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A Timeline of Hydrogen Sulfide (HS) Research: From Environmental Toxin to Biological Mediator

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Date 2017 Sep 27
PMID 28947277
Citations 100
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Abstract

The history of HS - as an environmental toxin - dates back to 1700, to the observations of the Italian physician Bernardino Ramazzini, whose book "De Morbis Artificum Diatriba" described the painful eye irritation and inflammation of "sewer gas" in sewer workers. The gas has subsequently been identified as hydrogen sulfide (HS), and opened three centuries of research into the biological roles of HS. The current article highlights the key discoveries in the field of HS research, including (a) the toxicological studies, which characterized HS as an environmental toxin, and identified some of its modes of action, including the inhibition of mitochondrial respiration; (b) work in the field of bacteriology, which, starting in the early 1900s, identified HS as a bacterial product - with subsequently defined roles in the regulation of periodontal disease (oral bacterial flora), intestinal epithelial cell function (enteral bacterial flora) as well as in the regulation of bacterial resistance to antibiotics; and (c), work in diverse fields of mammalian biology, which, starting in the 1940s, identified HS as an endogenous mammalian enzymatic product, the functions of which - among others, in the cardiovascular and nervous system - have become subjects of intensive investigation for the last decade. The current review not only enumerates the key discoveries related to HS made over the last three centuries, but also compiles the most frequently cited papers in the field which have been published over the last decade and highlights some of the current 'hot topics' in the field of HS biology.

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References
1.
Magierowski M, Magierowska K, Kwiecien S, Brzozowski T . Gaseous mediators nitric oxide and hydrogen sulfide in the mechanism of gastrointestinal integrity, protection and ulcer healing. Molecules. 2015; 20(5):9099-123. PMC: 6272495. DOI: 10.3390/molecules20059099. View

2.
Ju Y, Fu M, Stokes E, Wu L, Yang G . H₂S-Mediated Protein S-Sulfhydration: A Prediction for Its Formation and Regulation. Molecules. 2017; 22(8). PMC: 6152389. DOI: 10.3390/molecules22081334. View

3.
Hanson H, EISFELD G . [Intermediary sulfur metabolism. III. Formation of hydrogen sulfide from cystine and cysteine by the liver]. Z Gesamte Inn Med. 1952; 7(17):801-10. View

4.
Sen N, Paul B, Gadalla M, Mustafa A, Sen T, Xu R . Hydrogen sulfide-linked sulfhydration of NF-κB mediates its antiapoptotic actions. Mol Cell. 2012; 45(1):13-24. PMC: 3261430. DOI: 10.1016/j.molcel.2011.10.021. View

5.
Dorman D, Struve M, Gross E, Brenneman K . Respiratory tract toxicity of inhaled hydrogen sulfide in Fischer-344 rats, Sprague-Dawley rats, and B6C3F1 mice following subchronic (90-day) exposure. Toxicol Appl Pharmacol. 2004; 198(1):29-39. DOI: 10.1016/j.taap.2004.03.010. View