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Related Concept Videos

Type I Diabetes II: Pathophysiology01:26

Type I Diabetes II: Pathophysiology

Type 1 diabetes mellitus arises from an immune-mediated destruction of pancreatic β-cells, resulting in an absolute deficiency of insulin. This process develops in genetically susceptible individuals when autoimmunity, environmental exposures, and immunologic dysregulation converge to trigger a targeted attack on the insulin-producing cells of the pancreas. The β-cells are located within the islets of Langerhans and are essential for regulating blood glucose by facilitating cellular uptake of...
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Behavioral Assessment of Visual Function via Optomotor Response and Cognitive Function via Y-Maze in Diabetic Rats
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Vasomotion becomes less random as diabetes progresses in monkeys.

Xenia T Tigno1, Barbara C Hansen, Salasa Nawang

  • 1Department of Molecular Pharmacology and Physiology, College of Medicine, University of South Florida, Tampa, Florida, USA. xtigno@yahoo.com

Microcirculation (New York, N.Y. : 1994)
|March 26, 2011
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Summary

As diabetes progresses in monkeys, vasomotion becomes less random, indicating a reduced capacity of the peripheral circulation to adapt. Insulin

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Area of Science:

  • Cardiovascular Physiology
  • Metabolic Disease Research
  • Autonomic Nervous System Function

Background:

  • Vasomotion changes may signal early autonomic dysfunction in diabetes.
  • Previous studies demonstrated that spectral properties of vasomotion can differentiate between normal, pre-diabetic, and type 2 diabetic nonhuman primates.

Purpose of the Study:

  • To investigate the time-dependent changes and complexity of vasomotion's spectral properties across three metabolic groups of monkeys.
  • To assess the impact of heat-induced vasodilation on the vasomotion power spectrum.
  • To compare the effects of exogenous insulin administration on vasomotion.

Main Methods:

  • Laser Doppler flowmetry was used to measure foot blood flow in normal (N), pre-diabetic (PreDM), and type 2 diabetic (T2DM) monkeys.
  • Measurements were taken at baseline (34°C) and under heat stimulation (44°C).
  • Lempel-Ziv complexity, prediction error, and covariance complexity were calculated to quantify randomness.

Main Results:

  • Measures of vasomotion randomness decreased with diabetes progression, signifying a loss of peripheral circulatory homeostatic capacity.
  • In T2DM animals, power spectral density shifted to lower frequencies (0-1.45 Hz), suggesting a move towards local flow regulation.
  • Heat stimulation increased spectral power across all groups; insulin's effects varied by metabolic group, with T2DM showing impaired responses.

Conclusions:

  • Diabetes progression leads to decreased vasomotion randomness and a diminished capacity for peripheral circulation to adapt.
  • In advanced diabetes, circulatory regulation appears to shift from central autonomic control towards local mechanisms.
  • Insulin resistance affects vasomotion regulation, with varying responses observed in different stages of diabetes.