> Dissertation Defense Announcement > To: The George Mason University Community > > Candidate: Nachiket Dharker > Program: PhD Biosciences > > Date: Wednesday August 8, 2012 > Time: 2:00 p.m. > Place: George Mason University > Occoquan Bldg., #203 > Prince William Campus > <http://www.gmu.edu/resources/welcome/Directions-to-GMU.html> > > Dissertation Director/Committee Chair: Dr. Karl J. Fryxell > Committee members: Dr. Ancha Baranova, Dr. Daniel N. Cox, Dr. Timothy Born > > Title: "Gene Expression Responses to Single and Repeated Nicotine > Injections in Adolescent and Adult Mice" > > The dissertation is on reserve in the Johnson Center Library, Fairfax > campus. > The doctoral project will not be read at the meeting, but should be > read in advance. > > All members of the George Mason University community are invited to > attend. > > > *ABSTRACT:* > > The majority of smokers begin tobacco use during adolescence. > Relatively little is understood about the molecular effects of > nicotine on adolescents and its role in establishing future nicotine > dependence. Here we studied the mRNA expression of dopamine receptors > (Drd1, Drd2S, Drd2L, Drd3), cyclic nucleotide phosphodiesterases > [Pde4b (long isoforms), Pde4b1, Pde4d ], a tetraspanin (Cd81), opioid > peptides (Pdyn and Penk), and the anaplastic lymphoma kinase receptor > (Alk) after single or repeated nicotine injections in brain areas of > mice by quantitative reverse transcriptase PCR. We found that a single > nicotine injection caused dramatic gene expression responses in the > adolescent medial prefrontal cortex, where all inhibitory dopamine > receptor mRNAs (Drd2L, Drd2S, and Drd3) decreased by an average of > 3.5-fold after 24 hr in adolescents but not in adults. The > downregulation of Drd2 in adolescent males and females of the A/J and > C57BL/6J strains was strongly correlated (r = 0.99) with the nicotine > preference of those sexes and strains (measured as adults). More > generally, we found adolescent-specific gene expression responses to > nicotine in Drd2, Drd3, Pde4b (long isoforms), Alk, and Penk in medial > prefrontal cortex, and in Pde4b1 and Pde4d in ventral striatum. We > also found adolescent-specific sexually divergent gene expression > responses of Cd81. Another interesting finding was the significant > correlation between Drd2 and Penk expression in medial prefrontal > cortex (but not Drd1 and/or Pdyn). In contrast to the responses to a > single nicotine injection, repeated nicotine injections produced > significant gene expression responses for many of these genes in > ventral striatum that differed significantly between adolescents and > adults. In fact, the expression of Drd2S, and Drd2L decreased after > repeated nicotine injections in all adolescent sexes and strains, but > increased in most sexes and strains of adult ventral striatum. > Moreover, nicotine-induced changes in gene expression of all other > genes in ventral striatum were specific to adults. In medial > prefrontal cortex, fewer genes (Drd1 and Drd3) showed differential > gene expression responses between adolescents and adults, and none of > these gene expression responses were adolescent-specific. Our results > suggest that the initial adolescent-specific component of the gene > expression responses to nicotine occurs primarily in medial prefrontal > cortex, but the responses to repeated nicotine injections occur > primarily in ventral striatum. Results from other brain areas are also > reported. Our results help to elucidate several steps of > adolescent-specific gene expression response to nicotine by genes that > are implicated in drug abuse. > > ###