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Trujillo-Villarreal, L. A.

Publications and source records attributed to Trujillo-Villarreal, L. A..

3 recordsLinked to original sources

Cerebellar structural and functional alterations during morphine self-administration are associated with motivation and disrupted goal-directed actions in male Wistar rats

Opioid addiction is characterized by a strong motivational drive to obtain the drug, traditionally attributed to neuroadaptations within mesocorticolimbic reward circuits. Increasing evidence suggests that opioid-induced plasticity extends beyond these pathways, implicating the cerebellum in addiction, although its contribution to drug seeking remains poorly defined. Here, we hypothesized that morphine self-administration would induce cerebellum-associated behavioral alterations alongside structural and functional remodeling. Male Wistar rats (N = 27) were trained to self-administer morphine (0.1 mg/kg/infusion) or saline under fixed-ratio (FR1, 3 h/day, 20 days) and progressive-ratio (PR 9-4, 6 h/day, 25 days) schedules. Behavioral assessments included open field, elevated plus maze, novel object recognition, and Morris water maze tasks. Structural and functional magnetic resonance imaging was acquired longitudinally using a 7T scanner. Morphine self-administering rats showed a progressive increase in infusions and motivation. Exploratory activity increased without affecting anxiety-like behavior or recognition memory. In the Morris water maze, spatial learning was preserved; however, rats exhibited increased Whishaws error (path complexity) and a shift from serial to disorganized navigation strategies, indicating impaired movement sequencing. We also found cerebellar volume changes in Crus1, 7Cb, and 8Cb that were accompanied by altered cerebello-cerebral functional connectivity with insular, striatal, hippocampal, motor, and reticular networks. Multivariate analysis further suggested a brain-behavior covariance pattern in which motivational measures showed the strongest contribution, involving a distributed structural network including the cerebellum and insular cortex. These findings indicate that morphine self-administration preserves drug-seeking motivation while disrupting the organization of goal-directed actions, alongside cerebellar remodeling and altered cerebello-cerebral coupling.

neuroscience↗

Morphine self-administration induces region-specific brain volume changes and microglial phenotypic alterations without affecting neuronal density in male Wistar rats

Addiction to opioids, including morphine, is a major public health crisis in the U.S. It has been associated with brain volume changes in reward-related regions, neuronal death, and neuroinflammation. However, the link between structural changes and neuroinflammation is not well understood. In this study, we used operant conditioning to induce morphine self-administration in rats and examined brain volume and cellular changes, focusing on microglial phenotypes. Male Wistar rats were conditioned to morphine self-administration (0.01 mg/kg) for 20 days under a fixed-ratio 1 schedule. In vivo structural Magnetic Resonance Imaging (MRI) scans were conducted at the beginning and end of self-administration. Brains were stained for Iba1 and NeuN proteins, and confocal images were analyzed for cell counts and microglial morphology. We used Deformation-Based Morphometry for MRI volume analysis and Principal Component Analysis with K-means clustering for microglial phenotyping. Our results showed that morphine self-administration led to volume changes in addiction-related brain regions, including increased globus pallidus and decreased insular cortex volume. Additionally, morphine caused widespread neuroinflammation, evidenced by elevated microglial density in the caudate-putamen, dentate gyrus, globus pallidus, and insular cortex, without affecting neuron counts. Finally, we observed region-specific variations in microglial phenotypes, suggesting region-specific neuroinflammatory roles. In conclusion, our study shows that morphine self-administration induces structural and microglial changes in addiction-related brain regions without neuronal loss, highlighting the role of neuroinflammation in opioid-induced adaptations. The variability in microglial phenotypes underscores their complexity, emphasizing the need to study their progression in addiction and their potential as therapeutic targets.

neuroscience↗

The effect of chronic stress and chronic alcohol intake on behavior, brain structure, and functional connectivity in a rat model

Pathological chronic stress is stress exceeding the organisms ability to cope physiologically, which may act as a risk factor in the onset and relapse of alcohol use disorder. Chronic- restraint stress (CRS) and ethanol intake are independently known to induce changes in brain structure and function, however, their combined effects on neurodevelopment over long periods of time remains largely unexplored. We conducted an in vivo longitudinal rat model with three main goals. 1) to determine if chronic stress increases ethanol intake; 2) to determine the effect of chronic- stress and ethanol intake in behavioral measures, brain structure, and function; and 3) to investigate the effect of sex. This observational study included Wistar rats assigned to four groups: 1) ethanol consumption (EtOH+/CRS-), 2) stress exposure (EtOH-/CRS+), 3) both ethanol and stress exposure (EtOH+/CRS+), and 4) control group (EtOH-/CRS-). Our results showed that chronic stress did not affect ethanol intake but led to reduced body weight gain, elevated corticosterone levels, and impaired recognition memory. Structural MRI revealed that both exposures produced additive brain volume changes in regions such as the olfactory bulb, orbitofrontal cortex, caudate-putamen, hippocampus, and cerebellum. Functional connectivity analysis using network-based statistics identified disrupted cortical-subcortical connections. Results found here were sex-dependent in terms of volumetric changes (higher effects on males) and functional connectivity (higher effects on females). Findings suggest sex-dependent mechanisms where both chronic- ethanol intake and stress affect brain plasticity during neurodevelopment. Understanding these region-specific vulnerabilities is crucial for addressing alcohol use disorders and stress-related neuropathology. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=173 SRC="FIGDIR/small/638122v1_ufig1.gif" ALT="Figure 1"> View larger version (50K): org.highwire.dtl.DTLVardef@27094dorg.highwire.dtl.DTLVardef@d3b8faorg.highwire.dtl.DTLVardef@155deeorg.highwire.dtl.DTLVardef@c9bb7b_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOGraphical abstractC_FLOATNO Created with bioRender C_FIG

neuroscience↗