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Temperature-sensitive adenosine-mediated vasoconstriction in the skin microcirculation.

I Stojanov1, K G Proctor

  • 1Department of Physiology, University of Tennessee Health Science Center, Memphis.

The Journal of Pharmacology and Experimental Therapeutics
|June 1, 1990
PubMed
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Adenosine receptors (A1) in hamster skin arterioles show temperature-dependent vasoconstriction. This suggests temperature sensitivity is key for classifying adenosine receptors.

Area of Science:

  • Pharmacology
  • Physiology
  • Microcirculation

Background:

  • Adenosine receptors (A1 and A2) play crucial roles in regulating vascular tone.
  • Understanding the influence of temperature on adenosine receptor function is vital for interpreting physiological responses.

Purpose of the Study:

  • To investigate the effect of local skin temperature on adenosine receptor-mediated vasoconstriction and vasodilation in hamster arterioles.
  • To determine if A1 and A2 adenosine receptors exhibit temperature-dependent activity in vivo.

Main Methods:

  • Topical application of adenosine receptor agonists (e.g., adenosine, N6-cyclohexyladenosine) to arterioles in hamster skin microcirculation.
  • Vascular responses (vasoconstriction/vasodilation) were measured at varying local skin temperatures.

Related Experiment Videos

  • Pharmacological antagonism using 8-phenyltheophylline to identify receptor subtypes involved.
  • Main Results:

    • A1 receptor-mediated vasoconstrictions were enhanced by increased temperature and unaffected by decreased temperature.
    • Norepinephrine and angiotensin II responses showed different temperature dependencies, with angiotensin II being temperature-insensitive.
    • Adenosine-induced vasodilation was generally temperature-insensitive, with exceptions at higher concentrations.

    Conclusions:

    • A1 adenosine receptors, but not A2 receptors, demonstrate temperature-dependent actions in vivo.
    • Temperature sensitivity may serve as an additional criterion for classifying adenosine receptors.
    • These findings highlight the complex interplay between temperature and receptor pharmacology in microvascular regulation.