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Increased Fatty Acid Oxidation Protects Against Development of Metabolic Associated Steatotic Liver Disease
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Metabolic dysfunction-associated steatotic liver disease (MASLD), a
condition characterized by fat accumulation in the liver, affects over 30%
of Americans. Development of fatty liver is attributed to poor diet, lack of
exercise, and liver metabolic dysfunction. We found that liver fatty acid
oxidative (FAO) metabolism increases during the initiation of fatty liver
disease. FAO is the key pathway to harness energy from fats; however,
dysregulation of FAO is thought to contribute to numerous metabolic
diseases. Here, we questioned whether the contribution of increased FAO was
protective or detrimental towards the development of MASLD. To do so, we
generated a novel conditional mouse model of liver specific deletion of
carnitine-acylcarnitine translocase (Cact), a required and nonhomologous
enzyme in the FAO pathway (Cact Liv-/-). MASLD was initiated with a
fatty-liver diet feeding for 1 week in control and CACT Liv-/-, and tissues
were collected for RNA extraction, respirometry, and pathology analysis.
CACT Liv-/- mice display a more severe MASLD phenotype, suggesting that
increased liver FAO capacity is protective against MASLD pathology.
R01: DK125812
This abstract was presented at the American Physiology Summit 2025 and
is only available in HTML format. There is no downloadable file or PDF
version. The Physiology editorial board was not involved in the peer review
process.
American Physiological Society
Title: Increased Fatty Acid Oxidation Protects Against Development of Metabolic
Associated Steatotic Liver Disease
Description:
Metabolic dysfunction-associated steatotic liver disease (MASLD), a
condition characterized by fat accumulation in the liver, affects over 30%
of Americans.
Development of fatty liver is attributed to poor diet, lack of
exercise, and liver metabolic dysfunction.
We found that liver fatty acid
oxidative (FAO) metabolism increases during the initiation of fatty liver
disease.
FAO is the key pathway to harness energy from fats; however,
dysregulation of FAO is thought to contribute to numerous metabolic
diseases.
Here, we questioned whether the contribution of increased FAO was
protective or detrimental towards the development of MASLD.
To do so, we
generated a novel conditional mouse model of liver specific deletion of
carnitine-acylcarnitine translocase (Cact), a required and nonhomologous
enzyme in the FAO pathway (Cact Liv-/-).
MASLD was initiated with a
fatty-liver diet feeding for 1 week in control and CACT Liv-/-, and tissues
were collected for RNA extraction, respirometry, and pathology analysis.
CACT Liv-/- mice display a more severe MASLD phenotype, suggesting that
increased liver FAO capacity is protective against MASLD pathology.
R01: DK125812
This abstract was presented at the American Physiology Summit 2025 and
is only available in HTML format.
There is no downloadable file or PDF
version.
The Physiology editorial board was not involved in the peer review
process.
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