机构地区:[1]天津医科大学总医院内分泌科,300052 [2]内蒙古医学院附属医院神经内科 [3]南开大学生命科学院 [4]天津市武清区人民医院
出 处:《中华内科杂志》2009年第6期488-491,共4页Chinese Journal of Internal Medicine
基 金:天津市科委自然科学基金(05YFMJC04000)
摘 要:目的观察胰淀素对大鼠胰岛β细胞电压门控L-型钙通道的影响。方法用全细胞膜片钳技术观察胰淀素作用前后胰岛βB细胞电压门控L-型钙通道门控特性、电流变化。结果在葡萄糖5.5mmol/L条件下,大鼠胰岛β细胞L-型钙通道电流约在-40mV激活,+20mV左右达高峰,峰值约为-120pA,胰岛素分泌量为(0.76±0.12)μg/L;16.7mmol/L葡萄糖刺激下峰电流电压左移、峰电流达-140pA左右,胰岛素分泌量为(1.78±0.13)μg/L。用0.5、1.0.5.0、10.0μmo]/L浓度胰淀素分别孵育胰岛B细胞,在5.5、16.7mmoL/L葡萄糖条件下,0.5、1.0μmol/L胰淀素浓度的峰电位激活电压、电流、胰岛素分泌量与对照组相比,差异均无统计学意义,在5.5mmol/L葡萄糖条件下,5.0、10.0μmol/L胰淀素浓度的激活电压增加为一30mV,峰电流分别减小至-80pA、-60pA左右,胰岛素分泌量分别降低至(0.49±0.11)、(0.36±0.12)μg/L;在16.7mmol/L葡萄糖条件下,激活电压由-40mV增加到-30mV,峰电流分别减小至-80pA、-40pA,胰岛素分泌量分别降低至(1.20±0.13)、(0.89±0.14)μg/L,与对照组相比差异具有统计学意义。结论葡萄糖刺激胰岛β细胞电压门控L-型钙通道开放与胰岛素分泌同步,胰淀素抑制胰岛β细胞电压门控L-型钙通道开放和抑制胰岛素分泌作用同步并与其作用浓度正相关。Objective To observe the effect of amylin on the islet β-cells vohage-gated L-calcium channels in rats. Method Patch clamp technique was employed in the observation of the features and changes of electric current of islet β-cells vohage-gated L-calcium channels before and after using amylin. Results In the glucose environment of 5.5 mmol/L, the electric current of rat islet β-cells voltage-gated L-calcium channels was activated at -40 mV and reached the peak at about + 20 mV, with a peak value of about - 120 pA and the insulin secretion level was(0. 76 ±0. 12) p.g/L Under the stimulation of glucose of 16.7 mmol/L, the peak current voltage moved to the left and increased up to - 140 pA and the level of insulin secretion measured ( 1.78 ± 0. 13 )μg/L. Hatch islet β-cells in amylin at the concentrations of 0. 5, 1.0, 5.0 and 10. 0 μmol/L, respectively. It was observed that in the 0. 5μ mol/L and 1.0 μmol/L groups, there was no remarkable change in the peak potential activation voltage, current, and insulin secretion volume in comparison with the control group. However, in the environment of 5.5 mmol/L glucose, the increase of activation voltage of the 5.0 and 10. 0 μmoL/L groups was - 30 mV, with the peak current reduced to approximately -80 pA and -60 pA and the insulin secretion decreased to (0.49 ±0. 11 ) μg/L and (0. 36 ±0. 12) μg/L respectively. Under the concentration of 16.7 mmol/L glucose, the activation voltage increased from -40 mV up to -30 mV and the peak current reduced to -80 pA and -40 pA. In the meantime, the insulin secretion decreased respectively to ( 1.20 ±0. 13 ) μg/L and ( 0. 89 ±0. 14 ) μg/L, which is of significance. Conclusion The secretion of insulin is synchronized with the opening of the islet β-cells voltage-gated L-calcium channels at the stimulation of glucose. The amylin inhibition of the insulin secretion is also synchronized with the opening of islet β-cells vohage-gated L-calcium channels and it's in a positive concentration-dependen
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