Activation of TGR5 Increases Urine Concentration by Inducing AQP2 and AQP3 Expression in Renal Medullary Collecting Ducts.

Introduction: G protein-coupled bile acid receptor (TGR5), the first G protein-coupled receptor for bile acids identified, is capable of activating a variety of intracellular signaling pathways after interacting with bile acids. TGR5 plays an important role in multiple physiological processes and is considered to be a potential target for the treatment of various metabolic diseases, including type 2 diabetes. Evidence has emerged that genetic deletion of TGR5 results in an increase in basal urine output, suggesting that it may play a critical role in renal water and salt reabsorption. The present study aims to elucidate the effect and mechanism of TGR5 activation on urine concentration. Methods: Mice were treated with TGR5 agonists (LCA and INT-777) for 3 days. The 24-h urine of mice was collected and analyzed for urine biochemical parameters. The mRNA expressions were detected by real-time PCR, and the protein expressions were detected by western blot. Immunohistochemistry and immunofluorescence were performed to examine the cellular location of proteins. The cultured primary medullary collecting duct cells were pretreated with H89 (a PKA inhibitor) for 1 h, followed by 12-h treatment of LCA and INT-777. Luciferase reporter assays were used to detect the effect of CREB on the gene transcription of AQPs. Gel electrophoretic mobility shift assays were used to analyze DNA-protein interactions. Results: Treatment of mice with the TGR5 agonist LCA and INT-777 markedly reduced urine output and increased urine osmolality, accompanied by a marked increase in AQP2 and AQP3 protein expression and membrane translocation. In cultured primary medullary collecting duct cells, LCA and INT-777 dose-dependently upregulated AQP2 and AQP3 expression in a cAMP/PKA-dependent manner. Mechanistically, both AQP2 and AQP3 gene promoter contains a putative CREB-binding site, which can be bound and activated by CREB as assessed by both gene promoter-driven luciferase and gel shift assays. Conclusion: Collectively, our findings demonstrate that activation of TGR5 can promote urine concentration by upregulation of AQP2 and AQP3 expression in renal collecting ducts. TGR5 may represent an attractive target for the treatment of patients with urine concentration defect.

Bile acid receptors and renal regulation of water homeostasis.

The kidney is the key organ responsible for maintaining the body's water and electrolyte homeostasis. About 99% of the primary urine filtered from the Bowman's capsule is reabsorbed along various renal tubules every day, with only 1-2 L of urine excreted. Aquaporins (AQPs) play a vital role in water reabsorption in the kidney. Currently, a variety of molecules are found to be involved in the process of urine concentration by regulating the expression or activity of AQPs, such as antidiuretic hormone, renin-angiotensin-aldosterone system (RAAS), prostaglandin, and several nuclear receptors. As the main bile acid receptors, farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor 1 (TGR5) play important roles in bile acid, glucose, lipid, and energy metabolism. In the kidney, FXR and TGR5 exhibit broad expression across all segments of renal tubules, and their activation holds significant therapeutic potential for numerous acute and chronic kidney diseases through alleviating renal lipid accumulation, inflammation, oxidative stress, and fibrosis. Emerging evidence has demonstrated that the genetic deletion of FXR or TGR5 exhibits increased basal urine output, suggesting that bile acid receptors play a critical role in urine concentration. Here, we briefly summarize the function of bile acid receptors in renal water reabsorption and urine concentration.

Role of FXR in Renal Physiology and Kidney Diseases.

Farnesoid X receptor, also known as the bile acid receptor, belongs to the nuclear receptor (NR) superfamily of ligand-regulated transcription factors, which performs its functions by regulating the transcription of target genes. FXR is highly expressed in the liver, small intestine, kidney and adrenal gland, maintaining homeostasis of bile acid, glucose and lipids by regulating a diverse array of target genes. It also participates in several pathophysiological processes, such as inflammation, immune responses and fibrosis. The kidney is a key organ that manages water and solute homeostasis for the whole body, and kidney injury or dysfunction is associated with high morbidity and mortality. In the kidney, FXR plays an important role in renal water reabsorption and is thought to perform protective functions in acute kidney disease and chronic kidney disease, especially diabetic kidney disease. In this review, we summarize the recent advances in the understanding of the physiological and pathophysiological function of FXR in the kidney.

A Computational Toolbox to Investigate the Metabolic Potential and Resource Allocation in Fission Yeast.

The fission yeast, Schizosaccharomyces pombe, is a popular eukaryal model organism for cell division and cell cycle studies. With this extensive knowledge of its cell and molecular biology, S. pombe also holds promise for use in metabolism research and industrial applications. However, unlike the baker's yeast, Saccharomyces cerevisiae, a major workhorse in these areas, cell physiology and metabolism of S. pombe remain less explored. One way to advance understanding of organism-specific metabolism is construction of computational models and their use for hypothesis testing. To this end, we leverage existing knowledge of S. cerevisiae to generate a manually curated high-quality reconstruction of S. pombe's metabolic network, including a proteome-constrained version of the model. Using these models, we gain insights into the energy demands for growth, as well as ribosome kinetics in S. pombe. Furthermore, we predict proteome composition and identify growth-limiting constraints that determine optimal metabolic strategies under different glucose availability regimes and reproduce experimentally determined metabolic profiles. Notably, we find similarities in metabolic and proteome predictions of S. pombe with S. cerevisiae, which indicate that similar cellular resource constraints operate to dictate metabolic organization. With these cases, we show, on the one hand, how these models provide an efficient means to transfer metabolic knowledge from a well-studied to a lesser-studied organism, and on the other, how they can successfully be used to explore the metabolic behavior and the role of resource allocation in driving different strategies in fission yeast. IMPORTANCE Our understanding of microbial metabolism relies mostly on the knowledge we have obtained from a limited number of model organisms, and the diversity of metabolism beyond the handful of model species thus remains largely unexplored in mechanistic terms. Computational modeling of metabolic networks offers an attractive platform to bridge the knowledge gap and gain new insights into physiology of lesser-studied organisms. Here we showcase an example of successful knowledge transfer from the budding yeast Saccharomyces cerevisiae to a popular model organism in molecular and cell biology, fission yeast Schizosaccharomyces pombe, using computational models.

Intranasal administration of white tea alleviates the olfactory function deficit induced by chronic unpredictable mild stress.

CONTEXT: White tea [Camellia sinensis (L) O.Ktze. (Theaceae)] is popular in Asia, but its benefits on olfactory injury are unknown. OBJECTIVE: The present study explores the effects of white tea on the olfactory injury caused by chronic unpredictable mild stress (CUMS). MATERIALS AND METHODS: C57BL/6J mice (WT) were exposed to CUMS. CUMS mice (CU) were intranasally treated with white tea extract [low tea (LT), 20 mg/kg; high tea (HT), 40 mg/kg] and fluoxetine (CF, 20 mg/kg) for 7 days. Several behavioural tests were conducted to assess depression and olfactory function. The transmission electron microscope (TEM) and semi-quantitative reverse transcription PCR were performed separately to observe the changes of related structures and genes transcription level. RESULTS: The depressive behaviours of the LT and HT mice were reversed. The latency time of the buried food pellet test decreased from 280 s (CU) to 130 s (HT), while the olfactory sensitivity and olfactory avoidance test showed that the olfactory behaviours disorder of LT and HT mice were alleviated. The white tea increased the A490 nm values of the cortisol treated cells from 0.15 to 1.4. Reduced mitochondrial and synaptic damage in the olfactory bulb (OB), enhanced expression of the brain-derived neurotrophic factor (BDNF) and olfactory marker protein (OMP) were observed in the LT and HT mice. CONCLUSIONS AND DISCUSSION: White tea has the potential in curing the olfactory deficiency related to chronic stress. It lays the foundation for the development of new and reliable drug to improve olfactory.

Age-specific effects of P2X7 receptors on olfactory function in mice.

This study aimed to explore the age-specific effects of P2X7 receptor (P2X7R) knockout on olfactory function in mice. In this study, we analyzed olfactory functions of 2-month-old, 10-month-old and 18-month-old female P2X7R KO mice and age-matched female C57BL/6 wildtype mice (WT mice) by buried food seeking test and olfactory avoidance test. The structure of mitochondria and synapses in olfactory bulb were observed by electron microscopy. The content of interleukin-1 (IL-1ß) in olfactory bulb and transforming growth factor beta 1 (TGF-ß1) in olfactory epithelium were analyzed by ELISA. The results indicated that middle and old-aged P2X7R KO mice showed better olfactory function than middle and old-aged WT mice. Mitochondrial structures were complete and more spine synapses were observed in middle and old-aged P2X7R KO mice. Compared with middle and old-aged WT mice, IL-1ß content in olfactory bulb was decreased in middle and old-aged P2X7R KO mice, and there was no significant difference in TGF-ß1 content in olfactory epithelium. However, worse olfactory function was observed in young-aged P2X7R KO mice compared with young-aged WT mice. Abnormal mitochondrial structure and less synapses in olfactory bulb were observed. TGF-ß1 content in olfactory epithelium was significantly higher in P2X7R KO mice compared with young-aged WT mice. There was no significant difference in IL-1ß content in olfactory bulb of young-aged mice. In conclusion, P2X7R knockout can improve the olfactory function of middle and old-aged mice, while it may cause damage to young-aged mice, suggesting that P2X7R plays age-specific role on olfactory functions in mice.

The effects of P2X7 receptor knockout on emotional conditions over the lifespan of mice.

Neuroinflammation is one of the key factors contributing to depression. Recent studies have identified P2X7 receptor (P2X7r) as a major inflammatory regulator. However, the effects of P2X7r knockout (KO) on emotional conditions over the lifespan of mice are unknown. In this study, the effects of P2X7r deletion on emotional conditions over the lifespan of mice were investigated in young-aged (2 month old), middle-aged (10 month old), and old-aged (18 month old) female P2X7r KO mice and age-matched female C57BL/6 mice. Behavioral tasks were conducted by open field test, forced swimming test and sucrose preference test. Mitochondrial structures and spine synapses in hippocampus were examined by electron microscopy. Enzyme-linked immunosorbent assay was used to analyze the expression of interleukin-1ß and tumor necrosis factor-α. Western blot analysis was used to assess the expression of nuclear factor-kappa B (NF-κB) pathway-related proteins. The results indicated that middle-aged P2X7r KO mice displayed better emotional conditions than middle-aged WT mice. However, worse emotional conditions were observed in young-aged P2X7r KO mice. Moreover, abnormal mitochondrial structures and less spine synapses were observed in young-aged P2X7r KO mice. Mitochondrial structures were recovered and more spine synapses occurred in middle-aged P2X7r KO mice. In addition, expressions of interleukin-1ß, tumor necrosis factor-α, p-IKKα, p-IKKß, p-IκBα, and p-NF-κBp65 were decreased in middle-aged P2X7r KO mice, but increased in young-aged P2X7r KO mice. In conclusion, P2X7r KO improves the emotional conditions at later stages of the lifespan of mice, but not in all ages, suggesting time-specific roles of immune response in nervous system through NF-κB signaling pathway. Video abstract: http://links.lww.com/WNR/A494.

A perspective demonstration on the importance of variable selection in inverse calibration for complex analytical systems.

Classical calibration and inverse calibration are two kinds of multivariate calibration in chemical modeling. They use strategies of modeling in component spectral space and in measured variable space, respectively. However, the intrinsic difference between these two calibration models is not fully investigated. Besides, in the case of complex analytical systems, the net analyte signal (NAS) cannot be well defined in inverse calibration due to the existence of uninformative and/or interfering variables. Therefore, application of the NAS cannot improve the predictive performance for this kind of calibration, since it is essentially a technique based on the full-spectrum. From our perspective, variable selection can significantly improve the predictive performance through removing uninformative and/or interfering variables. Although the need for variable selection in the inverse calibration model has already been experimentally demonstrated, it has not aroused so much attention. In this study, we first clarify the intrinsic difference between these two calibration models and then use a new perspective to intrinsically prove the importance of variable selection in the inverse calibration model for complex analytical systems. In addition, we have experimentally validated our viewpoint through the use of one UV dataset and two generated near infrared (NIR) datasets.

Numerical model for the investigation of countercurrent chromatography.

A numerical model is developed to describe the separation process of countercurrent chromatography (CCC) in this work. The theory of countercurrent extraction table (TCCET) is first proposed to calculate concentration distributions of chemical components in the CCC, which is essential for a numerical model to describe the dynamic equilibrium of mass transfer. According to the theory of countercurrent extraction, the concentration in chromatography obeys binomial distribution, while the outflow from the n-th stage is a negative binomial distribution. As a result of the central limit theorem, they will obey normal distribution for sufficiently large n. Row-stage ratio (R(RS)) is then defined to determine the K value or retention time because it has a linear relationship to K value and retention time. The stage for a certain K value can be subsequently obtained with a very simple form, n(k)=1/(2piq(k)X(2)(k, max)), which can be calculated from the peak height obtained from experiments. Finally, the actual stage for a separation chromatogram can be acquired with using this simple expression. The agreement between theoretic and experimental results is quite satisfactory in the normal-phase and reversed-phase elution mode.

Enhancing the photoelectrical performance of dye-sensitized solar cells using TiO2:Eu3+ nanorods.

TiO(2):Eu(3+) nanorods are hydrothermally grown and used to fabricate a bilayer film electrode in a dye-sensitized solar cell. A light-to-electrical energy conversion efficiency of 8.0% and a quantum efficiency of 93.7% (at 575 nm) is achieved in this solar cell. The high efficiency is due to the improvement of ultraviolet light harvesting via a down-conversion luminescence process by the Eu(3+) ion and the increase of light scattering by one-dimensional TiO(2).