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肽AF3(AVPGVLRFamide)和AF4(GDVPGVLRFamide)对寄生线虫猪蛔虫和鸡蛔虫体壁肌肉的影响。

The effects of the peptides AF3 (AVPGVLRFamide) and AF4 (GDVPGVLRFamide) on the somatic muscle of the parasitic nematodes Ascaris suum and Ascaridia galli.

作者信息

Trim N, Holden-Dye L, Ruddell R, Walker R J

机构信息

Department of Physiology and Pharmacology, University of Southampton, UK.

出版信息

Parasitology. 1997 Aug;115 ( Pt 2):213-22. doi: 10.1017/s0031182097001224.

Abstract

AF3 (AVPGVLRFamide) and AF4 (GDVPGVLRFamide) are endogenous RFamide-like peptides isolated from the parasitic nematode Ascaris suum. Here the actions of these peptides on the somatic musculature of Ascaris have been investigated and compared to the action of acetylcholine (ACh), the excitatory transmitter at the neuromuscular junction. ACh, AF3 and AF4 contracted muscle with EC50S of 13 +/- 1 microM, 24 +/- 6 nM and 37 +/- 2 nM, respectively (n = 6). The muscle cells were depolarized by ACh (3 microM; 5.2 +/- 0.4 mV, n = 42), AF3 (1 microM; 2.6 +/- 0.3 mV, n = 19) and AF4 (1 microM; 3.3 +/- 0.4 mV, n = 19). EC50S were 681 +/- 329 nM (AF3) and 901 +/- 229 nM (AF4), but an estimate could not be made for ACh due to muscle contraction at concentrations greater than 10 microM. The depolarization to 3 microM ACh was abolished by the nicotinic receptor antagonist mecamylamine (10 microM; n = 5) but the responses to the peptides were not (111 +/- 7% and 108 +/- 17% with respect to control; n = 5). The depolarization elicited by ACh was reduced to a greater extent by a 50% reduction in extracellular Na+ concentration than the response to AF3 and AF4 (P < 0.02). Cobalt was more effective at blocking the AF3 and AF4 depolarizations than those to ACh. These observations suggest that AF3 and AF4 contract Ascaris muscle without an action at the Ascaris nicotinic receptor. Furthermore, the ionic mechanism through which AF3 and AF4 depolarize Ascaris muscle is different from that for ACh. ACh, AF3 and AF4 were also found to contract Ascaridia galli somatic muscle with EC50S of 13 +/- 3 microM, 721 +/- 236 nM and 371 +/- 177 nM, respectively (n = 7). The muscle cells were depolarized by ACh (EC50 = 14 +/- 5 microM, n = 5), AF3 (EC50 = 5 +/- 3 microM, n = 4) and AF4 (EC50 = 10 +/- 5 microM, n = 4). Therefore the response to these peptides is not unique to Ascaris and they may subserve a functional role in the motor nervous system of parasitic nematodes.

摘要

AF3(AVPGVLRFamide)和AF4(GDVPGVLRFamide)是从寄生线虫猪蛔虫中分离出的内源性类RFamide肽。本文研究了这些肽对猪蛔虫体壁肌肉组织的作用,并与神经肌肉接头处的兴奋性递质乙酰胆碱(ACh)的作用进行了比较。ACh、AF3和AF4均可使肌肉收缩,其半数有效浓度(EC50)分别为13±1μM、24±6 nM和37±2 nM(n = 6)。ACh(3μM)、AF3(1μM)和AF4(1μM)可使肌肉细胞去极化,去极化幅度分别为5.2±0.4 mV(n = 42)、2.6±0.3 mV(n = 19)和3.3±0.4 mV(n = 19)。AF3和AF4的EC50分别为681±329 nM和901±229 nM,但由于ACh在浓度大于10μM时会引起肌肉收缩,因此无法对其进行估计。烟碱受体拮抗剂美加明(10μM)可消除3μM ACh引起的去极化,但对肽类的反应无影响(相对于对照组分别为111±7%和108±17%;n = 5)。细胞外Na+浓度降低50%时,ACh引起的去极化程度比AF3和AF4引起的去极化程度降低得更多(P < 0.02)。钴对AF3和AF4去极化的阻断作用比对ACh去极化的阻断作用更有效。这些观察结果表明,AF3和AF4可使猪蛔虫肌肉收缩,且对猪蛔虫烟碱受体无作用。此外,AF3和AF4使猪蛔虫肌肉去极化的离子机制与ACh不同。还发现ACh、AF3和AF4均可使鸡蛔虫体壁肌肉收缩,其EC50分别为13±3μM、721±236 nM和371±177 nM(n = 7)。ACh(EC50 = 14±5μM,n = 5)、AF3(EC50 = 5±3μM,n = 4)和AF4(EC50 = 10±5μM,n = 4)可使肌肉细胞去极化。因此,这些肽的反应并非猪蛔虫所特有,它们可能在寄生线虫的运动神经系统中发挥功能作用。

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