Publications by authors named "A K Bekish"

A right aortic arch is an anomaly of prenatal development characterized by location of aortic arch to the right from tracheal-esophageal complex. This variant of anatomy is usually asymptomatic and diagnosed accidentally. We performed open upper lobectomy for cancer of the upper lobe of the right lung in a patient with aortic arch dextraposition.

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Ru-based catalysis results in highly unsaturated fatty acid (HUFA) ethyl esters (EE) deuterated to various extents. The products carry H (D) mainly at their -allylic positions, where they are resistant to autoxidation compared to natural HUFA and are promising as neurological and retinal drugs. We characterized the extent of deuteration at each allylic position of docosa-4,7,10,13,16,19-hexaenoic acid deuterated to completion at -allylic and allylic positions (D-DHA) by two-dimensional (2D) and high-field (600 and 950 MHz) NMR.

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Arachidonic acid (ARA) is a major component of lipid bilayers as well as the key substrate for the eicosanoid cascades. ARA is readily oxidized, and its non-enzymatic and enzymatic oxidation products induce inflammatory responses in nearly all tissues, including lung tissues. Deuteration at bis-allylic positions substantially decreases the overall rate of ARA oxidation when hydrogen abstraction is an initiating event.

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Lipid peroxidation (LPO) plays a key role in many age-related neurodegenerative conditions and other disorders. Light irradiation can initiate LPO through various mechanisms and is of importance in retinal and dermatological pathologies. The introduction of deuterated polyunsaturated fatty acids (D-PUFA) into membrane lipids is a promising approach for protection against LPO.

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Article Synopsis
  • No general method exists for quantitatively determining the position of deuterium (D) in hydrocarbon chains, making it difficult to analyze a new class of deuterated fatty acid drugs known as -allylic deuterated highly unsaturated fatty acids (D-HUFA).
  • Researchers have adapted the Paternó-Büchi reaction combined with shotgun lipidomics to effectively analyze and quantify specific D abundances in D-HUFA, allowing for detailed characterization of various isotopologues.
  • Their findings reveal that certain D-HUFA isotopologues, such as D5-7 linolenic acid and D9-11 docosahexaenoic acid, can achieve over 80% deuteration at specific allylic positions
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