2017
DOI: 10.24966/dmd-201x/100019
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Nutrition Therapy Regulates Caffeine Metabolism with Relevance to NAFLD and Induction of Type 3 Diabetes

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Cited by 39 publications
(39 citation statements)
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References 111 publications
(131 reference statements)
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“…The calculated fat content in man has now been determined by author's calculations to be approximately 20-30 g/day [13] and differs from other international researchers [111]. In several laboratories, cellular cholesterol levels are associated with increased amyloid beta formation in the brain and periphery [37], and Sirt 1 downregulation is associated with defective caffeine and cholesterol metabolism (Figure 4) with relevance to hepatic amyloid beta clearance and induction of NAFLD [112]. Increased plasma caffeine levels displace amyloid beta and fatty acids from albumin by competition for albumin binding sites [113] with relevance to amyloid beta aggregation [114].…”
Section: Defective Adipose Tissue-liver Crosstalk In the Induction Ofmentioning
confidence: 99%
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“…The calculated fat content in man has now been determined by author's calculations to be approximately 20-30 g/day [13] and differs from other international researchers [111]. In several laboratories, cellular cholesterol levels are associated with increased amyloid beta formation in the brain and periphery [37], and Sirt 1 downregulation is associated with defective caffeine and cholesterol metabolism (Figure 4) with relevance to hepatic amyloid beta clearance and induction of NAFLD [112]. Increased plasma caffeine levels displace amyloid beta and fatty acids from albumin by competition for albumin binding sites [113] with relevance to amyloid beta aggregation [114].…”
Section: Defective Adipose Tissue-liver Crosstalk In the Induction Ofmentioning
confidence: 99%
“…LPS interferes with the SCN and adipose tissue-liver crosstalk [10,85,135,136] and delays hepatic drug metabolism [165,166] with premature brain aging and chronic disease progression (Figure 6). LPS induces changes in plasma albumin contents [112] in individuals in the developing world with relevance to interference with caffeine and its therapeutic properties with relevance to SCN regulation of adipose tissue-liver crosstalk. In recent studies, caffeine intake and glucose dyshomeostasis that supersede insulin therapy [142,143] has raised concerns with relevance to glucose/amyloid beta-induced mitochondrial apoptosis and the induction of NAFLD.…”
Section: Nutritional Diets Maintain Brain and Adipose Tissue-liver Crmentioning
confidence: 99%
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“…Caffeine and its metabolism is critical to cardiovascular disease [50][51][52] with Indian spice intake (mg/day) now important with relevance to interference with caffeine's therapeutic properties in man and various species. Delayed caffeine clearance leads to interference with caffeine's bene icial effect on adipogenesis with increased transport to the brain relevant to mitochondrial induced apoptosis and the induction of Type 3 diabetes [26][27][28].…”
Section: Editorialmentioning
confidence: 99%
“…Sirt 1 is the heat shock gene [22,23] with its repression involved with dysregulation of heat shock protein 70 (HSP70), natural killer cell activation and mitophagy [24]. Defective adipose tissue-liver interaction has been treated with caffeine to prevent mitophagy [25,26] linked to adipocyte dysfunction and reversal of NAFLD [27]. Nutrition therapy that allows co-ordination between the brain, adipose tissue and liver activates the apelinergic-Sirt 1 interaction essential for hepatic caffeine metabolism and caffeine's critical role as modulation of Sirt 1 in the brain [28] important to the prevention of obesity.…”
Section: Editorialmentioning
confidence: 99%