Tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation

Background: Tyrosine hydroxylase (TH) activity and its possible participation in the control of insulin secretion were studied in pancreatic islets of adult Wistar rats fed a standard commercial diet (SD) or carbohydrates alone (CHD) for one week. TH activity, norepinephrine (NE) content, and glucos...

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Autores principales: Borelli, María Inés, Rubio, Modesto Carlos, García, María Elisa, Flores, Luis Emilio, Gagliardino, Juan José
Formato: Articulo
Lenguaje:Español
Publicado: 2003
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/36459
http://www.biomedcentral.com/content/pdf/1472-6823-3-2.pdf
Aporte de:
id I19-R120-10915-36459
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Español
topic Ciencias Médicas
carbohydrate
catecholamine
glucose
insulin
enzyme activity
hormonal regulation
spellingShingle Ciencias Médicas
carbohydrate
catecholamine
glucose
insulin
enzyme activity
hormonal regulation
Borelli, María Inés
Rubio, Modesto Carlos
García, María Elisa
Flores, Luis Emilio
Gagliardino, Juan José
Tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation
topic_facet Ciencias Médicas
carbohydrate
catecholamine
glucose
insulin
enzyme activity
hormonal regulation
description Background: Tyrosine hydroxylase (TH) activity and its possible participation in the control of insulin secretion were studied in pancreatic islets of adult Wistar rats fed a standard commercial diet (SD) or carbohydrates alone (CHD) for one week. TH activity, norepinephrine (NE) content, and glucose-induced insulin secretion were assessed. Blood glucose and insulin levels were measured at the time of sacrifice. Results: CHD rats had significantly higher blood glucose and lower insulin levels than SD rats (114.5 ± 6.7 vs 80.7 ± 7.25 mg/dl, p < 0.001; 20.25 ± 2.45 vs 42.5 ± 4.99 μU/ml, p < 0.01, respectively). Whereas TH activity was significantly higher in CHD isolated islets (600 ± 60 vs 330 ± 40 pmol/mg protein/h; p < 0.001), NE content was significantly lower (18 ± 1 vs 31 ± 5 pmol/mg protein), suggesting that TH activity would be inhibited by the end-products of catecholamines (CAs) biosynthetic pathway. A similar TH activity was found in control and solarectomized rats (330 ± 40 vs 300 ± 80 pmol/mg protein/h), suggesting an endogenous rather than a neural origin of TH activity. CHD islets released significantly less insulin in response to glucose than SD islets (7.4 ± 0.9 vs 11.4 ± 1.1 ng/islet/h; p < 0.02). Conclusions: TH activity is present in islet cells; dietary manipulation simultaneously induces an increase in this activity together with a decrease in glucose-induced insulin secretion in rat islets. TH activity - and the consequent endogenous CAs turnover - would participate in the paracrine control of insulin secretion.
format Articulo
Articulo
author Borelli, María Inés
Rubio, Modesto Carlos
García, María Elisa
Flores, Luis Emilio
Gagliardino, Juan José
author_facet Borelli, María Inés
Rubio, Modesto Carlos
García, María Elisa
Flores, Luis Emilio
Gagliardino, Juan José
author_sort Borelli, María Inés
title Tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation
title_short Tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation
title_full Tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation
title_fullStr Tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation
title_full_unstemmed Tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation
title_sort tyrosine hydroxylase activity in the endocrine pancreas: changes induced by short-term dietary manipulation
publishDate 2003
url http://sedici.unlp.edu.ar/handle/10915/36459
http://www.biomedcentral.com/content/pdf/1472-6823-3-2.pdf
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