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A cembranoid from tobacco prevents the expression of nicotine-induced withdrawal behavior in planarian worms.

Oné R Pagán | Amanda L Rowlands | Angela L Fattore | Tamara Coudron | Kimberly R Urban | Apurva H Bidja | Vesna A Eterović
European journal of pharmacology | 2009

Using an adaptation of published behavioral protocols, we determined that acute exposure to the cholinergic compounds nicotine and carbamylcholine decreased planarian motility in a concentration-dependent manner. A tobacco cembranoid (1S,2E,4R,6R,7E,11E)-cembra-2,7,11-triene-4,6-diol (4R-cembranoid), also decreased planarian motility. Experiments in the presence of 1 microM 4R-cembranoid did increase the IC50 for nicotine- but not carbamylcholine-induced decrease in planarian motility. When planarians were exposed for 24 h to either nicotine or carbamylcholine at concentrations near their respective IC50 values and then transferred to plain media, nicotine-exposed, but not carbamylcholine- or cembranoid-exposed worms displayed withdrawal-like distress behaviors. In experiments where planarians were pre-exposed to 100 microM nicotine for 24 h in the presence of 1 microM 4R-cembranoid, the withdrawal-like effects were significantly reduced. These results indicate that the 4R-cembranoid might have valuable applications for tobacco abuse research. This experimental approach using planarians is useful for the initial screening of compounds relevant to drug abuse and dependence.

Pubmed ID: 19490913

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Associated grants

  • Agency: NCRR NIH HHS, United States
    Id: G12 RR003035
  • Agency: NCRR NIH HHS, United States
    Id: G12 RR003035-24
  • Agency: NCRR NIH HHS, United States
    Id: 2G12RR03035

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Schmidtea mediterranea Genome Database (tool)

RRID:SCR_007934

A database that integrates all available data associated with the planarian genome, including predicted and annotated genes, ESTs, protein homologies, gene expression patterns and RNAi phenotypes. It is GMOD compliant. The planarian Schmidtea mediterranea is rapidly emerging as a key model organism for the study of regeneration, tissue homeostasis and stem cell biology. Thus, SmedGD features a genome browser, BLAST capability, and other search options in order to facilitate the advancement of scientific knowledge of this organism.<

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