Literature DB >> 15800054

Gender dimorphism in rat liver mitochondrial oxidative metabolism and biogenesis.

Roberto Justo1, Jordi Boada, Margalida Frontera, Jordi Oliver, Jordi Bermúdez, Magdalena Gianotti.   

Abstract

In the present study, we have investigated gender differences in rat liver mitochondrial oxidative metabolism. Total mitochondrial population (M) as well as the heavy (M1), medium (M3), and light (M8) mitochondrial fractions obtained by means of differential centrifugation steps at 1,000, 3,000, and 8,000 g, respectively, were isolated. Electron microscopic analysis was performed and mitochondrial protein content and cardiolipin levels, mitochondrial O(2) flux, ATP synthase activity, mitochondrial membrane potential, and mitochondrial transcription factor A (TFAM) protein levels were measured in each sample. Our results indicate that mitochondria from females have higher protein content and higher cardiolipin levels, greater respiratory and phosphorylative capacities, and more-energized mitochondria in respiratory state 3. Moreover, protein levels of TFAM were four times greater in females than in males. Gender differences in the aforementioned parameters were more patent in the isolated heavy M1 and M3 mitochondrial fractions. The present study demonstrates that gender-related differences in liver mitochondrial function are due mainly to a higher capacity and efficiency of substrate oxidation, likely related to greater mitochondrial machinery in females than in males, which is in accord with greater mitochondrial differentiation in females.

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Year:  2005        PMID: 15800054     DOI: 10.1152/ajpcell.00035.2005

Source DB:  PubMed          Journal:  Am J Physiol Cell Physiol        ISSN: 0363-6143            Impact factor:   4.249


  31 in total

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3.  Copper modulates sex-specific fructose hepatoxicity in nonalcoholic fatty liver disease (NALFD) Wistar rat models.

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4.  Impaired mitochondrial function in human placenta with increased maternal adiposity.

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Review 5.  Sex differences in renal mitochondrial function: a hormone-gous opportunity for research.

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6.  Genomics of sex hormone receptor signaling in hepatic sexual dimorphism.

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Journal:  Mol Cell Endocrinol       Date:  2017-05-26       Impact factor: 4.102

7.  Gemfibrozil pretreatment resulted in a sexually dimorphic outcome in the rat models of global cerebral ischemia-reperfusion via modulation of mitochondrial pro-survival and apoptotic cell death factors as well as MAPKs.

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8.  Estrogen receptor beta interacts and colocalizes with HADHB in mitochondria.

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Review 9.  Regulation of energy metabolism pathways by estrogens and estrogenic chemicals and potential implications in obesity associated with increased exposure to endocrine disruptors.

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10.  Gastrocnemius mitochondrial respiration: are there any differences between men and women?

Authors:  Jonathan R Thompson; Stanley A Swanson; George P Casale; Jason M Johanning; Evlampia Papoutsi; Panagiotis Koutakis; Dimitrios Miserlis; Zhen Zhu; Iraklis I Pipinos
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