Cellular and Molecular Actions of Methylene Blue in the Nervous System

被引:332
作者
Oz, Murat [1 ,2 ]
Lorke, Dietrich E. [3 ]
Hasan, Mohammed [2 ]
Petroianu, George A. [2 ]
机构
[1] NIDA, Integrat Neurosci Sect, Intramural Res Program, NIH,DHHS, Baltimore, MD 21224 USA
[2] UAE Univ, Dept Pharmacol, Fac Med & Hlth Sci, Al Ain, U Arab Emirates
[3] UAE Univ, Dept Anat, Fac Med & Hlth Sci, Al Ain, U Arab Emirates
关键词
methylene blue; nervous system; phenothiazines; NITRIC-OXIDE SYNTHASE; PROLONGED POSTOPERATIVE DISORIENTATION; MONOAMINE-OXIDASE; IFOSFAMIDE ENCEPHALOPATHY; INTRATHECAL INJECTION; BETA OLIGOMERIZATION; PHOTODYNAMIC THERAPY; SEROTONIN TOXICITY; PARATHYROID-GLANDS; PROSTAGLANDIN E(2);
D O I
10.1002/med.20177
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Methylene Blue (MB), following its introduction to biology in the 19th century by Ehrlich, has found uses in various areas of medicine and biology. At present, MB is the first line of treatment in methemoglobinemias, is used frequently in the treatment of ifosfamide-induced encephalopathy, and is routinely employed as a diagnostic tool in surgical procedures. Furthermore, recent studies suggest that MB has beneficial effects in Alzheimer's disease and memory improvement. Although the modulation of the cGMP pathway is considered the most significant effect of MB, mediating its pharmacological actions, recent studies indicate that it has multiple cellular and molecular targets. In the majority of cases, biological effects and clinical applications of MB are dictated by its unique physicochemical properties including its planar structure, redox chemistry, ionic charges, and light spectrum characteristics. In this review article, these physicochemical features and the actions of MB on multiple cellular and molecular targets are discussed with regard to their relevance to the nervous system. (C) 2009 Wiley Periodicals, Inc. Med Res Rev, 31, No. 1, 93-117, 2010
引用
收藏
页码:93 / 117
页数:25
相关论文
共 238 条
[101]  
Klamer D, 2004, BASIC CLIN PHARMACOL, V94, P65, DOI 10.1111/j.1742-7843.2004.pto940203.x
[102]   New inhibitors of scrapie-associated prion protein formation in a library of 2,000 drugs and natural products [J].
Kocisko, DA ;
Baron, GS ;
Rubenstein, R ;
Chen, JC ;
Kuizon, S ;
Caughey, B .
JOURNAL OF VIROLOGY, 2003, 77 (19) :10288-10294
[103]   Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease [J].
Korth, C ;
May, BCH ;
Cohen, FE ;
Prusiner, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9836-9841
[104]   DRUG DISTRIBUTION IN THE BODY .4. DOSE DEPENDENCY OF APPARENT VOLUMES OF DISTRIBUTION FOR METHYLENE-BLUE IN RABBITS [J].
KOZAKI, A ;
WATANABE, J .
JOURNAL OF PHARMACOBIO-DYNAMICS, 1981, 4 (01) :49-57
[105]   Methylene blue induces ongoing activity in rat cutaneous primary afferents and depolarization of DRG neurons via a photosensitive mechanism [J].
Kress, M ;
Petersen, M ;
Reeh, PW .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1997, 356 (05) :619-625
[106]  
KRISTIANSEN JE, 1989, DAN MED BULL, V36, P178
[107]   Multi-site inhibition of human plasma cholinesterase by cationic phenoxazine and phenothiazine dyes [J].
Kucukkilinc, Tuba ;
Ozer, Inci .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2007, 461 (02) :294-298
[108]   PROPHYLAXIS AND REVERSAL OF IFOSFAMIDE ENCEPHALOPATHY WITH METHYLENE-BLUE [J].
KUPFER, A ;
AESCHLIMANN, C ;
WERMUTH, B ;
CERNY, T .
LANCET, 1994, 343 (8900) :763-764
[109]   Rapid intraoperative localization of parathyroid glands utilizing methylene blue infusion [J].
Kuriloff, DB ;
Sanborn, KV .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2004, 131 (05) :616-622
[110]  
Lee SK, 2003, CHEM COMMUN, V18, P2347