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The Rhodococcus sp cocaine esterase: A bacterial candidate for novel pharmacokinetic-based therapies for cocaine abuse RID A-4573-2009

机译:Rhodococcus sp可卡因酯酶:可卡因滥用的基于新药代动力学疗法的细菌候选物RID A-4573-2009

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摘要

Cocaine is a powerful central nervous stimulant and among the most abused of drugs. Despite decades of efforts, however, no effective pharmacological treatments are available against cocaine addiction or toxic effects. Classical receptor-antagonist therapeutic approaches have not yielded significant effects, although cocaine targets are well known, thus fostering development of alternative therapeutic strategies. Recent evidence indicates that a sensible approach for treatment of cocaine abuse could be to interfere with cocaine pharmacokinetics, i.e. by preventing the drug from reaching the receptors responsible for its biological effects. Administration of cocaine binding antibodies as well as catalytic antibodies and enzymes that hydrolyze cocaine represent potential alternative therapeutic approach(es). The discovery of the cocaine esterase from the strain MB1 of the bacterium Rhodococcus sp. (cocE) could be a major breakthrough in this field; cocE hydrolyzes cocaine faster than any known cocaine esterase and catalytic antibody.
机译:可卡因是一种强大的中枢神经兴奋剂,也是滥用最多的药物之一。然而,尽管经过数十年的努力,仍没有有效的药理疗法可卡因成瘾或毒性作用。尽管可卡因靶标是众所周知的,但是经典的受体-拮抗剂治疗方法并未产生明显的效果,从而促进了其他治疗策略的发展。最近的证据表明,治疗可卡因滥用的明智方法可能是干扰可卡因的药代动力学,即通过阻止药物到达负责其生物作用的受体。可卡因结合抗体以及水解可卡因的催化抗体和酶的施用代表了潜在的替代治疗方法。从Rhodococcus sp。细菌MB1菌株中发现可卡因酯酶。 (cocE)可能是该领域的重大突破;与任何已知的可卡因酯酶和催化抗体相比,cocE水解可卡因的速度更快。

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