2011
DOI: 10.1016/j.zool.2010.11.002
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FaRP cell distribution in the developing CNS suggests the involvement of FaRPs in all parts of the chromatophore control pathway in Sepia officinalis (Cephalopoda)

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Cited by 18 publications
(16 citation statements)
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References 60 publications
(68 reference statements)
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“…Additionally, FMRFamide may be contained in small fibers within the pallial nerve connecting the CNS to the peripheral SG, and it is present in fibers of the stellate neuropil. A similar distribution of FMRFamide immunoreactivity has been observed for Sepia officinalis (Aroua et al, 2011). FMRFamide may be an important neurotransmitter through which the CNS engages the SG in control of movement and respiration.…”
Section: Discussionsupporting
confidence: 81%
“…Additionally, FMRFamide may be contained in small fibers within the pallial nerve connecting the CNS to the peripheral SG, and it is present in fibers of the stellate neuropil. A similar distribution of FMRFamide immunoreactivity has been observed for Sepia officinalis (Aroua et al, 2011). FMRFamide may be an important neurotransmitter through which the CNS engages the SG in control of movement and respiration.…”
Section: Discussionsupporting
confidence: 81%
“…This suggests that FMRFamide may be a main player in the regulation of chromatophores which role is already fully established before hatching. Our data are consistent with several studies on Sepia officinalis highlighting the role of FMRFamide peptides in the regulation of color changes during development and in the adult (Aroua et al, 2011;Loi and Tublitz, 2000;Loi et al, 1996). Notably, FMRFamide immunoreactivity is present in all trajectories of the neural pathways controlling chromatophore function (Aroua et al, 2011).…”
Section: Discussionsupporting
confidence: 93%
“…The overall distribution of FMRFamide in Doryteuthis pealei corresponds broadly with the distribution of FMRFamide-positive cells found in the nervous systems of other cephalopods, Sepia officinalis and Idiosepius notoides, as far as comparable in the published data (Aroua et al, 2011;Wollesen et al, 2008;Wollesen et al, 2010). In particular, the central palliovisceral lobe, chromatophore and magnocellular lobes seem to be shared as lobes with relatively dense FMRFamide neurons.…”
Section: Discussionsupporting
confidence: 85%
“…The embryonic development of S. officinalis is arbitrarily subdivided into 30 stages based on major morphological changes (Lemaire, 1970). Organogenesis and neurogenesis start at around stage 12 and quickly form the nervous system with all of its components (Figure 1c) including the sensory organs and sensory cells (Baratte & Bonnaud, 2009;Buresi et al, 2014;Darmaillacq, Lesimple, & Dickel, 2008;Imarazene, Andouche, Bassaglia, Lopez, & Bonnaud-Ponticelli, 2017;Shigeno, Kidokoro, Tsuchiya, Segawa, & Yamamoto, 2001a;Shigeno, Tsuchiya, & Segawa, 2001b;Yamamoto, Shimazaki, & Shigeno, 2003), the integrative centers (Aroua, Andouche, Martin, Baratte, & Bonnaud, 2011;Buresi et al, 2014), and the connection of motor fibers to their target organs (Baratte & Bonnaud, 2009) early during organogenesis (Romagny, Darmaillacq, Guibe, Bellanger, & Dickel, 2012) soon after the differentiation of the associated sensory neurons ( Figure 1d). As we aimed to describe the distribution of HAergic neurons, this early sensory system development, in addition to the cephalopod's direct development life history, makes late-stage embryos (stages 27-30) a convenient model for sensory system and CNS observations.…”
Section: Embryos Of S Officinalis Develop Inside Eggs Laid In Intertmentioning
confidence: 99%