Insulin, cortisol and catecholamines do not regulate circadian variations in fibrinolytic activity

Thromb Res. 1990 Apr 1;58(1):1-12. doi: 10.1016/0049-3848(90)90238-8.

Abstract

To evaluate possible hormonal regulators of the diurnal rhythm in fibrinolytic activity, we measured tissue plasminogen activator (t-PA) activity, plasminogen activator inhibitor activity (PAI-1), t-PA antigen, insulin, cortisol, and catecholamines in 6 healthy males (age 34 +/- 5) every 2 hours for 24 hours. Fibrinolysis was characterized by a peak in PAI-1 activity and a trough in t-PA activity at 0600 h. PAI-1 activity increased 92% and t-PA activity decreased 56% between 2400 h and 0600 h. t-PA antigen (principally a measure of t-PA/PAI-1 complex), peaked at 0800 h. In comparison, insulin levels were lowest at night when PAI-1 activity was rising. The weak inverse correlation between insulin and PAI-1 activity (r = -0.28, p less than 0.02), was not sufficient to explain the diurnal change in fibrinolysis. While cortisol demonstrated the expected circadian change, the increase in cortisol did not occur until 0400 h, 4-6 hours after the rise in PAI-1 and decrease in t-PA activity started. Supine resting plasma epinephrine and norepinephrine showed no circadian rhythm. From this data, we hypothesize that the increased level of PAI-1 in the morning consumes t-PA, leading to decreased t-PA activity and increased t-PA/PAI-1 complex. Further, we conclude that insulin, cortisol, and catecholamines are not responsible for the circadian rhythm of fibrinolysis.

Publication types

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

MeSH terms

  • Adult
  • Catecholamines / physiology*
  • Circadian Rhythm / physiology*
  • Epinephrine / blood
  • Fibrinolysis / physiology*
  • Humans
  • Hydrocortisone / blood
  • Hydrocortisone / physiology*
  • Insulin / blood
  • Insulin / physiology*
  • Male
  • Norepinephrine / blood
  • Plasminogen Inactivators / metabolism
  • Tissue Plasminogen Activator / metabolism

Substances

  • Catecholamines
  • Insulin
  • Plasminogen Inactivators
  • Tissue Plasminogen Activator
  • Hydrocortisone
  • Norepinephrine
  • Epinephrine