Capron L, Jarnet J, Kazandjian S, Housset E
Diabetes. 1986 Sep;35(9):973-8. doi: 10.2337/diab.35.9.973.
Proliferation of arterial smooth muscle cells is regarded as an important event in atherogenesis, which according to in vitro culture studies is influenced by diabetes and insulin. To assess whether this holds true in vivo, we studied the cellular kinetics of thoracic aorta in normal and streptozocin-induced diabetic rats with and without insulin treatment. We measured the incorporation of [3H]thymidine into intima-media, as well as its DNA content, 2 and 14 days after endothelial denudation. We found that the mitotic response of an injured artery is not modified by diabetes but is depressed by insulin treatment in nondiabetic rats, probably due to hypoglycemia. Our data in insulin-treated diabetic rats support but do not definitely settle the view that insulin is mitogenic as long as the treatment does not cause sustained hypoglycemia.
动脉平滑肌细胞的增殖被认为是动脉粥样硬化形成过程中的一个重要事件。根据体外培养研究,这一过程受糖尿病和胰岛素的影响。为了评估这在体内是否也成立,我们研究了正常大鼠以及链脲佐菌素诱导的糖尿病大鼠在接受或未接受胰岛素治疗的情况下胸主动脉的细胞动力学。我们在内皮剥脱术后第2天和第14天测量了胸主动脉中[3H]胸腺嘧啶核苷掺入内膜 - 中膜的情况及其DNA含量。我们发现,糖尿病不会改变受损动脉的有丝分裂反应,但在非糖尿病大鼠中,胰岛素治疗会抑制这种反应,这可能是由于低血糖所致。我们在接受胰岛素治疗的糖尿病大鼠中的数据支持但并未明确证实这样一种观点,即只要治疗不会导致持续性低血糖,胰岛素就具有促有丝分裂作用。