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

被引:17
作者
María I Borelli
Modesto Rubio
María E García
Luis E Flores
Juan J Gagliardino
机构
[1] CENEXA, National University of La Plata, School of Medical Sciences, La Plata
[2] Institute of Pharmacological Invest., CONICET, Buenos Aires
关键词
Insulin Secretion; Tyrosine Hydroxylase; Catecholamines; Endocrine pancreas;
D O I
10.1186/1472-6823-3-2
中图分类号
学科分类号
摘要
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. © 2003 Borell et al; licensee BioMed Central Ltd.
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