Literature DB >> 16702989

Excitatory P2-receptors at sympathetic axon terminals: role in temperature control of cutaneous blood flow.

Ivar von Kügelgen1.   

Abstract

The mechanisms underlying the reduction in cutaneous blood flow in response to cooling are only partially understood. A study published in this issue of the British Journal of Pharmacology now provides evidence for the involvement of excitatory P2-receptors located at sympathetic axon terminals in the cooling-induced vasoconstriction in the skin. Cooling appears to cause the release of adenine nucleotides followed by the activation of excitatory presynaptic P2-receptors at noradrenergic axon terminals. Activation of these excitatory P2-receptors induces the release of noradrenaline, which subsequently causes constriction of blood vessels in the skin by action on smooth muscle alpha(1)- and alpha(2)-adrenoceptors. The commentary discusses the implication of the results and remaining questions.

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Year:  2006        PMID: 16702989      PMCID: PMC1751880          DOI: 10.1038/sj.bjp.0706767

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  25 in total

1.  Silent alpha(2C)-adrenergic receptors enable cold-induced vasoconstriction in cutaneous arteries.

Authors:  M A Chotani; S Flavahan; S Mitra; D Daunt; N A Flavahan
Journal:  Am J Physiol Heart Circ Physiol       Date:  2000-04       Impact factor: 4.733

Review 2.  International union of pharmacology. XXIV. Current status of the nomenclature and properties of P2X receptors and their subunits.

Authors:  B S Khakh; G Burnstock; C Kennedy; B F King; R A North; P Séguéla; M Voigt; P P Humphrey
Journal:  Pharmacol Rev       Date:  2001-03       Impact factor: 25.468

Review 3.  Neuronal P2X receptors: localisation and functional properties.

Authors:  W Nörenberg; P Illes
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2000-11       Impact factor: 3.000

4.  Local regulation of skin blood flow during cooling involving presynaptic P2 purinoceptors in rats.

Authors:  Tadachika Koganezawa; Tomohisa Ishikawa; Yukiyoshi Fujita; Tomonari Yamashita; Takako Tajima; Masaki Honda; Koichi Nakayama
Journal:  Br J Pharmacol       Date:  2006-05-15       Impact factor: 8.739

5.  Differences in the mode of stimulation of cultured rat sympathetic neurons between ATP and UDP.

Authors:  I von Kügelgen; W Nörenberg; P Illes; A Schobert; K Starke
Journal:  Neuroscience       Date:  1997-06       Impact factor: 3.590

Review 6.  Pharmacological profiles of cloned mammalian P2Y-receptor subtypes.

Authors:  Ivar von Kügelgen
Journal:  Pharmacol Ther       Date:  2005-10-28       Impact factor: 12.310

7.  Role of action potentials and calcium influx in ATP- and UDP-induced noradrenaline release from rat cultured sympathetic neurones.

Authors:  I von Kügelgen; W Nörenberg; A Meyer; P Illes; K Starke
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1999-05       Impact factor: 3.000

8.  Local regulation of [(3)H]-noradrenaline release from the isolated guinea-pig right atrium by P(2X)-receptors located on axon terminals.

Authors:  B Sperlágh; F Erdélyi; G Szabó; E S Vizi
Journal:  Br J Pharmacol       Date:  2000-12       Impact factor: 8.739

9.  Evidence that release of adenosine triphosphate from endothelial cells during increased shear stress is vesicular.

Authors:  P Bodin; G Burnstock
Journal:  J Cardiovasc Pharmacol       Date:  2001-12       Impact factor: 3.105

10.  ATP stimulates sympathetic transmitter release via presynaptic P2X purinoceptors.

Authors:  S Boehm
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

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