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糖尿病大鼠的神经缺血:发展的时间进程、胰岛素治疗的效果以及链脲佐菌素和BB模型的比较

Nerve ischaemia in diabetic rats: time-course of development, effect of insulin treatment plus comparison of streptozotocin and BB models.

作者信息

Stevens E J, Carrington A L, Tomlinson D R

机构信息

William Harvey Research Institute, Department of Pharmacology, Queen Mary and Westfield College, London, UK.

出版信息

Diabetologia. 1994 Jan;37(1):43-8. doi: 10.1007/BF00428776.

Abstract

This study sought to determine the time-course of development of reduced nerve laser Doppler flux in experimental diabetes and the effect on this anomaly of insulin treatment. In addition, we aimed to compare nerve laser Doppler flux in streptozotocin- and genetically-diabetic BB rat models. Sciatic nerve laser Doppler flux in diabetic rats was variable during the 2 days following streptozotocin injection; from day 4, when the measurement was 80% of control, fluxes fell steadily and formed a plateau at 40% of control values after 4 weeks of diabetes. In a second study, using rats with 4-week streptozotocin-diabetes, sciatic nerve laser Doppler flux was reduced to 44% of the value measured in control rats. Treatment of a parallel group of diabetic rats with insulin, by sustained release implants, prevented this ischaemia, so that nerve laser Doppler flux was 91% of controls. Nerve Doppler flux in BB rats with 6-week genetic diabetes was 57% of a control (non-diabetic) BB group. There were no differences in mean arterial pressures between control and diabetic rats in any of the studies. Heart rates of control and insulin-treated diabetic animals were higher than those of the untreated diabetic group; in the other studies heart rates of diabetic animals were numerically lower than controls, but not significantly so. These observations suggest that sciatic nerves of rats with short-term diabetes, whether induced with streptozotocin or of genetic origin, are markedly ischaemic and that this ischaemia in streptozotocin-diabetes is evident within a week of diabetes onset, forms a plateau after 4 weeks and is maintained for at least 2 months.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在确定实验性糖尿病中神经激光多普勒血流减少的发展时间进程以及胰岛素治疗对这种异常情况的影响。此外,我们旨在比较链脲佐菌素诱导糖尿病和基因糖尿病BB大鼠模型中的神经激光多普勒血流。链脲佐菌素注射后2天内,糖尿病大鼠的坐骨神经激光多普勒血流变化不定;从第4天起,测量值为对照值的80%,此后血流稳步下降,糖尿病4周后达到对照值40%的平台期。在第二项研究中,对患有4周链脲佐菌素诱导糖尿病的大鼠进行测量,坐骨神经激光多普勒血流降至对照大鼠测量值的44%。通过缓释植入物对一组平行的糖尿病大鼠进行胰岛素治疗,可预防这种缺血情况,使神经激光多普勒血流达到对照值的91%。患有6周基因糖尿病的BB大鼠的神经多普勒血流为对照(非糖尿病)BB组的57%。在任何一项研究中,对照大鼠和糖尿病大鼠的平均动脉压均无差异。对照动物和胰岛素治疗的糖尿病动物的心率高于未治疗的糖尿病组;在其他研究中,糖尿病动物的心率在数值上低于对照组,但差异不显著。这些观察结果表明,无论是由链脲佐菌素诱导还是基因起源的短期糖尿病大鼠的坐骨神经均明显缺血,且链脲佐菌素诱导糖尿病中的这种缺血在糖尿病发病后一周内明显,4周后形成平台期并至少维持2个月。(摘要截断于250字)

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