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1.
Front Psychiatry ; 4: 38, 2013.
Article in English | MEDLINE | ID: mdl-23730292

ABSTRACT

Stress is a major factor that promotes tobacco use and relapse during withdrawal. Although women are more vulnerable to tobacco use than men, the manner in which stress contributes to tobacco use in women versus men is unclear. Thus, the goal of this study was to compare behavioral and biological indices of stress in male and female rats during nicotine withdrawal. Since the effects of nicotine withdrawal are age-dependent, this study also included adolescent rats. An initial study was conducted to provide comparable nicotine doses across age and sex during nicotine exposure and withdrawal. Rats received sham surgery or an osmotic pump that delivered nicotine. After 14 days of nicotine, the pumps were removed and controls received a sham surgery. Twenty-four hours later, anxiety-like behavior and plasma corticosterone were assessed. The nucleus accumbens (NAcc), amygdala, and hypothalamus were examined for changes in corticotropin-releasing factor (CRF) gene expression. In order to differentiate the effects of nicotine withdrawal from exposure to nicotine, a cohort of rats did not have their pumps removed. The major finding is that during nicotine withdrawal, adult females display higher levels of anxiety-like behavior, plasma corticosterone, and CRF mRNA expression in the NAcc relative to adult males. However, during nicotine exposure, adult males exhibited higher levels of corticosterone and CRF mRNA in the amygdala relative to females. Adolescents displayed less nicotine withdrawal than adults. Moreover, adolescent males displayed an increase in anxiety-like behavior and an up-regulation of CRF mRNA in the amygdala during nicotine exposure and withdrawal. These findings are likely related to stress produced by the high doses of nicotine that were administered to adolescents to produce equivalent levels of cotinine as adults. In conclusion, these findings suggest that intense stress produced by nicotine withdrawal may contribute to tobacco use in women.

2.
J Proteome Res ; 8(7): 3642-52, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19374451

ABSTRACT

The cell surface of Trypanosoma cruzi, the etiologic agent of Chagas disease, is covered by a dense layer of glycosylphosphatidylinositol (GPI)-anchored molecules. These molecules are involved in a variety of interactions between this parasite and its mammalian and insect hosts. Here, using the neutral detergent Triton X-114, we obtained fractions rich in GPI-anchored and other membrane proteins from insect developmental stages of T. cruzi. These fractions were analyzed by two-dimensional liquid chromatography coupled to tandem mass spectrometry (2D-LC-MS/MS), resulting in the identification of 98 proteins of metacyclic trypomastigotes and 280 of epimastigotes. Of those, approximately 65% (n=245) had predicted lipid post-translational modification sites (i.e., GPI-anchor, myristoylation, or prenylation), signal-anchor sequence, or transmembrane domains that could explain their solubility in detergent solution. The identification of some of these modified proteins was also validated by immunoblotting. We also present evidence that, in contrast to the noninfective proliferative epimastigote forms, the infective nonproliferative metacyclic trypomastigote forms express a large repertoire of surface glycoproteins, such as GP90 and GP82, which are involved in adhesion and invasion of host cells. Taken together, our results unequivocally show stage-specific protein profiles that appear to be related to the biology of each T. cruzi insect-derived developmental form.


Subject(s)
Detergents/pharmacology , Proteomics/methods , Trypanosoma cruzi/drug effects , Amino Acid Sequence , Animals , Chromatography, Liquid/methods , Computational Biology/methods , Glycoproteins/chemistry , Glycosylphosphatidylinositols/chemistry , Mass Spectrometry/methods , Membrane Proteins/chemistry , Mice , Molecular Sequence Data , Octoxynol , Polyethylene Glycols/pharmacology , Protein Processing, Post-Translational , Sequence Homology, Amino Acid
3.
Exp Parasitol ; 120(1): 98-102, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18511047

ABSTRACT

Pentamidine is a second-line agent used in the treatment of leishmaniasis and its mode of action and mechanism of resistance is not well understood. It was previously demonstrated that transfection of promastigotes and amastigotes with the ABC transporter PRP1 gene confers resistance to pentamidine. To further clarify this point, we generated Leishmania amazonensis mutants resistant to pentamidine. Our results indicated that this ABC transporter is not associated with pentamidine resistance in lines generated by drug pressure through amplification or overexpression mechanisms of PRP1 gene.


Subject(s)
Antiprotozoal Agents/pharmacology , Drug Resistance/genetics , Leishmania mexicana/drug effects , Pentamidine/pharmacology , ATP-Binding Cassette Transporters/genetics , ATP-Binding Cassette Transporters/physiology , Animals , Blotting, Southern , DNA, Protozoan/chemistry , DNA, Protozoan/isolation & purification , Electrophoresis, Gel, Pulsed-Field , Fluorescent Dyes , Indoles , Inhibitory Concentration 50 , Leishmania mexicana/genetics , Microscopy, Fluorescence , Mutation , Phenotype , Protozoan Proteins/genetics , Protozoan Proteins/physiology
4.
Acta Trop ; 105(1): 87-91, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17889817

ABSTRACT

Trypanosoma cruzi, the parasite causing Chagas' disease, relies on triatomines for its transmission. T. cruzi metacyclic trypomastigotes express GP82 and GP90, which are developmentally regulated surface proteins that have been implicated in host cell invasion. We used quantitative RT-PCR to quantify GP90 and GP82 mRNA levels expressed by T. cruzi in the digestive tract of experimentally infected Rhodnius prolixus at different times post infection. Translation of these transcripts was assessed by immunofluorescence using specific monoclonal antibodies against GP90 and GP82. We found that although GP82 and GP90 proteins were not detected in epimastigote cells by immunofluorescence, transcripts were present at lower levels. Increased levels of GP90 and GP82 transcripts and the appearance of these proteins on the parasite surface were accompanied by morphological differentiation from epimastigotes into metacyclic forms. Our data suggest that during in vivo metacyclogenesis there is a coordinated mechanism that links stabilization of GP90 and GP82 mRNAs with their translation.


Subject(s)
Gastrointestinal Tract/parasitology , Insect Vectors/parasitology , Membrane Glycoproteins/biosynthesis , Protozoan Proteins/biosynthesis , Rhodnius/parasitology , Trypanosoma cruzi/metabolism , Variant Surface Glycoproteins, Trypanosoma/biosynthesis , Animals , Gene Expression , Membrane Glycoproteins/genetics , Microscopy, Fluorescence , Protozoan Proteins/genetics , RNA, Protozoan/genetics , RNA, Protozoan/isolation & purification , Reverse Transcriptase Polymerase Chain Reaction , Variant Surface Glycoproteins, Trypanosoma/genetics
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