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Lopez-Tremoleda, J.

Publications and source records attributed to Lopez-Tremoleda, J..

3 recordsLinked to original sources

Brief, repeated isoflurane anaesthesia elicits sex-dependent behavioural, cerebrovascular, and microglial alterations in mice

General anaesthetics are indispensable tools in biomedical research, yet growing evidence shows that their effects on brain function extend beyond the transient loss of consciousness for which they are used. Although numerous preclinical studies have examined the impact of a single anaesthetic exposure, far less is known about the cumulative consequences of repeated administration protocols, despite their widespread use in longitudinal imaging, behavioural testing, and disease model studies. Here, we show that brief, repeated isoflurane exposures induce alterations in behaviour, cerebrovascular patterns, and microglial phenotype in adult CD1 mice, with several responses exhibiting pronounced sex specificity. Repeated anaesthesia suppressed locomotor activity selectively in females and impaired ethologically important maintenance behaviours, including nesting and burrowing, in both sexes. These behavioural effects were accompanied by sex-dependent changes in cerebral blood flow dynamics, with females displaying elevated cerebrovascular flow, yet males showing higher reactivity to isoflurane exposure. At the molecular level, repeated isoflurane exposure altered endothelial marker expression without modifying capillary density and shifted microglia toward a hyporeactive state. Together, these data reveal that even short, routine anaesthetic events produce biologically meaningful and sex-dependent effects on neural, vascular, and immune systems. These results indicate that the anaesthetic regimen is an often overlooked but influential factor that deserves careful consideration in pre-clinical neuroscience.

neuroscience↗

Mitochondria drive microglial NRLP3 inflammasome activation via TSPO

Uncontrolled microglial response is core to neuroinflammatory brain diseases. The correlation between the mitochondrial protein TSPO and inflammation has so far failed to explain whether TSPO positively or negatively regulates microglial function. The recent evidence on the species specificity of TSPO in microglia demands a deeper understanding of the protein biology in these brain-resident macrophages. To this end, we have here enrolled a murine model of microglial cells showing that TSPO is required for the priming of mitochondria to inflammation and a conduit for its escalation. Namely, in response to inflammatory cues TSPO is stabilised on the mitochondria where it binds and sequesters NOD-like receptor (NLR) protein (i), represses the PARK2-mediated mitophagy (ii) and engages the retrograde communication with the nucleus via the accumulation of the Nf-kB to promote the expression of pro-inflammatory genes (iii). Notably, the TSPO sustained inflammatory response drives cellular demise and ultimately leads to excitotoxicity (iv). Our findings advance the current knowledge of TSPO widening the understanding of mitochondria in inflammation and indicating a target for their regulation.

cell biology↗

Rejection in early life is associated with high and long-lasting stress and higher incidence of infections in owl monkeys

1.BackgroundThe mothers of owl monkeys sometimes reject their new-borns. When this occurs in captive colonies, the rejected infants are manually raised by veterinarians, allowing them to survive. However, maternal rejection can induce chronic stress, which in turn is associated with infectious diseases. Rescued, rejected owl monkeys might experience high rates of stress and infections which go undetected. MethodologyTo test this hypothesis, we evaluated the connection between maternal rejection, stress and infections in owl monkeys (Aotus nancymaae) from the IVITA Center for Conservation and Reproduction of Primates (UNMSM, Peru). Specifically, we compared the stress rates and frequency of infection treatment in juveniles (19-24 months) rejected in the first month of life and controls. To assess stress, we compared cortisol levels in hair using a competitive ELISA and recorded behaviours using cameras. We analysed past medical treatments and medication to compare incidence of infection treatment in subjects. We then studied the correlation between the frequency of infection treatments and cortisol using a linear regression. ResultsRejected owl monkeys showed significantly higher cortisol levels (p=0.0123), a higher incidence of stereotypical behaviour and overeating (pacing p=0.0159; head twirling p=0.0476, eating p=0.0238) compared to controls. Rejected owl monkeys also received significantly more treatment for infections than controls per month lived (p=0.0009). Moreover, infection rates observed in this population were positively although weakly associated with concentration of cortisol in hair (R2=0.307, p=0.0075). ConclusionMaternal rejection in the first month of life is associated with high and long-lasting stress levels and infections in the IVITA owl monkey colony. IVITA owl monkeys will be a useful model for studying the long-term effects of early life stress at the population level.

neuroscience↗