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首页> 外文期刊>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:蛔虫细胞的胆碱能受体蛔虫细胞和左旋吲哚的活化

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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, Ascaris suum, using RT-PCR and RNAscope in situ hybridization and detected mRNA of nAChR subunits in the cells. These subunits include components of the putative levamisole receptor in A. suum muscle: Asu-unc-38, Asu-unc-29, Asu-unc-63 and Asu-acr-8 . Relative expression of these mRNAs in A. suum intestine was quantified by qPCR. We also looked for and found expression of G protein-linked acetylcholine receptors ( Asu-gar-1 ). 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 A. suum, 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:像vamisole一样的胆碱能性激动剂是左旋药物的主要类药物,该主要药物被众所周知,在Nicotinic乙酰胆碱受体(NACHRS)上是在线虫寄生虫的躯体肌肉和神经上选择性的,以产生它们的收缩和痉挛性麻痹。以前的研究表明,除了在肌肉和神经上发现的NACHR,NAMATODE寄生虫的非激发组织有NACHRS。我们寻找NACHRS在大猪Nematode,Ascaris Sum的细胞中表达的证据,使用RT-PCR和Rnascope原位杂交,并检测细胞中NACHR亚基的mRNA。这些亚基包括A. sum肌肉中推定的左旋氨基受体的组分:ASU-UNC-38,ASU-UNC-29,ASU-UNC-63和ASU-ACR-8。通过QPCR量化了这些MRNA中这些MRNA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(ASU-GAR-1)的表达。我们使用Fluo-3 AM响应于受乙酰胆碱(作为非选择性激动剂)和左旋吲哚(作为L型NACHR激动剂)来检测细胞内钙变化,以寻找在肠道中运作NACHR的证据。我们发现,乙酰胆碱和左旋吲哚均引发细胞内钙的增加,但它们在分离的肠组织中的信号谱不同,表明不同受体集的激活。左旋胺应答被咪酰胺,烟碱受体拮抗剂中的甲胺胺封闭,表明左旋吲哚的激活肠道NACHR而不是G蛋白连接的乙酰胆碱受体(GARS)。除了肌肉和神经的细胞中,检测肠道细胞中的NACHRS揭示了胆碱能结构和可能有助于胆碱能结构与影响肠道的其他胆管的协同相互作用(Cry5B )。

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