Ridray S, Ktorza A, Picon L, Capron L
Laboratory of Pathophysiology of Nutrition, Broussais Hospital, University of Paris, France.
Arterioscler Thromb. 1992 May;12(5):633-8. doi: 10.1161/01.atv.12.5.633.
The objective of our study was to investigate the effect of hyperinsulinemia associated with either euglycemia, hypoglycemia, or hyperglycemia on the short-term mitotic activity of arterial smooth muscle cells (SMCs) after aortic injury. The proliferative reaction of arterial SMCs was provoked by the passage of an embolectomy catheter with a tightly inflated balloon. DNA synthesis was measured as DNA specific activity after incubation of the aorta in a medium containing 3[H]thymidine. Unrestrained rats were rendered hyperinsulinemic (4-7 nM versus 0.3 nM in controls) immediately after aortic injury by insulin infusion (10 units/day) and either euglycemic (about 5.6 mM), hyperglycemic (14-17 mM), or hypoglycemic (about 2.8 mM) by adjusting the flow rate of hypertonic glucose (30% wt/vol) that was infused simultaneously. The infusion was performed via a catheter inserted into the jugular vein and lasted 2 or 4 days after the aortic injury. After the injury, SMC mitotic activity was dramatically increased on day 2 in control rats with deendothelialized aortas and declined between days 2 and 4. In euglycemic-hyperinsulinemic and hyperglycemic-hyperinsulinemic rats, SMC proliferation showed the same pattern as in controls. At no time was a significant difference observed among the three groups of rats. In hypoglycemic-hyperinsulinemic rats, SMC mitotic activity increased to a lesser extent than in controls on day 2 after deendothelialization. These data indicate that hyperinsulinemia with or without hyperglycemia does not stimulate the early stages of arterial SMC proliferation in the rat although a long-lasting effect of hyperinsulinemia cannot be excluded.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究的目的是调查与正常血糖、低血糖或高血糖相关的高胰岛素血症对主动脉损伤后动脉平滑肌细胞(SMC)短期有丝分裂活性的影响。通过使用带有紧密充气气球的取栓导管来激发动脉SMC的增殖反应。在含有3[H]胸腺嘧啶核苷的培养基中孵育主动脉后,将DNA合成作为DNA比活性进行测量。在主动脉损伤后,通过胰岛素输注(10单位/天)使未受限制的大鼠立即出现高胰岛素血症(4 - 7 nM,而对照组为0.3 nM),并通过调整同时输注的高渗葡萄糖(30% wt/vol)的流速使其维持正常血糖(约5.6 mM)、高血糖(14 - 17 mM)或低血糖(约2.8 mM)状态。输注通过插入颈静脉的导管进行,在主动脉损伤后持续2或4天。损伤后,在去内皮主动脉的对照大鼠中,SMC有丝分裂活性在第2天显著增加,并在第2天至第4天之间下降。在正常血糖 - 高胰岛素血症和高血糖 - 高胰岛素血症大鼠中,SMC增殖表现出与对照组相同的模式。三组大鼠在任何时候均未观察到显著差异。在低血糖 - 高胰岛素血症大鼠中,去内皮后第2天SMC有丝分裂活性的增加程度低于对照组。这些数据表明,无论有无高血糖,高胰岛素血症均不会刺激大鼠动脉SMC增殖的早期阶段,尽管不能排除高胰岛素血症的长期影响。(摘要截短于250字)