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The xerogenic potency and mechanism of action of tramadol inhibition of salivary secretion in rats.

Götrick, Bengt (author)
Malmö högskola,Odontologiska fakulteten (OD)
Tobin, Gunnar, 1954 (author)
Gothenburg University,Göteborgs universitet,Institutionen för fysiologi och farmakologi, Avdelningen för farmakologi,Institute of Physiology and Pharmacology, Dept of Pharmacology
 (creator_code:org_t)
Elsevier BV, 2004
2004
English.
In: Archives of oral biology. - : Elsevier BV. - 0003-9969 .- 1879-1506. ; 49:12, s. 969-73
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Tramadol is a centrally acting analgesic with weak opioid agonist properties, which also has monoaminergic activity, exerted via inhibition of neuronal uptake of serotonin and norepinephrine. Tramadol is generally well tolerated and the most common adverse events are nausea, dizziness, drowsiness, sweating, vomiting and dry mouth. Currently it was examined by which principal mechanism tramadol induces oral dryness. The effects of intravenous administration (+/-)-tramadol were studied in rats on the flow of saliva in response to a peripheral cholinergic stimulus or to reflex activation involving the relay of impulses in the central nervous system. In pentobarbitone-anaesthetized rats, the salivary secretion to acetylcholine (0.1-10 micromol/kg IV) was increased by up to 110% by tramadol (1-5 mg/kg IV) and the protein concentration therein by up to 400%. The administration alpha- and beta-adrenoceptor antagonists resulted in almost identical acetylcholine-evoked responses as in the absence of tramadol. The secretory response to the application of citric acid on the tongue of the rat was reduced by 38% and by 64%, respectively, at 5 and 10 mg/kg IV of tramadol (p < 0.05-0.01). Thus, tramadol exerts its principal xerogenic effect by activating inhibitory pathways in the central nervous system and has no anticholinergic effect on the salivary glands at dosages that may be clinically relevant. Furthermore, the tramadol-induced increase of the acetylcholine-evoked secretion occurred at a glandular level and depended most likely on a release of noradrenaline from glandular nerve terminals.

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)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Physiology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Odontologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dentistry (hsv//eng)

Keyword

Acetylcholine
administration & dosage
Adrenergic alpha-Antagonists
pharmacology
Adrenergic beta-Antagonists
pharmacology
Analgesics
Opioid
administration & dosage
Animals
Chelating Agents
pharmacology
Citric Acid
pharmacology
Dose-Response Relationship
Drug
Drug Interactions
Female
Injections
Intravenous
Phentolamine
pharmacology
Propranolol
pharmacology
Rats
Rats
Sprague-Dawley
Reflex
Salivation
drug effects
Tramadol
administration & dosage

Publication and Content Type

ref (subject category)
art (subject category)

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Götrick, Bengt
Tobin, Gunnar, 1 ...
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MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Pharmacology and ...
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Physiology
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Dentistry
Articles in the publication
Archives of oral ...
By the university
University of Gothenburg
Malmö University

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