Fellowes R A, Maule A G, Marks N J, Geary T G, Thompson D P, Halton D W
Parasitology Research Group, School of Biology and Biochemistry, Queen's University of Belfast, UK.
Parasitology. 2000 Jan;120 ( Pt 1):79-89. doi: 10.1017/s0031182099005260.
Ascaris suum possesses a large number of FMRFamide-related peptides (FaRPs) of which KNEFIRFamide (AF1), KHEYLRFamide (AF2) and KSAYMRFamide (AF8/PF3) have been shown to modulate the intrinsic, rhythmic activity of the vagina vera of A. suum in vitro. In the present study, the effects of the nematode FaRPs, SDPNFLRFamide (PF1), SADPNFLREamide (PF2) and KPNFIRFamide (PF4) (from Panagrellus redivivus) and AVPGVLRFamide (AF3) and GDVPGVLRFamide (AF4) (from A. suum) on the in vitro activity of the vagina vera were examined. The effects of each of the peptides were qualitatively and quantitatively distinct. All 3 FaRPs from P. redivivus were inhibitory, causing a cessation of contractions. PF2 was 3 times more potent than PF1, with a threshold of 1 nM. Although PF4 was the least potent (threshold, 10 nM), its effects at > or = 10 nM were quantitatively the greatest. Both AF3 and AF4 (1 microM) induced complex, multiphasic responses consisting of an initial contraction and spastic paralysis followed by a return of contractile activity of increased amplitude. AF3 was 3 times more potent than AF4. The effects of these peptides had some similarities to those observed on A. suum somatic body wall muscle in vitro, with PF1, PF2 and PF4 being inhibitory and AF3 and AF4 being excitatory.
猪蛔虫拥有大量FMRF酰胺相关肽(FaRPs),其中KNEFIRF酰胺(AF1)、KHEYLRF酰胺(AF2)和KSAYMRF酰胺(AF8/PF3)已被证明可在体外调节猪蛔虫真阴道的内在节律性活动。在本研究中,检测了线虫FaRPs,即来自复生滑刃线虫的SDPNFLRF酰胺(PF1)、SADPNFLRE酰胺(PF2)和KPNFIRF酰胺(PF4),以及来自猪蛔虫的AVPGVLRF酰胺(AF3)和GDVPGVLRF酰胺(AF4)对真阴道体外活性的影响。每种肽的作用在定性和定量上都有所不同。来自复生滑刃线虫的所有3种FaRPs均具有抑制作用,可导致收缩停止。PF2的效力比PF1高3倍,阈值为1 nM。尽管PF4效力最低(阈值为10 nM),但其在≥10 nM时的作用在数量上最大。AF3和AF4(1 μM)均诱导出复杂的多相反应,包括初始收缩和痉挛性麻痹,随后收缩活性恢复且幅度增加。AF3的效力比AF4高3倍。这些肽的作用与在体外观察到的对猪蛔虫体壁肌肉的作用有一些相似之处,PF1、PF2和PF4具有抑制作用,而AF3和AF4具有兴奋作用。