Literature DB >> 792417

The association of octopamine with specific neurones along lobster nerve trunks.

P D Evans, E A Kravitz, B R Talamo, B G Wallace.   

Abstract

Octapamine and its synthetic enzyme, tyramine beta-hydroxylase (TBH), are found in high concentrations at two points along second thoracic nerve roots in lobsters. The first is in the proximal section of the second root between the ventral nerve cord and the bifurcation of the root into medial (to flexor muscles) and lateral (to extensors) branches. The second region of high concentration is within a well known crustacean neurosecretory system, the pericardial organ, located close to the ends of the lateral branches of the roots. 2. With several different staining procedures, small clusters of nerve cell bodies are found within the connective tissue sheath in the proximal regions of the second roots. No cell bodies are seen in the pericardial organ regions. Cell bodies are variable in number and position between corresponding roots in the same animal and homologous roots among different animals. The average numbers of cell bodies, however, correlate well with TBH and octopamine content, and with the synthesis of octopamine in these same regions of roots. 3. Small clusters of root cell bodies dissected from preparations have greater than 500-fold higher activities of TBH than isolated efferent excitatory and inhibitory or afferent sensory axons. 4. Along with octopamine, the preferential synthesis of acetylcholine and serotonin is also seen in proximal segments of roots. Acetylcholine synthesis in these regions may represent transmitter synthesized in the nerve terminals innervating the root cells. The role of serotonin in these regions is not understood at this time but the amounts of endogenous serotonin found are only a tenth of the amounts of octopamine present. 5. Dopamine is not synthesized from tyrosine in second thoracic roots. However, if DOPA or dopamine are used as precursor compounds, then noradrenaline, which is usually not found in lobsters, can be accumulated in proximal segments of roots. 6. Phenolamines are converted to two further metabolites by lobster tissues. The compounds are unidentified and are named fast and slow product on the basis of their migration on electrophoresis at acid pH. Some partial characterization of slow product reveals that it is a mixture of compounds that can be converted on mild acid hydrolysis to fast product and the parent phenolamine. 7. The several lines of evidence presented suggest that nerve cells found in the proximal segments of the second thoracic roots contain and can synthesize octopamine. Since not all the cells in any single root have been analysed for octopamine or TBH, however, the possibility that one or more of the cells contain physiologically interesting substances other than octopamine is not eliminated.

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Year:  1976        PMID: 792417      PMCID: PMC1307630          DOI: 10.1113/jphysiol.1976.sp011585

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  25 in total

1.  The normal occurrence of octopamine in neural tissue of the Octopus and other cephalopods.

Authors:  A V Juorio; P B Molinoff
Journal:  J Neurochem       Date:  1974-02       Impact factor: 5.372

2.  Octopamine in the insect central nervous system: distribution, biosynthesis and possible physiological role.

Authors:  H A Robertson; J E Steele
Journal:  J Physiol       Date:  1974-03       Impact factor: 5.182

3.  Octopamine in the lobster nervous system.

Authors:  D L Barker; P B Molinoff; E A Kravitz
Journal:  Nat New Biol       Date:  1972-03-15

4.  Octopamine-sensitive adenylate cyclse: evidence for a biological role of octopamine in nervous tissue.

Authors:  J A Nathanson; P Greengard
Journal:  Science       Date:  1973-04-20       Impact factor: 47.728

5.  Screening for neurotransmitters: a rapid radiochemical procedure.

Authors:  J G Hildebrand; D L Barker; E Herbert; E A Kravitz
Journal:  J Neurobiol       Date:  1971

6.  An electron-microscopic study of zinc iodide-osmium impregnation of neurons. I. Staining of synaptic vesicles at cholinergic junctions.

Authors:  K Akert; C Sandri
Journal:  Brain Res       Date:  1968-02       Impact factor: 3.252

7.  An enzymatic assay for octopamine and other beta-hydroxylated phenylethylamines.

Authors:  P B Molinoff; L Landsberg; J Axelrod
Journal:  J Pharmacol Exp Ther       Date:  1969-12       Impact factor: 4.030

8.  Octopamine: selective association with specific neurons in the lobster nervous system.

Authors:  B G Wallace; B R Talamo; P D Evans; E A Kravitz
Journal:  Brain Res       Date:  1974-07-12       Impact factor: 3.252

9.  Octopamine: presence in single neurons of Aplysia suggests neurotransmitter function.

Authors:  J M Saavedra; M J Brownstein; D O Carpenter; J Axelrod
Journal:  Science       Date:  1974-07-26       Impact factor: 47.728

10.  Octopamine- and serotonin-stimulated phosphorylation of specific protein in the abdominal ganglion of Aplysia californica.

Authors:  I B Levitan; S H Barondes
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

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  13 in total

1.  Octopamine potentiates intracellular Na+ and Cl- reductions during cell volume regulation in Limulus exposed to hypoosmotic stress.

Authors:  S C Edwards; S K Pierce
Journal:  J Comp Physiol B       Date:  1986       Impact factor: 2.200

2.  The roles of central and peripheral eclosion hormone release in the control of ecdysis behavior in Manduca sexta.

Authors:  R S Hewes; J W Truman
Journal:  J Comp Physiol A       Date:  1991-06       Impact factor: 1.836

3.  A voltage-sensitive cation channel present in clusters in lobster skeletal muscle membrane.

Authors:  M K Worden; R Rahamimoff; E A Kravitz
Journal:  J Membr Biol       Date:  1994-08       Impact factor: 1.843

4.  Neurotransmitter synthesis in Limulus ventral nerve photoreceptors.

Authors:  B A Battelle; E A Kravitz; H Stieve
Journal:  Experientia       Date:  1979-06-15

5.  Effects of biogenic amines and adrenergic drugs on oviposition in the cattle tick Boophilus: evidence for octopaminergic innervation of the oviduct.

Authors:  T F Booth
Journal:  Exp Appl Acarol       Date:  1989-09       Impact factor: 2.132

6.  State-dependent responses of two motor systems in the crayfish, Pacifastacus leniusculus.

Authors:  A Chrachri; D Neil; B Mulloney
Journal:  J Comp Physiol A       Date:  1994-09       Impact factor: 1.836

7.  Electrical excitability: a spectrum of properties in the progeny of a single embryonic neuroblast.

Authors:  C S Goodman; K G Pearson; N C Spitzer
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

8.  The physiological properties of amine-containing neurones in the lobster nervous system.

Authors:  S Konishi; E A Kravitz
Journal:  J Physiol       Date:  1978-06       Impact factor: 5.182

9.  Octopamine release at two points along lobster nerve trunks.

Authors:  P D Evans; E A Kravitz; B R Talamo
Journal:  J Physiol       Date:  1976-10       Impact factor: 5.182

10.  Multiple receptor types for octopamine in the locust.

Authors:  P D Evans
Journal:  J Physiol       Date:  1981-09       Impact factor: 5.182

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