Abstract

Aims: Iodine is critical for synthesis of thyroid hormones (TH). And iodine deficiency (ID) is one of the most significant reasons of intellectual disability and motor memory impairment, although the potential mechanisms are still under investigation. Presently, mild ID and marginal ID are largely ignored problems for women of child bearing age. Mild ID is a subtle form of TH deficiency, which shows low levels of free thyroxine (FT4) and relatively normal free triiodothyronine (FT3) or thyroid stimulation hormone (TSH). And marginal ID is a milder form of ID with decreased total T4 (TT4) but relatively normal FT3, FT4, and TSH. Therefore, we investigated the effects of maternal different degrees of ID on the development of pinceau in cerebellar purkinje cells (PCs) and studied the expression of pinceau related protein, which is crucial for the development and maturation of pinceau.Methods and Results: Three developmental iodine deficient rat models were created by feeding dam rats with an iodine-deficient diet and deionized water supplemented with potassiumiodide. Our study showed that different degrees of ID inhibited cerebellar pinceau synapse development and maturation on postnatal day (PN) 14 and PN21. What's more, mild and severe ID reduced the expression of AnkG, β4-spectrin, neurofascin186 and NrCAM on PN7, PN14, and PN21. However, marginal ID rarely altered expression of these proteins in the offspring.Conclusion: These results suggested that maternal mild and severe ID impaired the development and maturation of cerebellar pinceau, which may be attributed to the decrease of AnkG, β4-spectrin, neurofascin 186, and NrCAM. And the alteration of development and maturation in cerebellar pinceau in the offspring were also observed following maternal marginal ID, which is slighter than that of mild ID.

Highlights

  • Monitoring data have indicated that a large percentage of women during pregnancy and lactation have urinary iodine concentrations (UIC) of 100–150 μg/l in the developing country, which is slightly lower than the WHO criteria for sufficient iodine supply (World Health Organization/UNICEF/ICCIDD, 2007; Ferreir et al, 2014; Méndez-Villa et al, 2014)

  • The pinceau labeled by GAD65+ Calbindin+ or neurofascin 186 (NF186)+ Calbindin+ was observed in cerebellar purkinje cells (PCs)

  • Compared with the control group, the mean intensity of GAD65 and NF186 positive staining in treated group were found to be significantly reduced on PN14 (Figures 1B, 3B; p < 0.05) and PN21 (Figures 2B, 4B; p < 0.05)

Read more

Summary

Introduction

Iodine is drawn into the thyroid and combined the tyrosyl residues of thyroprotein to form triiodothyronine (T3) and thyroxine (T4) It is well-known that iodine deficiency (ID) can lead. Hypothyroxinemia shows low levels of free thyroxine (FT4) and relatively normal free triiodothyronine (FT3) or thyroid stimulation hormone (TSH), which is a subtle form of TH deficiency. Marginal ID is milder than mild ID, which shows decreased total T4 (TT4) but relatively normal circulating levels of FT3, FT4, and TSH (Versloot et al, 1998) This is alarming given that it is necessary to pay more attention to the effect of the mild thyroid hormone change on the neurodevelopment of the offspring

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call