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Calcium channels at the adrenergic neuroeffector junction in the rabbit ear artery

Zygmunt, P M (author)
Lund University,Lunds universitet,Avdelningen för klinisk kemi och farmakologi,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Clinical Chemistry and Pharmacology,Department of Laboratory Medicine,Faculty of Medicine
Högestätt, E D (author)
Lund University,Lunds universitet,Avdelningen för klinisk kemi och farmakologi,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Clinical Chemistry and Pharmacology,Department of Laboratory Medicine,Faculty of Medicine
 (creator_code:org_t)
1993
1993
English 7 s.
In: Naunyn-Schmiedeberg's Archives of Pharmacology. - 0028-1298. ; 347:6, s. 23-617
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Neurotransmitter release is dependent on influx of Ca2+ through voltage-operated calcium channels (VOCCs). These channels may be divided into L, N, T and P subtypes. To investigate the subtypes of VOCC involved in transmitter release from adrenergic nerves in the isolated rabbit ear artery, the effects of some subtype selective VOCC antagonists were examined on contractile responses induced by electrical field stimulation (EFS), and exposure to an isosmolar (low Na+, normal Cl- content) or a hyperosmolar (normal Na+, high Cl- content) 60 mM K+ solution. Tetrodotoxin (TTX) and the L channel blocker nimodipine were present in the latter experiments to inhibit sodium-dependent action potential discharge and the direct contractile effect of K+ depolarization on the smooth muscle cells. Prazosin abolished the contractile effect of EFS, indicating that the response was elicited by activation of adrenergic nerves. The EFS-induced contractions were concentration-dependently inhibited by the N channel blocker omega-conotoxin (pIC50 = 9.0) and the proposed L channel blocker T-cadinol (pIC50 = 4.5), while nimodipine and the T channel blocker tetramethrin had no effect. The isosmolar and hyperosmolar K+ solutions induced a prazosin-sensitive contraction, amounting to 46% and 10% of the response to 10(-5) M noradrenaline (NA), respectively. omega-Conotoxin inhibited the contractile response to the hyperosmolar K+ solution, but not that to the isosmolar K+ solution. T-cadinol preferentially inhibited the response to the hyperosmolar K+ solution. Tetramethrin had no effect on contractions induced by either type of K+ solution.(ABSTRACT TRUNCATED AT 250 WORDS)

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

Animals
Arteries/metabolism
Calcium Channel Blockers/pharmacology
Calcium Channels/drug effects
Ear/blood supply
Electric Stimulation
Female
In Vitro Techniques
Male
Muscle Contraction/drug effects
Muscle, Smooth, Vascular/drug effects
Neuroeffector Junction/drug effects
Nimodipine/pharmacology
Norepinephrine/pharmacology
Peptides/pharmacology
Potassium Chloride/pharmacology
Prazosin/pharmacology
Pyrethrins/pharmacology
Rabbits
Regional Blood Flow/physiology
Sesquiterpenes/pharmacology
Sympathetic Nervous System/drug effects
Tetrodotoxin/pharmacology
omega-Conotoxins

Publication and Content Type

art (subject category)
ref (subject category)

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Zygmunt, P M
Högestätt, E D
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MEDICAL AND HEALTH SCIENCES
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Naunyn-Schmiedeb ...
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Lund University

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