Effect of middle cerebral artery occlusion on mRNA expression for the sodium-coupled vitamin C transporter SVCT2 in rat brain

被引:56
作者
Berger, UV
Lu, XCM
Liu, WL
Tang, ZC
Slusher, BS
Hediger, MA
机构
[1] Brigham & Womens Hosp, Membrane Biol Program, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Div Renal, Boston, MA 02115 USA
[3] Guilford Pharmaceut Inc, Baltimore, MD USA
关键词
ascorbate; astrocytes; astrocytosis; ischemia; oxidative stress; SVCT2;
D O I
10.1046/j.1471-4159.2003.01891.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sodium-vitamin C co-transporter SVCT2 is primarily responsible for the accumulation of the important antioxidant ascorbate into brain cells. In vitro studies have demonstrated strong expression of this transporter in cultured astrocytes, whereas in situ hybridization analysis has so far detected SVCT2 only in neurons. In the present study, we examined the response of SVCT2 mRNA expression in the brain to focal ischemia induced for 2 h by unilateral middle cerebral artery occlusion. The mRNA expression patterns of SVCT2 and the glutamate-activated immediate early gene Arc were investigated at 2 and 22 h after ischemia. SVCT2 and Arc mRNA expression was lost in the ischemic core at both time points. In areas outside the core, Arc was strongly up-regulated, primarily at 2 h, whereas SVCT2 showed an increase at 2 and 22 h. SVCT2 expression was increased in neurons as well as in astrocytes, providing the first evidence for SVCT2 expression in astrocytes in situ . These findings underscore the importance of ascorbate as a neuroprotective agent and may have implications for therapeutic strategies. In addition, the increase of SVCT2 in astrocytes after ischemia suggests that cultured astrocytes are exposed to chronic oxidative stress.
引用
收藏
页码:896 / 906
页数:11
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