Evidence map›Paper›PMID 19196796›Full record

ArticleEndocrinology2009

Life without thyroxine to 3,5,3'-triiodothyronine conversion: studies in mice devoid of the 5'-deiodinases.

Valerie Anne Galton, Mark J Schneider, Ann S Clark, Donald L St Germain

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 1 pooled it
10.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

85 citing papers in PubMed, 1 synthesis or guideline pooled it, 177 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Emerging Therapies in Hypothyroidism.Annual review of medicine · 2024
    Review
  9. Cross-species applicability of an adverse outcome pathway network for thyroid hormone system disruption.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Review
  10. Article
  11. Reducing uncertainties in quantitative adverse outcome pathways by analysis of thyroid hormone in the neonatal rat brain.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
  12. Thyroid Hormone Metabolism: A Historical Perspective.Thyroid : official journal of the American Thyroid Association · 2023
    Article
  13. Review
  14. The relevance of TThe lancet. Diabetes & endocrinology · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

25 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Valerie Anne GaltonDepartment of Physiology, Dartmouth Medical School, Lebanon, New Hampshire 03756, USA. val.galton@dartmouth.edu
Mark J Schneider
Ann S Clark
Donald L St Germain
Dartmouth College · US

Funding

MECHANISMS OF THYROID HORMONE ACTION IN DEVELOPMENTR01HD009020 · NICHD · DARTMOUTH COLLEGE · PI GALTON, VALERIE ANNE · 1985 to 2006
$2.5M
THE ROLE OF THE TYPE 3 DEIODINASE IN DEVELOPMENTR01DK054716 · NIDDK · DARTMOUTH COLLEGE · PI ST. GERMAIN, DONALD L. · 1999 to 2007
$2.4M
NICHD NIH HHS HD09020NICHD NIH HHS R01 HD009020NIDDK NIH HHS DK 54716NIDDK NIH HHS R01 DK054716
6 · The paper itself

Abstract

Considerable indirect evidence suggests that the type 2 deiodinase (D2) generates T(3) from T(4) for local use in specific tissues including pituitary, brown fat, and brain, whereas the type I deiodinase (D1) generates T(3) from T(4) in the thyroid and peripheral tissues primarily for export to plasma. From studies in deiodinase-deficient mice, the importance of the D2 for local T(3) generation has been confirmed. However, the phenotypes of these D1 knockout (KO) and D2KO mice are surprisingly mild and their serum T(3) level, general health, and reproductive capacity are unimpaired. To explore further the importance of 5'deiodination in thyroid hormone economy, we used a mouse devoid of both D1 and D2 activity. In general, the phenotype of the D1/D2KO mouse is the sum of the phenotypes of the D1KO and D2KO mice. It appears healthy and breeds well, and most surprisingly its serum T(3) level is normal. However, impairments in brain gene expression and possibly neurological function are somewhat greater than those seen in the D2KO mouse, and the serum rT(3) level is elevated 6-fold in the D1/D2KO mouse but only 2-fold in the D1KO mouse and not at all in the D2KO mouse. The data suggest that whereas D1 and D2 are not essential for the maintenance of the serum T(3) level, they do serve important roles in thyroid hormone homeostasis, the D2 being critical for local T(3) production and the D1 playing an important role in iodide conservation by serving as a scavenger enzyme in peripheral tissues and the thyroid.

Indexed as

AnimalsBrainHomeostasisIodide PeroxidaseIodineIodothyronine Deiodinase Type IILearningLocomotionMemoryMiceMice, Inbred C57BLMice, KnockoutRNA, MessengerThyroid GlandThyrotropinThyroxineIodide PeroxidaseIodineiodothyronine deiodinase type IIodothyronine Deiodinase Type IIRNA, MessengerThyrotropinThyroxineTriiodothyronine

Identifiers

PMID19196796
PMCPMC2689801
OpenAlexW2109458276

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.