首页> 美国卫生研究院文献>International Journal for Parasitology: Drugs and Drug Resistance >Cholinergic receptors on intestine cells of Ascaris suum and activation of nAChRs by levamisole
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Cholinergic receptors on intestine cells of Ascaris suum and activation of nAChRs by levamisole

机译:A虫肠细胞上的胆碱能受体和左旋咪唑激活nAChRs

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摘要

Cholinergic agonists, like levamisole, are a major class of anthelmintic drugs that are known to act selectively on nicotinic acetylcholine receptors (nAChRs) on the somatic muscle and nerves of nematode parasites to produce their contraction and spastic paralysis. Previous studies have suggested that in addition to the nAChRs found on muscle and nerves, there are nAChRs on non-excitable tissues of nematode parasites. We looked for evidence of nAChRs expression in the cells of the intestine of the large pig nematode, using RT-PCR and RNAscope hybridization and detected mRNA of nAChR subunits in the cells. These subunits include components of the putative levamisole receptor in muscle: and . Relative expression of these mRNAs in intestine was quantified by qPCR. We also looked for and found expression of G protein-linked acetylcholine receptors ( ). We used Fluo-3 AM to detect intracellular calcium changes in response to receptor activation by acetylcholine (as a non-selective agonist) and levamisole (as an L-type nAChR agonist) to look for evidence of functioning nAChRs in the intestine. We found that both acetylcholine and levamisole elicited increases in intracellular calcium but their signal profiles in isolated intestinal tissues were different, suggesting activation of different receptor sets. The levamisole responses were blocked by mecamylamine, a nicotinic receptor antagonist in indicating the activation of intestinal nAChRs rather than G protein-linked acetylcholine receptors (GARs) by levamisole The detection of nAChRs in cells of the intestine, in addition to those on muscles and nerves, reveals another site of action of the cholinergic anthelmintics and a site that may contribute to the synergistic interactions of cholinergic anthelmintics with other anthelmintics that affect the intestine (Cry5B).
机译:胆碱能激动剂,如左旋咪唑,是一类驱虫药,已知能选择性地作用于线虫寄生虫的体肌和神经上的烟碱乙酰胆碱受体(nAChRs),以产生收缩和痉挛性麻痹。先前的研究表明,除了在肌肉和神经上发现的nAChRs外,在线虫寄生虫的非兴奋性组织上也存在nAChRs。我们使用RT-PCR和RNAscope杂交寻找在大型猪线虫肠细胞中nAChRs表达的证据,并检测到细胞中nAChR亚基的mRNA。这些亚基包括肌肉中假定的左旋咪唑受体的成分。通过mPCR定量这些mRNA在肠中的相对表达。我们还寻找并发现了G蛋白连接的乙酰胆碱受体()的表达。我们使用Fluo-3 AM检测乙酰胆碱(作为非选择性激动剂)和左旋咪唑(作为L型nAChR激动剂)对受体激活的反应中的细胞内钙变化,以寻找在肠道中起作用的nAChRs的证据。我们发现乙酰胆碱和左旋咪唑都引起细胞内钙的增加,但是它们在分离的肠组织中的信号特征是不同的,表明不同受体集的激活。左旋咪唑的反应被烟酰胺受体拮抗剂美卡明胺所阻断,它表明左旋咪唑激活了肠道nAChRs而不是G蛋白连接的乙酰胆碱受体(GARs)。检测肠道细胞中nAChR的含量,以及肌肉和神经中的含量。 ,揭示了胆碱能驱虫药的另一个作用位点和可能有助于胆碱能驱虫药与影响肠道的其他驱虫药的协同相互作用的位点(Cry5B)。

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