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Biology subjects

Farina, N.

Publications and source records attributed to Farina, N..

2 recordsLinked to original sources

Alternative strategies of orthographic processing: the case of skilled deaf readers

The cognitive factors that enable us to be proficient readers can greatly vary across individuals. The case of skilled deaf readers is emblematic as it shows that high reading performances can be achieved even when lifelong acoustic experience is absent or minimal. Here we present a set of experiments investigating how alternative strategies of orthographic processing can lead to high levels of reading proficiency. Four EEG studies compared behavioral and brain correlates of orthographic processing in skilled deaf readers and matched hearing controls. Using single word recognition and priming paradigms, we investigated two pillars of orthographic processing: letter identity and letter position. Our findings show that, although both groups had similarly accurate reading performance, skilled deaf readers were faster, and they consistently differ from hearing controls in the way they process letter identity. This group difference was observed in both lexical and sublexical tasks and was specifically related to the identity of orthographic representations, regardless of the visual form of the written stimuli (such as character visual similarity and letter case). These findings uncover alternative strategies that make possible high reading performance, even in the absence of acoustic experience. Public Significance StatementThis research identifies alternative orthographic strategies that improve single-word reading efficiency and can potentially serve as effective compensatory tools when phonological processing is impaired.

neuroscience↗

Sustained morphine delivery suppresses bone formation and alters metabolic and circulating miRNA profiles in male C57BL/6J mice

Opioid use is detrimental to bone health, causing both indirect and direct effects on bone turnover. While the mechanisms of these effects are not entirely clear, recent studies have linked chronic opioid use to alterations in circulating miRNAs. Our aim was to develop a model of opioid-induced bone loss to understand bone turnover and identify candidate miRNA-mediated regulatory mechanisms. We evaluated the effects of sustained morphine treatment on the skeleton, metabolism, and body composition of male and female C57BL/6J mice by treating with vehicle (0.9% saline) or morphine (18 mg/kg) using subcutaneous osmotic minipumps for 25 days. Morphine-treated mice had higher energy expenditure and respiratory quotient, indicating a shift toward carbohydrate metabolism. Microcomputed tomography ({micro}CT) analysis indicated that male mice treated with morphine had reduced trabecular bone volume fraction (Tb.BV/TV) (15%) and Tb. bone mineral density (BMD) (14%) in the distal femur compared to vehicle. Conversely, bone microarchitecture was not changed in females after morphine treatment. Histomorphometric analysis demonstrated that in males, morphine reduced bone formation rate compared to vehicle, but osteoclast parameters were not different. Furthermore, morphine reduced bone formation marker gene expression in the tibia of males (Bglap and Dmp1). Circulating miRNA profile changes were evident in males, with 14 differentially expressed miRNAs associated with morphine treatment. Target analysis indicated hypoxia inducible factor (HIF) signaling pathway was targeted by miR-223-3p and fatty acid metabolism by miR-484, - 223-3p, and -328-3p. In summary, we have established a model where morphine leads to a lower trabecular bone formation in males. Further, understanding the mechanisms of bone loss from opioid treatment will be important for improving management of the adverse effects of opioids on the skeleton.

physiology↗