ABSTRACT
Cocaine abuse continues to be a significant problem in the USA and elsewhere. Cocaine is an indirect agonist for dopamine, norepinephrine and serotonin with numerous potential downstream effects, including processes and signals associated with adult neurogenesis. Since drug addiction is associated with brain plasticity, we hypothesized that cocaine exposure would alter cellular proliferation in two adult neurogenic regions (the subventricular and subgranular zones). We used bromodeoxyuridine (BrdU) to track newly generated cells in the brains of adult mice after chronic cocaine or saline exposures. No differences were found in the number or migration patterns of BrdU-labeled cells in the forebrain neurogenic areas. However, cocaine produced a significant increase in the number of hippocampal BrdU-labeled cells.
Subject(s)
Cell Proliferation/drug effects , Cocaine-Related Disorders/pathology , Cocaine/toxicity , Hippocampus/cytology , Hippocampus/drug effects , Neurogenesis/drug effects , Animals , Disease Models, Animal , Dopamine Uptake Inhibitors/toxicity , Male , Mice , Mice, Inbred C57BL , Neurogenesis/physiology , Neuronal Plasticity/drug effects , Neuronal Plasticity/physiologyABSTRACT
Studies of chemoreception in crustaceans have shown that flesh-eating species can detect amino acids, nucleotides and derivatives, and amines, while most herbivorous and omnivorous species are additionally sensitive to carbohydrates. We used extracellular recording techniques to evaluate the effectiveness of a range of nitrogen-containing compounds (mostly amino acids), bile acids, and carbohydrates in stimulating chemoreceptor cells present in the second and third pereopods of the omnivorous crayfish Procambarus clarkii. When applied at a final concentration of approximately 100 microM, effective stimuli were trehalose, leucine, cellobiose, glycine, sucrose, maltose, and ammonium (from most to least effective). The other 17 compounds tested, many chosen because they are potent stimuli for other crustaceans, were ineffective stimuli for P. clarkii. Concentration-response functions were determined for three single cells that were sensitive to ammonium, for five multiunit fibers sensitive to glycine, and for six multiunit fibers sensitive to leucine. Thresholds ranged from 10 nM to 10 micro, functions were generally linear when plotted against the log of the stimulus concentration, and there was little evidence of saturation. While P. clarkii is sensitive to only seven of 24 compounds tested, the compounds that proved stimulatory should serve as cues for location and identification of food items preferred by this omnivorous crustacean.
