Vitamin D3 attenuates cortical infarction induced by middle cerebral arterial ligation in rats

被引:178
作者
Wang, Y [1 ]
Chiang, YH
Su, TP
Hayashi, T
Morales, M
Hoffer, BJ
Lin, SZ
机构
[1] NIDA, NIH, Baltimore, MD 21224 USA
[2] Natl Def Med Ctr, Tri Serv Gen Hosp, Taipei, Taiwan
关键词
vitamin D-3; infarction; ischemia; neuroprotection; glial cell line-derived neurotrophic factor;
D O I
10.1016/S0028-3908(99)00255-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have previously reported that intracerebral administration of glial cell line derived neurotrophic factor (GDNF) reduces the extent of middle cerebral arterial (MCA) ligation-induced cortical infarction in rats. Recent studies have shown that application of 1,25 dihydroxyvitamin D-3 (D3) enhances GDNF mRNA expression in vitro. The purpose of the present study was to investigate if administration of D3 in vivo will protect against ischemic brain injury. Adult male Sprague-Dawley rats were injected daily with D3 or with saline for four or eight days. Animals received a 90-min right MCA ligation on the 4(th) or 8(th) day after anesthesia with chloral hydrate. Animals were sacrificed for tri-phenyl-tetrazolium chloride (TTC) staining 24 h after the onset of reperfusion. A subset of animals receiving eight days of D3 or saline treatment were used for blood gas and cerebral GDNF protein level analysis. We found that pretreatment with D3 for four days did not attenuate the ischemic injury. However, animals receiving eight days of D3 injections showed a significant reduction in the amount of infarction in the cortex. Eight day D3 treatment did not alter blood gases or blood pressure; however, it did increase calcium levels. Pretreatment with D3 significantly increased GDNF levels in the cortex. In conclusion, our data indicate that D3 reduces ischemia- induced brain damage and supports the hypothesis that this effect may be through the up-regulation of GDNF mechanisms in cortex. Published by Elsevier Science Ltd.
引用
收藏
页码:873 / 880
页数:8
相关论文
共 45 条
[1]   Amelioration of brain edema by topical application of glial cells line-derived neurotrophic factor in reperfused rat brain [J].
Abe, K ;
Hayashi, T ;
Itoyama, Y .
NEUROSCIENCE LETTERS, 1997, 231 (01) :37-40
[2]   Expression of the glial cell line-derived neurotrophic factor gene in rat brain after transient MCA occlusion [J].
Abe, K ;
Hayashi, T .
BRAIN RESEARCH, 1997, 776 (1-2) :230-234
[3]  
BARNETT RN, 1973, AM J CLIN PATHOL, V59, P836
[4]   Cytotoxic effects of 1 alpha,25-dihydroxyvitamin D-3 and synthetic vitamin D-3 analogues on a glioma cell line [J].
Baudet, C ;
Chevalier, G ;
Naveilhan, P ;
Binderup, L ;
Brachet, P ;
Wion, D .
CANCER LETTERS, 1996, 100 (1-2) :3-10
[5]  
Brown RD, 1996, STROKE, V27, P373
[6]   Mechanisms of neuronal damage in brain hypoxia/ischemia: Focus on the role of mitochondrial calcium accumulation [J].
Budd, SL .
PHARMACOLOGY & THERAPEUTICS, 1998, 80 (02) :203-229
[7]   A MODEL OF FOCAL ISCHEMIC STROKE IN THE RAT - REPRODUCIBLE EXTENSIVE CORTICAL INFARCTION [J].
CHEN, ST ;
HSU, CY ;
HOGAN, EL ;
MARICQ, H ;
BALENTINE, JD .
STROKE, 1986, 17 (04) :738-743
[8]   Transplantation of fetal kidney tissue reduces cerebral infarction induced by middle cerebral artery ligation [J].
Chiang, YH ;
Lin, SZ ;
Borlongan, CV ;
Hoffer, BJ ;
Morales, M ;
Wang, Y .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (12) :1329-1335
[9]   Very delayed infarction after mild focal cerebral ischemia: A role for apoptosis? [J].
Du, C ;
Hu, R ;
Csernansky, CA ;
Hsu, CY ;
Choi, DW .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (02) :195-201
[10]   1,25-Dihydroxyvitamin D-3 inhibits the expression of inducible nitric oxide synthase in rat central nervous system during experimental allergic encephalomyelitis [J].
Garcion, E ;
Nataf, S ;
Berod, A ;
Darcy, F ;
Brachet, P .
MOLECULAR BRAIN RESEARCH, 1997, 45 (02) :255-267