2350
[16]   The role of calcium in the regulation of apoptosis [J].
McConkey, DJ ;
Orrenius, S .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 59 (06) :775-783
[17]   NOVEL MECHANISMS IN CHEMICALLY-INDUCED HEPATOTOXICITY [J].
MEHENDALE, HM ;
ROTH, RA ;
GANDOLFI, AJ ;
KLAUNIG, JE ;
LEMASTERS, JJ ;
CURTIS, LR .
FASEB JOURNAL, 1994, 8 (15) :1285-1295
[18]   IN-VITRO ISCHEMIA-INDUCED INTRACELLULAR CA2+ ELEVATION IN CEREBELLAR SLICES - A COMPARATIVE-STUDY WITH THE VALUES FOUND IN HIPPOCAMPAL SLICES [J].
MITANI, A ;
YANASE, H ;
NAMBA, S ;
SHUDO, M ;
KATAOKA, K .
ACTA NEUROPATHOLOGICA, 1995, 89 (01) :2-7
[19]  
PALNITKAR SS, 1995, ANESTHESIOLOGY, V83, pA729
[20]   Disturbances of the functioning of endoplasmic reticulum: A key mechanism underlying neuronal cell injury? [J].
Paschen, W ;
Doutheil, J .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (01) :1-18