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The antimanic-like effect of tamoxifen: Behavioural comparison with other PKC-inhibiting and antiestrogenic drugs.

Abstract
Protein kinase C (PKC) is an important cellular target for mood stabilizers such as lithium and valproate, and tamoxifen, an antiestrogenic drug with PKC inhibition activity, also demonstrates an antimanic effect. Thus, the aim of the present study was to evaluate whether the antimanic effect of tamoxifen is mediated through the PKC inhibitory and/or the antiestrogenic action(s) of the drug. In the present study, the effects of tamoxifen, chelerythrine (a PKC inhibitor) and medroxyprogesterone (an antiestrogenic drug) were investigated in amphetamine-induced hyperlocomotion of mice, an animal model of a manic state. Lithium carbonate (100 and 150 mg/kg, i.p.), tamoxifen (1.0 mg/kg, i.p.) and chelerythrine (1 microg/site, i.c.v.) completely blocked the amphetamine-induced hyperlocomotion. However, while the intermediate medroxyprogesterone dose (3.0 mg/kg, i.p.) partially reduced the amphetamine-induced hyperlocomotion, lower (1.0 mg/g) and higher (6.0 mg/kg) doses produced no effect. Our results indicate a major role for PKC inhibition in the antimanic-like effect of tamoxifen, although its antiestrogenic action may also contribute to this effect.
AuthorsPamela Sabioni, Irinéia P Baretta, Ester M Ninomiya, Lianna Gustafson, Ana Lúcia S Rodrigues, Roberto Andreatini
JournalProgress in neuro-psychopharmacology & biological psychiatry (Prog Neuropsychopharmacol Biol Psychiatry) Vol. 32 Issue 8 Pg. 1927-31 (Dec 12 2008) ISSN: 0278-5846 [Print] England
PMID18930105 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antimanic Agents
  • Benzophenanthridines
  • Contraceptives, Oral, Synthetic
  • Enzyme Inhibitors
  • Tamoxifen
  • Lithium Carbonate
  • Amphetamine
  • chelerythrine
  • Protein Kinase C
  • Medroxyprogesterone
Topics
  • Amphetamine
  • Analysis of Variance
  • Animals
  • Antimanic Agents (therapeutic use)
  • Behavior, Animal (drug effects)
  • Benzophenanthridines (pharmacology)
  • Contraceptives, Oral, Synthetic (pharmacology)
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Enzyme Inhibitors (pharmacology)
  • Hyperkinesis (chemically induced, drug therapy)
  • Lithium Carbonate (pharmacology, therapeutic use)
  • Medroxyprogesterone (pharmacology)
  • Mice
  • Protein Kinase C (antagonists & inhibitors, metabolism)
  • Tamoxifen (therapeutic use)

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