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FMRF酰胺相关肽对小龙虾心脏的调节作用

Modulation of Crayfish Hearts by FMRFamide-related Peptides.

作者信息

Mercier A J, Russenes R T

出版信息

Biol Bull. 1992 Jun;182(3):333-340. doi: 10.2307/1542253.

Abstract

The present study examines effects of FMRFamide-related peptides (FaRPs) on crayfish heart. Lobster peptides F1 (TNRNFLRFamide) and F2 (SDRNFLRFamide) increase the rate and amplitude of heart beat in hearts isolated from Procambarus clarkii. Thresholds for these effects were between 10-10 and 10-9 M for F2 and between 10-9 and 10-8 M for F1. FMRFamide and FLRFamide elicited similar cardioexcitatory effects, but at thresholds of approximately 10-7 M. Thus, the aminoterminal extensions "TNRN" and "SDRN" enhance the excitatory actions of FMRFamide and FLRFamide. SchistoFLRFamide (PDVDHVFLRFamide) and leucomyosuppressin (pQDVDHVFLRFamide) markedly decrease the rate of cardiac contractions at 10-9 to 10-8 M and can suppress the cardiac rhythm for one minute or more at 10-7 M. The amino-terminal extensions of these two peptides, therefore, are necessary for inhibition of heart rate. Both of these peptides cause an initial reduction in contraction amplitude, but contractions subsequently increase in the presence of schistoFLRFamide. Thus, crayfish hearts are sensitive to several FMRFamide-related peptides, but the sites and mechanisms of action remain to be determined.

摘要

本研究考察了FMRF酰胺相关肽(FaRPs)对小龙虾心脏的影响。龙虾肽F1(TNRNFLRF酰胺)和F2(SDRNFLRF酰胺)可提高克氏原螯虾离体心脏的心跳速率和幅度。F2产生这些效应的阈值在10⁻¹⁰至10⁻⁹ M之间,F1的阈值在10⁻⁹至10⁻⁸ M之间。FMRF酰胺和FLRF酰胺引发类似的心脏兴奋效应,但阈值约为10⁻⁷ M。因此,氨基末端延伸序列“TNRN”和“SDRN”增强了FMRF酰胺和FLRF酰胺的兴奋作用。血吸虫FLRF酰胺(PDVDHVFLRF酰胺)和白细胞抑制素(pQDVDHVFLRF酰胺)在10⁻⁹至10⁻⁸ M时显著降低心脏收缩速率,在10⁻⁷ M时可抑制心脏节律一分钟或更长时间。因此,这两种肽的氨基末端延伸序列是抑制心率所必需 的。这两种肽都会使收缩幅度最初降低,但在血吸虫FLRF酰胺存在的情况下,收缩随后会增加。因此,小龙虾心脏对几种FMRF酰胺相关肽敏感,但其作用位点和机制仍有待确定。

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