scholarly journals Long-Term Feeding of Conjugated Linoleic Acid and Fish Oil to Laying Hens: Effects on Hepatic Histopathology, Egg Quality, and Lipid Components

2007 ◽  
Vol 16 (3) ◽  
pp. 420-428 ◽  
Author(s):  
G. Cherian ◽  
D. Gonzalez ◽  
K.S. Ryu ◽  
M.P. Goeger
2000 ◽  
Vol 83 (11) ◽  
pp. 2620-2628 ◽  
Author(s):  
D.C. Donovan ◽  
D.J. Schingoethe ◽  
R.J. Baer ◽  
J. Ryali ◽  
A.R. Hippen ◽  
...  

2013 ◽  
Vol 92 (7) ◽  
pp. 1824-1829 ◽  
Author(s):  
Q.H. Zhai ◽  
X.F. Dong ◽  
J.M. Tong ◽  
Y.M. Guo ◽  
Y.E. Bao

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Orli Binyamin ◽  
Keren Nitzan ◽  
Kati Frid ◽  
Yael Ungar ◽  
Hanna Rosenmann ◽  
...  

AbstractDeregulation of Cyclin-dependent kinase 5 (CDK5) by binding to the activated calpain product p25, is associated with the onset of neurodegenerative diseases, such as Alzheimer’s disease (AD). Conjugated Linoleic Acid (CLA), a calpain inhibitor, is a metabolite of Punicic Acid (PA), the main component of Pomegranate seed oil (PSO). We have shown recently that long-term administration of Nano-PSO, a nanodroplet formulation of PSO, delays mitochondrial damage and disease advance in a mouse model of genetic Creutzfeldt Jacob disease (CJD). In this project, we first demonstrated that treatment of mice with Nano-PSO, but not with natural PSO, results in the accumulation of CLA in their brains. Next, we tested the cognitive, biochemical and pathological effects of long-term administration of Nano-PSO to 5XFAD mice, modeling for Alzheimer’s disease. We show that Nano-PSO treatment prevented age-related cognitive deterioration and mitochondrial oxidative damage in 5XFAD mice. Also, brains of the Nano-PSO treated mice presented reduced accumulation of Aβ and of p25, a calpain product, and increased expression of COX IV-1, a key mitochondrial enzyme. We conclude that administration of Nano-PSO results in the brain targeting of CLA, and suggest that this treatment may prevent/delay the onset of neurodegenerative diseases, such as AD and CJD.


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