Literature DB >> 18775723

Neuropeptides associated with the regulation of feeding in insects.

N Audsley1, R J Weaver.   

Abstract

The stomatogastric nervous system plays a pivotal role in feeding behaviour. Central to this system is the frontal ganglion, which is responsible for foregut motor activity, and hence the passage of food through the gut. Many insect peptides, which exhibit myoactivity on the visceral muscles of the gut in vitro, have been detected in the stomatogastric nervous system by immunochemical or mass spectrometric techniques. This localisation of myoactive peptides, particularly in the frontal ganglion, implies roles for these peptides in the neural control and modulation of feeding in insects. Insect sulfakinins, tachykinins, allatotropin and proctolin have all been shown to stimulate the foregut muscles, whereas myosuppressins, myoinhibitory peptides and allatostatins all inhibited spontaneous contractions of the foregut in a variety of insects. Some of these peptides, when injected, inhibited feeding in vivo. Both the A-type and B-type allatostatins suppressed feeding activity when injected into the cockroach, Blattella germanica and the Manduca sexta C-type allatostatin and allatotropin inhibited feeding when injected into the larvae of two noctuid moths, Lacanobia oleracea and Spodoptera frugiperda, respectively. Injection of sulfakinins into the fly Phormia regina, the locust Schistocera gregaria and the cockroach B. germanica also suppressed feeding, whereas silencing the sulfakinin gene through the injection of double stranded RNA resulted in an increase in food consumption in the cricket Gryllus bimaculatus. The regulation of feeding in insects is clearly very complex, and involves the interaction of a number of mechanisms, one of which is the release, either centrally or locally, of neuropeptides. However, the role of neuropeptides, their mechanisms of action, interactions with each other, and their release are still poorly understood. It is also unclear why insects possess such a number of different peptides, some with multiples copies or homologues, which stimulate or inhibit gut motility, and how their release, sometimes from the same neurone, is regulated. These neuropeptides may also act at sites other than visceral muscles, such as centrally through the brain or on gut stretch receptors.

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Year:  2008        PMID: 18775723     DOI: 10.1016/j.ygcen.2008.08.003

Source DB:  PubMed          Journal:  Gen Comp Endocrinol        ISSN: 0016-6480            Impact factor:   2.822


  46 in total

1.  Distribution of C-type allatostatin (C-AST)-like immunoreactivity in the central nervous system of the copepod Calanus finmarchicus.

Authors:  Caroline H Wilson; Andrew E Christie
Journal:  Gen Comp Endocrinol       Date:  2010-03-23       Impact factor: 2.822

2.  Distribution and physiological effects of B-type allatostatins (myoinhibitory peptides, MIPs) in the stomatogastric nervous system of the crab Cancer borealis.

Authors:  Theresa M Szabo; Ruibing Chen; Marie L Goeritz; Ryan T Maloney; Lamont S Tang; Lingjun Li; Eve Marder
Journal:  J Comp Neurol       Date:  2011-09-01       Impact factor: 3.215

3.  Gastric and pyloric motor pattern control by a modulatory projection neuron in the intact crab Cancer pagurus.

Authors:  Ulrike B S Hedrich; Florian Diehl; Wolfgang Stein
Journal:  J Neurophysiol       Date:  2011-02-16       Impact factor: 2.714

4.  A review of FMRFamide- and RFamide-like peptides in metazoa.

Authors:  Robert J Walker; Sylvana Papaioannou; Lindy Holden-Dye
Journal:  Invert Neurosci       Date:  2010-02-26

5.  Data Independent Acquisition Mass Spectrometry Method for Improved Neuropeptidomic Coverage in Crustacean Neural Tissue Extracts.

Authors:  Kellen DeLaney; Lingjun Li
Journal:  Anal Chem       Date:  2019-04-04       Impact factor: 6.986

6.  More than two decades of research on insect neuropeptide GPCRs: an overview.

Authors:  Jelle Caers; Heleen Verlinden; Sven Zels; Hans Peter Vandersmissen; Kristel Vuerinckx; Liliane Schoofs
Journal:  Front Endocrinol (Lausanne)       Date:  2012-11-30       Impact factor: 5.555

7.  bHLH proneural genes as cell fate determinants of entero-endocrine cells, an evolutionarily conserved lineage sharing a common root with sensory neurons.

Authors:  Volker Hartenstein; Shigeo Takashima; Parvana Hartenstein; Samuel Asanad; Kian Asanad
Journal:  Dev Biol       Date:  2017-07-24       Impact factor: 3.582

8.  Comparative Neuropeptidomic Analysis of Food Intake via a Multi-faceted Mass Spectrometric Approach.

Authors:  Ruibing Chen; Limei Hui; Stephanie S Cape; Junhua Wang; Lingjun Li
Journal:  ACS Chem Neurosci       Date:  2010-03-17       Impact factor: 4.418

9.  Peristalsis in the junction region of the Drosophila larval midgut is modulated by DH31 expressing enteroendocrine cells.

Authors:  Dennis R LaJeunesse; Brooke Johnson; Jason S Presnell; Kathleen Kay Catignas; Grzegorz Zapotoczny
Journal:  BMC Physiol       Date:  2010-08-10

Review 10.  The complexity of small circuits: the stomatogastric nervous system.

Authors:  Nelly Daur; Farzan Nadim; Dirk Bucher
Journal:  Curr Opin Neurobiol       Date:  2016-07-21       Impact factor: 6.627

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