Publications by authors named "Kala P Nair"

Chronic diabetic conditions have been associated with certain cerebral complications, that include neurobehavioral dysfunctional patterns and morphological alterations of neurons, especially the hippocampus. Neuroanatomical studies done by the authors have shown decreased total dendritic length, intersections, dendritic length per branch order and nodes in the CA1 hippocampal region of the diabetic brain as compared to its normal control group, indicating reduced dendritic arborization of the hippocampal CA1 neurons. Epigenetic alterations in the brain are well known to affect age-associated disorders, however its association with the evolving diabetes-induced damage in the brain is still not fully understood.

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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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Objective: Neurosteroids are known to exert diverse functions in the brain. 5α-reductase (5α-R), a rate-limiting enzyme involved in the biosynthesis of neurosteroids is inhibited by finasteride. Clinical studies suggest that administration of finasteride causes the emergence of affective symptoms and cognitive dysfunction.

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