823 research outputs found
Guanosine nucleotides regulate B2 kinin receptor affinity of agonists but not of antagonists: Discussion of a model proposing receptor precoupling to G protein
The effect of nucleotides on binding of the B2 kinin (BK) receptor agonist {[}H-3]BK and the antagonist {[}H-3]NPC17731 to particulate fractions of human foreskin fibroblasts was studied. At 0 degrees C, particulate fractions exhibited a single class of binding sites with a Kd of 2.3 nM for {[}H-3]BK and a K-d Of 3.8 nM for the antagonist {[}H-3]NPC17731. Incubation with radioligands at 37 degrees C for 5 min gave a reduction of agonist, as well as antagonist, binding that was between 0-40% depending on the preparation, even in the absence of guanosine nucleotides. As shown by Scatchard analysis, this reduction in specific binding was due to a shift in the affinity of at least a fraction of the receptors. The presence at 37 degrees C of the guanine nucleotides GTP, GDP and their poorly hydrolyzable analogs left {[}H-3]-NPC17731 binding unaffected, but reduced the receptor affinity for {[}H-3]BK to a K-d Of about 15 nM. The maximal number of receptors, however, was unchanged. This affinity change was strongly dependent on the presence of bivalent cations, in particular Mg2+. It was reversed by incubation at 0 degrees C, The rank order of the guanosine nucleotides for {[}H-3]BK binding reduction was GTP{[}gamma S] = Gpp{[}NH]p > GTP = GDP > GDP{[}beta S]. GMP, ATP, ADP and AMP showed no influence on agonist binding. A model for the interaction of the B2 kinin receptor with G proteins is discussed
Evidences for a quasi 60-year North Atlantic Oscillation since 1700 and its meaning for global climate change
The North Atlantic Oscillation (NAO) obtained using instrumental and
documentary proxy predictors from Eurasia is found to be characterized by a
quasi 60-year dominant oscillation since 1650. This pattern emerges clearly
once the NAO record is time integrated to stress its comparison with the
temperature record. The integrated NAO (INAO) is found to well correlate with
the length of the day (since 1650) and the global surface sea temperature
record HadSST2 and HadSST3 (since 1850). These findings suggest that INAO can
be used as a good proxy for global climate change, and that a 60-year cycle
exists in the global climate since at least 1700. Finally, the INAO ~60-year
oscillation well correlates with the ~60- year oscillations found in the
historical European aurora record since 1700, which suggests that this 60-year
dominant climatic cycle has a solar-astronomical origin
A new approach to long-term reconstruction of the solar irradiance leads to large historical solar forcing
The variable Sun is the most likely candidate for natural forcing of past
climate change on time scales of 50 to 1000 years. Evidence for this
understanding is that the terrestrial climate correlates positively with solar
activity. During the past 10,000 years, the Sun has experienced substantial
variations in activity and there have been numerous attempts to reconstruct
solar irradiance. While there is general agreement on how solar forcing varied
during the last several hundred years --- all reconstructions are proportional
to the solar activity --- there is scientific controversy on the magnitude of
solar forcing. We present a reconstruction of the Total and Spectral Solar
Irradiance covering 130 nm--10 m from 1610 to the present with annual
resolution and for the Holocene with 22-year resolution. We assume that the
minimum state of the quiet Sun in time corresponds to the observed quietest
area on the present Sun. Then we use available long-term proxies of the solar
activity, which are Be isotope concentrations in ice cores and 22-year
smoothed neutron monitor data, to interpolate between the present quiet Sun and
the minimum state of the quiet Sun. This determines the long-term trend in the
solar variability which is then superposed with the 11-year activity cycle
calculated from the sunspot number. The time-dependent solar spectral
irradiance from about 7000 BC to the present is then derived using a
state-of-the-art radiation code. We derive a total and spectral solar
irradiance that was substantially lower during the Maunder minimum than
observed today. The difference is remarkably larger than other estimations
published in the recent literature. The magnitude of the solar UV variability,
which indirectly affects climate is also found to exceed previous estimates. We
discuss in details the assumptions which leaded us to this conclusion.Comment: 9 pages, 5 figures, accepted for publication in
Astronomy&Astrophysic
Discriminant analysis of solar bright points and faculae I. Classification method and center-to-limb distribution
While photospheric magnetic elements appear mainly as Bright Points (BPs) at
the disk center and as faculae near the limb, high-resolution images reveal the
coexistence of BPs and faculae over a range of heliocentric angles. This is not
explained by a "hot wall" effect through vertical flux tubes, and suggests that
the transition from BPs to faculae needs to be quantitatively investigated. To
achieve this, we made the first recorded attempt to discriminate BPs and
faculae, using a statistical classification approach based on Linear
Discriminant Analysis(LDA). This paper gives a detailed description of our
method, and shows its application on high-resolution images of active regions
to retrieve a center-to-limb distribution of BPs and faculae. Bright "magnetic"
features were detected at various disk positions by a segmentation algorithm
using simultaneous G-band and continuum information. By using a selected sample
of those features to represent BPs and faculae, suitable photometric parameters
were identified in order to carry out LDA. We thus obtained a Center-to-Limb
Variation (CLV) of the relative number of BPs and faculae, revealing the
predominance of faculae at all disk positions except close to disk center (mu >
0.9). Although the present dataset suffers from limited statistics, our results
are consistent with other observations of BPs and faculae at various disk
positions. The retrieved CLV indicates that at high resolution, faculae are an
essential constituent of active regions all across the solar disk. We speculate
that the faculae near disk center as well as the BPs away from disk center are
associated with inclined fields
Photoaffinity labelling of atrial natriuretic factor (ANF)-R1 receptor by underivatized 125I-ANF. Involvement of lipid peroxidation
Brown adipose tissue mitochondria: modulation by GDP and fatty acids depends on the respiratory substrates
The UCP1 [first UCP (uncoupling protein)] that is found in the mitochondria of brown adipocytes [BAT (brown adipose tissue)] regulates the heat production, a process linked to non-shivering thermogenesis. The activity of UCP1 is modulated by GDP and fatty acids. In this report, we demonstrate that respiration and heat released by BAT mitochondria vary depending on the respiratory substrate utilized and the coupling state of the mitochondria. It has already been established that, in the presence of pyruvate/malate, BAT mitochondria are coupled by faf-BSA (fatty-acid-free BSA) and GDP, leading to an increase in ATP synthesis and mitochondrial membrane potential along with simultaneous decreases in both the rates of respiration and heat production. Oleate restores the uncoupled state, inhibiting ATP synthesis and increasing the rates of both respiration and heat production. We now show that in the presence of succinate: (i) the rates of uncoupled mitochondria respiration and heat production are five times slower than in the presence of pyruvate/malate; (ii) faf-BSA and GDP accelerate heat and respiration as a result and, in coupled mitochondria, these two rates are accelerated compared with pyruvate/malate; (iii) in spite of the differences in respiration and heat production noted with the two substrates, the membrane potential and the ATP synthesized were the same; and (iv) oleate promoted a decrease in heat production and respiration in coupled mitochondria, an effect different from that observed using pyruvate/malate. These effects are not related to the production of ROS (reactive oxygen species). We suggest that succinate could stimulate a new route to heat production in BAT mitochondria
A bi-directional relationship between obesity and health-related quality of life : evidence from the longitudinal AusDiab study
Objective: To assess the prospective relationship between obesity and health-related quality of life, including a novel assessment of the impact of health-related quality of life on weight gain.Design and setting: Longitudinal, national, population-based Australian Diabetes, Obesity and Lifestyle (AusDiab) study, with surveys conducted in 1999/2000 and 2004/2005.Participants: A total of 5985 men and women aged 25 years at study entry.Main outcome measure(s): At both time points, height, weight and waist circumference were measured and self-report data on health-related quality of life from the SF-36 questionnaire were obtained. Cross-sectional and bi-directional, prospective associations between obesity categories and health-related quality of life were assessed.Results: Higher body mass index (BMI) at baseline was associated with deterioration in health-related quality of life over 5 years for seven of the eight health-related quality of life domains in women (all P0.01, with the exception of mental health, P>0.05), and six out of eight in men (all P<0.05, with the exception of role-emotional, P=0.055, and mental health, P>0.05). Each of the quality-of-life domains related to mental health as well as the mental component summary were inversely associated with BMI change (all P<0.0001 for women and P0.01 for men), with the exception of vitality, which was significant in women only (P=0.008). For the physical domains, change in BMI was inversely associated with baseline general health in women only (P=0.023).Conclusions: Obesity was associated with a deterioration in health-related quality of life (including both physical and mental health domains) in this cohort of Australian adults followed over 5 years. Health-related quality of life was also a predictor of weight gain over 5 years, indicating a bi-directional association between obesity and health-related quality of life. The identification of those with poor health-related quality of life may be important in assessing the risk of future weight gain, and a focus on health-related quality of life may be beneficial in weight management strategies.<br /
Peeking at G-protein-coupled receptors through the molecular dynamics keyhole
Molecular dynamics is a state of the art computational tool for the investigation of biophysics phenomenon at a molecular scale, as it enables the modeling of dynamic processes, such as conformational motions, molecular solvation and ligand binding. The recent advances in structural biology have led to a bloom in published G-protein-coupled receptor structures, representing a solid and valuable resource for molecular dynamics studies. During the last decade, indeed, a plethora of physiological and pharmacological facets of this membrane protein superfamily have been addressed by means of molecular dynamics simulations, including the activation mechanism, allosterism and, very recently, biased signaling. Here, we try to recapitulate some of the main contributions that molecular dynamics has recently produced in the field
Percentile reference values for anthropometric body composition indices in European children from the IDEFICS study
INTRODUCTION: To characterise the nutritional status in children with obesity or wasting conditions, European anthropometric reference values for body composition measures beyond the body mass index (BMI) are needed. Differentiated assessment of body composition in children has long been hampered by the lack of appropriate references.
OBJECTIVES: The aim of our study is to provide percentiles for body composition indices in normal weight European children, based on the IDEFICS cohort (Identification and prevention of Dietary-and lifestyle-induced health Effects in Children and infantS).
METHODS: Overall 18 745 2.0-10.9-year-old children from eight countries participated in the study. Children classified as overweight/obese or underweight according to IOTF (N = 5915) were excluded from the analysis. Anthropometric measurements (BMI (N = 12 830); triceps, subscapular, fat mass and fat mass index (N = 11 845-11 901); biceps, suprailiac skinfolds, sum of skinfolds calculated from skinfold thicknesses (N = 8129-8205), neck circumference (N = 12 241); waist circumference and waist-to-height ratio (N = 12 381)) were analysed stratified by sex and smoothed 1st, 3rd, 10th, 25th, 50th, 75th, 90th, 97th and 99th percentile curves were calculated using GAMLSS.
RESULTS: Percentile values of the most important anthropometric measures related to the degree of adiposity are depicted for European girls and boys. Age-and sex-specific differences were investigated for all measures. As an example, the 50th and 99th percentile values of waist circumference ranged from 50.7-59.2 cm and from 51.3-58.7 cm in 4.5-to < 5.0-year-old girls and boys, respectively, to 60.6-74.5 cm in girls and to 59.9-76.7 cm in boys at the age of 10.5-10.9 years.
CONCLUSION: The presented percentile curves may aid a differentiated assessment of total and abdominal adiposity in European children
Evidence for a role of NTS2 receptors in the modulation of tonic pain sensitivity
<p>Abstract</p> <p>Background</p> <p>Central neurotensin (NT) administration results in a naloxone-insensitive antinociceptive response in animal models of acute and persistent pain. Both NTS1 and NTS2 receptors were shown to be required for different aspects of NT-induced analgesia. We recently demonstrated that NTS2 receptors were extensively associated with ascending nociceptive pathways, both at the level of the dorsal root ganglia and of the spinal dorsal horn. Then, we found that spinally administered NTS2-selective agonists induced dose-dependent antinociceptive responses in the acute tail-flick test. In the present study, we therefore investigated whether activation of spinal NTS2 receptors suppressed the persistent inflammatory pain symptoms observed after intraplantar injection of formalin.</p> <p>Results</p> <p>We first demonstrated that spinally administered NT and NT69L agonists, which bind to both NTS1 and NTS2 receptors, significantly reduced pain-evoked responses during the inflammatory phase of the formalin test. Accordingly, pretreatment with the NTS2-selective analogs JMV-431 and levocabastine was effective in inhibiting the aversive behaviors induced by formalin. With resolution at the single-cell level, we also found that activation of spinal NTS2 receptors reduced formalin-induced <it>c-fos </it>expression in dorsal horn neurons. However, our results also suggest that NTS2-selective agonists and NTS1/NTS2 mixed compounds differently modulated the early (21–39 min) and late (40–60 min) tonic phase 2 and recruited endogenous pain inhibitory mechanisms integrated at different levels of the central nervous system. Indeed, while non-selective drugs suppressed pain-related behaviors activity in both part of phase 2, intrathecal injection of NTS2-selective agonists was only efficient in reducing pain during the late phase 2. Furthermore, assessment of the stereotypic pain behaviors of lifting, shaking, licking and biting to formalin also revealed that unlike non-discriminative NTS1/NTS2 analogs reversing all nociceptive endpoint behaviors, pure NTS2 agonists specifically inhibited paw lifting, supporting a role of NTS2 in spinal modulation of persistent nociception.</p> <p>Conclusion</p> <p>The present study provides the first demonstration that activation of NTS2 receptors produces analgesia in the persistent inflammatory pain model of formalin. The dichotomy between these two classes of compounds also indicates that both NTS1 and NTS2 receptors are involved in tonic pain inhibition and implies that these two NT receptors modulate the pain-induced behavioral responses by acting on distinct spinal and/or supraspinal neural circuits. In conclusion, development of NT agonists targeting both NTS1 and NTS2 receptors could be useful for chronic pain management.</p
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