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Lifespan effects in male UM-HET3 mice treated with sodium thiosulfate, 16-hydroxyestriol, and late-start canagliflozin
by
Salmon, Adam B.
, Strong, Randy
, Ginsburg, Brett C.
, Korstanje, Ron
, Garratt, Michael
, Mitchell, James R.
, Lopez-Cruzan, Marisa
, Dehghan, Ishmael
, Milne, Ginger
, Harrison, David E.
, Geisler, John G.
, Han, Melissa L.
, Leiser, Scott F.
, Nelson, James F.
, Kaczorowski, Catherine C.
, Rosenthal, Nadia
, Kumar, Navasuja
, Fernandez, Elizabeth
, Miller, Richard A.
, Reifsnyder, Peter C.
, Cortopassi, Gino A.
in
2,4-Dinitrophenol
/ Age
/ Aging
/ Animals
/ Antidiabetics
/ Biomedical and Life Sciences
/ Blood levels
/ Canagliflozin - pharmacology
/ Cell Biology
/ Drug dosages
/ Drugs
/ Expressed sequence tags
/ Female
/ Females
/ Genetics
/ Geriatrics/Gerontology
/ Hydrogen sulfide
/ Ketoglutaric acid
/ Life Sciences
/ Life span
/ Longevity - drug effects
/ Male
/ Males
/ Mice
/ Molecular Medicine
/ Original
/ Original Article
/ Oxidation
/ Proteins
/ Sex Factors
/ Sexes
/ Sexual dimorphism
/ Sodium
/ Sodium thiosulfate
/ Sodium-Glucose Transporter 2 Inhibitors - pharmacology
/ Tests
/ Thiosulfates - pharmacology
/ Toxicity
/ Young men
2024
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Lifespan effects in male UM-HET3 mice treated with sodium thiosulfate, 16-hydroxyestriol, and late-start canagliflozin
by
Salmon, Adam B.
, Strong, Randy
, Ginsburg, Brett C.
, Korstanje, Ron
, Garratt, Michael
, Mitchell, James R.
, Lopez-Cruzan, Marisa
, Dehghan, Ishmael
, Milne, Ginger
, Harrison, David E.
, Geisler, John G.
, Han, Melissa L.
, Leiser, Scott F.
, Nelson, James F.
, Kaczorowski, Catherine C.
, Rosenthal, Nadia
, Kumar, Navasuja
, Fernandez, Elizabeth
, Miller, Richard A.
, Reifsnyder, Peter C.
, Cortopassi, Gino A.
in
2,4-Dinitrophenol
/ Age
/ Aging
/ Animals
/ Antidiabetics
/ Biomedical and Life Sciences
/ Blood levels
/ Canagliflozin - pharmacology
/ Cell Biology
/ Drug dosages
/ Drugs
/ Expressed sequence tags
/ Female
/ Females
/ Genetics
/ Geriatrics/Gerontology
/ Hydrogen sulfide
/ Ketoglutaric acid
/ Life Sciences
/ Life span
/ Longevity - drug effects
/ Male
/ Males
/ Mice
/ Molecular Medicine
/ Original
/ Original Article
/ Oxidation
/ Proteins
/ Sex Factors
/ Sexes
/ Sexual dimorphism
/ Sodium
/ Sodium thiosulfate
/ Sodium-Glucose Transporter 2 Inhibitors - pharmacology
/ Tests
/ Thiosulfates - pharmacology
/ Toxicity
/ Young men
2024
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Lifespan effects in male UM-HET3 mice treated with sodium thiosulfate, 16-hydroxyestriol, and late-start canagliflozin
by
Salmon, Adam B.
, Strong, Randy
, Ginsburg, Brett C.
, Korstanje, Ron
, Garratt, Michael
, Mitchell, James R.
, Lopez-Cruzan, Marisa
, Dehghan, Ishmael
, Milne, Ginger
, Harrison, David E.
, Geisler, John G.
, Han, Melissa L.
, Leiser, Scott F.
, Nelson, James F.
, Kaczorowski, Catherine C.
, Rosenthal, Nadia
, Kumar, Navasuja
, Fernandez, Elizabeth
, Miller, Richard A.
, Reifsnyder, Peter C.
, Cortopassi, Gino A.
in
2,4-Dinitrophenol
/ Age
/ Aging
/ Animals
/ Antidiabetics
/ Biomedical and Life Sciences
/ Blood levels
/ Canagliflozin - pharmacology
/ Cell Biology
/ Drug dosages
/ Drugs
/ Expressed sequence tags
/ Female
/ Females
/ Genetics
/ Geriatrics/Gerontology
/ Hydrogen sulfide
/ Ketoglutaric acid
/ Life Sciences
/ Life span
/ Longevity - drug effects
/ Male
/ Males
/ Mice
/ Molecular Medicine
/ Original
/ Original Article
/ Oxidation
/ Proteins
/ Sex Factors
/ Sexes
/ Sexual dimorphism
/ Sodium
/ Sodium thiosulfate
/ Sodium-Glucose Transporter 2 Inhibitors - pharmacology
/ Tests
/ Thiosulfates - pharmacology
/ Toxicity
/ Young men
2024
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Lifespan effects in male UM-HET3 mice treated with sodium thiosulfate, 16-hydroxyestriol, and late-start canagliflozin
Journal Article
Lifespan effects in male UM-HET3 mice treated with sodium thiosulfate, 16-hydroxyestriol, and late-start canagliflozin
2024
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Overview
Genetically heterogeneous UM-HET3 mice born in 2020 were used to test possible lifespan effects of alpha-ketoglutarate (AKG), 2,4-dinitrophenol (DNP), hydralazine (HYD), nebivolol (NEBI), 16α-hydroxyestriol (OH_Est), and sodium thiosulfate (THIO), and to evaluate the effects of canagliflozin (Cana) when started at 16 months of age. OH_Est produced a 15% increase (
p
= 0.0001) in median lifespan in males but led to a significant (7%) decline in female lifespan. Cana, started at 16 months, also led to a significant increase (14%,
p
= 0.004) in males and a significant decline (6%,
p
= 0.03) in females. Cana given to mice at 6 months led, as in our previous study, to an increase in male lifespan without any change in female lifespan, suggesting that this agent may lead to female-specific late-life harm. We found that blood levels of Cana were approximately 20-fold higher in aged females than in young males, suggesting a possible mechanism for the sex-specific disparities in its effects. NEBI was also found to produce a female-specific decline (4%,
p
= 0.03) in lifespan. None of the other tested drugs provided a lifespan benefit in either sex. These data bring to 7 the list of ITP-tested drugs that induce at least a 10% lifespan increase in one or both sexes, add a fourth drug with demonstrated mid-life benefits on lifespan, and provide a testable hypothesis that might explain the sexual dimorphism in lifespan effects of the SGLT2 inhibitor Cana.
Publisher
Springer International Publishing,Springer Nature B.V
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