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Muscle-Liver Substrate Fluxes in Exercising Humans and Potential Effects on Hepatic Metabolism
by
Weigert, Cora
,
Zhao, Xinjie
,
Secher, Niels H
in
Adaptation, Physiological
,
Adult
,
Bioenergetics
2020
Abstract
Context
The liver is crucial to maintain energy homeostasis during exercise. Skeletal muscle-derived metabolites can contribute to the regulation of hepatic metabolism.
Objective
We aim to elucidate which metabolites are released from the working muscles and taken up by the liver in exercising humans and their potential influence on hepatic function.
Methods
In two separate studies, young healthy men fasted overnight and then performed an acute bout of exercise. Arterial-to-venous differences of metabolites over the hepato-splanchnic bed and over the exercising and resting leg were investigated by capillary electrophoresis- and liquid chromatography-mass spectrometry metabolomics platforms. Liver transcriptome data of exercising mice were analyzed by pathway analysis to find a potential overlap between exercise-regulated metabolites and activators of hepatic transcription.
Results
During exercise, hepatic O2 uptake and CO2 delivery were increased two-fold. In contrast to all other free fatty acids (FFA), those FFA with 18 or more carbon atoms and a high degree of saturation showed a constant release in the liver vein and only minor changes by exercise. FFA 6:0 and 8:0 were released from the working leg and taken up by the hepato-splanchnic bed. Succinate and malate showed a pronounced hepatic uptake during exercise and were also released from the exercising leg. The transcriptional response in the liver of exercising mice indicates the activation of HIF-, NRF2-, and cAMP-dependent gene transcription. These pathways can also be activated by succinate.
Conclusion
Metabolites circulate between working muscles and the liver and may support the metabolic adaption to exercise by acting both as substrates and as signaling molecules.
Journal Article
Effects of 4-week very-high-fructose/glucose diets on insulin sensitivity, visceral fat and intrahepatic lipids: an exploratory trial
by
Schick, Fritz
,
Silbernagel, Guenther
,
Unmuth, Susanne
in
abdominal fat
,
administration & dosage
,
Adult
2011
An increasing amount of fructose in the diet is suggested to play a causal role in the pathogenesis of the metabolic syndrome, type 2 diabetes and fatty liver. Our aim was to investigate and compare the effects of very high fructose and very high glucose in hyperenergetic diets on glucose and lipid metabolism and on fat depots in healthy humans. We conducted an exploratory, prospective, randomised, single-blinded, intervention trial. Participants in addition to a balanced weight-maintaining diet received 150 g of fructose or glucose/d for 4 weeks. Insulin sensitivity was estimated from oral glucose tolerance tests. Visceral and subcutaneous abdominal fat was determined with MRI. Liver fat and intramyocellular lipids of the tibialis anterior muscle were measured with 1H magnetic resonance spectroscopy. A total of twenty healthy subjects (fructose group n 10 and glucose group n 10; twelve males and eight females) completed the study. They had a mean age of 30·5 (sem 2·0) years and a mean BMI of 25·9 (sem 0·5) kg/m2. Insulin sensitivity appeared to decrease both in the fructose and glucose groups. TAG markedly increased in the fructose group. No strong alterations or treatment effects were found for liver fat, visceral fat, subcutaneous abdominal fat and intramyocellular lipids of the tibialis anterior muscle. In conclusion, the effects of very high fructose and very high glucose in hyperenergetic diets on glucose metabolism and body fat composition were not different in the healthy participants of the present study. However, elevation of plasma TAG seemed to be fructose-specific.
Journal Article
A characterization of alternating links in thickened surfaces
2023
We use an extension of Gordon–Litherland pairing to thickened surfaces to give a topological characterization of alternating links in thickened surfaces. If $\\Sigma$ is a closed oriented surface and $F$ is a compact unoriented surface in $\\Sigma \\times I$, then the Gordon–Litherland pairing defines a symmetric bilinear pairing on the first homology of $F$. A compact surface in $\\Sigma \\times I$ is called definite if its Gordon–Litherland pairing is a definite form. We prove that a link $L$ in a thickened surface is non-split, alternating, and of minimal genus if and only if it bounds two definite surfaces of opposite sign.
Journal Article
Carnot and the Archetype of Waterfalls
2024
Carnot treats Heat as a Force of Nature, with its typical fundamental characteristics of intensity and thermal tension (temperature and temperature difference), extension (amount of heat, i.e., caloric), and power. To suggest how the three aspects are related, he applies the imagery of waterfalls to causative thermal processes: heat powers motion in a heat engine just as falling water does when activating rotation in a water wheel. We understand Carnot’s waterfall imagery as an archetype of human reasoning—as an embodiment of how we experience and understand causative (agentive) phenomena. We project it onto the macroscopic phenomena identified in physical science and so unlock the power of analogical structure mapping between theories of fluids, electricity and magnetism, heat, substances, gravity, and linear and rotational motion. In particular, the notion of (motive) power of a waterfall lets us create imaginative explanations of the interactions of Forces of Nature and helps us construct a generalized energy principle. Two-hundred years after Carnot made us aware of it, his Waterfall Analogy is a powerful example of theory construction with roots deep in how we experience phenomena as caused by natural agents.
Journal Article
Spin dynamics of molecular nanomagnets unravelled at atomic scale by four-dimensional inelastic neutron scattering
by
Baker, Michael L.
,
Ollivier, Jacques
,
Carretta, Stefano
in
639/766/119/997
,
639/766/119/998
,
Atomic
2012
Molecular nanomagnets are among the first examples of finite-size spin systems and have been test beds for addressing several phenomena in quantum dynamics. In fact, for short-enough timescales the spin wavefunctions evolve coherently according to an appropriate spin Hamiltonian, which can be engineered to meet specific requirements. Unfortunately, so far it has been impossible to determine these spin dynamics directly. Here we show that recently developed instrumentation yields the four-dimensional inelastic-neutron scattering function in vast portions of reciprocal space and enables the spin dynamics to be determined directly. We use the Cr
8
antiferromagnetic ring as a benchmark to demonstrate the potential of this approach which allows us, for example, to examine how quantum fluctuations propagate along the ring or to test the degree of validity of the Néel-vector-tunnelling framework.
Understanding the spin dynamics in magnetic nanostructures is important for spintronics, but so far it has been impossible to probe the spin dynamics directly. A neutron-scattering technique providing direct information about dynamical two-spin correlations in a molecular nanomagnet has now been demonstrated.
Journal Article
Estrogen induces St6gal1 expression and increases IgG sialylation in mice and patients with rheumatoid arthritis: a potential explanation for the increased risk of rheumatoid arthritis in postmenopausal women
by
Mårtensson, Inga-Lill
,
Schett, Georg
,
Forsblad-d’Elia, Helena
in
animal experiment
,
animal model
,
Animals
2018
Background
Rheumatoid arthritis (RA) preferentially affects women, with the peak incidence coinciding with estrogen decrease in menopause. Estrogen (E2) may therefore have intrinsic immune-regulatory properties that vanish with menopause. Fc sialylation is a crucial factor determining the inflammatory effector function of antibodies. We therefore analyzed whether E2 affects immunoglobulin G (IgG) sialylation.
Methods
Postmenopausal (ovariectomized) mice were immunized with ovalbumin and treated with E2 or vehicle. Total and ovalbumin-specific IgG concentrations, sialylation, and Fcγ receptor expression were analyzed. Postmenopausal women with RA receiving hormone replacement therapy, including E2, or no treatment were analyzed for IgG sialylation. Furthermore, effects of E2 on the expression of the sialylation enzyme β-galactoside α2,6-sialyltransferase 1 (St6Gal1) were studied in mouse and human antibody-producing cells.
Results
E2 treatment significantly increased Fc sialylation of total and ovalbumin-specific IgG in postmenopausal mice. Furthermore, E2 led to increased expression of inhibitory Fcγ receptor IIb on bone marrow leukocytes. Treatment with E2 also increased St6Gal1 expression in mouse and human antibody-producing cells, providing a mechanistic explanation for the increase in IgG-Fc sialylation. In postmenopausal women with RA, treatment with E2 significantly increased the Fc sialylation of IgG.
Conclusions
E2 induces anti-inflammatory effector functions in IgG by inducing St6Gal1 expression in antibody-producing cells and by increasing Fc sialylation. These observations provide a mechanistic explanation for the increased risk of RA in conditions with low estrogen levels such as menopause.
Journal Article
Extensive glycosylation of ACPA-IgG variable domains modulates binding to citrullinated antigens in rheumatoid arthritis
2016
ObjectivesTo understand the molecular features distinguishing anti-citrullinated protein antibodies (ACPA) from ‘conventional’ antibodies in rheumatoid arthritis (RA).MethodsSerum of ACPA-positive RA patients was fractionated by size exclusion chromatography and analysed for the presence of ACPA-IgG by ELISA. ACPA-IgG and non-citrulline-specific IgG were affinity purified from serum, plasma and/or synovial fluid and analysed by gel electrophoresis. Electrophoresis bands were excised, enzymatically digested and analysed by mass spectrometry. Binding affinity to citrullinated antigens was measured by ELISA and imaging surface plasmon resonance using recombinant monoclonal ACPA with molecular modifications.ResultsIn all donor samples studied (n=24), ACPA-IgG exhibited a 10–20 kDa higher molecular weight compared with non-autoreactive IgG. This feature also distinguished ACPA-IgG from antibodies against recall antigens or other disease-specific autoantibodies. Structural analysis revealed that a high frequency of N-glycans in the (hyper)variable domains of ACPA is responsible for this observation. In line with their localisation, these N-glycans were found to modulate binding avidity of ACPA to citrullinated antigens.ConclusionsThe vast majority of ACPA-IgG harbour N-glycans in their variable domains. As N-linked glycosylation requires glycosylation consensus sites in the protein sequence and as these are lacking in the ‘germline-counterparts’ of identified variable domains, our data indicate that the N-glycosylation sites in ACPA variable domains have been introduced by somatic hypermutation. This finding also suggests that ACPA-hyperglycosylation confers a selective advantage to ACPA-producing B cells. This unique and completely novel feature of the citrulline-specific immune response in RA elucidates our understanding of the underlying B cell response.
Journal Article
Growth study under combined effects of temperature, pH and salinity and transcriptome analysis revealed adaptations of Aspergillus terreus NTOU4989 to the extreme conditions at Kueishan Island Hydrothermal Vent Field, Taiwan
by
Hwang, Jiang-Shiou
,
Shih, Chi-Yu
,
Cha, Hyo-Jung
in
Adaptation
,
Amino acid oxidase
,
Amino acids
2020
A high diversity of fungi was discovered on various substrates collected at the marine shallow-water Kueishan Island Hydrothermal Vent Field, Taiwan, using culture and metabarcoding methods but whether these fungi can grow and play an active role in such an extreme environment is unknown. We investigated the combined effects of different salinity, temperature and pH on growth of ten fungi (in the genera Aspergillus, Penicillium, Fodinomyces, Microascus, Trichoderma, Verticillium) isolated from the sediment and the vent crab Xenograpsus testudinatus. The growth responses of the tested fungi could be referred to three groups: (1) wide pH, salinity and temperature ranges, (2) salinity-dependent and temperature-sensitive, and (3) temperature-tolerant. Aspergillus terreus NTOU4989 was the only fungus which showed growth at 45 °C, pH 3 and 30 ‰ salinity, and might be active near the vents. We also carried out a transcriptome analysis to understand the molecular adaptations of A. terreus NTOU4989 under these extreme conditions. Data revealed that stress-related genes were differentially expressed at high temperature (45 °C); for instance, mannitol biosynthetic genes were up-regulated while glutathione S-transferase and amino acid oxidase genes down-regulated in response to high temperature. On the other hand, hydrogen ion transmembrane transport genes and phenylalanine ammonia lyase were up-regulated while pH-response transcription factor was down-regulated at pH 3, a relative acidic environment. However, genes related to salt tolerance, such as glycerol lipid metabolism and mitogen-activated protein kinase, were up-regulated in both conditions, possibly related to maintaining water homeostasis. The results of this study revealed the genetic evidence of adaptation in A. terreus NTOU4989 to changes of environmental conditions.
Journal Article