Analysis of nitroxyl spin probes in mouse brain by X-band ESR with microdialysis technique

被引:5
作者
Shiba, Takeshi [1 ]
Yamato, Mayumi [1 ]
Kudou, Wataru [1 ]
Ichikawa, Kazuhiro [2 ]
Yamada, Ken-Ichi [2 ]
Watanabe, Toshiaki [1 ]
Utsumi, Hideo [2 ]
机构
[1] Kyushu Univ, Fac Pharmaceut Sci, Dept REDOX Med Sci, Fukuoka 8128582, Japan
[2] Kyushu Univ, Fac Pharmaceut Sci, Dept Biofunct Sci, Fukuoka 8128582, Japan
关键词
nitroxyl radical; microdialysis; electron spin resonance; blood-brain barrier; free radical; pharmacokinetics;
D O I
10.1002/jps.21258
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Stable nitroxyl radicals are widely used in electron spin resonance (ESR) studies in vivo to determine ROS generation, but there are insufficient data on how their distribution to various tissues, excretion, and/or systemic signal decay affect the signal decay in a region of interest. Here, we evaluated the level of spin probe in the brain using a microdialysis combined with X-band ESR spectroscopy, to clarify the BBB permeability of different spin probes. We also determined the association between PROXYL spin probe signal decay in the head and the probe's level in the brain, its excretion in urine, and its rate of signal decay in other areas and tissues. Dialysate recovered from the mouse prefrontal cortex was used to determine the total spin probe level in the brain by X-band ESR spectroscopy. There was a positive correlation between the level of spin probes in the brain and their partition coefficients. Furthermore, the in vivo decay rate of the nitroxyl radical signal in the head was associated with the probes' level in the brain, but not with its systemic signal decay rate or excretion into urine. These basic data may support the use of PROXYLs as site-specific ROS probes in the brain. (C) 2008 Wiley-Liss, Inc. and the American Pharmacists Association.
引用
收藏
页码:4101 / 4107
页数:7
相关论文
共 32 条
[11]   Metabolism of the stable nitroxyl radical 4-oxo-2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPONE) [J].
Kroll, C ;
Borchert, HH .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1999, 8 (01) :5-9
[12]  
Kuppusamy P, 2002, CANCER RES, V62, P307
[14]   Electron paramagnetic resonance imaging of tumor hypoxia:: Enhanced spatial and temporal resolution for in vivo pO2 determination [J].
Matsumoto, K ;
Subramanian, S ;
Devasahayam, N ;
Aravalluvan, T ;
Murugesan, R ;
Cook, JA ;
Mitchell, JB ;
Krishna, MC .
MAGNETIC RESONANCE IN MEDICINE, 2006, 55 (05) :1157-1163
[15]  
MEHLHORN RJ, 1991, J BIOL CHEM, V266, P2724
[16]   In vivo L-band ESR and quantitative pharmacokinetic analysis of stable spin probes in rats and mice [J].
Nishino, N ;
Yasui, H ;
Sakurai, H .
FREE RADICAL RESEARCH, 1999, 31 (01) :35-51
[17]   Noninvasive evaluation of in vivo free radical reactions catalyzed by iron using in vivo ESR spectroscopy [J].
Phumala, N ;
Ide, T ;
Utsumi, H .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (9-10) :1209-1217
[18]   An improved external loop resonator for in vivo L-band EPR spectroscopy [J].
Salikhov, I ;
Hirata, H ;
Walczak, T ;
Swartz, HM .
JOURNAL OF MAGNETIC RESONANCE, 2003, 164 (01) :54-59
[19]  
Sano H, 1997, BIOCHEM MOL BIOL INT, V42, P641
[20]   A new nitroxyl-probe with high retention in the brain and its application for brain imaging [J].
Sano, H ;
Naruse, M ;
Matsumoto, K ;
Oi, T ;
Utsumi, H .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (06) :959-969