Abstract

Ansell's mole-rats (Fukomys anselli) are subterranean, long-lived rodents, which live in eusocial families, where the maximum lifespan of breeders is twice as long as that of non-breeders. Their metabolic rate is significantly lower than expected based on allometry, and their retinae show a high density of S-cone opsins. Both features may indicate naturally low thyroid hormone levels. In the present study, we sequenced several major components of the thyroid hormone pathways and analyzed free and total thyroxine and triiodothyronine in serum samples of breeding and non-breeding F. anselli to examine whether a) their thyroid hormone system shows any peculiarities on the genetic level, b) these animals have lower hormone levels compared to euthyroid rodents (rats and guinea pigs), and c) reproductive status, lifespan and free hormone levels are correlated. Genetic analyses confirmed that Ansell's mole-rats have a conserved thyroid hormone system as known from other mammalian species. Interspecific comparisons revealed that free thyroxine levels of F. anselli were about ten times lower than of guinea pigs and rats, whereas the free triiodothyronine levels, the main biologically active form, did not differ significantly amongst species. The resulting fT4:fT3 ratio is unusual for a mammal and potentially represents a case of natural hypothyroxinemia. Comparisons with total thyroxine levels suggest that mole-rats seem to possess two distinct mechanisms that work hand in hand to downregulate fT4 levels reliably. We could not find any correlation between free hormone levels and reproductive status, gender or weight. Free thyroxine may slightly increase with age, based on sub-significant evidence. Hence, thyroid hormones do not seem to explain the different ageing rates of breeders and non-breeders. Further research is required to investigate the regulatory mechanisms responsible for the unusual proportion of free thyroxine and free triiodothyronine.

Highlights

  • Most ageing theories assume a link between metabolism and ageing because of several inevitable side effects of metabolic processes that potentially impair somatic integrity in the long term

  • The aim of our study was to characterize the Thyroid hormones (THs) system of Ansell’s mole-rats and to determine T4 and T3 levels in this species to investigate if these animals are hypothyroid, and if their hormone concentrations correlate with their extraordinary lifespan and the bimodal ageing pattern of reproductive and nonreproductive animals

  • In F. anselli, the major molecular constituents of the mammalian TH system could be identified via their mRNAs, namely TG, TPO, TSHB, D1, D2, TTR, MCT8, TBG and natrium/ iodide symporter (NIS)

Read more

Summary

Introduction

Most ageing theories assume a link between metabolism and ageing because of several inevitable side effects of metabolic processes that potentially impair somatic integrity in the long term. Examples of such side effects are the production of reactive oxygen species [1,2], formation of advanced glycation end products [3,4,5], and telomere shortening with every cell proliferation cycle [6]. Ames dwarf mice and Snell dwarf mice, which have extraordinary low levels of THs, and other hormones related to growth and development (e.g., somatropin, insulin-like growth factor 1), live significantly longer than wild type mice [11]. There is a significant correlation between low TH metabolism and longevity [7,18]

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

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

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.