To the extent possible under law, AOP-Wiki has waived all copyright and related or neighboring rights to KER:1505
TH synthesis, Decreased leads to GABAergic interneurons, Decreased
Key Event Relationship Overview
AOPs Referencing Relationship
|AOP Name||Adjacency||Weight of Evidence||Quantitative Understanding||Point of Contact||Author Status||OECD Status|
|Inhibition of Na+/I- symporter (NIS) leads to learning and memory impairment||non-adjacent||Low||Low||Arthur Author (send email)||Open for citation & comment||WPHA/WNT Endorsed|
Life Stage Applicability
|During brain development||Moderate|
Key Event Relationship Description
Thyroid hormone synthesis is responsible for physiological TH serum levels that subsequently correlate with TH brain concentrations. It has been shown that TH regulates function of different neuronal subtypes, including GABAergic neurons. TH increases glutamic acid decarboxylase (GAD) activity (responsible for GABA-synthesis) in neonatal brain, and GABA transaminase (responsible for GABA degradation) activity (Shulga and Rivera, 2013). GABAergic interneurons are remarkably diverse and complex in nature and they are believed to play a key role in numerous neurodevelopmental processes (Southwell et al., 2014). During the early cortical network development TH has been shown to regulate the morphology and function of the GABAergic neurons (Westerholz et al., 2010). It is well documented that decreased TH synthesis triggered by TPO and NIS inhibitors affects survival of GABAergic interneurons, as well as their morphology and function.
Evidence Collection Strategy
Evidence Supporting this KER
TH levels influence the development of cortical GABAergic circuits (Friauf et al., 2008; Westerholz et al., 2010). In hypothyroid rats the expression of parvalbumin, the marker of a subpopulation of GABAergic neurons, is reduced (Gilbert et al., 2007). TH increase glutamic acid decarboxylase (GAD, GABA-synthesizing enzyme) activity in neonatal brain. Also GABA transaminase (GABA-T, GABA-degrading enzyme) activity appears to be increased by TH. Therefore, both GABA synthesis and degradation are increased by TH. This might reflect either the specific regulation of GABA levels, or general regulation of gene expression maintenance by TH, as commented by Shulga and Rivera, 2013. This strongly supports the link between the two KEs described in this indirect KER (decrease of TH synthesis leads to GABAergic interneuron decrease). It was also shown that low concentrations of T3 increase by non-genomic mechanism the depolarization-dependent release of GABA. GABA appears to provide negative feedback to thyroid endocrine axis, as TSH release is inhibited by GABA (Wiens and Trudeau, 2006).
Uncertainties and Inconsistencies
While some in vivo studies (Sawano et al., 2013; Shiraki et al., 2012) have shown a decrease of GABAergic cell populations upon induction of hypothyroidism, Saegusa and co-workers (Saegusa et al., 2010) reported about an increase of GABAergic interneurons. In Saegusa's study, rat dams were treated with either PTU or MMI in the drinking water, and male offspring were immunohistochemically examined on PND 20 and at the adult stage (i.e., 11-week-old). MMI and PTU caused in the offspring growth retardation, lasting into the adult stage. All exposure groups showed a sustained increase of GAD67+ cells in the adult stage, indicating an increase in GABAergic interneurons.
It should be noticed that in Saegusa et al., 2010 in vivo study, increase of GAD67+ cells was mainly observed in the adult stage (11-week-old rats) and analysis of GABAergic interneurons. PV+ cells, which appear to be the GABAergic population most affected by TH dysregulation, was not evaluated. On the opposite, Sawano's and Shiraki's in vivo studies reported a decrease of GABAergic PV+ neurons at earlier stages, respectively on PND 15 and 21 induced by hypothyroidism (Sawano et al., 2013; Shiraki et al., 2012). Discrepancies in results are due to the fact that THs have effects on multiple components of the GABA system. For instance, in the developing brain, hypothyroidism generally decreases enzyme activities and GABA levels, whereas in adult brain, hypothyroidism generally increases enzyme activities and GABA levels.
There are also conflicting results on effects of long term changes in TH levels on GABA reuptake. Therefore, results variability from study to study is due to different experimental study designs, accounting for differences in brain development stages (PND vs adult), times of exposures to chemicals, and regional brain differences (Wiens and Trudeau, 2006).
Known modulating factors
Known Feedforward/Feedback loops influencing this KER
Domain of Applicability
Empirical evidence comes from work with laboratory rodents (rats and mice).
Aguado F, Carmona MA, Pozas E, Aguiló A, Martínez-Guijarro FJ, Alcantara S, Borrell V, Yuste R, Ibañez CF, SorianoE. (2003). BDNF regulates spontaneous correlated activity at early developmental stages by increasing synaptogenesis and expression of the K+/Cl–co-transporter KCC2. Development 130:1267-1280.
Blaesse P, Airaksinen MS, Rivera C, Kaila K. (2009). Cation chloride co-transporters and neuronal function. Neuron 61:820–838
Friauf E, Wenz M, Oberhofer M, Nothwang HG, Balakrishnan V, Knipper M, Lohrke S. (2008). Hypothyroidism impairs chloride homeostasis and onset of inhibitory neurotransmission in developing auditory brainstem and hippocampal neurons. Eur J Neurosci, 28, pp. 2371–2380
Gilbert ME, Sui L, Walker MJ, Anderson W, Thomas S, Smoller SN, Schon JP, Phani S, Goodman JH. (2007). Thyroid hormone insufficiency during brain development reduces parvalbumin immunoreactivity and inhibitory function in the hippocampus. Endocrinology. Jan;148(1):92-102.
Madeira MD, Cadete-Leite A, Andrade JP, Paula-Barbosa MM. (1991). Effects of hypothyroidism upon the granular layer of the dentate gyrus in male and female adult rats: a morphometric study. J Comp Neurol 314:171-186.
Rami A, Patel AJ, Rabie A. (1986a). Thyroid hormone and development of the rat hippocampus: morphological alterations in granule and pyramidal cells. Neuroscience 19:1217-1226.
Rami A, Rabie A, Patel AJ. (1986b). Thyroid hormone and development of the rat hippocampus: cell acquisition in the dentate gyrus. Neuroscience 19:1207-1216.
Rami A, Rabie A. (1990). Delayed synaptogenesis in the dentate gyrus of the thyroid-deficient developing rat. Dev Neurosci 12:398-405.
Rivera, C., Li, H., Thomas-Crusells, J., Lahtinen, H., Vilkman, V., Nanobashvili, A., Kokaia, Z., Airaksinen, M.S., Voipio, J., Kaila, K. & Saarma, M. (2002). BDNF-induced TrkB activation down-regulates the K+–Cl− cotransporter KCC2 and impairs neuronal Cl− extrusion. J. Cell Biol., 159, 747–752.
Rivera, C., Voipio, J., Thomas-Crusells, J., Li, H., Emri, Z., Sipilä, S., Payne, J.A., Minichiello, L., Saarma, M. & Kaila, K. (2004). Mechanism of activity-dependent downregulation of the neuron-specific K-Cl cotransporter KCC2. J. Neurosci., 24, 4683–4691.
Sawano E, Takahashi M, Negishi T, Tashiro T. (2013). Thyroid hormone-dependent development of the GABAergic pre- and post-synaptic components in the rat hippocampus. Int J Dev Neurosci. Dec;31(8):751-61.
Shiraki A, Akane H, Ohishi T, Wang L, Morita R, Suzuki K, Mitsumori K, Shibutani M. (2012). Similar distribution changes of GABAergic interneuron subpopulations in contrast to the different impact on neurogenesis between developmental and adult-stage hypothyroidism in the hippocampal dentate gyrus in rats. Arch Toxicol. Oct;86(10):1559-69.
Shulga A, Rivera C. (2013). Interplay between thyroxin, BDNF and GABA in injured neurons. Neuroscience. Jun 3;239:241-52.
Southwell DG, Nicholas CR, Basbaum AI, Stryker MP, Kriegstein AR, Rubenstein JL, Alvarez-Buylla A. (2014). Interneurons from embryonic development to cell-based therapy. Science. 44:1240622.
Wake, H., Watanabe, M., Moorhouse, A.J., Kanematsu, T., Horibe, S., Matsukawa, N., Asai, K., Ojika, K., Hirata, M. & Nabekura, J. (2007). Early changes in KCC2 phosphorylation in response to neuronal stress result in functional downregulation. J. Neurosci., 27, 1642–1650.
Westerholz S, de Lima AD, Voigt T. (2010). Regulation of early spontaneous network activity and GABAergic neurons development by thyroid hormone. Neuroscience 168:573-589.
Westerholz S, de Lima AD, Voigt T. (2013). Thyroid hormone-dependent development of early cortical networks: temporal specificity and the contribution of trkB and mTOR pathways. Front Cell Neurosci 7:121.
Wiens SC, Trudeau VL. (2006). Thyroid hormone and gamma-aminobutyric acid (GABA) interactions in neuroendocrine systems. Comp Biochem Physiol A Mol Integr Physiol. Jul;144(3):332-44. Epub 2006 Mar 9.