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Biology subjects

Bodard, S.

Publications and source records attributed to Bodard, S..

3 recordsLinked to original sources

Environmental enrichment selectively restores brain metabolic activity during cocaine abstinence

BackgroundEnvironmental enrichment (EE) is a promising strategy to promote recovery from addiction, but its neurobiological mechanisms remain poorly understood. This study investigates how exposure to EE during abstinence dynamically affects brain neuroadaptations induced by voluntary intake of cocaine. MethodsUsing longitudinal 18FDG microPET imaging, we examined brain metabolic activity in rats following extended access cocaine self-administration. After establishing escalation of cocaine intake, rats were housed in either enriched or standard environments during a four-week abstinence period. Brain metabolic activity was assessed after one and four weeks of abstinence. ResultsCocaine self-administration produced widespread decreases in cortical metabolic activity, particularly in regions involved in executive function (orbitofrontal cortex, anterior cingulate) and interoception (insula), while increasing activity in emotional and motivational circuits (nucleus accumbens, amygdala, mesencephalon). EE selectively normalized these alterations through temporally distinct mechanisms: rapidly restoring nucleus accumbens and amygdala function while gradually affecting prefrontal cortical activity. After four weeks, rats housed in enriched environments showed significantly normalized metabolic activity in the orbitofrontal cortex and dorsolateral striatum compared to those in standard housing, with persistent changes in anterior cingulate cortex and ventral posterior hippocampus. ConclusionsOur findings reveal circuit-specific and temporally distinct effects of environmental enrichment on cocaine-induced brain alterations. These insights could inform the development of more targeted therapeutic approaches for addiction recovery.

neuroscience↗

3D Transcranial ultrasound localization microscopy reveals major arteries in the sheep brain

ObjectiveStroke, a leading cause of mortality and disability globally, demands swift and accurate diagnosis for effective treatment. Although MRI and CT scans serve as conventional methods, their accessibility remains a challenge, prompting exploration into alternative, portable, and non-ionizing imaging solutions like ultrasound with reduced costs. While Ultrasound Localization Microscopy (ULM) displays potential in high-resolution vessel imaging, its 2D constraints limit its emergency utility. Materials and MethodsThis study delves into the feasibility of 3D ULM with multiplexed probe for transcranial vessel imaging in sheep brains, emulating human skull characteristics. Three sheep underwent 3D ULM imaging, compared with angiographic MRI, while skull characterization was conducted in vivo using ultrashort bone MRI sequences and ex vivo via micro CT. Results and conclusionsThe study showcased 3D ULMs ability to highlight vessels, down to the Circle of Willis, yet within a confined 3D field-of-view. Future enhancements in signal, aberration correction, and human trials hold promise for a portable, volumetric, transcranial ultrasound angiography system. Summary statement3D Ultrasound localization microscopy, using a low-frequency matrix probe, enables transcranial reconstruction of the main vessels in sheep brains.

physiology↗

Whole organ volumetric sensing Ultrasound Localization Microscopy for characterization of kidney structure

Glomeruli are the filtration units of the kidney and their function relies heavily on their microcirculation. Despite its obvious diagnostic importance, an accurate estimation of blood flow in the capillary bundle within glomeruli defies the resolution of conventional imaging modalities. Ultrasound Localization Microscopy (ULM) has demonstrated its ability to image in-vivo deep organs in the body. Recently, the concept of sensing ULM or sULM was introduced to classify individual microbubble behavior based on the expected physiological conditions at the micrometric scale. In the kidney of both rats and humans, it revealed glomerular structures in 2D but was severely limited by planar projection. In this work, we aim to extend sULM in 3D to image the whole organ and in order to perform an accurate characterization of the entire kidney structure. The extension of sULM into the 3D domain allows better localization and more robust tracking. The 3D metrics of velocity and pathway angular shift made glomerular mask possible. This approach facilitated the quantification of glomerular physiological parameter such as an interior traveled distance of approximately 7.5 {+/-} 0.6 microns within the glomerulus. This study introduces a technique that characterize the complete kidney phisiology which can serve as a method to facilite pathology assessment. Furthermore, its potential for clinical relevance could serve as a bridge between research and practical application, leading to innovative diagnostics and improved patient care.

physiology↗