TY - JOUR
T1 - Tryptophan metabolism is differently regulated between large and small dogs
AU - Hoffman, Jessica M.
AU - Kiklevich, J. Veronika
AU - Austad, Marika
AU - Tran, Vi Linh
AU - Jones, Dean P.
AU - Royal, Angela
AU - Henry, Carolyn
AU - Austad, Steven N.
N1 - Funding Information:
This work was funded by a Glenn/AFAR Postdoctoral Fellowship to JMH and NIH/NIA AG050886 and an award from the Glenn Foundation for Medical Research to SNA
Funding Information:
First and foremost, we would like to thank all the dogs that were sampled during the course of this study and their owners for permitting sampling. We would also like to thank Andrew Brown for insights on the statistical analyses in this manuscript.
Publisher Copyright:
© 2019, The Author(s).
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Companion dogs have recently been promoted as an animal model for the study of aging due to their similar disease profile to humans, the sophistication of health assessment and disease diagnosis, and the shared environments with their owners. In addition, dogs show an interesting life history trait pattern where smaller individuals are up to two-fold longer lived than their larger counterparts. While some of the mechanisms underlying this size and longevity trade-off are strongly suspected (i.e., growth hormone/IGF-I), there are likely a number of undiscovered mechanisms as well. Accordingly, we have completed a large-scale global metabolomic profiling of dogs encompassing a range of sizes and ages from three cities across the USA. We found a surprisingly strong location signal in the metabolome, stronger in fact than any signal related to age, breed, or sex. However, after controlling for the effects of location, tryptophan metabolism emerged as significantly associated with weight of the dogs, with small dogs having significantly higher levels of tryptophan pathway metabolites. Overall, our results point toward novel, testable hypotheses about the underlying physiological mechanisms that influence size and longevity in the companion dog and suggest that dogs may be useful in sorting out the complexities of the tryptophan metabolic network.
AB - Companion dogs have recently been promoted as an animal model for the study of aging due to their similar disease profile to humans, the sophistication of health assessment and disease diagnosis, and the shared environments with their owners. In addition, dogs show an interesting life history trait pattern where smaller individuals are up to two-fold longer lived than their larger counterparts. While some of the mechanisms underlying this size and longevity trade-off are strongly suspected (i.e., growth hormone/IGF-I), there are likely a number of undiscovered mechanisms as well. Accordingly, we have completed a large-scale global metabolomic profiling of dogs encompassing a range of sizes and ages from three cities across the USA. We found a surprisingly strong location signal in the metabolome, stronger in fact than any signal related to age, breed, or sex. However, after controlling for the effects of location, tryptophan metabolism emerged as significantly associated with weight of the dogs, with small dogs having significantly higher levels of tryptophan pathway metabolites. Overall, our results point toward novel, testable hypotheses about the underlying physiological mechanisms that influence size and longevity in the companion dog and suggest that dogs may be useful in sorting out the complexities of the tryptophan metabolic network.
KW - Body size
KW - Dog
KW - Metabolomics
KW - Tryptophan metabolism
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U2 - 10.1007/s11357-019-00114-x
DO - 10.1007/s11357-019-00114-x
M3 - Article
C2 - 31784886
AN - SCOPUS:85075881235
SN - 2509-2715
VL - 42
SP - 881
EP - 896
JO - GeroScience
JF - GeroScience
IS - 3
ER -