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在神经性疼痛模型中评估的天然产物——一项系统综述。

Natural products evaluated in neuropathic pain models - a systematic review.

作者信息

Quintans Jullyana S S, Antoniolli Angelo R, Almeida Jackson R G S, Santana-Filho Valter J, Quintans-Júnior Lucindo J

机构信息

Department of Physiology, Federal University of Sergipe, São Cristóvão, Brazil.

出版信息

Basic Clin Pharmacol Toxicol. 2014 Jun;114(6):442-50. doi: 10.1111/bcpt.12178. Epub 2013 Dec 19.

Abstract

Chronic pain conditions, such as neuropathic pain, are a common problem that poses a major challenge to health-care providers due to its complex natural history, unclear aetiology and poor response towards therapy. Despite the large number of drugs available, the adherence is limited by the large range of side effects and pharmacological ineffectiveness. Thus, the search for new chemical entities that can act as promising molecules to treat chronic pain conditions has emerged. The natural products remain as the most promising sources of new chemical entities with applicability for the medical approach. Hence, we performed a systematic review analysing pre-clinical studies shown to be promising in a possible applicability in neuropathic pain. The search terms neuropathic pain, phytotherapy and medicinal plants were used to retrieve English language articles in LILACS, PUBMED and EMBASE published until 10 April 2013. From a total of 1529 articles surveyed, 28 met the inclusion and exclusion criteria established. The main chemical compounds studied were flavonoids (28%), terpenes (17%), alkaloids (14%), phenols (10%), carotenoids (10%) and others (21%). The mostly described animal models for the study of neuropathic pain included were chronic constriction injury (CCI - 32%), partial sciatic nerve ligation (PSNL - 28%), streptozotocin - induced diabetic (28%), alcoholic neuropathy (3.5%), sodium monoiodoacetate (MIA - 3.5%) and neuropathic pain induced by paclitaxel (3.5%). The opioids, serotonergic and cannabinoid systems are suggested as the most promising targets for the natural products described. Therefore, the data reviewed here suggest that these compounds are possible candidates for the treatment of chronic painful conditions, such as neuropathic pain.

摘要

慢性疼痛病症,如神经性疼痛,是一个常见问题,由于其复杂的自然病史、不明病因以及对治疗的不良反应,给医疗保健提供者带来了重大挑战。尽管有大量药物可用,但由于副作用范围广泛和药理无效,药物依从性受到限制。因此,寻找能够作为治疗慢性疼痛病症的有前景分子的新化学实体的研究应运而生。天然产物仍然是具有医学应用前景的新化学实体的最有希望的来源。因此,我们进行了一项系统综述,分析了在神经性疼痛的可能适用性方面显示出有前景的临床前研究。使用搜索词“神经性疼痛”、“植物疗法”和“药用植物”在LILACS、PUBMED和EMBASE中检索截至2013年4月10日发表的英文文章。在总共调查的1529篇文章中,有28篇符合既定的纳入和排除标准。研究的主要化合物为黄酮类化合物(28%)、萜类化合物(17%)、生物碱(14%)、酚类(10%)、类胡萝卜素(10%)和其他(21%)。研究神经性疼痛时最常描述的动物模型包括慢性缩窄损伤(CCI - 32%)、坐骨神经部分结扎(PSNL - 28%)、链脲佐菌素诱导的糖尿病(28%)、酒精性神经病变(3.5%)、单碘乙酸钠(MIA - 3.5%)和紫杉醇诱导的神经性疼痛(3.5%)。阿片类、血清素能和大麻素系统被认为是所描述的天然产物最有前景的靶点。因此,这里综述的数据表明,这些化合物可能是治疗慢性疼痛病症,如神经性疼痛的候选药物。

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