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用作用于神经肌肉系统的药剂控制线虫寄生虫:神经肽配体发现的启示。

Control of nematode parasites with agents acting on neuro-musculature systems: lessons for neuropeptide ligand discovery.

机构信息

Department of Biomedical Sciences, Iowa State University, Ames, Iowa, USA.

出版信息

Adv Exp Med Biol. 2010;692:138-54. doi: 10.1007/978-1-4419-6902-6_7.

Abstract

There are a number of reasons why the development of novel anthelmintics is very necessary. In domestic animals, parasites cause serious loss of production and are a welfare concern. The control of these parasites requires changes in management practices to reduce the spread of infection and the use of therapeutic agents to treat affected animals. The development of vaccines against parasites is desirable but their development so far has been very limited. One notable exception is the vaccination of calves against infection by Dictyocaulus viviparous (lungworm) which has proved to be very effective. In domestic animals, the total market for anti-parasitic agents (both ecto- and endo-parasites) is in excess of a billion U.S. dollars. In humans there are serious problems ofmorbidity and mortality associated with parasite infections. 1.6 billion People throughout the world are infected with ascariasis (Fig. 1A) and/or hookworm. Approximately one-third of the world's population is suffering from the effects of intestinal nematode parasites, causing low growth-rates in infants, ill-thrift, diarrhea and in 2% of cases, loss of life. Despite the huge number of affected individuals, the market for anti-parasitic drugs for humans is not big enough to foster the development of anthelmintics because most infestations that occur are in undeveloped countries that lack the ability to pay for the development of these drugs. The major economic motivator then, is for the development of animal anthelmintics. In both domestic animals and now in humans, there is now a level of resistance to the available anthelmintic compounds. The resistance is either: constitutive, where a given species of parasite has never been sensitive to the compound; or acquired, where the resistance has developed through Darwinian selection fostered by the continued exposure to the anti-parasitic drugs. The continued use of all anthelmintics has and will, continue to increase the level of resistance. Cure rates are now often less than 100% and resistance of parasites to agents acting on the neuromuscular systems is present in a wide range of parasites of animals and humans hosts. In the face of this resistance the development of novel and effective agents is an urgent and imperative need. New drugs which act on the neuromuscular system have an advantage for medication for animals and humans because they have a rapid therapeutic effect within 3 hours of administration. The effects on the neuromuscular system include: spastic paralysis with drugs like levamisole and pyrantel; flaccid paralysis as with piperazine; or disruption of other vital muscular activity as with ivermectin. Figure 1 B and C, illustrates an example ofa spastic effect oflevamisole on infectious L3 larvae of Ostertagia ostertagiae, a parasite of pigs. The effect was produced within minutes of the in vitro application oflevamisole. In this chapter we comment on the properties of existing agents that have been used to control nematode parasites and that have an action on neuromuscular systems. We then draw attention to resistance that has developed to these compounds and comment on their toxicity and spectra of actions. We hope that some of the lessons that the use of these compounds has taught us may to be applied to any novel neuropeptide ligand that may be introduced. Our aim is then is to provide some warning signs for recognized but dangerous obstacles.

摘要

有许多原因说明开发新型驱虫药是非常必要的。在家畜中,寄生虫会导致严重的生产损失,并且是动物福利关注的问题。控制这些寄生虫需要改变管理实践,以减少感染的传播,并使用治疗剂来治疗受感染的动物。寄生虫疫苗的开发是理想的,但到目前为止,它们的开发非常有限。一个值得注意的例外是对感染旋毛虫(肺线虫)的小牛进行疫苗接种,事实证明这非常有效。在家畜中,抗寄生虫剂(包括外寄生虫和内寄生虫)的总市场超过 10 亿美元。在人类中,寄生虫感染与发病率和死亡率有关,存在严重问题。全世界有 16 亿人感染了蛔虫(图 1A)和/或钩虫。大约三分之一的世界人口受到肠道线虫寄生虫的影响,导致婴儿生长缓慢、身体不适、腹泻,在 2%的情况下导致死亡。尽管受影响的人数众多,但人类驱虫药市场还不够大,无法促进驱虫药的开发,因为大多数发生的寄生虫感染都发生在发展中国家,这些国家没有能力为这些药物的开发支付费用。那么,主要的经济动机是开发动物驱虫药。在家畜和现在的人类中,现有的驱虫化合物已经出现了耐药性。这种耐药性要么是:组成型的,即特定的寄生虫种类从未对化合物敏感;要么是获得性的,即通过对驱虫药物的持续暴露,通过达尔文选择而产生的耐药性。持续使用所有驱虫药都会并将继续增加耐药性水平。现在的治愈率通常低于 100%,并且对作用于神经肌肉系统的药物的寄生虫耐药性存在于动物和人类宿主的广泛寄生虫中。面对这种耐药性,开发新型有效的药物是当务之急。作用于神经肌肉系统的新药对动物和人类的药物治疗具有优势,因为它们在给药后 3 小时内具有快速的治疗效果。对神经肌肉系统的影响包括:像左旋咪唑和噻嘧啶这样的药物会引起痉挛性瘫痪;像哌嗪一样引起弛缓性瘫痪;或像伊维菌素一样破坏其他重要的肌肉活动。图 1B 和 1C 说明了左旋咪唑对感染性 L3 幼虫的 Ostertagia ostertagiae(一种猪寄生虫)的痉挛作用,这种寄生虫在体外应用左旋咪唑后几分钟内就产生了这种作用。在这一章中,我们将评论已用于控制线虫寄生虫并作用于神经肌肉系统的现有药物的特性。然后,我们将提请注意对这些化合物产生的耐药性,并对其毒性和作用谱进行评论。我们希望,从这些化合物的使用中吸取的一些经验教训可以应用于任何可能引入的新型神经肽配体。我们的目标是为公认但危险的障碍提供一些警告信号。

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