Differential trophic effects of ORG 2766, an ACTH(4–9)/MSH(4–9) analogue, on peptidergic neurons and glial cells in the snail Lymnaea stagnalis

Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10 −6 M ORG 2766 for 10 and 20 h, with or without regular refreshment of the medium. Quantitative ultrastructural study of cross sections of the cerebral commissure showed that the number of microtubules in large axons o...

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Published inPeptides (New York, N.Y. : 1980) Vol. 15; no. 1; pp. 143 - 149
Main Authors Müller, Linda J., Kiburg, Barbara, Moorer-van Delft, Carry M., Boer, Harry H.
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 1994
Elsevier Science
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Abstract Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10 −6 M ORG 2766 for 10 and 20 h, with or without regular refreshment of the medium. Quantitative ultrastructural study of cross sections of the cerebral commissure showed that the number of microtubules in large axons of all ORG 2766-treated groups had increased after 10 h by approximately 40%. In a separate experiment, central nervous systems were incubated in ORG 2766 for only 15 min and then kept in Ringer's for 9 h and 45 min. Maximal stimulation (40% increase of microtubules) in these specimens was also observed. The results would seem to support the hypothesis that ORG 2766 binds to a receptor and initiates a long-lasting effect. It is argued that ORG 2766 stimulates novel synthesis of tubulin rather than being involved in the assembly of microtubules. Also, glial cells were found to be activated by ORG 2766. This was concluded from the fact that the number of heterochromatin clumps and the size of the clumps in these cells had decreased and the amount of glial tissue surrounding the axons had increased (approximately 50%). In contrast to the activating effects of ORG 2766 on glial tissue, this drug did not affect nucleoli, number, and size of the heterochromatin clumps and the Golgi apparatus in the neuropeptidergic caudodorsal cells. The data indicate that ORG 2766 exerts differential trophic effects.
AbstractList Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10(-6) M ORG 2766 for 10 and 20 h, with or without regular refreshment of the medium. Quantitative ultrastructural study of cross sections of the cerebral commissure showed that the number of microtubules in large axons of all ORG 2766-treated groups had increased after 10 h by approximately 40%. In a separate experiment, central nervous systems were incubated in ORG 2766 for only 15 min and then kept in Ringer's for 9 h and 45 min. Maximal stimulation (40% increase of microtubules) in these specimens was also observed. The results would seem to support the hypothesis that ORG 2766 binds to a receptor and initiates a long-lasting effect. It is argued that ORG 2766 stimulates novel synthesis of tubulin rather than being involved in the assembly of microtubules. Also, glial cells were found to be activated by ORG 2766. This was concluded from the fact that the number of heterochromatin clumps and the size of the clumps in these cells had decreased and the amount of glial tissue surrounding the axons had increased (approximately 50%). In contrast to the activating effects of ORG 2766 on glial tissue, this drug did not affect nucleoli, number, and size of the heterochromatin clumps and the Golgi apparatus in the neuropeptidergic caudodorsal cells. The data indicate that ORG 2766 exerts differential trophic effects.
Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10 super(-6) M ORG 2766 for 10 and 20 h, with or without regular refreshment of the medium. Quantitative ultrastructural study of cross sections of the cerebral commissure showed that the number of microtubules in large axons of all ORG 2766-treated groups had increased after 10 h by approximately 40%. In a separate experiment, central nervous systems were incubated in ORG 2766 for only 15 min and then kept in Ringer's for 9 h and 45 min. Maximal stimulation (40% increase of microtubules) in these specimens was also observed. The results would seem to support the hypothesis that ORG 2766 binds to a receptor and initiates a long-lasting effect. It is argued that ORG 2766 stimulates novel synthesis of tubulin rather than being involved in the assembly of microtubules. Also, glial cells were found to be activated by ORG 2766. The data indicate that ORG 2766 exerts differential trophic effects.
Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10 −6 M ORG 2766 for 10 and 20 h, with or without regular refreshment of the medium. Quantitative ultrastructural study of cross sections of the cerebral commissure showed that the number of microtubules in large axons of all ORG 2766-treated groups had increased after 10 h by approximately 40%. In a separate experiment, central nervous systems were incubated in ORG 2766 for only 15 min and then kept in Ringer's for 9 h and 45 min. Maximal stimulation (40% increase of microtubules) in these specimens was also observed. The results would seem to support the hypothesis that ORG 2766 binds to a receptor and initiates a long-lasting effect. It is argued that ORG 2766 stimulates novel synthesis of tubulin rather than being involved in the assembly of microtubules. Also, glial cells were found to be activated by ORG 2766. This was concluded from the fact that the number of heterochromatin clumps and the size of the clumps in these cells had decreased and the amount of glial tissue surrounding the axons had increased (approximately 50%). In contrast to the activating effects of ORG 2766 on glial tissue, this drug did not affect nucleoli, number, and size of the heterochromatin clumps and the Golgi apparatus in the neuropeptidergic caudodorsal cells. The data indicate that ORG 2766 exerts differential trophic effects.
Author Boer, Harry H.
Kiburg, Barbara
Moorer-van Delft, Carry M.
Müller, Linda J.
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Issue 1
Keywords Electron microscope
Nucleoli
Quantitative morphology
Cerebral commissure
Glial cells
Caudodorsal cells
Golgi apparatus
Lymnaea stagnalis
Glial cell
MSH
ACTH
Nervous system
Gastropoda
Neuropeptide
Pituitary hormone
Peptidergic neuron
Ultrastructure
Analog
Invertebrata
Mollusca
Quantitative analysis
Language English
License CC BY 4.0
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Snippet Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10 −6 M ORG 2766 for 10 and 20 h, with or without regular refreshment of the...
Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10(-6) M ORG 2766 for 10 and 20 h, with or without regular refreshment of the...
Cerebral ganglia of the pond snail Lymnaea stagnalis were incubated in vitro in 10 super(-6) M ORG 2766 for 10 and 20 h, with or without regular refreshment of...
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SubjectTerms Adrenocorticotropic Hormone - analogs & derivatives
Adrenocorticotropic Hormone - pharmacology
Animals
Biochemistry. Physiology. Immunology
Biological and medical sciences
Brain - drug effects
Brain - ultrastructure
Caudodorsal cells
Cell Nucleolus - drug effects
Cerebral commissure
Chromatin - drug effects
Electron microscope
Freshwater
Fundamental and applied biological sciences. Psychology
Glial cells
Golgi apparatus
Golgi Apparatus - drug effects
Invertebrates
Lymnaea - drug effects
Lymnaea stagnalis
Microtubules - drug effects
Mollusca
Nerve Growth Factors - pharmacology
Neuroglia - drug effects
Neuroglia - ultrastructure
Neurons - drug effects
Neurons - ultrastructure
Neuropeptides - biosynthesis
Neuropeptides - metabolism
Nucleoli
Peptide Fragments - pharmacology
Physiology. Development
Quantitative morphology
Title Differential trophic effects of ORG 2766, an ACTH(4–9)/MSH(4–9) analogue, on peptidergic neurons and glial cells in the snail Lymnaea stagnalis
URI https://dx.doi.org/10.1016/0196-9781(94)90183-X
https://www.ncbi.nlm.nih.gov/pubmed/8015971
https://search.proquest.com/docview/16810752
https://search.proquest.com/docview/76578725
Volume 15
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