Ghr knockout
Intervention1 paper4 findings
- Animals1
Outcomes
4Hepatic steatosis
upin mice1
1 study
Hepatic steatosis
upin mice1
Ghr knockout induces hepatic steatosis in mice.
“Elevated circulating GH following hepatocyte-specific GHR ablation mediates adipose-liver crosstalk that promotes adipose lipolysis and CD36-dependent hepatic steatosis.”
Animalshepatocyte-specifichepatocyte-specific knockoutliver
Deleting liver growth hormone receptors accelerates aging phenotypes and shortens lifespan in mice · Aging cell · 26 Sep 2026
Cognitive function
downin mice1
1 study
Cognitive function
downin mice1
Ghr knockout impairs cognitive function in mice.
“reduced metabolic stress resilience, cognitive decline, impaired bone mineralization, and exacerbated inflammaging.”
Animalshepatocyte-specifichepatocyte-specific knockout
Deleting liver growth hormone receptors accelerates aging phenotypes and shortens lifespan in mice · Aging cell · 26 Sep 2026
Cellular senescence
upin mice1
1 study
Cellular senescence
upin mice1
Ghr knockout increases cellular senescence in mice.
“hepatocyte-specific GHR knockout mice display accelerated aging-related phenotypes, characterized by shortened lifespan, enhanced cellular senescence”
Animalshepatocyte-specifichepatocyte-specific knockoutliver
Deleting liver growth hormone receptors accelerates aging phenotypes and shortens lifespan in mice · Aging cell · 26 Sep 2026
Lifespan
downin mice1
1 study
Lifespan
downin mice1
Ghr knockout shortens lifespan in mice.
“hepatocyte-specific GHR knockout mice display accelerated aging-related phenotypes, characterized by shortened lifespan”
Animalshepatocyte-specifichepatocyte-specific knockoutliver
Deleting liver growth hormone receptors accelerates aging phenotypes and shortens lifespan in mice · Aging cell · 26 Sep 2026
Latest
1Deleting liver growth hormone receptors accelerates aging phenotypes and shortens lifespan in mice
The loss of hepatic growth hormone signaling disrupts lipid metabolism and causes mitochondrial damage that can be counteracted by inhibiting PDK4.