Citrobacter freundii infection in silver catfish (Rhamdia quelen): Hematological and histological alterations.

Citrobacter freundii is a fish pathogen known for its ability to cause injury and high mortality. There have been no studies reporting the effect of this bacterium on hematological parameters and internal organ histology in silver catfish (Rhamdia quelen). Therefore, the aim of this study is to evaluate the hematological and histopathological effects of an experimentally induced C. freundii infection in silver catfish. Twenty fish were divided into healthy and infected groups. The fish of the infected group were inoculated intramuscularly with 100 µL of bacterial suspension (6.4 × 108 CFU mL-1), while healthy control animals received 100 µL of sterile saline. On day 18 post-infection, blood and tissues (cephalic kidneys, livers, and spleens) were collected for histological analysis. The infected animals presented high mortality, as well as hematological and histological changes. In relation to hematology, the infected fish presented aregenerative anemia, protein loss, leukopenia with neutropenia, lymphocytosis, and leukoblastosis. Regarding histology, there was liver degeneration, decrease in the amount of renal hematopoietic tissue, and the presence of melanomacrophage centers (MMCs) in the spleen and cephalic kidney of infected fish. In summary, these alterations may contribute to disease pathophysiology, contributing to high mortality of affected fish.

Inflammatory cytokines in vitro production are associated with Ala16Val superoxide dismutase gene polymorphism of peripheral blood mononuclear cells.

Obesity is considered a chronic low-grade inflammatory state associated with a chronic oxidative stress caused by superoxide production (O(2)(-)). The superoxide dismutase manganese dependent (SOD2) catalyzes O(2)(-) in H(2)O(2) into mitochondria and is encoded by a single gene that presents a common polymorphism that results in the replacement of alanine (A) with a valine (V) in the 16 codon. This polymorphism has been implicated in a decreased efficiency of SOD2 transport into targeted mitochondria in V allele carriers. Previous studies described an association between VV genotype and metabolic diseases, including obesity and diabetes. However, the causal mechanisms to explain this association need to be more elucidated. We postulated that the polymorphism could influence the inflammatory response. To test our hypothesis, we evaluated the in vitro cytokines production by human peripheral blood mononuclear cells (PBMCs) carrier's different Ala16Val-SOD2 genotypes (IL-1, IL-6, IL-10, TNF-α, IFN-γ). Additionally, we evaluated if the culture medium glucose, enriched insulin, could influence the cytokine production. Higher levels of proinflammatory cytokines were observed in VV-PBMCs when compared to AA-PBMCs. However, the culture medium glucose and enriched insulin did not affect cytokine production. The results suggest that Ala16Val-SOD2 gene polymorphism could trigger the PBMCs proinflammatory cytokines level. However, discerning if a similar mechanism occurs in fat cells is an open question.

Habitual intake of guaraná and metabolic morbidities: an epidemiological study of an elderly Amazonian population.

The aim of the present study was to evaluate the associations of metabolic disorders and anthropometric and biochemical biomarkers of lipid, glucose and oxidative metabolism and the habitual ingestion of guaraná (Paullinia cupana, Mart. Var. sorbilis) by an elderly population residing in the Amazon Riverine region of the Maués municipality (Brazil). A case-controlled study was performed that included 637 elderly (≥60 years of age) patients classified as either those who habitually drank guaraná (GI, n = 421) or those who never drank guaraná (NG, n = 239) based upon their self-reported intake of guaraná. Indeed, the prevalence of various metabolic disorders was associated with guaraná ingestion. The prevalence of hypertension, obesity and metabolic syndrome in the GI group was lower than the prevalence found in the NG group. The NG group exhibited lower systolic and diastolic blood pressure values. The males in the GI group exhibited a lower waist circumference, on average, than the circumference found in the NG group, whereas the females in the GI group had lower cholesterol (total and LDL-c) levels than the control cohort. Additionally, a significant association was found between lower levels of advanced oxidative protein product (AOPP) and habitual guaraná consumption. The results constitute the first epidemiological study to suggest a potentially protective effect of habitual guaraná ingestion against metabolic disorders in elderly subjects.

Association between the Gln223Arg polymorphism of the leptin receptor and metabolic syndrome in free-living community elderly.

BACKGROUND: Metabolic syndrome is a cluster of cardiovascular risk factors. Aging and gene-environmental interactions are involved in the pathophysiology of metabolic syndrome. The LEPR gene Gln223Arg polymorphism has been associated with energy metabolism and body weight. METHODS: The association of the Gln223Arg polymorphism with metabolic syndrome was evaluated in a case-control study with elderly subjects (> or = 60 years old). The case-control groups were: (1) healthy group (HG), individuals without any cardio-metabolic diseases (CMD) or previous cardiovascular events (n = 64); (2) metabolic disorder group (MD), subjects with at least one metabolic disorder (hypertension, obesity, dyslipidemia, and impaired glucose tolerance, n = 306); and (3) metabolic syndrome group (MS) (n = 98). The Gln223Arg polymorphism of the LEPR gene was determined by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) using Msp I endonuclease enzyme restriction. RESULTS: The mean age of the HG subjects was 70.12 +/- 7.7, and the MD and MS subjects were 69.7 +/- 6.4 and 69.68 +/- 5.0 years old, respectively. The MS group showed higher body mass index (BMI), waist circumference, systolic and diastolic blood pressure, glucose, cholesterol, triglycerides, and low-density lipoprotein cholesterol (LDL-C) levels than did the HG individuals. The analysis showed differences in genotype frequencies: reduction in the Gln/Gln genotype and an excess of the Arg/Arg genotype in MD (chi(2) = 7.886, P = 0.019) and MS (chi(2) = 14.941, P = 0.001) when compared to the HG group. CONCLUSIONS: This study provides evidence for a role of the LEPR gene Gln223Arg polymorphism in predisposition to metabolic syndrome in the elderly.