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噻嘧啶抗性改变线虫烟碱型乙酰胆碱受体单通道特性。

Pyrantel resistance alters nematode nicotinic acetylcholine receptor single-channel properties.

作者信息

Robertson A P, Bjørn H E, Martin R J

机构信息

Department of Preclinical Veterinary Sciences, R.(D.)S.V.S., Summerhall Square, University of Edinburgh, Edinburgh, UK.

出版信息

Eur J Pharmacol. 2000 Apr 7;394(1):1-8. doi: 10.1016/s0014-2999(00)00135-7.

Abstract

Resistance to the anthelmintics pyrantel ((E)-1,4,5, 6-tetrahydro-1-methyl-2-[2-(2thienyl)ethenyl]pyrimidine) and levamisole ((S)-2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazole) is an increasingly widespread problem in gastro-intestinal nematode infestations. Both compounds act on the nicotinic acetylcholine receptors on the surface of nematode somatic muscle. The patch-clamp technique was used to measure nematode nicotinic acetylcholine receptor properties at 75, 50, -50 and -75 mV in a pyrantel-resistant isolate of Oesophagostomum dentatum. Patch pipettes contained 30 microM levamisole as agonist. We found that 28. 1% of membrane patches contained active receptors. At -50 mV, the single-channel conductance was 36.2+/-1.4 pS, the mean open-time (tau) was 1.45+/-0.14 ms and the mean probability of opening (P(o)) was 0.004+/-0.002. We compared these results with previous work on an anthelmintic sensitive isolate and a levamisole-resistant isolate [Robertson, A.P., Bjorn, H.E., Martin, R.J., 1999. Levamisole resistance resolved at the single-channel level. FASEB J. 13, 749-760.]. We found that pyrantel-resistant parasites had a reduced percentage of active patches and a reduced P(o) value when compared to anthelmintic sensitive worms. We concluded that pyrantel resistance is associated with a modification of the target nicotinic receptor properties.

摘要

对驱虫药噻嘧啶((E)-1,4,5,6-四氢-1-甲基-2-[2-(2-噻吩基)乙烯基]嘧啶)和左旋咪唑((S)-2,3,5,6-四氢-6-苯基咪唑并[2,1-b]噻唑)产生抗性是胃肠道线虫感染中一个日益普遍的问题。这两种化合物都作用于线虫体壁肌肉表面的烟碱型乙酰胆碱受体。采用膜片钳技术在75、50、-50和-75 mV下测量了对噻嘧啶耐药的齿食道口线虫分离株的线虫烟碱型乙酰胆碱受体特性。膜片钳微电极中含有30 μM左旋咪唑作为激动剂。我们发现28.1%的膜片含有活性受体。在-50 mV时,单通道电导为36.2±1.4 pS,平均开放时间(τ)为1.45±0.14 ms,平均开放概率(P(o))为0.004±0.002。我们将这些结果与之前关于驱虫药敏感分离株和左旋咪唑耐药分离株的研究结果进行了比较[罗伯逊,A.P.,比约恩,H.E.,马丁,R.J.,1999年。左旋咪唑抗性在单通道水平得到解决。《美国实验生物学会联合会杂志》13,749 - 760]。我们发现,与驱虫药敏感的蠕虫相比,对噻嘧啶耐药的寄生虫活性膜片的百分比降低,P(o)值降低。我们得出结论,噻嘧啶抗性与靶标烟碱型受体特性的改变有关。

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