Astiz Lab

Laboratory of Circadian Physiology | Achucarro Basque Center for Neuroscience

Rodent Models for the Analysis of Tissue Clock Function in Metabolic Rhythms Research


Journal article


A. H. Tsang, M. Astiz, Brinja Leinweber, H. Oster
Frontiers in Endocrinology, 2017

Semantic Scholar DOI PubMedCentral PubMed
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APA   Click to copy
Tsang, A. H., Astiz, M., Leinweber, B., & Oster, H. (2017). Rodent Models for the Analysis of Tissue Clock Function in Metabolic Rhythms Research. Frontiers in Endocrinology.


Chicago/Turabian   Click to copy
Tsang, A. H., M. Astiz, Brinja Leinweber, and H. Oster. “Rodent Models for the Analysis of Tissue Clock Function in Metabolic Rhythms Research.” Frontiers in Endocrinology (2017).


MLA   Click to copy
Tsang, A. H., et al. “Rodent Models for the Analysis of Tissue Clock Function in Metabolic Rhythms Research.” Frontiers in Endocrinology, 2017.


BibTeX   Click to copy

@article{a2017a,
  title = {Rodent Models for the Analysis of Tissue Clock Function in Metabolic Rhythms Research},
  year = {2017},
  journal = {Frontiers in Endocrinology},
  author = {Tsang, A. H. and Astiz, M. and Leinweber, Brinja and Oster, H.}
}

Abstract

The circadian timing system consists on a distributed network of cellular clocks that together coordinate 24-h rhythms of physiology and behavior. Clock function and metabolism are tightly coupled, from the cellular to the organismal level. Genetic and non-genetic approaches in rodents have been employed to study circadian clock function in the living organism. Due to the ubiquitous expression of clock genes and the intricate interaction between the circadian system and energy metabolism, genetic approaches targeting specific tissue clocks have been used to assess their contribution in systemic metabolic processes. However, special requirements regarding specificity and efficiency have to be met to allow for valid conclusions from such studies. In this review, we provide a brief summary of different approaches developed for dissecting tissue clock function in the metabolic context in rodents, compare their strengths and weaknesses, and suggest new strategies in assessing tissue clock output and the consequences of circadian clock disruption in vivo.





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