TY - JOUR
T1 - Canagliflozin extends life span in genetically heterogeneous male but not female mice
AU - Miller, Richard A.
AU - Harrison, David E.
AU - Allison, David B.
AU - Bogue, Molly
AU - Debarba, Lucas
AU - Diaz, Vivian
AU - Fernandez, Elizabeth
AU - Galecki, Andrzej
AU - Timothy Garvey, W.
AU - Jayarathne, Hashan
AU - Kumar, Navasuja
AU - Javors, Martin A.
AU - Ladiges, Warren C.
AU - Macchiarini, Francesca
AU - Nelson, James
AU - Reifsnyder, Peter
AU - Rosenthal, Nadia A.
AU - Sadagurski, Marianna
AU - Salmon, Adam B.
AU - Smith, Daniel L.
AU - Snyder, Jessica M.
AU - Lombard, David B.
AU - Strong, Randy
N1 - Publisher Copyright:
Copyright: © 2020, Miller et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.
PY - 2020/11/5
Y1 - 2020/11/5
N2 - Canagliflozin (Cana) is an FDA-approved diabetes drug that protects against cardiovascular and kidney diseases. It also inhibits the sodium glucose transporter 2 by blocking renal reuptake and intestinal absorption of glucose. In the context of the mouse Interventions Testing Program, genetically heterogeneous mice were given chow containing Cana at 180 ppm at 7 months of age until their death. Cana extended median survival of male mice by 14%. Cana also increased by 9% the age for 90th percentile survival, with parallel effects seen at each of 3 test sites. Neither the distribution of inferred cause of death nor incidental pathology findings at end-of-life necropsies were altered by Cana. Moreover, although no life span benefits were seen in female mice, Cana led to lower fasting glucose and improved glucose tolerance in both sexes, diminishing fat mass in females only. Therefore, the life span benefit of Cana is likely to reflect blunting of peak glucose levels, because similar longevity effects are seen in male mice given acarbose, a diabetes drug that blocks glucose surges through a distinct mechanism, i.e., slowing breakdown of carbohydrate in the intestine. Interventions that control daily peak glucose levels deserve attention as possible preventive medicines to protect from a wide range of late-life neoplastic and degenerative diseases.
AB - Canagliflozin (Cana) is an FDA-approved diabetes drug that protects against cardiovascular and kidney diseases. It also inhibits the sodium glucose transporter 2 by blocking renal reuptake and intestinal absorption of glucose. In the context of the mouse Interventions Testing Program, genetically heterogeneous mice were given chow containing Cana at 180 ppm at 7 months of age until their death. Cana extended median survival of male mice by 14%. Cana also increased by 9% the age for 90th percentile survival, with parallel effects seen at each of 3 test sites. Neither the distribution of inferred cause of death nor incidental pathology findings at end-of-life necropsies were altered by Cana. Moreover, although no life span benefits were seen in female mice, Cana led to lower fasting glucose and improved glucose tolerance in both sexes, diminishing fat mass in females only. Therefore, the life span benefit of Cana is likely to reflect blunting of peak glucose levels, because similar longevity effects are seen in male mice given acarbose, a diabetes drug that blocks glucose surges through a distinct mechanism, i.e., slowing breakdown of carbohydrate in the intestine. Interventions that control daily peak glucose levels deserve attention as possible preventive medicines to protect from a wide range of late-life neoplastic and degenerative diseases.
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U2 - 10.1172/jci.insight.140019
DO - 10.1172/jci.insight.140019
M3 - Article
C2 - 32990681
AN - SCOPUS:85095774730
SN - 2379-3708
VL - 5
JO - JCI Insight
JF - JCI Insight
IS - 21
M1 - e140019
ER -