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Peris, M.

Publications and source records attributed to Peris, M..

2 recordsLinked to original sources

Inter-unit variability and rapid depletion of 2,3-diphosphoglycerate in stored red blood cells: implications for transfusion practice in neurocritical care

Red blood cell (RBC) transfusion aims to restore tissue oxygen delivery, yet a stored unit's capacity to unload oxygen depends on 2,3-diphosphoglycerate (2,3-DPG), the principal allosteric modulator of hemoglobin-oxygen affinity. Randomized trials comparing fresher with older units have been consistently null, and all have used storage duration as the exposure variable. We asked whether storage age reflects the metabolic state of individual units. Twenty-four leukodepleted packed RBC units were sampled serially from day 3 to day 42 of standard cold storage. 2,3-DPG was quanti-fied by liquid chromatography-mass spectrometry (LC-MS) with isotopically labelled internal standards, pH was measured in parallel, and trajectories were modelled by linear mixed effects with unit-level random intercepts. At day 3, 2,3-DPG spanned a twenty-fold range across units of identical age (0.8-14.7 mol/g Hb; median 4.8): some were already near-depleted at the earliest sampled timepoint, while others retained near-physiological concentrations. This heterogeneity collapsed rapidly - median val-ues fell to 27% of day-3 levels by day 7 and by more than 90% by day 14 ({beta} = -0.298 mol/g Hb per day, p < 0.001) - and were below the limit of detection in most units af-ter day 17. pH declined monotonically to 6.40 {+/-} 0.04 by day 42 ({beta} = -0.0163 units per day, p < 0.001). Units of identical storage age therefore differ markedly in the metabo-lite that governs oxygen unloading, and virtually all are depleted long before the 42-day expiry, indicating that storage-age dichotomies misclassify the exposure they are intended to represent.

biochemistry↗

Chronic IL-6 overproduction induces a tolerogenic response in aged mice after peripheral nerve injury

Highlights/Main pointsO_LIAstrocyte-targeted IL-6 overproduction during aging increases basal microglial acivation in the facial nucleus. C_LIO_LIDuring aging, chronic IL-6 overproduction does not modify microglial response after peripheral nerve injury but increases T-lymphocyte infiltration. C_LIO_LIChronic IL-6 overproduction in aged mice does not modify facial motor neuron survival after facial nerve axotomy. C_LI Interleukin-6 (IL-6) is the main cytokine controlling neuroinflammation and microglial activation during aging, and the increase of IL-6 levels correlate well with chronic neuroinflammation and age-related neurodegenerative diseases. Despite the relevance of IL-6 in these conditions, the effect of this cytokine in microglia activation and neuroinflammation upon CNS injuries during aging has been scarcely explored. Previous results from our group showed that adult and aged transgenic mice with astrocyte-targeted overproduction of IL-6 (GFAP-IL6Tg) presented features of a primed microglial phenotype in basal conditions compared to wild-type (WT) mice, and that after CNS lesions, microglia showed and exacerbated response associated with increased neuronal death in adult mice. In this work, we aimed to study whether chronic IL-6 overproduction influenced microglia response to CNS injury during aging. With this aim, we performed facial nerve axotomy (FNA) in aged 21-23-month-old WT and GFAP-IL6Tg animals, and analysed facial motor neuron (FMN) survival, glial reactivity, antigen presentation, and lymphocyte infiltration both at basal conditions (non-lesioned) and after FNA. Our results showed that non-lesioned aged transgenic mice presented higher Iba1, CD11b, and CD68 levels than aged WT mice, indicative of a priming effect in the aged facial nucleus. After FNA, we detected similar levels of microglial and astroglia activation, but a remarkable increase in T-lymphocyte infiltration in GFAP-IL6Tg axotomized group. Despite slight differences in the neuroinflammatory response, aged GFAP-IL6Tg animals showed a similar rate of FMN death compared to aged WT mice. Overall, our work shows that transgenic IL-6 overproduction induces a primed microglial phenotype under basal conditions in aged animals, with a reduced fold-increase in the microglial response after FNA compared to aged WT mice and similar lesion outcomes, suggestive of a tolerant microglial phenotype. This study suggests a tolerant effect of chronic IL-6 overproduction in microglia during aging in basal conditions and after CNS lesions.

neuroscience↗