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Biology subjects

Hashmi, M. A.

Publications and source records attributed to Hashmi, M. A..

2 recordsLinked to original sources

Pain-regulation circuitry as a predictor of chronic pain phenotypes

Chronic pain involves sensory, emotional, and functional disruption, yet diagnostic labels rarely capture this variability, limiting individualized care. Multidimensional models, such as fear-avoidance and predictive coding, suggest that high emotional burden may disrupt expectation-based pain modulation and midbrain pain regulatory pathways, particularly within the periaqueductal gray (PAG). We tested whether chronic pain phenotypes defined by pain intensity, disability, and affective distress (PDA) differ in expectation-induced pain modulation, PAG connectivity, and behavioral markers including catastrophizing, hypervigilance, and medication use, and whether these features aid phenotype classification. We studied 159 patients with fibromyalgia or chronic low back pain and 72 controls. Our data-driven clustering approach identified high and low PDA groups. High PDA patients showed impaired modulation when positive expectations were violated and reported greater cognitive and behavioral burden (P<0.05). They also exhibited more negative connectivity between the dorsolateral/lateral PAG (dl/lPAG) and the dorsomedial prefrontal cortex (dmPFC) (corrected). Machine learning models classified PDA subtypes above chance, with accuracy improving when PAG connectivity was included. Findings highlight disrupted expectation-driven regulation and altered PAG pathways as markers for chronic pain stratification.

neuroscience↗

PROTEOMICS OF HYPOTHERMIC ADAPTATION REVEALS THAT RBM3 ENHANCES MITOCHONDRIAL METABOLISM AND MUSCLE STEM-CELL DIFFERENTIATION

Adaptation to hypothermic stress is important for skeletal muscle cells, but a comprehensive knowledge of molecular mediators is lacking. We show that adaptation to mild hypothermia (320C) improves the ability of skeletal muscle myoblasts to differentiate into myotubes in vitro. We performed proteomic analysis of mouse myoblasts exposed to mild hypothermia for various time points and identified dynamic changes in mitochondrial metabolism and proteostasis. This revealed that RBM3, an RNA-binding protein, increases progressively with acute and chronic exposure to hypothermic stress, and is necessary for the enhanced differentiation upon hypothermic adaptation. We also demonstrate that overexpression of RBM3 at physiological temperatures is sufficient to (i) enhance mitochondrial metabolism as judged by a decrease in the AMPK energy-sensing pathway, (ii) increase levels of proteins associated with translation and increase levels of 4E-BP1 phosphorylation, (iii) increase stem cell markers (MyoD1, PAX7), and improve differentiation of myoblasts from both young and aged mice.

biochemistry↗