Literature DB >> 33128215

Effects of endogenous H2S production inhibition on the homeostatic responses induced by acute high-salt diet consumption.

Andreia Mara Moreira1, Samuel Amorin Grisote1, Heloisa Della Colleta Francescato2, Terezila Machado Coimbra2, Lucila Leico Kagohara Elias2, José Antunes-Rodrigues2, Silvia Graciela Ruginsk3.   

Abstract

The gaseous modulator hydrogen sulfide (H2S) is synthesized, among other routes, by the action of cystathionine-γ-lyase (CSE) and importantly participates in body fluid homeostasis. Therefore, the present study aimed to evaluate the participation of H2S in behavioral, renal and neuroendocrine homeostatic responses triggered by the acute consumption of a high Na+ diet. After habituation, adult male Wistar rats were randomly distributed and maintained for seven days on a control [CD (0.27% of Na+)] or hypersodic diet [HD (0.81% of Na+)]. CD and HD-fed animals were treated with DL-Propargylglycine (PAG, 25 mg/kg/day, ip) or vehicle (0.9% NaCl in equivalent volume) for the same period. At the end of the experiment, animals were euthanized for blood and tissue collection. We demonstrated that a short-term increase in dietary Na+ intake, in values that mimic the variations in human consumption (two times the recommended) significantly modified hydroelectrolytic homeostasis, with repercussions in the hypothalamic-neurohypophysial system and hypothalamic-pituitary-adrenal axis function. These findings were accompanied by the development of a clear inflammatory response in renal tubular cells and microvascular components. On the other hand, the inhibition of the endogenous production of H2S by CSE provided by PAG treatment prevented the inflammation induced by HD. In the kidney, PAG treatment induced the overexpression of inducible nitric oxide synthase in animals fed with HD. Taken together, these data suggest, therefore, that HD-induced H2S production plays an important proinflammatory role in the kidney, apparently counter regulating nitric oxide actions in renal tissue.

Entities:  

Keywords:  High-salt diet; Homeostasis; Hydrogen sulfide; Kidney inflammation

Mesh:

Substances:

Year:  2020        PMID: 33128215     DOI: 10.1007/s11010-020-03938-w

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  27 in total

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Authors:  Ling Li; Peter Rose; Philip K Moore
Journal:  Annu Rev Pharmacol Toxicol       Date:  2011       Impact factor: 13.820

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6.  Dysregulation of cystathionine γ-lyase (CSE)/hydrogen sulfide pathway contributes to ox-LDL-induced inflammation in macrophage.

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Review 7.  Hydrogen sulfide as a gasotransmitter.

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8.  [Estimated sodium intake for the Brazilian population, 2008-2009].

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Journal:  Br J Pharmacol       Date:  2013-06       Impact factor: 8.739

10.  Variation in dietary salt intake induces coordinated dynamics of monocyte subsets and monocyte-platelet aggregates in humans: implications in end organ inflammation.

Authors:  Xin Zhou; Ling Zhang; Wen-Jie Ji; Fei Yuan; Zhao-Zeng Guo; Bo Pang; Tao Luo; Xing Liu; Wen-Cheng Zhang; Tie-Min Jiang; Zhuoli Zhang; Yu-Ming Li
Journal:  PLoS One       Date:  2013-04-04       Impact factor: 3.240

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  1 in total

1.  NLRP3 inflammasome activation in gestational diabetes mellitus placentas is associated with hydrogen sulfide synthetase deficiency.

Authors:  Wei Wu; Qing-Ying Tan; Fang-Fang Xi; Yun Ruan; Jing Wang; Qiong Luo; Xiao-Bing Dou; Tian-Xiao Hu
Journal:  Exp Ther Med       Date:  2021-11-30       Impact factor: 2.447

  1 in total

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