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Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry

In the present study, pancreas of rats were dissected and transferred to HEPES buffer (25 mM, pH 7.4). The control tissue pieces were kept in culture medium for one hour and the treated tissues were kept in same medium for 30 minutes and incubated with Insulin (10 nm and 100 nm) for another half hou...

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Detalles Bibliográficos
Autores principales: Aswar, MK, Aswar, UM, Subhedar, NK
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021688/
https://www.ncbi.nlm.nih.gov/pubmed/21264116
http://dx.doi.org/10.4103/0975-1483.63154
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author Aswar, MK
Aswar, UM
Subhedar, NK
author_facet Aswar, MK
Aswar, UM
Subhedar, NK
author_sort Aswar, MK
collection PubMed
description In the present study, pancreas of rats were dissected and transferred to HEPES buffer (25 mM, pH 7.4). The control tissue pieces were kept in culture medium for one hour and the treated tissues were kept in same medium for 30 minutes and incubated with Insulin (10 nm and 100 nm) for another half hour, then tissues were transferred to Bouin‘s fixative (overnight at 40 ° Cc), cryosectioned (15 µm at -16 0 c) and subjected to immunocytochemical labeling with antibodies against Glucagon. RESULTS: In the sections of control tissue, the Glucagon Immunoreactive Cells (GIC) were distinctly visible; on average 40-50 cells were counted in each islet. However in vitro treatment with 10 nm insulin caused 285.89 % increase in the GIC and was found to be highly significant (P< 0.001). Whereas in 100 nm Insulin treatment, 206.41% increase in GIC was seen, this was significant with the control but non-significant with 10 nm Insulin treatment
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spelling pubmed-30216882011-01-24 Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry Aswar, MK Aswar, UM Subhedar, NK J Young Pharm Pharmacology In the present study, pancreas of rats were dissected and transferred to HEPES buffer (25 mM, pH 7.4). The control tissue pieces were kept in culture medium for one hour and the treated tissues were kept in same medium for 30 minutes and incubated with Insulin (10 nm and 100 nm) for another half hour, then tissues were transferred to Bouin‘s fixative (overnight at 40 ° Cc), cryosectioned (15 µm at -16 0 c) and subjected to immunocytochemical labeling with antibodies against Glucagon. RESULTS: In the sections of control tissue, the Glucagon Immunoreactive Cells (GIC) were distinctly visible; on average 40-50 cells were counted in each islet. However in vitro treatment with 10 nm insulin caused 285.89 % increase in the GIC and was found to be highly significant (P< 0.001). Whereas in 100 nm Insulin treatment, 206.41% increase in GIC was seen, this was significant with the control but non-significant with 10 nm Insulin treatment Medknow Publications 2010 /pmc/articles/PMC3021688/ /pubmed/21264116 http://dx.doi.org/10.4103/0975-1483.63154 Text en © Journal of Young Pharmacists http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pharmacology
Aswar, MK
Aswar, UM
Subhedar, NK
Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry
title Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry
title_full Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry
title_fullStr Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry
title_full_unstemmed Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry
title_short Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry
title_sort glucagon secreting cells responds to insulin secretion in vitro using immunocytochemistry
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021688/
https://www.ncbi.nlm.nih.gov/pubmed/21264116
http://dx.doi.org/10.4103/0975-1483.63154
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