Sexual conflict over mating duration drives the evolution of male and female adaptations that facilitate the manipulation of mating interactions in their favor. This conflict drives the evolution of traits that improve the fitness of the focal sex despite inflicting costs on mates. However, males can express multiple traits that increase and decrease female fitness simultaneously. When the effects of male traits on female fitness increase or decrease with duration of exposure, females traits that influence mating duration are selected upon. Females of Callosobruchus maculatus, a bruchid bean beetle, kick mates to forcefully end copulation. Although both negative effects of male genital spines and positive of effects ejaculatory materials on female fitness have been documented, it is not yet clear how these male traits interact to influence the timing of female kicking. In this study, we observed the effect of male genital spine size, ejaculate size and mating history, and manipulated mating duration to disentangle the effects of male traits on the timing of female kicking behavior. We found that male mating history and mate body size dimorphism predicted the timing and duration of female kicking, but that male ejaculate size and spine length did not predict female kicking timing.

Thesis (Ph. D.)--University of Alabama at Birmingham, 2008. / Title from first page of PDF file (viewed Sept. 16, 2008). Includes bibliographical references.

Thesis (Ph.D. in Pharmacology) -- University of Colorado Denver, 2008. / Typescript. Includes bibliographical references (leaves 135-162). Free to UCD affiliates. Online version available via ProQuest Digital Dissertations;

No description available.

abstract: One explanation for membrane accommodation in response to a slowly rising current, and the phenomenon underlying the dynamics of elliptic bursting in nerves, is the mathematical problem of dynamic Hopf bifurcation. This problem has been studied extensively for linear (deterministic and stochastic) current ramps, nonlinear ramps, and elliptic bursting. These studies primarily investigated dynamic Hopf bifurcation in space-clamped excitable cells. In this study we introduce a new phenomenon associated with dynamic Hopf bifurcation. We show that for excitable spiny cables injected at one end with a slow current ramp, the generation of oscillations may occur an order one distance away from the current injection site. The phenomenon is significant since in the model the geometric and electrical parameters, as well as the ion channels, are uniformly distributed. In addition to demonstrating the phenomenon computationally, we analyze the problem using a singular perturbation method that provides a way to predict when and where the onset will occur in response to the input stimulus. We do not see this phenomenon for excitable cables in which the ion channels are embedded in the cable membrane itself, suggesting that it is essential for the channels to be isolated in the spines. / Dissertation/Thesis / Ph.D. Applied Mathematics 2012

No description available.

Les événements vécus peuvent laisser une trace durable au niveau des réseaux cérébraux. Ces réseaux sont constitués de neurones connectés par des synapses, dont l'efficacité de transmission est régulée sur le plan fonctionnel et structural. Les drogues d'abus détournent les circuits neuronaux impliqués dans l'apprentissage régulé par la récompense, induisant une plasticité des neurones striataux de projection (SPN) du noyau Accumbens (NAc), notamment via l'activation de la voie de signalisation Extracellular Regulated Kinase (ERK) et l'augmentation de la densité en épines dendritiques -qui sont les protrusions portant l'élément post-synaptique glutamatergique-. L'objectif de ma thèse était d'étudier l'impact de l'exposition répétée ou unique à la cocaïne sur le mode formation des synapses des SPN du NAc et d'élucider les rôles précis de la voie ERK dans ce phénomène. J'ai pu montrer qu'une ou plusieurs injections de cocaïne chez la souris induisaient la formation de synapses glutamatergiques persistantes au sein des SPN in vivo. Par des expériences d'imagerie en temps-réel sur tranches striatales, j'ai dissocié les phases de pousse et de stabilisation de nouvelles épines dendritiques. J'ai pu mettre en évidence que la voie ERK joue un rôle prépondérant dans ces deux phases via des processus moléculaires distincts. Ainsi, la phase de pousse des épines est directement régulée par ERK, tandis que le maintien est régulé par MNK-1, une kinase cytoplasmique en aval de ERK, et par la synthèse protéique. Ce travail apporte des données nouvelles sur le mode de formation de ces synapses et les mécanismes moléculaires associés. / Brief life occurrences can leave durable changes at the level of neuronal networks. These networks consist of neurons connected by synapses, which transmission efficacy is regulated at the functional and structural levels. Drugs of abuse highjack neuronal circuits involved in reward-driven learning by activating the Extracellular Regulated Kinase (ERK) pathway and induce an increase in the dendritic spines density –protrusions which host the glutamatergic pre-synaptic element- of SPN. The goal of my thesis work was to study the consequences of acute and chronic cocaine exposures on the mode of synapse formation in SPN from the NAc and to decipher the precise roles of ERK pathway in this phenomenon. I demonstrated that acute and chronic cocaine treatments induced the formation of persisting glutamatergic synapses in SPN in vivo. Time-lapse imaging using two-photon microscopy in acute striatal slices allowed me to dissociate the phases of growth and stabilization of the new dendritic spines. I could indeed demonstrate a key role for ERK in those two phases, although through distinct molecular mechanisms. Firstly, the growth phase is dependent on ERK. Secondly, the stabilization of newly grown spines is controlled by MNK-1, a cytosolic kinase downstream ERK, and by protein synthesis. This work brings new results on the mode of synapse formation as well as on the associated molecular mechanisms.

Dendritic spines are the major sites for receiving excitatory synaptic inputs and play important roles in neuronal signal transduction, memory storage and neuronal circuit organization. Structural plasticity of dendritic spines is correlated with functional plasticity, and is critical for learning and memory. Visualization of the changes of dendritic spines at the ultrastructural level that specifically correlated with their function changes in high throughput would shed light on detailed mechanisms of synaptic plasticity. Here we developed a correlative light and electron microscopy workflow which combines two-photon MNI-glutamate uncaging, pre-embedding immunolabeling, Automatic Tape-collecting Ultramicrotome sectioning and scanning electron microscopy imaging. This method bridges two different visualization platforms, directly linking ultrastructure and function at the level of individual synapses. With this method, we successfully relocated single dendritic spines that underwent long-term potentiation (LTP) induced by two-photon MNI-glutamate uncaging, and visualized their ultrastructures and AMPA receptors distribution at different phases of LTP in high throughput. / Includes bibliography. / Dissertation (Ph.D.)--Florida Atlantic University, 2020. / FAU Electronic Theses and Dissertations Collection

The red lionfish, Pterois volitans, has arguably become the most successful marine invasive species to date. Yet, despite the invasion success of P. volitans, little is known about the morphology, physiology, and ecology of this species in their native and invaded habitats. The majority of recent studies have focused on the migration of P. volitans into new regions, digestion, and bacterial infections. Knowledge is lacking on the body plan of the invasive lionfish, specifically the numerous venomous spines that are protruding outward, making the body less streamlined. In this study we quantified the mechanical properties (bending and puncture) of the venomous spines of P. volitans, and related these properties to the cross-sectional morphology. We also documented variation in the cross-sectional morphology of spines from other lionfish species in their native regions. Lastly, we documented the dorsal spine joint morphology of the first three dorsal spines and the in situ range of motion as tissues were removed. We found that the long, numerous dorsal spines absorb more energy but are less stiff than the pelvic and anal spines. In addition, we found that the anal and pelvic spines are more effective at puncturing buccal skin from sharks and grouper. We found that the removal of connective tissue significantly changes lateral movement (abduction) for the first three dorsal spines. The removal of the fin sheath significantly alters forward movement (extension) for the first two dorsal spines. From morphology, mechanical property, and range of motion data for P. volitans, we propose that the numerous long dorsal spines are primarily used for intimidation, and are not as effective defense structures as the pelvic and anal spines. Having a substantial amount of intimidating, venomous spines may allow for the lionfish to conserve energy for other highly metabolically costly activities other than warding off predators, such as digestion and reproduction. Future studies could focus on the amount of venom in each spine, how long it takes for the venom to be made and replaced, how the venomous spines affect hydrodynamic flow, and in vivo range of motion during swimming and striking. / Includes bibliography. / Dissertation (Ph.D.)--Florida Atlantic University, 2020. / FAU Electronic Theses and Dissertations Collection

Schizophrenia postmortem brain is characterized by γ aminobutyric acid downregulation and by decreased dendritic spine density in frontal cortex. Protracted L-methionine treatment exacerbates schizophrenia symptoms, and our earlier work (Tremolizzo et al. and Dong et al.) has shown that L-methionine decreases reelin and GAD67 transcription in mice which is prevented by co-administration of valproate. In this study, we observed a decrease in spine density following L-methionine treatment, which was prevented by co-administration of valproate. Together with our earlier findings conducted under the same experimental conditions, we suggest that downregulation of spine density in L-methionine-treated mice may be because of the decreased expression of reelin and that valproate may prevent spine downregulation by inhibiting the methylation induced decrease in reelin.