| Literature DB >> 26362394 |
Seyedeh Masoumeh Seyedhoseini Tamijani1, Benyamin Karimi2, Elham Amini2, Mojtaba Golpich2, Leila Dargahi3, Raymond Azman Ali2, Norlinah Mohamed Ibrahim2, Zahurin Mohamed4, Rasoul Ghasemi5, Abolhassan Ahmadiani6.
Abstract
Thyroid hormones (THs) L-thyroxine and L-triiodothyronine, primarily known as metabolism regulators, are tyrosine-derived hormones produced by the thyroid gland. They play an essential role in normal central nervous system development and physiological function. By binding to nuclear receptors and modulating gene expression, THs influence neuronal migration, differentiation, myelination, synaptogenesis and neurogenesis in developing and adult brains. Any uncorrected THs supply deficiency in early life may result in irreversible neurological and motor deficits. The development and function of GABAergic neurons as well as glutamatergic transmission are also affected by THs. Though the underlying molecular mechanisms still remain unknown, the effects of THs on inhibitory and excitatory neurons may affect brain seizure activity. The enduring predisposition of the brain to generate epileptic seizures leads to a complex chronic brain disorder known as epilepsy. Pathologically, epilepsy may be accompanied by mitochondrial dysfunction, oxidative stress and eventually dysregulation of excitatory glutamatergic and inhibitory GABAergic neurotransmission. Based on the latest evidence on the association between THs and epilepsy, we hypothesize that THs abnormalities may contribute to the pathogenesis of epilepsy. We also review gender differences and the presumed underlying mechanisms through which TH abnormalities may affect epilepsy here.Entities:
Keywords: Brain development; Epileptogenesis; Hyperthyroidism; Hypothyroidism; Seizures; Temporal lobe epilepsy (TLE)
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Year: 2015 PMID: 26362394 DOI: 10.1016/j.seizure.2015.07.021
Source DB: PubMed Journal: Seizure ISSN: 1059-1311 Impact factor: 3.184