2,233 research outputs found
Pour en finir avec le Bronze final ? Les haches à douille de type armoricain en France
A discussion about socket armorican bronze axes datation. They are from Ha D period (VII th & VIt h century B.C.)Révision de la datation des haches à douille de type armoricain, au seul Hallstatt D (VIIe-VIe s; av. J.-C.
Making Green Polymers Even Greener:Towards Sustainable Production of Polyhydroxyalkanoates from Agroindustrial By-Products
Induction of Engineered Residual Stresses Fields and Associate Surface Properties Modification by Short Pulse Laser Shock Processing
Laser shock processing (LSP) is consolidating as an effective technology for the improvement of metallic materials surface properties involving their fatigue life. The main acknowledged advantage of the LSP technique consists on its capability of inducing a relatively deep compression residual stresses field into metallic alloy pieces allowing an improved mechanical behaviour, explicitly the life improvement of the treated specimens against wear, crack growth and stress corrosion cracking. Progress accomplished by the authors in the line of practical development of the LSP technique at an experimental level, aiming its integral assessment from an interrelated theoretical and experimental point of view, is presented in this paper. Concretely, experimental results on the residual stress profiles and associated surface properties modification successfully reached in typical materials (especially Al and Ti alloys) under different LSP irradiation conditions are presented, a correlated analysis of the residual stress profiles obtained under different irradiation strategies and the evaluation of the corresponding induced surface properties as roughness and wear resistance being also presented. Through a coupled theoretical- experimental analysis the real possibilities of the LSP technique as a possible substitutive of related traditional surface modification techniques as, for example, shot peening
The obestatin receptor (GPR39) is expressed in human adipose tissue and is down-regulated in obesity-associated type 2 diabetes mellitus
The G protein-coupled receptor 39 (GPR39) has recently been identified
as the receptor for obestatin, a peptidic hormone involved in energy homeostasis.
However, the expression levels of this receptor in human adipose tissue in
obesity and obesity-associated type 2 diabetes mellitus (T2DM) remain unknown.
Therefore, we evaluated the actual presence of GPR39 mRNA in human adipose tissue
and whether GPR39 expression levels are altered in obesity and obesity-associated
T2DM. DESIGN: Omental adipose tissue biopsies obtained from 15 women were used in
the study. Patients were classified as lean (body mass index 20.8 +/- 1.0
kg/m(2)), obese normoglycaemic (body mass index 48.4 +/- 2.1 kg/m(2)) and obese
T2DM patients (body mass index 52.6 +/- 4.9 kg/m(2)). Anthropometric measurements
and biochemical profiles were assessed for each subject. Real-time RT-PCR
analyses were performed to quantify transcript levels of GPR39 and adiponectin.
RESULTS: Obese T2DM patients exhibited significantly lower GPR39 expression
levels compared to lean (P = 0.016) and obese normoglycaemic subjects (P =
0.008), while no differences between lean and obese normoglycaemic patients were
observed. The mRNA expression levels of GPR39 were negatively correlated to
fasting glucose concentrations (r = -0.581, P = 0.023), while exhibiting a
positive correlation to adiponectin mRNA expression levels (r = 0.674, P =
0.006). CONCLUSION: GPR39 is expressed in human adipose tissue. The reduced
expression levels of GPR39 in omental adipose tissue observed in obese patients
with T2DM suggest an involvement of obestatin signalling in glucose homeostasis
and T2DM development
Expression of caveolin-1 in human adipose tissue is upregulated in obesity and obesity-associated type 2 diabetes mellitus and related to inflammation
Caveolin-1 (CAV-1) plays important roles in many aspects of cellular
biology, including vesicular transport, cholesterol homeostasis and signal
transduction. The aim of the present study was to explore gene expression levels
of CAV-1 in human adipose tissue in obesity and obesity-associated type 2
diabetes mellitus (T2DM) and to analyse its potential implication in the
inflammatory state associated with obesity. DESIGN AND METHODS: Visceral adipose
tissue (VAT) and subcutaneous adipose tissue (SAT) obtained from 15 females were
used in the study. Patients were classified as lean (BMI 20.8 +/- 1.0 kg/m(2)) or
obese (BMI 50.5 +/- 2.6 kg/m(2)). The obese group was further subclassified as
normoglycaemic (NG) or patients with T2DM. Anthropometric measurements as well as
circulating metabolites, hormones and adipokines were determined. Real-time
polymerase chain reaction (PCR) analyses were performed to quantify transcript
levels of CAV-1 and monocyte chemoattractant protein (MCP-1). RESULTS: The
presence of CAV-1 protein was detected in VAT and SAT by immunohistochemistry.
Both obese NG and with T2DM patients exhibited significantly higher CAV-1
expression levels in VAT and SAT compared with lean subjects (P < 0.05). No
differences between obese NG and T2DM patients were observed in VAT. However,
obese T2DM patients were found to have higher CAV-1 expression levels in SAT (P <
0.05) compared with obese NG patients. A significant correlation was found
between CAV-1 mRNA expression levels in VAT and different circulating
inflammatory markers such as sialic acid (SA) (P < 0.001) and fibrinogen (P <
0.001) as well as with MCP1 mRNA expression (P < 0.05). CONCLUSION: Our findings
show for the first time the upregulation of mRNA CAV-1 expression levels in VAT
and SAT of obese NG and obese T2DM patients compared with lean controls,
suggesting a role for CAV-1 in obesity and T2DM development. The association with
different inflammatory markers further suggests an implication of CAV-1 in the
low-grade inflammation accompanying obesity
Increased circulating and visceral adipose tissue expression levels of YKL-40 in obesity-associated type 2 diabetes are related to inflammation: impact of conventional weight loss and gastric bypass
Context: Plasma YKL-40 is elevated in patients with type 2 diabetes. The potential role of visceral
adipose tissue (VAT) as a significant source of YKL-40 is unknown.
Objective: In the study circulating and expression levels of YKL-40 were examined in VAT analyzing
the contribution of adipocytes and stromovascular fraction cells (SVFCs).Wealso explored YKL-40’s
implication in insulin resistance and inflammation and the effect of weight loss on plasma YKL-40
concentrations.
PatientsandMethods: Samples obtained from 53 subjects were used in the study.Geneandprotein
expression levels of YKL-40 were analyzed in VAT as well as in both adipocytes and SVFCs. In
addition, circulating YKL-40 concentrations were measured before and after weight loss achieved
either by Roux-en-Y gastric bypass (n 26) or after a conventional dietetic program (n 20).
Results: Circulating concentrations and VAT expression of YKL-40 were increased in obese patients
with type 2 diabetes (P 0.01) as well as associated with variables of insulin resistance and inflammation.
No differences in YKL-40 expression levels between adipocytes and SVFCs were detected.
Monocyte chemoattractant protein-1 and homeostasis model assessment emerged (P
0.01) as independent factors predicting circulating YKL-40. Elevated levels of YKL-40 in obese
patients decreased after weight loss following a conventional hypocaloric diet (P 0.05) but not
via a surgery-induced negative energy balance mediated by the Roux-en-Y gastric bypass.
Conclusions: The association of increased YKL-40 mRNA and protein levels in VAT with its circulating
concentrations indicates an important contribution of VAT in YKL-40 regulation. Furthermore,
our data suggest a relevant role of glucose metabolism and inflammation on YKL-40
regulation
Plasma osteopontin levels and expression in adipose tissue are increased in obesity
Obesity acts as a cardiovascular risk factor by mechanisms that are not
fully understood. Osteopontin (OPN) is a proinflammatory mediator involved in
tissue remodeling that plays a role in atherosclerosis and diabetes. OBJECTIVE:
The aim of the present study was to compare the circulating concentrations of OPN
and its mRNA expression in omental adipose tissue of lean, overweight, and obese
individuals and to analyze the effect of weight loss. SUBJECTS AND METHODS:
Plasma concentrations of OPN were measured in 77 volunteers. OPN mRNA expression
in omental adipose tissue obtained from 12 women was quantified by real-time PCR.
In addition, the concentrations of OPN in 12 obese men were measured before and
after weight loss following a dietetic program. SETTING: The study was conducted
at a University Hospital. RESULTS: Obese and overweight patients exhibited
significantly increased circulating OPN concentrations as compared with lean
subjects (obese 72.6 +/- 28.5, overweight 68.2 +/- 20.8, lean 42.7 +/- 27.9
ng/ml; P < 0.001). A significant positive correlation was found between OPN
levels and body fat (r = 0.45; P < 0.0001). Obese individuals showed
significantly increased (P < 0.05) mRNA expression of OPN in omental adipose
tissue as compared with lean volunteers, which was further increased in obese
diabetic patients. Diet-induced weight loss significantly decreased OPN
concentrations from 64.7 +/- 22.1 to 36.6 +/- 20.1 ng/ml (P = 0.006).
CONCLUSIONS: These findings represent the first observation that plasma OPN and
mRNA expression of OPN in omental adipose tissue are increased in
overweight/obese patients with the latter being further elevated in
obesity-associated diabetes. Moreover, weight loss reduces OPN concentrations,
which may contribute to the beneficial effects accompanying weight reduction.
Measurement of OPN might be useful for evaluating the outcomes of various
clinical interventions for obesity-related cardiovascular disease
3 Making Green Polymers Even Greener: Towards Sustainable Production of Polyhydroxyalkanoates from Agroindustrial By-Products
Histological and ultrastructural comparison of cauterization and thrombosis stroke models in immune-deficient mice
Background: Stroke models are essential tools in experimental stroke. Although several models of stroke have
been developed in a variety of animals, with the development of transgenic mice there is the need to develop a
reliable and reproducible stroke model in mice, which mimics as close as possible human stroke.
Methods: BALB/Ca-RAG2-/-gc-/- mice were subjected to cauterization or thrombosis stroke model and sacrificed at
different time points (48hr, 1wk, 2wk and 4wk) after stroke. Mice received BrdU to estimate activation of cell
proliferation in the SVZ. Brains were processed for immunohistochemical and EM.
Results: In both stroke models, after inflammation the same glial scar formation process and damage evolution
takes place. After stroke, necrotic tissue is progressively removed, and healthy tissue is preserved from injury
through the glial scar formation. Cauterization stroke model produced unspecific damage, was less efficient and
the infarct was less homogeneous compared to thrombosis infarct. Finally, thrombosis stroke model produces
activation of SVZ proliferation.
Conclusions: Our results provide an exhaustive analysis of the histopathological changes (inflammation, necrosis,
tissue remodeling, scarring...) that occur after stroke in the ischemic boundary zone, which are of key importance
for the final stroke outcome. This analysis would allow evaluating how different therapies would affect wound and
regeneration. Moreover, this stroke model in RAG 2-/- gC -/- allows cell transplant from different species, even
human, to be analyzed
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