In this paper, we present a comparative study of the pseudomorphic carbonatation of gypsum and anhydrite single crystals in Mg-bearing aqueous solutions at room temperature. We have found that carbonatation of gypsum an anhydrite occurs via a similar coupled dissolution–crystallization mechanism. However, whereas pseudomorphization of anhydrite precisely preserves the external form and dimension of the initial crystals, pseudomorphs after gypsum are less perfect and the shape and volume of the original crystals are partially lost. Furthermore, the mineralogical compositions of the pseudomorphs after anhydrite and gypsum are different, because gypsum is replaced by relatively large calcite crystals, while anhydrite pseudomorphs consist of aggregates of calcite and aragonite. Such textural and compositional differences can be clearly related to the length scale of the coupling between dissolution and crystallization at the replacement fronts. In situ atomic force microscopy observations of the early stages of carbonatation have shown that dissolution and crystallization are very tightly coupled on anhydrite rather than on gypsum surfaces. This clearly indicates that during the replacement of anhydrite and gypsum, dissolution and precipitation, respectively, are the rate-limiting steps. On the other hand, the higher supersaturation levels reached during the replacement of anhydrite lead to a competition between calcite and aragonite crystallization. This explains the fact that calcite and aragonite coexist within the replacement layers after anhydrite. Finally, we have found that dissolved magnesium in the reacting solutions is almost equally incorporated into the pseudomorphs, regardless of both the precursor phase and the mineralogical composition of the replacements. Our calculations and chemical analyses have shown that the compositions of the Mg x Ca1–x CO3 solid solution for which supersaturations reach maximum values correspond quite well with maximum Mg/Ca ratios in the replacement layers.
Background and Aims:The molecular mechanisms driving non-alcoholic fatty liver disease (NAFLD) are poorly understood; however, microRNAs might play a key role in these processes. We hypothesize that let-7d-5p could contribute to the pathophysiology of NAFLD and serve as a potential diagnostic biomarker. Methods:We evaluated let-7d-5p levels and its targets in liver biopsies from a crosssectional study including patients with NAFLD and healthy donors, and from a mouse model of NAFLD. Moreover, the induction of let-7d-5p expression by fatty acids was evaluated in vitro. Further, we overexpressed let-7d-5p in vitro to corroborate the results observed in vivo. Circulating let-7d-5p and its potential as a NAFLD biomarker was determined in isolated extracellular vesicles from human plasma by RT-qPCR. Results:Our results demonstrate that hepatic let-7d-5p was significantly up-regulated in patients with steatosis, and this increase correlated with obesity and a decreased | 1715 INFANTE-MENÉNDEZ et al.
Background: Cardiovascular dysfunction is linked to insulin-resistant states. In this paper, we analyzed whether the severe hepatic insulin resistance of an inducible liver-specific insulin receptor knockout (iLIRKO) might generate vascular insulin resistance and dysfunction, and whether insulin receptor (IR) isoforms gene therapy might revert it. Methods: We studied in vivo insulin signaling in aorta artery and heart from iLIRKO. Vascular reactivity and the mRNA levels of genes involved in vascular dysfunction were analyzed in thoracic aorta rings by qRT-PCR. Finally, iLIRKO mice were treated with hepatic-specific gene therapy to analyze vascular dysfunction improvement. Results: Our results suggest that severe hepatic insulin resistance was expanded to cardiovascular tissues. This vascular insulin resistance observed in aorta artery from iLIRKO mice correlated with a reduction in both PI3K/AKT/eNOS and p42/44 MAPK pathways, and it might be implicated in their vascular alterations characterized by endothelial dysfunction, hypercontractility and eNOS/iNOS levels’ imbalance. Finally, regarding long-term hepatic expression of IR isoforms, IRA was more efficient than IRB in the improvement of vascular dysfunction observed in iLIRKO mice. Conclusion: Severe hepatic insulin resistance is sufficient to produce cardiovascular insulin resistance and dysfunction. Long-term hepatic expression of IRA restored the vascular damage observed in iLIRKO mice.
Background: Cardiovascular diseases (CVDs) are the main cause of death in first world countries, being atherosclerosis, a recurring process underlying their apparition. MicroRNAs (miRNAs) are small non-coding RNAs that modulate the expression of their target proteins. Therefore, they have emerged as key players in diseases like cancer, diabetes, or CVDs.Methods: Apolipoprotein E-deficient (ApoE-/-) mice fed a standard type diet (STD) or high fat diet (HFD) for 8 and 18 weeks was compared to wild type (WT) STD-fed groups for the same time. 18 miRNAs were selected (from pubmed and GEO database) for their possible role in promoting atherosclerosis and were analysed by RT-qPCR in the aorta from the experimental model. Afterwards, the altered miRNAs in the aorta from 18 weeks-ApoE-/- mice were studied in human healthy aortic samples, human early aortic atherosclerotic plaques, and human advanced carotid atherosclerotic plaques. Results: From the 18 miRNAs analyzed, miR-155-5p was overexpressed and miR-143-3p was downregulated in mouse and human atherosclerotic lesions. In addition, a significant decrease of protein kinase B (AKT), target of miR-155-5p, and an increase of insulin-like growth factor type II receptor (IGF-IIR), target of miR-143-3p, were noted in aortic roots from ApoE-/- mice and in carotid plaques from ACA patients. Finally, both miRNAs were studied on vascular endothelial and smooth muscle cell lines. The overexpression of miR-155-5p reduced AKT levels and its phosphorylation in vascular smooth muscle cells. MiR-143-3p overexpression decreased IGF-IIR reducing apoptosis in vascular cells. Conclusions: Our results suggest that miR-155-5p and miR-143-3p may be implicated in insulin resistance and plaque instability by the modulation of their targets AKT and IGF-IIR, contributing to the progression of experimental and human atherosclerosis.Trial Registration: authorization numbers PFS09-007 and PI1442016.
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