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Two groups of diabetic KK-CAy mice specifically bred for high and low sensitivity to exogenous acetylcholine and beta 1-adrenergic stimulation: interaction of higenamine and aconitine on pulse rate.

Abstract
Diabetic KK-CAy mice were specifically bred for high and low sensitivity to the addition of exogenous acetylcholine (ACh). The sensitivity to ACh was measured by the change in pulse rate 2 min after the administration of ACh (10 mg/kg, s.c.). The two groups of mice, with high and low sensitivity to ACh, were specially selected and mated sequentially until the 12th filial generation. Although higenamine (100 micrograms/kg, i.p.), a beta 1-adrenergic agonist (a compound derived from aconite), had no effect per se, it inhibited aconitine (another compound derived from aconite extract)-induced bradycardia within 30 s of administration in ACh-low sensitive mice but not in ACh-high sensitive mice. The effects of aconitine and higenamine alone did not differ between these two groups of mice. This demonstrates that the high muscarinic and high beta 1-adrenergic sensitive mice may be stratified into two groups based upon an antagonistic interaction between higenamine and aconitine.
AuthorsI Kimura, M Makino, R Honda, M Kimura
JournalBiological & pharmaceutical bulletin (Biol Pharm Bull) Vol. 18 Issue 10 Pg. 1356-61 (Oct 1995) ISSN: 0918-6158 [Print] Japan
PMID8593436 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Adrenergic beta-1 Receptor Agonists
  • Adrenergic beta-Agonists
  • Alkaloids
  • Tetrahydroisoquinolines
  • Acetylcholine
  • higenamine
  • Aconitine
Topics
  • Acetylcholine (metabolism, pharmacology)
  • Aconitine (pharmacology)
  • Adrenergic beta-1 Receptor Agonists
  • Adrenergic beta-Agonists (pharmacology)
  • Alkaloids (pharmacology)
  • Animals
  • Autonomic Nervous System (metabolism)
  • Blood Pressure (drug effects)
  • Diabetes Mellitus, Type 2 (genetics, metabolism)
  • Heart Rate (drug effects)
  • In Vitro Techniques
  • Male
  • Mice
  • Mice, Inbred Strains
  • Obesity (genetics, metabolism)
  • Pulse (drug effects)
  • Tetrahydroisoquinolines

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