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  1. Article ; Online: Soluble Klotho, a Potential Biomarker of Chronic Kidney Disease-Mineral Bone Disorders Involved in Healthy Ageing: Lights and Shadows.

    Martín-Vírgala, Julia / Martín-Carro, Beatriz / Fernández-Villabrille, Sara / Ruiz-Torres, María Piedad / Gómez-Alonso, Carlos / Rodríguez-García, Minerva / Fernández-Martín, José Luis / Alonso-Montes, Cristina / Panizo, Sara / Cannata-Andía, Jorge B / Naves-Díaz, Manuel / Carrillo-López, Natalia

    International journal of molecular sciences

    2024  Volume 25, Issue 3

    Abstract: Shortly after the discovery of Klotho, interest grew in its potential role in chronic kidney disease (CKD). There are three isoforms of the Klotho protein: αKlotho, βKlotho and γKlotho. This review will focus on αKlotho due to its relevance as a ... ...

    Abstract Shortly after the discovery of Klotho, interest grew in its potential role in chronic kidney disease (CKD). There are three isoforms of the Klotho protein: αKlotho, βKlotho and γKlotho. This review will focus on αKlotho due to its relevance as a biomarker in CKD. αKlotho is synthesized mainly in the kidneys, but it can be released into the bloodstream and urine as soluble Klotho (sKlotho), which undertakes systemic actions, independently or in combination with FGF23. It is usually accepted that sKlotho levels are reduced early in CKD and that lower levels of sKlotho might be associated with the main chronic kidney disease-mineral bone disorders (CKD-MBDs): cardiovascular and bone disease. However, as results are inconsistent, the applicability of sKlotho as a CKD-MBD biomarker is still a matter of controversy. Much of the inconsistency can be explained due to low sample numbers, the low quality of clinical studies, the lack of standardized assays to assess sKlotho and a lack of consensus on sample processing, especially in urine. In recent decades, because of our longer life expectancies, the prevalence of accelerated-ageing diseases, such as CKD, has increased. Exercise, social interaction and caloric restriction are considered key factors for healthy ageing. While exercise and social interaction seem to be related to higher serum sKlotho levels, it is not clear whether serum sKlotho might be influenced by caloric restriction. This review focuses on the possible role of sKlotho as a biomarker in CKD-MBD, highlighting the difference between solid knowledge and areas requiring further research, including the role of sKlotho in healthy ageing.
    MeSH term(s) Humans ; Biomarkers ; Chronic Kidney Disease-Mineral and Bone Disorder/diagnosis ; Fibroblast Growth Factors ; Glucuronidase ; Healthy Aging/metabolism ; Minerals ; Renal Insufficiency, Chronic/complications ; Klotho Proteins/blood ; Klotho Proteins/metabolism
    Chemical Substances Biomarkers ; Fibroblast Growth Factors (62031-54-3) ; Glucuronidase (EC 3.2.1.31) ; Minerals ; Klotho Proteins (EC 3.2.1.31)
    Language English
    Publishing date 2024-02-03
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms25031843
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  2. Article ; Online: Novel Biomarkers of Bone Metabolism.

    Fernández-Villabrille, Sara / Martín-Carro, Beatriz / Martín-Vírgala, Julia / Rodríguez-Santamaria, Mª Del Mar / Baena-Huerta, Francisco / Muñoz-Castañeda, Juan Rafael / Fernández-Martín, José Luis / Alonso-Montes, Cristina / Naves-Díaz, Manuel / Carrillo-López, Natalia / Panizo, Sara

    Nutrients

    2024  Volume 16, Issue 5

    Abstract: Bone represents a metabolically active tissue subject to continuous remodeling orchestrated by the dynamic interplay between osteoblasts and osteoclasts. These cellular processes are modulated by a complex interplay of biochemical and mechanical factors, ...

    Abstract Bone represents a metabolically active tissue subject to continuous remodeling orchestrated by the dynamic interplay between osteoblasts and osteoclasts. These cellular processes are modulated by a complex interplay of biochemical and mechanical factors, which are instrumental in assessing bone remodeling. This comprehensive evaluation aids in detecting disorders arising from imbalances between bone formation and reabsorption. Osteoporosis, characterized by a reduction in bone mass and strength leading to heightened bone fragility and susceptibility to fractures, is one of the more prevalent chronic diseases. Some epidemiological studies, especially in patients with chronic kidney disease (CKD), have identified an association between osteoporosis and vascular calcification. Notably, low bone mineral density has been linked to an increased incidence of aortic calcification, with shared molecules, mechanisms, and pathways between the two processes. Certain molecules emerging from these shared pathways can serve as biomarkers for bone and mineral metabolism. Detecting and evaluating these alterations early is crucial, requiring the identification of biomarkers that are reliable for early intervention. While traditional biomarkers for bone remodeling and vascular calcification exist, they suffer from limitations such as low specificity, low sensitivity, and conflicting results across studies. In response, efforts are underway to explore new, more specific biomarkers that can detect alterations at earlier stages. The aim of this review is to comprehensively examine some of the emerging biomarkers in mineral metabolism and their correlation with bone mineral density, fracture risk, and vascular calcification as well as their potential use in clinical practice.
    MeSH term(s) Humans ; Chronic Kidney Disease-Mineral and Bone Disorder/complications ; Osteoporosis/etiology ; Bone Density/physiology ; Renal Insufficiency, Chronic/complications ; Fractures, Bone/etiology ; Vascular Calcification/complications ; Biomarkers ; Minerals
    Chemical Substances Biomarkers ; Minerals
    Language English
    Publishing date 2024-02-22
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu16050605
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  3. Article ; Online: Influence of Kv11.1 (hERG1) K

    Fernández-Villabrille, Sara / Álvarez-González, Enol / Barros, Francisco / de la Peña, Pilar / Sierra, Luisa María

    Pflugers Archiv : European journal of physiology

    2021  Volume 473, Issue 2, Page(s) 197–217

    Abstract: Besides their crucial role in cell electrogenesis and maintenance of basal membrane potential, the voltage-dependent ... ...

    Abstract Besides their crucial role in cell electrogenesis and maintenance of basal membrane potential, the voltage-dependent K
    MeSH term(s) Antineoplastic Agents/pharmacology ; Apoptosis/drug effects ; Cell Cycle/drug effects ; Cell Survival/drug effects ; DNA Damage ; ERG1 Potassium Channel/genetics ; ERG1 Potassium Channel/metabolism ; HEK293 Cells ; Humans ; Membrane Potentials ; Methyl Methanesulfonate/pharmacology ; Poly (ADP-Ribose) Polymerase-1/genetics ; Poly (ADP-Ribose) Polymerase-1/metabolism
    Chemical Substances Antineoplastic Agents ; ERG1 Potassium Channel ; KCNH2 protein, human ; Methyl Methanesulfonate (AT5C31J09G) ; PARP1 protein, human (EC 2.4.2.30) ; Poly (ADP-Ribose) Polymerase-1 (EC 2.4.2.30)
    Language English
    Publishing date 2021-01-15
    Publishing country Germany
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 6380-0
    ISSN 1432-2013 ; 0031-6768
    ISSN (online) 1432-2013
    ISSN 0031-6768
    DOI 10.1007/s00424-021-02517-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Effects of a Losartan-Antioxidant Hybrid (GGN1231) on Vascular and Cardiac Health in an Experimental Model of Chronic Renal Failure.

    Martínez-Arias, Laura / Fernández-Villabrille, Sara / Alonso-Montes, Cristina / García-Navazo, Gonzalo / Ruíz-Torres, María P / Alajarín, Ramón / Alvarez-Builla, Julio / Gutiérrez-Calabres, Elena / Vaquero-López, Juan José / Carrillo-López, Natalia / Rodríguez-Puyol, Diego / Cannata-Andía, Jorge B / Panizo, Sara / Naves-Díaz, Manuel

    Nutrients

    2023  Volume 15, Issue 8

    Abstract: Drugs providing antihypertensive and protective cardiovascular actions are of clinical interest in controlling cardiovascular events and slowing the progression of kidney disease. We studied the effect of a hybrid compound, GGN1231 (derived from losartan ...

    Abstract Drugs providing antihypertensive and protective cardiovascular actions are of clinical interest in controlling cardiovascular events and slowing the progression of kidney disease. We studied the effect of a hybrid compound, GGN1231 (derived from losartan in which a powerful antioxidant was attached), on the prevention of cardiovascular damage, cardiac hypertrophy, and fibrosis in a rat model of severe chronic renal failure (CRF). CRF by a 7/8 nephrectomy was carried out in male Wistar rats fed with a diet rich in phosphorous (0.9%) and normal calcium (0.6%) for a period of 12 weeks until sacrifice. In week 8, rats were randomized in five groups receiving different drugs including dihydrocaffeic acid as antioxidant (Aox), losartan (Los), dihydrocaffeic acid+losartan (Aox+Los) and GGN1231 as follows: Group 1 (CRF+vehicle group), Group 2 (CRF+Aox group), Group 3 (CRF+Los group), Group 4 (CRF+Aox+Los group), and Group 5 (CRF+GGN1231 group). Group 5, the CRF+GGN1231 group, displayed reduced proteinuria, aortic TNF-α, blood pressure, LV wall thickness, diameter of the cardiomyocytes, ATR1, cardiac TNF-α and fibrosis, cardiac collagen I, and TGF-β1 expression. A non-significant 20% reduction in the mortality was also observed. This study showed the possible advantages of GGN1231, which could help in the management of cardiovascular and inflammatory processes. Further research is needed to confirm and even expand the positive aspects of this compound.
    MeSH term(s) Rats ; Male ; Animals ; Losartan/pharmacology ; Losartan/therapeutic use ; Antioxidants/pharmacology ; Antioxidants/therapeutic use ; Tumor Necrosis Factor-alpha/pharmacology ; Rats, Wistar ; Kidney Failure, Chronic ; Models, Theoretical ; Fibrosis ; Kidney/metabolism
    Chemical Substances Losartan (JMS50MPO89) ; 3,4-dihydroxyphenylpropionic acid (1078-61-1) ; Antioxidants ; Tumor Necrosis Factor-alpha
    Language English
    Publishing date 2023-04-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu15081820
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  5. Article ; Online: Experimental Models to Study Diabetes Mellitus and Its Complications: Limitations and New Opportunities.

    Martín-Carro, Beatriz / Donate-Correa, Javier / Fernández-Villabrille, Sara / Martín-Vírgala, Julia / Panizo, Sara / Carrillo-López, Natalia / Martínez-Arias, Laura / Navarro-González, Juan F / Naves-Díaz, Manuel / Fernández-Martín, José L / Alonso-Montes, Cristina / Cannata-Andía, Jorge B

    International journal of molecular sciences

    2023  Volume 24, Issue 12

    Abstract: Preclinical biomedical models are a fundamental tool to improve the knowledge and management of diseases, particularly in diabetes mellitus (DM) since, currently, the pathophysiological and molecular mechanisms involved in its development are not fully ... ...

    Abstract Preclinical biomedical models are a fundamental tool to improve the knowledge and management of diseases, particularly in diabetes mellitus (DM) since, currently, the pathophysiological and molecular mechanisms involved in its development are not fully clarified, and there is no treatment to cure DM. This review will focus on the features, advantages and limitations of some of the most used DM models in rats, such as the spontaneous models: Bio-Breeding Diabetes-Prone (BB-DP) and LEW.1AR1-
    MeSH term(s) Humans ; Rats ; Animals ; Disease Models, Animal ; Streptozocin ; Rats, Zucker ; Diabetes Mellitus, Type 1/complications ; Diabetes Mellitus, Type 2/complications
    Chemical Substances Streptozocin (5W494URQ81)
    Language English
    Publishing date 2023-06-18
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms241210309
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  6. Article ; Online: MicroRNA-145 and microRNA-486 are potential serum biomarkers for vascular calcification.

    Fernández-Villabrille, Sara / Martín-Carro, Beatriz / Martín-Vírgala, Julia / Alonso-Montes, Cristina / Palomo-Antequera, Carmen / García-Castro, Raúl / López-Ongil, Susana / Dusso, Adriana S / Fernández-Martín, José Luis / Naves-Díaz, Manuel / Cannata-Andía, Jorge B / Carrillo-López, Natalia / Panizo, Sara

    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

    2023  Volume 38, Issue 7, Page(s) 1729–1740

    Abstract: Introduction: MicroRNAs (miRs) regulate vascular calcification (VC), and their quantification may contribute to suspicion of the presence of VC.: Methods: The study was performed in four phases. Phase 1: miRs sequencing of rat calcified and non- ... ...

    Abstract Introduction: MicroRNAs (miRs) regulate vascular calcification (VC), and their quantification may contribute to suspicion of the presence of VC.
    Methods: The study was performed in four phases. Phase 1: miRs sequencing of rat calcified and non-calcified aortas. Phase 2: miRs with the highest rate of change, plus miR-145 [the most abundant miR in vascular smooth muscle cells (VSMCs)], were validated in aortas and serum from rats with and without VC. Phase 3: the selected miRs were analyzed in epigastric arteries from kidney donors and recipients, and serum samples from general population. Phase 4: VSMCs were exposed to different phosphorus concentrations, and miR-145 and miR-486 were overexpressed to investigate their role in VC.
    Results: miR-145, miR-122-5p, miR-486 and miR-598-3p decreased in the rat calcified aortas, but only miR-145 and miR-486 were detected in serum. In human epigastric arteries, miR-145 and miR-486 were lower in kidney transplant recipients compared with donors. Both miRs inversely correlated with arterial calcium content and with VC (Kauppila index). In the general population, the severe VC was associated with the lowest serum levels of both miRs. The receiver operating characteristic curve showed that serum miR-145 was a good biomarker of VC. In VSMCs exposed to high phosphorus, calcium content, osteogenic markers (Runx2 and Osterix) increased, and the contractile marker (α-actin), miR-145 and miR-486 decreased. Overexpression of miR-145, and to a lesser extent miR-486, prevented the increase in calcium content induced by high phosphorus, the osteogenic differentiation and the loss of the contractile phenotype.
    Conclusion: miR-145 and miR-486 regulate the osteogenic differentiation of VSMCs, and their quantification in serum could serve as a marker of VC.
    MeSH term(s) Animals ; Humans ; Rats ; Biomarkers ; Calcium ; MicroRNAs/genetics ; Muscle, Smooth, Vascular ; Myocytes, Smooth Muscle ; Osteogenesis/genetics ; Phosphorus ; Vascular Calcification/genetics
    Chemical Substances Biomarkers ; Calcium (SY7Q814VUP) ; MicroRNAs ; MIRN-598 microRNA, human ; MIRN145 microRNA, human ; MIRN145 microRNA, rat ; MIRN486 microRNA, human ; Phosphorus (27YLU75U4W)
    Language English
    Publishing date 2023-01-30
    Publishing country England
    Document type Journal Article
    ZDB-ID 90594-x
    ISSN 1460-2385 ; 0931-0509
    ISSN (online) 1460-2385
    ISSN 0931-0509
    DOI 10.1093/ndt/gfad027
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  7. Article ; Online: Phosphorus May Induce Phenotypic Transdifferentiation of Vascular Smooth Muscle Cells through the Reduction of microRNA-145.

    Fernández-Villabrille, Sara / Martín-Carro, Beatriz / Martín-Vírgala, Julia / Alonso-Montes, Cristina / Fernández-Fernández, Alejandra / Martínez-Salgado, Carlos / Fernández-Martín, José L / Naves-Díaz, Manuel / Cannata-Andía, Jorge B / Carrillo-López, Natalia / Panizo, Sara

    Nutrients

    2023  Volume 15, Issue 13

    Abstract: Phosphorus is a vital element for life found in most foods as a natural component, but it is also one of the most used preservatives added during food processing. High serum phosphorus contributes to develop vascular calcification in chronic kidney ... ...

    Abstract Phosphorus is a vital element for life found in most foods as a natural component, but it is also one of the most used preservatives added during food processing. High serum phosphorus contributes to develop vascular calcification in chronic kidney disease; however, it is not clear its effect in a population without kidney damage. The objective of this in vivo and in vitro study was to investigate the effect of high phosphorus exposure on the aortic and serum levels of miR-145 and its effect on vascular smooth muscle cell (VSMCs) changes towards less contractile phenotypes. The study was performed in aortas and serum from rats fed standard and high-phosphorus diets, and in VSMCs exposed to different concentrations of phosphorus. In addition, miR-145 silencing and overexpression experiments were carried out. In vivo results showed that in rats with normal renal function fed a high P diet, a significant increase in serum phosphorus was observed which was associated to a significant decrease in the aortic α-actin expression which paralleled the decrease in aortic and serum miR-145 levels, with no changes in the osteogenic markers. In vitro results using VSMCs corroborated the in vivo findings. High phosphorus first reduced miR-145, and afterwards α-actin expression. The miR-145 overexpression significantly increased α-actin expression and partially prevented the increase in calcium content. These results suggest that miR-145 could be an early biomarker of vascular calcification, which could give information about the initiation of the transdifferentiation process in VSMCs.
    MeSH term(s) Rats ; Animals ; Phosphorus/metabolism ; Muscle, Smooth, Vascular ; Actins/metabolism ; Cell Transdifferentiation ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Phenotype ; Vascular Calcification/genetics ; Vascular Calcification/metabolism ; Myocytes, Smooth Muscle ; Cells, Cultured
    Chemical Substances Phosphorus (27YLU75U4W) ; Actins ; MicroRNAs ; MIRN145 microRNA, rat
    Language English
    Publishing date 2023-06-27
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu15132918
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  8. Article ; Online: Contribution of phosphorus and PTH to the development of cardiac hypertrophy and fibrosis in an experimental model of chronic renal failure.

    Martínez-Arias, Laura / Panizo-García, Sara / Martín-Vírgala, Julia / Martín-Carro, Beatriz / Fernández-Villabrille, Sara / Avello-Llano, Noelia / Miguel-Fernández, Diego / Ruíz Torres, María Piedad / Cannata-Andía, Jorge B / Carrillo-López, Natalia / Naves-Díaz, Manuel

    Nefrologia

    2022  Volume 41, Issue 6, Page(s) 640–651

    Abstract: Background and objective: Adequate serum phosphorus levels in patients with chronic kidney disease is essential for their clinical management. However, the control of hyperphosphatemia is difficult because is normally associated with increases in serum ... ...

    Abstract Background and objective: Adequate serum phosphorus levels in patients with chronic kidney disease is essential for their clinical management. However, the control of hyperphosphatemia is difficult because is normally associated with increases in serum PTH. In the present study, the effects of hyperphosphatemia, in the presence of elevated and normal PTH, on cardiac inflammation, hypertrophy and fibrosis in an experimental renal failure model were analyzed.
    Materials and methods: 4 groups of rats were formed. Two groups underwent total parathyroidectomy (PTx). Rats with Ca <7.5 mg/dL and PTH < 50 pg/mL underwent 7/8 nephrectomy (CRF) and a subcutaneous pellet was placed that releases PTH 1-34 (5 µg/kg/day). One group received a diet with normal P (NP) (CRF + PTx + rPTH + NP group) and another with a high P diet (0.9% - HP) (CRF + PTx + rPTH + HP group). Other 2 groups that only had CRF received NP (CRF + NP) and HP (CRF + HP) diet. A SHAM group for nephrectomy and parathyroidectomy was also added. After 14 weeks the rats were sacrificed.
    Results: The groups with a diet high in phosphorus (CRF + H A and CRF + PTx + rPTH + HP) had a significant reduction in creatinine clearance and also in body weight with an increase in serum phosphorus regardless of parathyroidectomy, but not serum levels of calcium, FGF23 and calcitriol that were 2-3 times higher in the group with secondary hyperparathyroidism (CRF + HP). The diameter of the cardiomyocytes was greater in the CRF + HP group, while parathyroidectomy (CRF + PTx + rPTH + HP) significantly reduced them, despite the high and similar serum phosphorus values. TNF-α, Adam17 and cardiac fibrosis at the histological and molecular level showed a similar pattern with increases in the group with severe secondary hyperparathyroidism (CRF + HP).
    Conclusions: Hyperphosphatemia confirmed its importance in the genesis of secondary hyperparathyroidism, but also of kidney damage that was independent of PTH levels. However, inflammation, fibrosis, and cardiomyocyte growth were more closely related to PTH levels, since in the presence of similar severe hyperphosphatemia, parathyroidectomy reduced the values ​​of inflammatory parameters, cardiac hypertrophy, and fibrosis.
    MeSH term(s) Animals ; Calcitriol ; Calcium ; Cardiomegaly/complications ; Creatinine ; Fibrosis ; Humans ; Hyperparathyroidism, Secondary/complications ; Hyperparathyroidism, Secondary/surgery ; Hyperphosphatemia/etiology ; Inflammation ; Kidney Failure, Chronic/complications ; Models, Theoretical ; Phosphorus ; Rats ; Renal Insufficiency, Chronic/complications ; Tumor Necrosis Factor-alpha
    Chemical Substances Tumor Necrosis Factor-alpha ; Phosphorus (27YLU75U4W) ; Creatinine (AYI8EX34EU) ; Calcitriol (FXC9231JVH) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2022-01-03
    Publishing country Spain
    Document type Journal Article
    ZDB-ID 2837917-2
    ISSN 2013-2514 ; 2013-2514
    ISSN (online) 2013-2514
    ISSN 2013-2514
    DOI 10.1016/j.nefroe.2021.12.004
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  9. Article ; Online: Serum and Urinary Soluble α-Klotho as Markers of Kidney and Vascular Impairment.

    Martín-Vírgala, Julia / Fernández-Villabrille, Sara / Martín-Carro, Beatriz / Tamargo-Gómez, Isaac / Navarro-González, Juan F / Mora-Fernández, Carmen / Calleros, Laura / Astudillo-Cortés, Elena / Avello-Llano, Noelia / Mariño, Guillermo / Dusso, Adriana S / Alonso-Montes, Cristina / Panizo, Sara / Cannata-Andía, Jorge B / Naves-Díaz, Manuel / Carrillo-López, Natalia

    Nutrients

    2023  Volume 15, Issue 6

    Abstract: This study was designed to investigate the controversy on the potential role of sKlotho as an early biomarker in Chronic Kidney Disease-Mineral Bone Disorder (CKD-MBD), to assess whether sKlotho is a reliable marker of kidney α-Klotho, to deepen the ... ...

    Abstract This study was designed to investigate the controversy on the potential role of sKlotho as an early biomarker in Chronic Kidney Disease-Mineral Bone Disorder (CKD-MBD), to assess whether sKlotho is a reliable marker of kidney α-Klotho, to deepen the effects of sKlotho on vascular smooth muscle cells (VSMCs) osteogenic differentiation and to evaluate the role of autophagy in this process. Experimental studies were conducted in CKD mice fed a normal phosphorus (CKD+NP) or high phosphorus (CKD+HP) diet for 14 weeks. The patients' study was performed in CKD stages 2-5 and in vitro studies which used VSMCs exposed to non-calcifying medium or calcifying medium with or without sKlotho. The CKD experimental model showed that the CKD+HP group reached the highest serum PTH, P and FGF23 levels, but the lowest serum and urinary sKlotho levels. In addition, a positive correlation between serum sKlotho and kidney α-Klotho was found. CKD mice showed aortic osteogenic differentiation, together with increased autophagy. The human CKD study showed that the decline in serum sKlotho is previous to the rise in FGF23. In addition, both serum sKlotho and FGF23 levels correlated with kidney function. Finally, in VSMCs, the addition of sKlotho prevented osteogenic differentiation and induced autophagy. It can be concluded that serum sKlotho was the earliest CKD-MBD biomarker, a reliable indicator of kidney α-Klotho and that might protect against osteogenic differentiation by increasing autophagy. Nevertheless, further studies are needed to investigate the mechanisms of this possible protective effect.
    MeSH term(s) Humans ; Mice ; Animals ; Klotho Proteins ; Glucuronidase ; Chronic Kidney Disease-Mineral and Bone Disorder ; Osteogenesis ; Fibroblast Growth Factors ; Kidney ; Renal Insufficiency, Chronic ; Phosphorus ; Minerals ; Biomarkers
    Chemical Substances Klotho Proteins (EC 3.2.1.31) ; Glucuronidase (EC 3.2.1.31) ; Fibroblast Growth Factors (62031-54-3) ; Phosphorus (27YLU75U4W) ; Minerals ; Biomarkers
    Language English
    Publishing date 2023-03-18
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu15061470
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  10. Article ; Online: Redox Metabolism and Vascular Calcification in Chronic Kidney Disease.

    Carrillo-López, Natalia / Panizo, Sara / Martín-Carro, Beatriz / Mayo Barrallo, Juan Carlos / Román-García, Pablo / García-Castro, Raúl / Fernández-Gómez, Jesús María / Hevia-Suárez, Miguel Ángel / Martín-Vírgala, Julia / Fernández-Villabrille, Sara / Martínez-Arias, Laura / Vázquez, Sara Barrio / Calleros Basilio, Laura / Naves-Díaz, Manuel / Cannata-Andía, Jorge Benito / Quirós-González, Isabel / Alonso-Montes, Cristina / Fernández-Martín, José Luis

    Biomolecules

    2023  Volume 13, Issue 9

    Abstract: Vascular calcification (VC) is a common complication in patients with chronic kidney disease which increases their mortality. Although oxidative stress is involved in the onset and progression of this disorder, the specific role of some of the main redox ...

    Abstract Vascular calcification (VC) is a common complication in patients with chronic kidney disease which increases their mortality. Although oxidative stress is involved in the onset and progression of this disorder, the specific role of some of the main redox regulators, such as catalase, the main scavenger of H
    MeSH term(s) Humans ; Animals ; Rats ; Catalase ; Core Binding Factor Alpha 1 Subunit/genetics ; Hydrogen Peroxide ; Oxidation-Reduction ; Vascular Calcification ; Renal Insufficiency, Chronic
    Chemical Substances Catalase (EC 1.11.1.6) ; Core Binding Factor Alpha 1 Subunit ; Hydrogen Peroxide (BBX060AN9V)
    Language English
    Publishing date 2023-09-20
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom13091419
    Database MEDical Literature Analysis and Retrieval System OnLINE

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