scholarly journals Hydrogen sulfide (H2S) releasing agents: chemistry and biological applications

2014 ◽  
Vol 50 (80) ◽  
pp. 11788-11805 ◽  
Author(s):  
Yu Zhao ◽  
Tyler D. Biggs ◽  
Ming Xian

This Feature Article provides an overview of currently known hydrogen sulfide donors.

2017 ◽  
Vol 53 (35) ◽  
pp. 4748-4758 ◽  
Author(s):  
Balaram Mohapatra ◽  
Pratibha Pratibha ◽  
Sandeep Verma

This feature article outlines design strategies for modified adenine derivatives to construct discrete metal complexes, ring-expanded skeletons, coordination polymers, MOFs, and capped nanoparticles, for applications in gas adsorption, as bioimaging agents and as bioactive molecules.


ChemInform ◽  
2014 ◽  
Vol 45 (45) ◽  
pp. no-no ◽  
Author(s):  
Yu Zhao ◽  
Tyler D. Biggs ◽  
Ming Xian

2015 ◽  
Vol 51 (94) ◽  
pp. 16733-16749 ◽  
Author(s):  
Xinjun Xu ◽  
Ronghua Liu ◽  
Lidong Li

This feature article summarizes the recent applications of nanoparticles made of π-conjugated compounds in bio/chemo-sensing, disease therapy, and photoacoustic imaging.


2021 ◽  
Author(s):  
Huhui Fu ◽  
Yuhan Ma ◽  
Yongsheng Liu ◽  
Maochun Hong

This feature article overviews the recent advances in the local-structure-dependent luminescence in lanthanide-doped inorganic nanocrystals for various biological applications.


2014 ◽  
Vol 50 (82) ◽  
pp. 12234-12249 ◽  
Author(s):  
Fabiao Yu ◽  
Xiaoyue Han ◽  
Lingxin Chen

In this feature article, we address the synthesis and design strategies for the development of fluorescent probes for H2S, based on the reaction type between H2S and the probes.


Author(s):  
Philippe Fragu

The identification, localization and quantification of intracellular chemical elements is an area of scientific endeavour which has not ceased to develop over the past 30 years. Secondary Ion Mass Spectrometry (SIMS) microscopy is widely used for elemental localization problems in geochemistry, metallurgy and electronics. Although the first commercial instruments were available in 1968, biological applications have been gradual as investigators have systematically examined the potential source of artefacts inherent in the method and sought to develop strategies for the analysis of soft biological material with a lateral resolution equivalent to that of the light microscope. In 1992, the prospects offered by this technique are even more encouraging as prototypes of new ion probes appear capable of achieving the ultimate goal, namely the quantitative analysis of micron and submicron regions. The purpose of this review is to underline the requirements for biomedical applications of SIMS microscopy.Sample preparation methodology should preserve both the structural and the chemical integrity of the tissue.


2019 ◽  
Vol 133 (20) ◽  
pp. 2045-2059 ◽  
Author(s):  
Da Zhang ◽  
Xiuli Wang ◽  
Siyao Chen ◽  
Selena Chen ◽  
Wen Yu ◽  
...  

Abstract Background: Pulmonary artery endothelial cell (PAEC) inflammation is a critical event in the development of pulmonary arterial hypertension (PAH). However, the pathogenesis of PAEC inflammation remains unclear. Methods: Purified recombinant human inhibitor of κB kinase subunit β (IKKβ) protein, human PAECs and monocrotaline-induced pulmonary hypertensive rats were employed in the study. Site-directed mutagenesis, gene knockdown or overexpression were conducted to manipulate the expression or activity of a target protein. Results: We showed that hydrogen sulfide (H2S) inhibited IKKβ activation in the cell model of human PAEC inflammation induced by monocrotaline pyrrole-stimulation or knockdown of cystathionine γ-lyase (CSE), an H2S generating enzyme. Mechanistically, H2S was proved to inhibit IKKβ activity directly via sulfhydrating IKKβ at cysteinyl residue 179 (C179) in purified recombinant IKKβ protein in vitro, whereas thiol reductant dithiothreitol (DTT) reversed H2S-induced IKKβ inactivation. Furthermore, to demonstrate the significance of IKKβ sulfhydration by H2S in the development of PAEC inflammation, we mutated C179 to serine (C179S) in IKKβ. In purified IKKβ protein, C179S mutation of IKKβ abolished H2S-induced IKKβ sulfhydration and the subsequent IKKβ inactivation. In human PAECs, C179S mutation of IKKβ blocked H2S-inhibited IKKβ activation and PAEC inflammatory response. In pulmonary hypertensive rats, C179S mutation of IKKβ abolished the inhibitory effect of H2S on IKKβ activation and pulmonary vascular inflammation and remodeling. Conclusion: Collectively, our in vivo and in vitro findings demonstrated, for the first time, that endogenous H2S directly inactivated IKKβ via sulfhydrating IKKβ at Cys179 to inhibit nuclear factor-κB (NF-κB) pathway activation and thereby control PAEC inflammation in PAH.


Polymer News ◽  
2004 ◽  
Vol 29 (7) ◽  
pp. 205-212 ◽  
Author(s):  
Rengarajan Balaji ◽  
Sylvie Boileau ◽  
Philippe Guérin ◽  
Daniel Grande

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