Borelli María I, Rubio Modesto, García María E, Flores Luis E, Gagliardino Juan J
CENEXA- Center of Experimental and Applied Endocrinology (National University of La Plata-National Research Council, PAHO/WHO Collaborating Center), School of Medical Sciences, La Plata, Argentina.
BMC Endocr Disord. 2003 Mar 24;3(1):2. doi: 10.1186/1472-6823-3-2.
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 PlusMinus; 6.7 vs 80.7 PlusMinus; 7.25 mg/dl, p < 0.001; 20.25 PlusMinus; 2.45 vs 42.5 PlusMinus; 4.99 &mgr;U/ml, p < 0.01, respectively). Whereas TH activity was significantly higher in CHD isolated islets (600 PlusMinus; 60 vs 330 PlusMinus; 40 pmol/mg protein/h; p < 0.001), NE content was significantly lower (18 PlusMinus; 1 vs 31 PlusMinus; 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 PlusMinus; 40 vs 300 PlusMinus; 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 PlusMinus; 0.9 vs 11.4 PlusMinus; 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.
研究了成年Wistar大鼠胰岛中酪氨酸羟化酶(TH)活性及其在胰岛素分泌控制中的可能作用。这些大鼠被喂食标准商业饮食(SD)或仅碳水化合物饮食(CHD)一周,评估了TH活性、去甲肾上腺素(NE)含量和葡萄糖诱导的胰岛素分泌。在处死时测量血糖和胰岛素水平。结果:CHD大鼠的血糖显著高于SD大鼠,胰岛素水平显著低于SD大鼠(分别为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)。虽然CHD分离胰岛中的TH活性显著更高(600±60 vs 330±40 pmol/mg蛋白/h;p<0.001),但NE含量显著更低(18±1 vs 31±5 pmol/mg蛋白),这表明TH活性会被儿茶酚胺(CAs)生物合成途径的终产物抑制。在对照大鼠和去肾上腺大鼠中发现了相似的TH活性(330±40 vs 300±80 pmol/mg蛋白/h),这表明TH活性起源于内源性而非神经源性。CHD胰岛对葡萄糖刺激释放的胰岛素显著少于SD胰岛(7.4±0.9 vs 11.4±1.1 ng/胰岛/h;p<0.02)。结论:TH活性存在于胰岛细胞中;饮食调控同时诱导该活性增加以及大鼠胰岛中葡萄糖诱导的胰岛素分泌减少。TH活性以及随之而来的内源性CAs周转可能参与胰岛素分泌的旁分泌控制。