Romero-Sandoval E Alfonso, Curros-Criado M Mar, Gaitan Gema, Molina Carlos, Herrero Juan F
Department of Anesthesiology, Dartmouth College, Dartmouth Hitchcock Medical Center, Hanover, New Hampshire, USA.
CNS Drug Rev. 2007 Fall;13(3):279-95. doi: 10.1111/j.1527-3458.2007.00016.x.
The combination of numerous classic drugs with nitric oxide donors has led to the development of new compounds with promising therapeutic activities in a great variety of situations, including cardiovascular and respiratory systems, ocular pressure, inflammation, and pain. One of the first compounds developed was NCX-701 or nitroparacetamol, resulting from the combination of paracetamol, a classic and popular analgesic used in a great number of over-the-counter medications because of its antipyretic and analgesic properties, and a nitrooxybutyroyl moiety, which releases nitric oxide at a low but steady level. Although paracetamol is devoid of most of the gastrointestinal toxicity associated with aspirin-like drugs, this type of compounds was first designed to take advantage of the cytoprotective properties of nitric oxide when released at low concentrations. However, the combination of these molecules also resulted in an unexpected enhancement of the analgesic activity of paracetamol. In fact, NCX-701 has been shown to be effective in acute nociception as well as in neuropathic pain, situations in which paracetamol and other COX inhibitors are devoid of any effect. In addition, NCX-701 is more potent and, in some circumstances, more effective than its parent compound in different models of inflammatory pain. Furthermore, whereas paracetamol lacks any effective antiinflammatory action, NCX-701 might reduce inflammation. All these results taken together imply that the mechanism of action of NCX-701 is different from that of paracetamol, although it is not yet established for either molecule. NCX-701 appears to be a promising compound in the treatment of different types of pain, with a likely better profile of side effects than its parent molecule, paracetamol. Although recent clinical trials provided data consistent with the preclinical profile of NCX-701, further studies are needed to support its clinical use.
众多经典药物与一氧化氮供体的结合,已促使新型化合物的研发,这些化合物在多种情形下展现出颇具前景的治疗活性,涵盖心血管和呼吸系统、眼压、炎症及疼痛等领域。最早研发的化合物之一是NCX - 701或硝基对乙酰氨基酚,它由对乙酰氨基酚与一个硝基氧丁酰部分结合而成。对乙酰氨基酚是一种经典且常用的镇痛药,因其解热和镇痛特性被大量用于非处方药物中。硝基氧丁酰部分能以低但稳定的水平释放一氧化氮。尽管对乙酰氨基酚没有大多数与阿司匹林类药物相关的胃肠道毒性,但这类化合物最初设计的目的是利用低浓度释放的一氧化氮的细胞保护特性。然而,这些分子的结合还意外增强了对乙酰氨基酚的镇痛活性。事实上,NCX - 701已被证明在急性伤害性疼痛以及神经性疼痛中有效,而在这些情形下对乙酰氨基酚和其他环氧化酶抑制剂均无任何效果。此外,在不同的炎性疼痛模型中,NCX - 701比其母体化合物更有效力,在某些情况下也更具疗效。再者,虽然对乙酰氨基酚缺乏有效的抗炎作用,但NCX - 701可能会减轻炎症。综合所有这些结果表明,NCX - 701的作用机制与对乙酰氨基酚不同,尽管这两种分子的作用机制均尚未明确。NCX - 701似乎是一种治疗不同类型疼痛的颇具前景的化合物,其副作用可能比母体分子对乙酰氨基酚更好。尽管近期的临床试验提供的数据与NCX - 701临床前的特征相符,但仍需要进一步研究以支持其临床应用。