Use of carbon monoxide as a therapeutic agent: promises and challenges

被引:235
作者
Foresti, Roberta [1 ]
Bani-Hani, Mohamed G. [1 ]
Motterlini, Roberto [1 ]
机构
[1] Northwick Pk Inst Med Res, Vasc Biol Unit, Dept Surg Res, Harrow HA1 3UJ, Middx, England
关键词
D O I
10.1007/s00134-008-1011-1
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
As a by-product of heme catabolism by the heme oxygenase system, carbon monoxide (CO) has been neglected for many years, and only recently has its role as an essential signaling molecule been appreciated. In the past decade, the use of CO gas in pre-clinical experimental models of disease has produced some remarkable data indicating that its therapeutic delivery to mammals could alleviate inflammatory processes and cardiovascular disorders. However, the inherent toxic nature of CO cannot be ignored, knowing that inhalation of uncontrolled amounts of this gas can ultimately lead to serious systemic complications and neuronal derangements. From a clinical perspective, a key question is whether a safe and therapeutically effective threshold of CO can be reached locally in organs and tissues without delivering potentially toxic amounts through the lung. The advent of CO-releasing molecules (CO-RMs), a group of compounds capable of carrying and liberating controlled quantities of CO in cellular systems, appears a plausible alternative in the attempt to overcome the limitations of CO gas. Although in its infancy and far from being used for clinical applications, the CO-RMs technology is supported by very encouraging biological results and reflected by the chemical versatility of these compounds and their endless potential to be transformed into CO-based pharmaceuticals.
引用
收藏
页码:649 / 658
页数:10
相关论文
共 95 条
[11]   Cardioprotective actions by a water-soluble carbon monoxide-releasing molecule [J].
Clark, JE ;
Naughton, P ;
Shurey, S ;
Green, CJ ;
Johnson, TR ;
Mann, BE ;
Foresti, R ;
Motterlini, R .
CIRCULATION RESEARCH, 2003, 93 (02) :E2-E8
[12]   Inhaled carbon monoxide and hyperoxic lung injury in rats [J].
Clayton, CE ;
Carrawav, MS ;
Suliman, HB ;
Thalmann, ED ;
Thalmann, KN ;
Schmechel, DE ;
Piantadosi, CA .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 281 (04) :L949-L957
[13]   Stromal cell-derived factor 1 promotes angiogenesis via a heme oxygenase 1-dependent mechanism [J].
Deshane, Jessy ;
Chen, Sifeng ;
Caballero, Sergio ;
Grochot-Przeczek, Anna ;
Was, Halina ;
Calzi, Sergio Li ;
Lach, Radoslaw ;
Hock, Thomas D. ;
Chen, Bo ;
Hill-Kapturczak, Nathalie ;
Siegal, Gene P. ;
Dulak, Jozef ;
Jozkowicz, Alicja ;
Grant, Maria B. ;
Agarwal, Anupam .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (03) :605-618
[14]   Inhaled carbon monoxide confers antiinflammatory effects against ventilator-induced lung injury [J].
Dolinay, T ;
Szilasi, M ;
Liu, MY ;
Choi, AMK .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (06) :613-620
[15]   Carbon monoxide mediates vasodilator effects of glutamate in isolated pressurized cerebral arterioles of newborn pigs [J].
Fiumana, E ;
Parfenova, H ;
Jaggar, JH ;
Leffler, CW .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 284 (04) :H1073-H1079
[16]   Generation of bile pigments by haem oxygenase: a refined cellular strategy in response to stressful insults [J].
Foresti, R ;
Green, CJ ;
Motterlini, R .
FREE RADICALS: ENZYMOLOGY, SIGNALLING AND DISEASE, 2004, 71 :177-192
[17]   Vasoactive properties of CORM-3, a novel water-soluble carbon monoxide-releasing molecule [J].
Foresti, R ;
Hammad, J ;
Clark, JE ;
Johnson, TR ;
Mann, BE ;
Friebe, A ;
Green, CJ ;
Motterlini, R .
BRITISH JOURNAL OF PHARMACOLOGY, 2004, 142 (03) :453-460
[18]   Heme oxygenase/carbon monoxide-biliverdin pathway down regulates neutrophil rolling, adhesion and migration in acute inflammation [J].
Freitas, A. ;
Alves-Filho, J. C. ;
Secco, D. D. ;
Neto, A. F. ;
Ferreira, S. H. ;
Barja-Fidalgo, C. ;
Cunha, F. Q. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 149 (04) :345-354
[19]   Paradoxical rescue from ischemic lung injury by inhaled carbon monoxide driven by derepression of fibrinolysis [J].
Fujita, T ;
Toda, K ;
Karimova, A ;
Yan, SF ;
Naka, Y ;
Yet, SF ;
Pinsky, DJ .
NATURE MEDICINE, 2001, 7 (05) :598-604
[20]   The clinical toxicology of carbon monoxide [J].
Gorman, D ;
Drewry, A ;
Huang, YL ;
Sames, C .
TOXICOLOGY, 2003, 187 (01) :25-38