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Hypothermia in mice: D2 dopamine receptor mediation and absence of spare receptors.

Abstract
The nonselective dopamine (DA) receptor agonists R(-)apomorphine (APO) and R(-)-N-n-propylnorapomorphine (NPA) elicited dose- and time-dependent hypothermia in mice with ED50 values of 300 and 18 micrograms/kg, respectively. The selective D2 agonist quinpirole (LY 171555) also elicited dose-dependent hypothermia, whereas the selective D1 agonist SKF 38393 had no effect. The selective D1 and D2 antagonists SCH 23390 (1 mg/kg) and sulpiride (200 mg/kg), respectively, did not significantly alter body temperature. The hypothermic effect of a maximal dose of NPA (0.2 mg/kg) was not blocked by SCH 23390 (1 mg/kg) but was significantly attenuated (p less than 0.001) by pretreatment with sulpiride (200 mg/kg). Pretreatment with sulpiride (200 mg/kg) produced a parallel, 40-fold shift to the right of the dose-response curve for NPA. Partial, irreversible DA receptor inactivation by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) (2 mg/kg) reduced the maximal hypothermic effect of NPA (to 49% of control) without altering its ED50. Analysis of the data indicated a linear relationship between DA receptor occupancy and hypothermic response. The results demonstrate that DA agonist-induced hypothermia in mice is mediated by D2 receptors and that there is no receptor reserved for this response.
AuthorsE Meller, R Hizami, L Kreuter
JournalPharmacology, biochemistry, and behavior (Pharmacol Biochem Behav) Vol. 32 Issue 1 Pg. 141-5 (Jan 1989) ISSN: 0091-3057 [Print] United States
PMID2567521 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Adrenergic alpha-Antagonists
  • Benzazepines
  • Dopamine Agents
  • Dopamine Antagonists
  • Ergolines
  • Quinolines
  • Receptors, Dopamine
  • Receptors, Dopamine D2
  • Quinpirole
  • N-n-propylnorapomorphine
  • EEDQ
  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine
  • Sulpiride
  • Apomorphine
Topics
  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine
  • Adrenergic alpha-Antagonists (pharmacology)
  • Animals
  • Apomorphine (analogs & derivatives, pharmacology)
  • Benzazepines (pharmacology)
  • Body Temperature (drug effects)
  • Dopamine Agents (pharmacology)
  • Dopamine Antagonists
  • Ergolines (pharmacology)
  • Hypothermia (physiopathology)
  • Male
  • Mice
  • Mice, Inbred Strains
  • Quinolines (pharmacology)
  • Quinpirole
  • Receptors, Dopamine (physiology)
  • Receptors, Dopamine D2
  • Sulpiride (pharmacology)

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