Publications by authors named "Raghava Jagadeesh Salaka"

NMDA-type glutamate receptors (NMDARs) are widely recognized as master regulators of synaptic plasticity, most notably for driving long-term changes in synapse size and strength that support learning. NMDARs are unique among neurotransmitter receptors in that they require binding of both neurotransmitter (glutamate) and co-agonist (e.g.

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Unlabelled: NMDA-type glutamate receptors (NMDARs) are widely recognized as master regulators of synaptic plasticity, most notably for driving long-term changes in synapse size and strength that support learning. NMDARs are unique among neurotransmitter receptors in that they require binding of both neurotransmitter (glutamate) and co-agonist (e.g.

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Article Synopsis
  • Temporal lobe epilepsy (TLE) is the most prevalent focal epilepsy and is primarily managed with anti-seizure drugs (ASDs), such as levetiracetam (LEV), which target the SV2A protein.
  • Despite extensive research on LEV's effects in acute epilepsy models, its impact on chronic epilepsy regarding neuronal excitability, synaptic plasticity, neurogenesis, and histological changes remains understudied.
  • In a study of epileptic rats, LEV treatment improved synaptic transmission and structural changes in hippocampal regions but did not reverse all aspects of abnormal neurogenesis, sprouting, or anxiety-like behavior caused by chronic epilepsy.
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Sleep dysfunctions in epilepsy increase the burden of seizures and cognitive impairments. Seizures and certain anti-seizure drugs (ASDs) can affect sleep quality, leading to excessive daytime sleepiness and poor cognitive performance. Therefore, it is imperative to develop non-pharmacological strategies to curb epilepsy and related sleep dysfunction.

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Temporal lobe epilepsy (TLE) is the most common form of focal epilepsies. Pharmacoresistance and comorbidities pose significant challenges to its treatment necessitating the development of non-pharmacological approaches. In an earlier study, exposure to enriched environment (EE) reduced seizure frequency and duration and ameliorated chronic epilepsy-induced depression in rats.

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