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Androgens and cardiac diseases. [Monaldi Arch Chest Dis. 2013] - PubMed - NCBI - 0 views

www.ncbi.nlm.nih.gov/...25087292

CVD cardiovascular disease low T Testosterone hypogonadism men male hormone hormones

shared by Nathan Goodyear on 05 Aug 14 - No Cached

Nathan Goodyear on 05 Aug 14

Abstract only available here. Take home: individuals at risk for CVD should have T levels evaluated.

<div class="cArrow"> </div><div class="cContentInner">Abstract only available here. Take home: individuals at risk for CVD should have T levels evaluated.</div>

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Testosterone in Men with Advanced Li... [J Gastroenterol Hepatol. 2014] - PubMed - NCBI - 0 views

www.ncbi.nlm.nih.gov/...25087838

Testosterone men male hormone hormones cirrhosis liver disease

shared by Nathan Goodyear on 05 Aug 14 - No Cached

Nathan Goodyear on 05 Aug 14

published ahead of print. The authors conclude that the Testosterone therapy in hypogonadal men with cirrhosis requires further study. They, the authors, state that the risk of Testosterone and hepatocellular carcinoma is overstated. This risk is associated with oral Testosterone replacement and thus in that light is not overstated. The majority of treatment strategies today employ none oral routes of administration which would support their statement.

<div class="cArrow"> </div><div class="cContentInner">published ahead of print. The authors conclude that the Testosterone therapy in hypogonadal men with cirrhosis requires further study. They, the authors, state that the risk of Testosterone and hepatocellular carcinoma is overstated. This risk is associated with oral Testosterone replacement and thus in that light is not overstated. The majority of treatment strategies today employ none oral routes of administration which would support their statement.</div>

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Probiotics and gut health: A special focus on liver diseases - 0 views

www.ncbi.nlm.nih.gov/...PMC2811790

probiotic probiotics liver cancer disease IBD IBS cirrhosis NAFLD gut health

shared by Nathan Goodyear on 05 Aug 14 - No Cached

Nathan Goodyear on 05 Aug 14

Probiotics are not just for disease prevention, but also can be utilized as adjuncts for different liver disease states. This review article highlights probiotics in IBD, IBS, surgery, NAFLD, cancer, and cirrhosis.

<div class="cArrow"> </div><div class="cContentInner">Probiotics are not just for disease prevention, but also can be utilized as adjuncts for different liver disease states. This review article highlights probiotics in IBD, IBS, surgery, NAFLD, cancer, and cirrhosis.</div>

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The role of probiotic bacteria in cancer pre... [Microbes Infect. 2000] - PubMed - NCBI - 0 views

www.ncbi.nlm.nih.gov/...10884619

probiotic probiotics cancer colorectal Lactobacillus

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Nathan Goodyear on 05 Aug 14

The evidence of Lactobacillus probiotics to suppress colorectal cancer is limited to indirect evidence.

<div class="cArrow"> </div><div class="cContentInner">The evidence of Lactobacillus probiotics to suppress colorectal cancer is limited to indirect evidence.</div>

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Cancer-preventing attributes of probioti... [Int J Food Sci Nutr. 2010] - PubMed - NCBI - 0 views

www.ncbi.nlm.nih.gov/...20187714

protbiotics cancer SOD superoxide disumutase catalase glutathione peroxidase glutathione-S-transferase

shared by Nathan Goodyear on 05 Aug 14 - No Cached

Nathan Goodyear on 05 Aug 14

The evidence of probiotics in cancer is limited. The limited evidence points to an increase in anti-oxidative enzymes i.e. glutathion-S-transferase, glutathione perioxidase, catalase, SOD.

<div class="cArrow"> </div><div class="cContentInner">The evidence of probiotics in cancer is limited. The limited evidence points to an increase in anti-oxidative enzymes i.e. glutathion-S-transferase, glutathione perioxidase, catalase, SOD.</div>

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Metabolic endotoxemia: a molecular link between obesity and cardiovascular risk - 0 views

jme.endocrinology-journals.org/...R51.full

metabolic endotoxemia obesity insulin resistance cardiovascular disease LPS inflammation

shared by Nathan Goodyear on 04 Aug 14 - No Cached

Weight gain has been associated with a higher gut permeability
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a high-fat diet promotes LPS absorption
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higher concentrations of fatty acids impair intestinal barrier integrity
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...37 more annotations...
The starting point for innate immunity activation is the recognition of conserved structures of bacteria, viruses, and fungal components through pattern-recognition receptors
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TLRs are PRRs that recognize microbe-associated molecular patterns
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TLRs are transmembrane proteins containing extracellular domains rich in leucine repeat sequences and a cytosolic domain homologous to the IL1 receptor intracellular domain
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The major proinflammatory mediators produced by the TLR4 activation in response to endotoxin (LPS) are TNFα, IL1β and IL6, which are also elevated in obese and insulin-resistant patients
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Obesity, high-fat diet, diabetes, and NAFLD are associated with higher gut permeability leading to metabolic endotoxemia.
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Probiotics, prebiotics, and antibiotic treatment can reduce LPS absorption
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LPS promotes hepatic insulin resistance, hypertriglyceridemia, hepatic triglyceride accumulation, and secretion of pro-inflammatory cytokines promoting the progression of fatty liver disease.
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In the endothelium, LPS induces the expression of pro-inflammatory, chemotactic, and adhesion molecules, which promotes atherosclerosis development and progression.
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In the adipose tissue, LPS induces adipogenesis, insulin resistance, macrophage infiltration, oxidative stress, and release of pro-inflammatory cytokines and chemokines.
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the gut microbiota has been recently proposed to be an environmental factor involved in the control of body weight and energy homeostasis by modulating plasma LPS levels
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dietary fats alone might not be sufficient to cause overweight and obesity, suggesting that a bacterially related factor might be responsible for high-fat diet-induced obesity.
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This was accompanied in high-fat-fed mice by a change in gut microbiota composition, with reduction in Bifidobacterium and Eubacterium spp.
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n humans, it was also shown that meals with high-fat and high-carbohydrate content (fast-food style western diet) were able to decrease bifidobacteria levels and increase intestinal permeability and LPS concentrations
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it was demonstrated that, more than the fat amount, its composition was a critical modulator of ME (Laugerette et al. 2012). Very recently, Mani et al. (2013) demonstrated that LPS concentration was increased by a meal rich in saturated fatty acids (SFA), while decreased after a meal rich in n-3 polyunsaturated fatty acids (n-3 PUFA).
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this effect seems to be due to the fact that some SFA (e.g., lauric and mystiric acids) are part of the lipid-A component of LPS and also to n-3 PUFA's role on reducing LPS potency when substituting SFA in lipid-A
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these experimental results suggest a pivotal role of CD14-mediated TLR4 activation in the development of LPS-mediated nutritional changes.
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This suggests a link between gut microbiota, western diet, and obesity and indicates that gut microbiota manipulation can beneficially affect the host's weight and adiposity.
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endotoxemia was independently associated with energy intake but not fat intake in a multivariate analysis
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in vitro that endotoxemia activates pro-inflammatory cytokine/chemokine production via NFκB and MAPK signaling in preadipocytes and decreased peroxisome proliferator-activated receptor γ activity and insulin responsiveness in adipocytes.
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T2DM patients have mean values of LPS that are 76% higher than healthy controls
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LPS-induced release of glucagon, GH and cortisol, which inhibit glucose uptake, both peripheral and hepatic
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LPSs also seem to induce ROS-mediated apoptosis in pancreatic cells
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Recent evidence has been linking ME with dyslipidemia, increased intrahepatic triglycerides, development, and progression of alcoholic and nonalcoholic fatty liver disease
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The hepatocytes, rather than hepatic macrophages, are the cells responsible for its clearance, being ultimately excreted in bile
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All the subclasses of plasma lipoproteins can bind and neutralize the toxic effects of LPS, both in vitro (Eichbaum et al. 1991) and in vivo (Harris et al. 1990), and this phenomenon seems to be dependent on the number of phospholipids in the lipoprotein surface (Levels et al. 2001). LDL seems to be involved in LPS clearance, but this antiatherogenic effect is outweighed by its proatherogenic features
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LPS produces hypertriglyceridemia by several mechanisms, depending on LPS concentration. In animal models, low-dose LPS increases hepatic lipoprotein (such as VLDL) synthesis, whereas high-dose LPS decreases lipoprotein catabolism
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When a dose of LPS similar to that observed in ME was infused in humans, a 2.5-fold increase in endothelial lipase was observed, with consequent reduction in total and HDL. This mechanism may explain low HDL levels in ‘ME’ and other inflammatory conditions such as obesity and metabolic syndrome
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It is known that the high-fat diet and the ‘ME’ increase intrahepatic triglyceride accumulation, thus synergistically contributing to the development and progression of alcoholic and NAFLD, from the initial stages characterized by intrahepatic triglyceride accumulation up to chronic inflammation (nonalcoholic steatohepatitis), fibrosis, and cirrhosis
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On the other hand, LPS activates Kupffer cells leading to an increased production of ROS and pro-inflammatory cytokines like TNFα
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high-fat diet mice presented with ME, which positively and significantly correlated with plasminogen activator inhibitor (PAI-1), IL1, TNFα, STAMP2, NADPHox, MCP-1, and F4/80 (a specific marker of mature macrophages) mRNAs
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prebiotic administration reduces intestinal permeability to LPS in obese mice and is associated with decreased systemic inflammation when compared with controls
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Cani et al. also found that high-fat diet mice presented with not only ME but also higher levels of inflammatory markers, oxidative stress, and macrophage infiltration markers
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This suggests that important links between gut microbiota, ME, inflammation, and oxidative stress are implicated in a high-fat diet situation
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high-fat feeding is associated with adipose tissue macrophage infiltration (F4/80-positive cells) and increased levels of chemokine MCP-1, suggesting a strong link between ME, proinflammatory status, oxidative stress, and, lately, increased CV risk
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LPS has been shown to promote atherosclerosis
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markers of systemic inflammation such as circulating bacterial endotoxin were elevated in patients with chronic infections and were strong predictors of increased atherosclerotic risk
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As a TLR4 ligand, LPS has been suggested to induce atherosclerosis development and progression, via a TLR4-mediated inflammatory state.
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Nathan Goodyear on 04 Aug 14

Very nice updated review on Metabolic endotoxemia

<div class="cArrow"> </div><div class="cContentInner">Very nice updated review on Metabolic endotoxemia</div>

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Testosterone deficiency and quality of life in ... [Intern Med J. 2014] - PubMed - NCBI - 0 views

www.ncbi.nlm.nih.gov/...25081047

Testosterone quality of life QOL Testicular cancer low T men male hormone hormones

shared by Nathan Goodyear on 04 Aug 14 - No Cached

Nathan Goodyear on 04 Aug 14

Small study in men s/p Testicular cancer found no association between Testosterone levels and quality of life measures.

<div class="cArrow"> </div><div class="cContentInner">Small study in men s/p Testicular cancer found no association between Testosterone levels and quality of life measures.</div>

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Zearalenone inhibits testosterone biosynthe... [Toxicol In Vitro. 2014] - PubMed - NCBI - 0 views

www.ncbi.nlm.nih.gov/...24512812

mycotoxin Testosterone low T leydig cells

shared by Nathan Goodyear on 15 Feb 14 - No Cached

Nathan Goodyear on 15 Feb 14

Zearalenone, a mycotoxin, reduced testosterone by leydig cells in mice.

<div class="cArrow"> </div><div class="cContentInner">Zearalenone, a mycotoxin, reduced testosterone by leydig cells in mice.</div>

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Penile Growth in Response to Human Chorionic Gonadotropin (hCG) Treatment in Patients w... - 0 views

www.ncbi.nlm.nih.gov/...PMC3214853

hCG human chorionic gonadotropin idiopathic hypogonadotrophic hypogonadism hypogonadism low testosterone low T low testosterone

shared by Nathan Goodyear on 05 Feb 13 - No Cached

Nathan Goodyear on 05 Feb 13

HCG used to stimulate endogenous testosterone production in young men with idiopathic hypogonadotrophic hypogonadism.

<div class="cArrow"> </div><div class="cContentInner">HCG used to stimulate endogenous testosterone production in young men with idiopathic hypogonadotrophic hypogonadism.</div>

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