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Disease models & mechanisms, 2010-03, Vol.3 (3-4), p.156-166
2010

Details

Autor(en) / Beteiligte
Titel
Mouse models of the metabolic syndrome
Ist Teil von
  • Disease models & mechanisms, 2010-03, Vol.3 (3-4), p.156-166
Ort / Verlag
England: The Company of Biologists Limited
Erscheinungsjahr
2010
Link zum Volltext
Quelle
EZB Free E-Journals
Beschreibungen/Notizen
  • The metabolic syndrome (MetS) is characterized by obesity concomitant with other metabolic abnormalities such as hypertriglyceridemia, reduced high-density lipoprotein levels, elevated blood pressure and raised fasting glucose levels. The precise definition of MetS, the relationships of its metabolic features, and what initiates it, are debated. However, obesity is on the rise worldwide, and its association with these metabolic symptoms increases the risk for diabetes and cardiovascular disease (among many other diseases). Research needs to determine the mechanisms by which obesity and MetS increase the risk of disease. In light of this growing epidemic, it is imperative to develop animal models of MetS. These models will help determine the pathophysiological basis for MetS and how MetS increases the risk for other diseases. Among the various animal models available to study MetS, mice are the most commonly used for several reasons. First, there are several spontaneously occurring obese mouse strains that have been used for decades and that are very well characterized. Second, high-fat feeding studies require only months to induce MetS. Third, it is relatively easy to study the effects of single genes by developing transgenic or gene knockouts to determine the influence of a gene on MetS. For these reasons, this review will focus on the benefits and caveats of the most common mouse models of MetS. It is our hope that the reader will be able to use this review as a guide for the selection of mouse models for their own studies.
Sprache
Englisch
Identifikatoren
ISSN: 1754-8403
eISSN: 1754-8411
DOI: 10.1242/dmm.003467
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2869491

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