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Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata.
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Zeitschriftentitel: | European Journal of Neuroscience |
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Personen und Körperschaften: | , , |
In: | European Journal of Neuroscience, 17, 2003, 2, S. 239-248 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
Wiley
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Schlagwörter: |
author_facet |
Weiss, Torsten Kreissl, Sabine Rathmayer, Werner Weiss, Torsten Kreissl, Sabine Rathmayer, Werner |
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author |
Weiss, Torsten Kreissl, Sabine Rathmayer, Werner |
spellingShingle |
Weiss, Torsten Kreissl, Sabine Rathmayer, Werner European Journal of Neuroscience Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. General Neuroscience |
author_sort |
weiss, torsten |
spelling |
Weiss, Torsten Kreissl, Sabine Rathmayer, Werner 0953-816X 1460-9568 Wiley General Neuroscience http://dx.doi.org/10.1046/j.1460-9568.2003.02455.x <jats:title>Abstract</jats:title><jats:p>In the ventral nerve cord of the isopod <jats:italic>Idotea emarginata</jats:italic>, FMRFamide‐immunoreactive efferent neurons are confined to pereion ganglion 5 where a single pair of these neurons was identified. Each neuron projects an axon into the ipsilateral ventral and dorsal lateral nerves, which run through the entire animal. The immunoreactive axons form numerous varicosities on the ventral flexor and dorsal extensor muscle fibres, and in the pericardial organs. To analyse the neuromuscular effects of a FMRFamide, we used the DRNFLRFamide (DF<jats:sub>2</jats:sub>). DF<jats:sub>2</jats:sub> acted both pre‐ and postsynaptically. On the presynaptic side, DF<jats:sub>2</jats:sub> increased transmitter release from neuromuscular endings. Postsynaptically, DF<jats:sub>2</jats:sub> depolarized muscle fibres by approximately 10 mV. This effect was not observed in leg muscles of a crab. The depolarization required Ca<jats:sup>2+</jats:sup>, was blocked by substituting Ca<jats:sup>2+</jats:sup> with Co<jats:sup>2+</jats:sup>, but not affected by nifedipine or amiloride. In <jats:italic>Idotea</jats:italic>, DF<jats:sub>2</jats:sub> also potentiated evoked extensor muscle contractions. The amplitude of high K<jats:sup>+</jats:sup> contractures was increased in a dose dependent manner with an EC<jats:sub>50</jats:sub> value of 40 n<jats:sc>m</jats:sc>. In current‐clamped fibres, DF<jats:sub>2</jats:sub> strongly potentiated contractions evoked by current pulses exceeding excitation‐contraction threshold. In voltage‐clamped fibres, the inward current through <jats:sc>l</jats:sc>‐type Ca<jats:sup>2+</jats:sup> channels was increased by the peptide. The observed physiological effects together with the localization of FMRFamide‐immunoreactive efferent neurons suggest a role for this type of peptidergic modulation for the neuromuscular performance in <jats:italic>Idotea</jats:italic>. The pre‐ and postsynaptic effects of DF<jats:sub>2</jats:sub> act synergistically and, <jats:italic>in vivo</jats:italic>, all should increase the efficacy of motor input to muscles resulting in potentiation of contractions.</jats:p> Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF<sub>2</sub>) in the crustacean <i>Idotea emarginata</i>. European Journal of Neuroscience |
doi_str_mv |
10.1046/j.1460-9568.2003.02455.x |
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Online |
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ElectronicArticle |
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DE-105 DE-14 DE-Ch1 DE-L229 DE-D275 DE-Bn3 DE-Brt1 DE-D161 DE-Gla1 DE-Zi4 DE-15 DE-Pl11 DE-Rs1 |
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Wiley, 2003 |
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Wiley, 2003 |
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weiss2003localizationofafmrfamiderelatedpeptideinefferentneuronsandanalysisofneuromusculareffectsofdrnflrfamidedf2inthecrustaceanidoteaemarginata |
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2003 |
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Wiley |
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European Journal of Neuroscience |
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49 |
title |
Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_unstemmed |
Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_full |
Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_fullStr |
Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_full_unstemmed |
Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_short |
Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_sort |
localization of a fmrfamide‐related peptide in efferent neurons and analysis of neuromuscular effects of drnflrfamide (df<sub>2</sub>) in the crustacean <i>idotea emarginata</i>. |
topic |
General Neuroscience |
url |
http://dx.doi.org/10.1046/j.1460-9568.2003.02455.x |
publishDate |
2003 |
physical |
239-248 |
description |
<jats:title>Abstract</jats:title><jats:p>In the ventral nerve cord of the isopod <jats:italic>Idotea emarginata</jats:italic>, FMRFamide‐immunoreactive efferent neurons are confined to pereion ganglion 5 where a single pair of these neurons was identified. Each neuron projects an axon into the ipsilateral ventral and dorsal lateral nerves, which run through the entire animal. The immunoreactive axons form numerous varicosities on the ventral flexor and dorsal extensor muscle fibres, and in the pericardial organs. To analyse the neuromuscular effects of a FMRFamide, we used the DRNFLRFamide (DF<jats:sub>2</jats:sub>). DF<jats:sub>2</jats:sub> acted both pre‐ and postsynaptically. On the presynaptic side, DF<jats:sub>2</jats:sub> increased transmitter release from neuromuscular endings. Postsynaptically, DF<jats:sub>2</jats:sub> depolarized muscle fibres by approximately 10 mV. This effect was not observed in leg muscles of a crab. The depolarization required Ca<jats:sup>2+</jats:sup>, was blocked by substituting Ca<jats:sup>2+</jats:sup> with Co<jats:sup>2+</jats:sup>, but not affected by nifedipine or amiloride. In <jats:italic>Idotea</jats:italic>, DF<jats:sub>2</jats:sub> also potentiated evoked extensor muscle contractions. The amplitude of high K<jats:sup>+</jats:sup> contractures was increased in a dose dependent manner with an EC<jats:sub>50</jats:sub> value of 40 n<jats:sc>m</jats:sc>. In current‐clamped fibres, DF<jats:sub>2</jats:sub> strongly potentiated contractions evoked by current pulses exceeding excitation‐contraction threshold. In voltage‐clamped fibres, the inward current through <jats:sc>l</jats:sc>‐type Ca<jats:sup>2+</jats:sup> channels was increased by the peptide. The observed physiological effects together with the localization of FMRFamide‐immunoreactive efferent neurons suggest a role for this type of peptidergic modulation for the neuromuscular performance in <jats:italic>Idotea</jats:italic>. The pre‐ and postsynaptic effects of DF<jats:sub>2</jats:sub> act synergistically and, <jats:italic>in vivo</jats:italic>, all should increase the efficacy of motor input to muscles resulting in potentiation of contractions.</jats:p> |
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author | Weiss, Torsten, Kreissl, Sabine, Rathmayer, Werner |
author_facet | Weiss, Torsten, Kreissl, Sabine, Rathmayer, Werner, Weiss, Torsten, Kreissl, Sabine, Rathmayer, Werner |
author_sort | weiss, torsten |
container_issue | 2 |
container_start_page | 239 |
container_title | European Journal of Neuroscience |
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description | <jats:title>Abstract</jats:title><jats:p>In the ventral nerve cord of the isopod <jats:italic>Idotea emarginata</jats:italic>, FMRFamide‐immunoreactive efferent neurons are confined to pereion ganglion 5 where a single pair of these neurons was identified. Each neuron projects an axon into the ipsilateral ventral and dorsal lateral nerves, which run through the entire animal. The immunoreactive axons form numerous varicosities on the ventral flexor and dorsal extensor muscle fibres, and in the pericardial organs. To analyse the neuromuscular effects of a FMRFamide, we used the DRNFLRFamide (DF<jats:sub>2</jats:sub>). DF<jats:sub>2</jats:sub> acted both pre‐ and postsynaptically. On the presynaptic side, DF<jats:sub>2</jats:sub> increased transmitter release from neuromuscular endings. Postsynaptically, DF<jats:sub>2</jats:sub> depolarized muscle fibres by approximately 10 mV. This effect was not observed in leg muscles of a crab. The depolarization required Ca<jats:sup>2+</jats:sup>, was blocked by substituting Ca<jats:sup>2+</jats:sup> with Co<jats:sup>2+</jats:sup>, but not affected by nifedipine or amiloride. In <jats:italic>Idotea</jats:italic>, DF<jats:sub>2</jats:sub> also potentiated evoked extensor muscle contractions. The amplitude of high K<jats:sup>+</jats:sup> contractures was increased in a dose dependent manner with an EC<jats:sub>50</jats:sub> value of 40 n<jats:sc>m</jats:sc>. In current‐clamped fibres, DF<jats:sub>2</jats:sub> strongly potentiated contractions evoked by current pulses exceeding excitation‐contraction threshold. In voltage‐clamped fibres, the inward current through <jats:sc>l</jats:sc>‐type Ca<jats:sup>2+</jats:sup> channels was increased by the peptide. The observed physiological effects together with the localization of FMRFamide‐immunoreactive efferent neurons suggest a role for this type of peptidergic modulation for the neuromuscular performance in <jats:italic>Idotea</jats:italic>. The pre‐ and postsynaptic effects of DF<jats:sub>2</jats:sub> act synergistically and, <jats:italic>in vivo</jats:italic>, all should increase the efficacy of motor input to muscles resulting in potentiation of contractions.</jats:p> |
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imprint | Wiley, 2003 |
imprint_str_mv | Wiley, 2003 |
institution | DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1 |
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mega_collection | Wiley (CrossRef) |
physical | 239-248 |
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spelling | Weiss, Torsten Kreissl, Sabine Rathmayer, Werner 0953-816X 1460-9568 Wiley General Neuroscience http://dx.doi.org/10.1046/j.1460-9568.2003.02455.x <jats:title>Abstract</jats:title><jats:p>In the ventral nerve cord of the isopod <jats:italic>Idotea emarginata</jats:italic>, FMRFamide‐immunoreactive efferent neurons are confined to pereion ganglion 5 where a single pair of these neurons was identified. Each neuron projects an axon into the ipsilateral ventral and dorsal lateral nerves, which run through the entire animal. The immunoreactive axons form numerous varicosities on the ventral flexor and dorsal extensor muscle fibres, and in the pericardial organs. To analyse the neuromuscular effects of a FMRFamide, we used the DRNFLRFamide (DF<jats:sub>2</jats:sub>). DF<jats:sub>2</jats:sub> acted both pre‐ and postsynaptically. On the presynaptic side, DF<jats:sub>2</jats:sub> increased transmitter release from neuromuscular endings. Postsynaptically, DF<jats:sub>2</jats:sub> depolarized muscle fibres by approximately 10 mV. This effect was not observed in leg muscles of a crab. The depolarization required Ca<jats:sup>2+</jats:sup>, was blocked by substituting Ca<jats:sup>2+</jats:sup> with Co<jats:sup>2+</jats:sup>, but not affected by nifedipine or amiloride. In <jats:italic>Idotea</jats:italic>, DF<jats:sub>2</jats:sub> also potentiated evoked extensor muscle contractions. The amplitude of high K<jats:sup>+</jats:sup> contractures was increased in a dose dependent manner with an EC<jats:sub>50</jats:sub> value of 40 n<jats:sc>m</jats:sc>. In current‐clamped fibres, DF<jats:sub>2</jats:sub> strongly potentiated contractions evoked by current pulses exceeding excitation‐contraction threshold. In voltage‐clamped fibres, the inward current through <jats:sc>l</jats:sc>‐type Ca<jats:sup>2+</jats:sup> channels was increased by the peptide. The observed physiological effects together with the localization of FMRFamide‐immunoreactive efferent neurons suggest a role for this type of peptidergic modulation for the neuromuscular performance in <jats:italic>Idotea</jats:italic>. The pre‐ and postsynaptic effects of DF<jats:sub>2</jats:sub> act synergistically and, <jats:italic>in vivo</jats:italic>, all should increase the efficacy of motor input to muscles resulting in potentiation of contractions.</jats:p> Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF<sub>2</sub>) in the crustacean <i>Idotea emarginata</i>. European Journal of Neuroscience |
spellingShingle | Weiss, Torsten, Kreissl, Sabine, Rathmayer, Werner, European Journal of Neuroscience, Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata., General Neuroscience |
title | Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_full | Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_fullStr | Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_full_unstemmed | Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_short | Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
title_sort | localization of a fmrfamide‐related peptide in efferent neurons and analysis of neuromuscular effects of drnflrfamide (df<sub>2</sub>) in the crustacean <i>idotea emarginata</i>. |
title_unstemmed | Localization of a FMRFamide‐related peptide in efferent neurons and analysis of neuromuscular effects of DRNFLRFamide (DF2) in the crustacean Idotea emarginata. |
topic | General Neuroscience |
url | http://dx.doi.org/10.1046/j.1460-9568.2003.02455.x |