An age-dependent alteration of the respiratory exchange ratio in the db/db mouse

The leptin receptor-deficient db/db mouse is a rodent model of type 2 diabetes and obesity. Diabetes in db/db mice shows an age-dependent progression, with early insulin resistance followed by an insulin secretory defect resulting in profound hyperglycemia. However, there is insufficient data on age...

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Published inLaboratory animal research Vol. 31; no. 1; pp. 1 - 6
Main Authors Choi, H.M., KRIBB, Cheongju, Republic of Korea, Kim, H.R., KRIBB, Cheongju, Republic of Korea, Kim, E.K., KRIBB, Cheongju, Republic of Korea, Byun, Y.S., KRIBB, Cheongju, Republic of Korea, Won, Y.S., KRIBB, Cheongju, Republic of Korea, Yoon, W.K., KRIBB, Cheongju, Republic of Korea, Kim, H.C., KRIBB, Cheongju, Republic of Korea, Kang, J.G., Chungbuk National University, Cheongju, Republic of Korea, Nam, K.H., KRIBB, Cheongju, Republic of Korea
Format Journal Article
LanguageEnglish
Published England Korean Association for Laboratory Animal Science 01.03.2015
한국실험동물학회
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Summary:The leptin receptor-deficient db/db mouse is a rodent model of type 2 diabetes and obesity. Diabetes in db/db mice shows an age-dependent progression, with early insulin resistance followed by an insulin secretory defect resulting in profound hyperglycemia. However, there is insufficient data on agedependent changes of energy metabolism in db/db mice. We demonstrated an age-dependent decrease in the respiratory exchange ratio (RER), calculated by a ratio of VO2/VCO2, in db/db mice. The RER determined by indirect calorimetry, was 1.03 in db/db mice under 6 weeks of age, which were similar to those in heterozygote (db/+) and wild-type (+/+) mice. However, RER decreased from approximately 0.9 to 0.8 by 10 weeks of age and subsequently returned to approximately 0.9 at 22 weeks of age. The changes in RER were concurrent with the alterations in body weight and blood glucose level. However, other metabolic indicators such as glucose tolerance, changes in body fat mass, and urinary glucose levels, did not change with age. The results suggested that the energy source utilized in db/db mice changed with the age-related progression of diabetes.
Bibliography:L50
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
G704-001509.2015.31.1.004
ISSN:1738-6055
2233-7660
DOI:10.5625/lar.2015.31.1.1