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      The potential antioxidant bioactivity of date palm fruit against gentamicin-mediated hepato-renal injury in male albino rats

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          [13] Catalase in vitro

          Hugo Aebi (1984)
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            Determination of malonaldehyde precursor in tissues by thiobarbituric acid test.

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              Metabolic zonation of the liver: The oxygen gradient revisited

              The liver has a multitude of functions which are necessary to maintain whole body homeostasis. This requires that various metabolic pathways can run in parallel in the most efficient manner and that futile cycles are kept to a minimum. To a large extent this is achieved due to a functional specialization of the liver parenchyma known as metabolic zonation which is often lost in liver diseases. Although this phenomenon is known for about 40 years, the underlying regulatory pathways are not yet fully elucidated. The physiologically occurring oxygen gradient was considered to be crucial for the appearance of zonation; however, a number of reports during the last decade indicating that β-catenin signaling, and the hedgehog (Hh) pathway contribute to metabolic zonation may have shifted this view. In the current review we connect these new observations with the concept that the oxygen gradient within the liver acinus is a regulator of zonation. This is underlined by a number of facts showing that the β-catenin and the Hh pathway can be modulated by the hypoxia signaling system and the hypoxia-inducible transcription factors (HIFs). Altogether, we provide a view by which the dynamic interplay between all these pathways can drive liver zonation and thus contribute to its physiological function.
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                Author and article information

                Journal
                Biomedicine & Pharmacotherapy
                Biomedicine & Pharmacotherapy
                Elsevier BV
                07533322
                November 2021
                November 2021
                : 143
                : 112154
                Article
                10.1016/j.biopha.2021.112154
                34649332
                585afed6-9300-4aeb-ae51-a1e1216400f6
                © 2021

                https://www.elsevier.com/tdm/userlicense/1.0/

                http://creativecommons.org/licenses/by/4.0/

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