TY - JOUR
T1 - Isotope-reinforced polyunsaturated fatty acids protect yeast cells from oxidative stress
AU - Hill, Shauna
AU - Hirano, Kathleen
AU - Shmanai, Vadim V.
AU - Marbois, Beth N.
AU - Vidovic, Dragoslav
AU - Bekish, Andrei V.
AU - Kay, Bradley
AU - Tse, Vincent
AU - Fine, Jonathan
AU - Clarke, Catherine F.
AU - Shchepinov, Mikhail S.
PY - 2011/1/1
Y1 - 2011/1/1
N2 - The facile abstraction of bis-allylic hydrogens from polyunsaturated fatty acids (PUFAs) is the hallmark chemistry responsible for initiation and propagation of autoxidation reactions. The products of these autoxidation reactions can form cross-links to other membrane components and damage proteins and nucleic acids. We report that PUFAs deuterated at bis-allylic sites are much more resistant to autoxidation reactions, because of the isotope effect. This is shown using coenzyme Q-deficient Saccharomyces cerevisiae coq mutants with defects in the biosynthesis of coenzyme Q (Q). Q functions in respiratory energy metabolism and also functions as a lipid-soluble antioxidant. Yeast coq mutants incubated in the presence of the PUFA α-linolenic or linoleic acid exhibit 99% loss of colony formation after 4 h, demonstrating a profound loss of viability. In contrast, coq mutants treated with monounsaturated oleic acid or with one of the deuterated PUFAs, 11,11-D2-linoleic or 11,11,14,14-D4-α-linolenic acid, retain viability similar to wild-type yeast. Deuterated PUFAs also confer protection to wild-type yeast subjected to heat stress. These results indicate that isotope-reinforced PUFAs are stabilized compared to standard PUFAs, and they protect coq mutants and wild-type yeast cells against the toxic effects of lipid autoxidation products. These findings suggest new approaches to controlling ROS-inflicted cellular damage and oxidative stress.
AB - The facile abstraction of bis-allylic hydrogens from polyunsaturated fatty acids (PUFAs) is the hallmark chemistry responsible for initiation and propagation of autoxidation reactions. The products of these autoxidation reactions can form cross-links to other membrane components and damage proteins and nucleic acids. We report that PUFAs deuterated at bis-allylic sites are much more resistant to autoxidation reactions, because of the isotope effect. This is shown using coenzyme Q-deficient Saccharomyces cerevisiae coq mutants with defects in the biosynthesis of coenzyme Q (Q). Q functions in respiratory energy metabolism and also functions as a lipid-soluble antioxidant. Yeast coq mutants incubated in the presence of the PUFA α-linolenic or linoleic acid exhibit 99% loss of colony formation after 4 h, demonstrating a profound loss of viability. In contrast, coq mutants treated with monounsaturated oleic acid or with one of the deuterated PUFAs, 11,11-D2-linoleic or 11,11,14,14-D4-α-linolenic acid, retain viability similar to wild-type yeast. Deuterated PUFAs also confer protection to wild-type yeast subjected to heat stress. These results indicate that isotope-reinforced PUFAs are stabilized compared to standard PUFAs, and they protect coq mutants and wild-type yeast cells against the toxic effects of lipid autoxidation products. These findings suggest new approaches to controlling ROS-inflicted cellular damage and oxidative stress.
KW - Coenzyme Q
KW - Free radicals
KW - Isotope effect
KW - Lipid autoxidation
KW - Oxidative stress
KW - Ubiquinone
UR - https://www.scopus.com/pages/publications/78650704798
U2 - 10.1016/j.freeradbiomed.2010.10.690
DO - 10.1016/j.freeradbiomed.2010.10.690
M3 - Article
C2 - 20955788
AN - SCOPUS:78650704798
SN - 0891-5849
VL - 50
SP - 130
EP - 138
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
IS - 1
ER -