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Nataraj, A.

Publications and source records attributed to Nataraj, A..

2 recordsLinked to original sources

Spatial learning-specific remodeling of the hippocampal palmitoylome

Protein S-palmitoylation is a reversible lipid modification that regulates protein trafficking, membrane association, and synaptic signaling, yet its role in learning-induced neuronal plasticity remains incompletely understood. Here, we investigated how spatial learning remodels the hippocampal palmitoylome in rats trained in the Morris water maze using short-term (STT; one session, 15 trials; probe at 1 h) or long-term (LTT; four sessions over four days; probe at 24 h) paradigms. Palmitoylated proteins were profiled by acyl-biotin exchange coupled with tandem mass tag labeling and LC-MS/MS. We identified 5,260 proteins, including 763 palmitoylated species. Spatial learning induced extensive remodeling of protein S-palmitoylation, with markedly greater changes after STT than LTT. Using yoked controls, we distinguished palmitoylation changes associated with learning the hidden platform location from those induced by general behavioral experience. Comparison of trained and yoked animals identified 186 and 62 differentially palmitoylated proteins after STT and LTT, respectively, whereas yoked animals also exhibited extensive changes relative to naive controls, demonstrating that behavioral experience alone substantially reshapes the hippocampal palmitoylome. Functional enrichment revealed that STT preferentially engaged pathways related to synaptic transmission, cytoskeletal remodeling, GTPase signaling, and cellular metabolism, whereas LTT was associated with protein translation and synaptic organization. Site-specific analysis identified numerous previously unreported palmitoylation sites. Hierarchical analysis further identified diacylglycerol lipase- (DAGLA) as the only protein whose palmitoylation consistently reflected both general Morris water maze experience and learning the hidden platform location across both paradigms. Together, these findings establish S-palmitoylation as a dynamic regulator of experience-dependent hippocampal plasticity.

neuroscience↗

LPS-induced sepsis disrupts brain activity in a region- and vigilance-state specific manner

Sepsis-associated encephalopathy (SAE) is a common complication of sepsis and the systemic inflammatory response syndrome that leads to lasting consequences in survivors. It manifests as early EEG changes, that are region-, time- and state-specific, possibly reflecting distinct mechanisms of injury. Here, we investigated the effects of 5mg/kg lipopolysaccharide (LPS) on hippocampal and cortical sleep-wake states, oscillatory and non-oscillatory neuronal activity, as well as on within and between state dynamics using state-space analysis. LPS induced rapid-onset severe temporal and spatial vigilance state fragmentation, which preceded all other spectral changes by [~]90 minutes. Thereafter, LPS led to specific destabilization and increased delta oscillatory activity in wakefulness, but not NREM sleep, although state transitions remained largely normal. Instead, reduced NREM delta power resulted from aperiodic spectrum changes. LPS specifically reduced higher frequency hippocampal gamma oscillations (60-80Hz peak) in wakefulness, but not cortical high gamma or lower frequency gamma oscillations. These results suggest that disruption of sleep-wake patterns could serve as an early indicator of sepsis and associated encephalopathy, independent of spectral changes. Moreover, treatment aimed at stabilizing vigilance states in early stages of sepsis might prove to be a novel option preventing the development of further pathological neurophysiology, as well as limiting inflammation-related brain damage.

neuroscience↗