Therapeutic modulation of growth-promoting activity in platelets from diabetics

Diabetes. 1987 May;36(5):667-72. doi: 10.2337/diab.36.5.667.

Abstract

Proliferation of vascular smooth muscle is thought to be involved in the major diabetic complication atherosclerosis. We have previously reported an increase of growth-promoting activity (GA) in platelets from insulin-dependent diabetics. In this study, GA was measured in the platelet extract (PE) from eight diabetic patients who had been treated by conventional insulin therapy. Vascular smooth muscle cells from rat aorta were cultured and used as an assay system for GA. Incorporation of [3H]thymidine into DNA of cultured cells was stimulated by diabetic PE significantly more (P less than .05) than by normal PE. Diabetic PE incubated with cells for 4 days increased cell numbers significantly more (P less than .05) than normal PE. These abnormalities were corrected by long-term intensive insulin treatments (continuous subcutaneous insulin infusion and Pen infuser). The decrease of platelet extract GA appeared to correlate with the amount of insulin administered before meals as short-acting boluses, whereas the level of basal or long-acting insulin appeared to correlate with an increase of PE GA. Thus, the growth-promoting potential of platelets can be normalized by intensive insulin therapy. The relationship of insulin levels to this activity needs further evaluation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Animals
  • Biological Assay
  • Blood Platelets / metabolism*
  • Cells, Cultured
  • Cholesterol / blood
  • DNA / biosynthesis
  • Diabetes Mellitus, Type 1 / blood*
  • Diabetes Mellitus, Type 1 / drug therapy
  • Dose-Response Relationship, Drug
  • Female
  • Glycated Hemoglobin / metabolism
  • Growth Substances / blood*
  • Growth Substances / pharmacology
  • Humans
  • Insulin / administration & dosage
  • Insulin / therapeutic use*
  • Male
  • Muscle, Smooth, Vascular / metabolism
  • Rats

Substances

  • Glycated Hemoglobin A
  • Growth Substances
  • Insulin
  • DNA
  • Cholesterol