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      An Update on Hydrogen Sulfide and Nitric Oxide Interactions in the Cardiovascular System

      review-article
      1 , , 2 , 1 ,
      Oxidative Medicine and Cellular Longevity
      Hindawi

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          Abstract

          Hydrogen sulfide (H 2S) and nitric oxide (NO) are now recognized as important regulators in the cardiovascular system, although they were historically considered as toxic gases. As gaseous transmitters, H 2S and NO share a wide range of physical properties and physiological functions: they penetrate into the membrane freely; they are endogenously produced by special enzymes, they stimulate endothelial cell angiogenesis, they regulate vascular tone, they protect against heart injury, and they regulate target protein activity via posttranslational modification. Growing evidence has determined that these two gases are not independent regulators but have substantial overlapping pathophysiological functions and signaling transduction pathways. H 2S and NO not only affect each other's biosynthesis but also produce novel species through chemical interaction. They play a regulatory role in the cardiovascular system involving similar signaling mechanisms or molecular targets. However, the natural precise mechanism of the interactions between H 2S and NO remains unclear. In this review, we discuss the current understanding of individual and interactive regulatory functions of H 2S and NO in biosynthesis, angiogenesis, vascular one, cardioprotection, and posttranslational modification, indicating the importance of their cross-talk in the cardiovascular system.

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          Most cited references149

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          H2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine gamma-lyase.

          Studies of nitric oxide over the past two decades have highlighted the fundamental importance of gaseous signaling molecules in biology and medicine. The physiological role of other gases such as carbon monoxide and hydrogen sulfide (H2S) is now receiving increasing attention. Here we show that H2S is physiologically generated by cystathionine gamma-lyase (CSE) and that genetic deletion of this enzyme in mice markedly reduces H2S levels in the serum, heart, aorta, and other tissues. Mutant mice lacking CSE display pronounced hypertension and diminished endothelium-dependent vasorelaxation. CSE is physiologically activated by calcium-calmodulin, which is a mechanism for H2S formation in response to vascular activation. These findings provide direct evidence that H2S is a physiologic vasodilator and regulator of blood pressure.
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            A molecular view of microbial diversity and the biosphere.

            N Pace (1997)
            Over three decades of molecular-phylogenetic studies, researchers have compiled an increasingly robust map of evolutionary diversification showing that the main diversity of life is microbial, distributed among three primary relatedness groups or domains: Archaea, Bacteria, and Eucarya. The general properties of representatives of the three domains indicate that the earliest life was based on inorganic nutrition and that photosynthesis and use of organic compounds for carbon and energy metabolism came comparatively later. The application of molecular-phylogenetic methods to study natural microbial ecosystems without the traditional requirement for cultivation has resulted in the discovery of many unexpected evolutionary lineages; members of some of these lineages are only distantly related to known organisms but are sufficiently abundant that they are likely to have impact on the chemistry of the biosphere.
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              Two's company, three's a crowd: can H2S be the third endogenous gaseous transmitter?

              Rui Wang (2002)
              Bearing the public image of a deadly "gas of rotten eggs," hydrogen sulfide (H2S) can be generated in many types of mammalian cells. Functionally, H2S has been implicated in the induction of hippocampal long-term potentiation, brain development, and blood pressure regulation. By acting specifically on KATP channels, H2S can hyperpolarize cell membranes, relax smooth muscle cells, or decrease neuronal excitability. The endogenous metabolism and physiological functions of H2S position this gas well in the novel family of endogenous gaseous transmitters, termed "gasotransmitters." It is hypothesized that H2S is the third endogenous signaling gasotransmitter, besides nitric oxide and carbon monoxide. This positioning of H2S will open an exciting field-H2S physiology-encompassing realization of the interaction of H2S and other gasotransmitters, sulfurating modification of proteins, and the functional role of H2S in multiple systems. It may shed light on the pathogenesis of many diseases related to the abnormal metabolism of H2S.
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                Author and article information

                Contributors
                Journal
                Oxid Med Cell Longev
                Oxid Med Cell Longev
                OMCL
                Oxidative Medicine and Cellular Longevity
                Hindawi
                1942-0900
                1942-0994
                2018
                9 September 2018
                : 2018
                : 4579140
                Affiliations
                1Department of Pharmacy, Tongji Hospital, Tongji University School of Medicine, Shanghai, China
                2Mitochondria and Metabolism Center, Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, USA
                Author notes

                Academic Editor: Nazareno Paolocci

                Author information
                http://orcid.org/0000-0001-6117-5099
                http://orcid.org/0000-0001-9288-6491
                http://orcid.org/0000-0001-6038-7188
                Article
                10.1155/2018/4579140
                6151216
                30271527
                f3ca8960-ca5f-4444-8d23-df26db08e05d
                Copyright © 2018 Dan Wu et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 April 2018
                : 25 July 2018
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 81703499
                Funded by: Shanghai Chenguang Program
                Award ID: 17CG13
                Funded by: Shanghai Sailing Program
                Award ID: 16YF1410400
                Funded by: Foundation of Shanghai Municipal Commission of Health and Family Planning
                Award ID: ZHYY-ZXYJHZX-201618
                Funded by: Beijing Medical Award Foundation
                Award ID: YJHYXKYJJ-152
                Categories
                Review Article

                Molecular medicine
                Molecular medicine

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