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 in | Peptides (New York, N.Y. : 1980) Vol. 15; no. 1; pp. 143 - 149 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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. |
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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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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 |
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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 |
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