Literature DB >> 24898746

Common therapeutic targets in cardiometabolic disease.

Gabrielle Fredman1, Lale Ozcan1, Ira Tabas2.   

Abstract

The interactions between cardiovascular disease (CVD) and insulin resistance syndromes suggest the possibility of joint targets for cardiometabolic research. The best drugs would go beyond minimizing adverse effects and have protective actions against both metabolic disease and CVD. In this perspective, we will outline a few examples in which a deep mechanistic understanding of the many cellular pathways that contribute to type 2 diabetes and CVD, regardless of cell type, have resulted in common upstream pathogenic pathways that can be therapeutically targeted.
Copyright © 2014, American Association for the Advancement of Science.

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Year:  2014        PMID: 24898746      PMCID: PMC4176709          DOI: 10.1126/scitranslmed.3008908

Source DB:  PubMed          Journal:  Sci Transl Med        ISSN: 1946-6234            Impact factor:   17.956


  39 in total

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5.  The transcription factor CREB enhances interleukin-17A production and inflammation in a mouse model of atherosclerosis.

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7.  Increased endoplasmic reticulum stress in atherosclerotic plaques associated with acute coronary syndrome.

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9.  Enrichment of endoplasmic reticulum with cholesterol inhibits sarcoplasmic-endoplasmic reticulum calcium ATPase-2b activity in parallel with increased order of membrane lipids: implications for depletion of endoplasmic reticulum calcium stores and apoptosis in cholesterol-loaded macrophages.

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  7 in total

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Review 3.  Imaging and nanomedicine in inflammatory atherosclerosis.

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4.  Resolvin D1 limits 5-lipoxygenase nuclear localization and leukotriene B4 synthesis by inhibiting a calcium-activated kinase pathway.

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6.  The Role of Gut-brain Axis in Regulating Glucose Metabolism After Acute Pancreatitis.

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7.  A systematic review and meta-analysis of the effect of treadmill desks on energy expenditure, sitting time and cardiometabolic health in adults.

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  7 in total

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