• Content of nitrogen oxide and its metabolites in blood and esophageal mucosa in children sickly with respiratory diseases against the bachground of gastroesophagial reflux disease
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Content of nitrogen oxide and its metabolites in blood and esophageal mucosa in children sickly with respiratory diseases against the bachground of gastroesophagial reflux disease

SOVREMENNAYA PEDIATRIYA.2019.2(98):31-34; doi 10.15574/SP.2019.98.31

Pochinok T. V., Zhuravel O. V., Chernov O. V.
Bogomolets National Medical University, Kyiv, Ukraine
SI «Institute of Pediatrics, Obstetrics and Gynecology named after academician О. Lukyanova of the National Academy of Medical Sciences of Ukraine», Kyiv

Actuality. Nitric oxide provides vasodilatation of blood vessels, regulation of microcirculation, regulation of synthesis and secretion of hormones that affect the gastrointestinal motility (gastrointestinal tract), gastric secretion. There are few studies which confirm gastroprotective effect of this mediator. In other researches signed disorders of stomach motility when blocking NO-synthase.

The aim of research — to set the level of nitric oxide and its metabolites in blood plasma and esophagus mucous membrane in children with frequent respiratory diseases (FRD) and gastroesophageal reflux disease (GERD).

Materials and methods. 150 children of puberty age were examined and divided into three groups — children with frequent respiratory diseases (FRD) and concominant gastroesophageal reflux disease (90 children, group 1), children with FRD without GERD (30 children, group 2), healthy children (30 children, group 3).

Abstract. A significant increase of total NO (29.5%) in children with RRI and GERD, NO2 metabolite (27.4%) and NO3 metabolite (40.2%) was established. It has been found that frequent respiratory infections accompanied with significant increase of total NO and its metabolites in esophageal mucosa — total NO — 2.16 times, NO3 — 2.1 times, NO2 — 1.59 times, p<0.05; however, in RRI without GERD there is no significant difference revealed. After regression analisys it was set direct linear relations between the content nitric oxide and its metabolites in esophagus mucous membrane and blood plasma. The regression between total NO level in plasma and esophagus mucous membrane was r=0.30 (p<0.05), NO2 — r=0.29 (p<0.05), NO3 — r=0.34 (p<0.05).

Conclusion. It was set the probable increase of nitric oxide in blood plasma and esophagus mucous membrane in GERD, positive correlation between NO and its metabolites NO2 and NO3 in plasma and mucous membrane.

Key words: children with recurrent respiratory infections, gastroesophageal reflux disease, nitric oxide, esophageal mucosa, blood.

REFERANCES

1. Kireeva KV, Kankova NYu, Shabunina EI et al. (2015). Changes in the Content of Nitric Oxide Derivatives in Children with Inflammatory Diseases of the Esophagus and the Stomach. Medical Almanac. Pediatrics. 4 (39):118–121.

2. Kirnus NI, Artamonov RG, Smirnov IE. (2007). Nitric Oxide and Chronic Diseases of the Digestive Tract in Children. Pediatrics. 86 (5):113–116.

3. Metelskaya VA, Gumanova NG. (2005). Screening Method for Determining the Level of Nitric Oxide Metabolites in Blood Serum. Clinical Laboratory Diagnostics. 6:15–18.

4. Somova LM, Plekhova NG. (2006). Nitric Oxide as a Mediator of Inflammation. Bulletin of the Far East Branch of the Russian Academy of Sciences. 2:77–80.

5. Cirino G, Distrutti E, Wallace JL. (2006). Nitric oxide and inflammation. Inflammation & Allergy-Drug Targets (Formerly Current Drug Targets-Inflammation & Allergy). 5(2):115–119. https://doi.org/10.2174/187152806776383143; PMid:16613570

6. Kuiken SD, Tytgat GN, Boeckxstaens GE. (2002). Role of endogenous nitric oxide in regulating antropyloroduodenal motility in humans. The American journal of gastroenterology. 97(7):166–1667. https://doi.org/10.1016/S0002-9270(02)04180-1

7. Lane C, Knight D, Burgess S. et al. (2004). Epithelial inducible nitric oxide synthase activity is the major determinant of nitric oxide concentration in exhaled breath. Thorax. 59(9):757–760. https://doi.org/10.1136/thx.2003.014894; PMid:15333851 PMCid:PMC1747143

8. Lok HC, Sahni S, Jansson PJ. et al. (2016). A nitric oxide storage and transport system that protects activated macrophages from endogenous nitric oxide cytotoxicity. Journal of Biological Chemistry. 291(53): 27042–27061. https://doi.org/10.1074/jbc.M116.763714; PMid:27866158 PMCid:PMC5207136

9. Schmulson M. (2018). How to use Rome IV criteria in the evaluation of esophageal disorders. Current opinion in gastroenterology. 34(4):258–265. https://doi.org/10.1097/MOG.0000000000000443; PMid:29846258

10. Shah V, Lyford G, Gores G, Farrugia G. (2004). Nitric oxide in gastrointestinal health and disease. Gastroenterology. 126(3):903–913. https://doi.org/10.1053/j.gastro.2003.11.046; PMid:14988844

11. Sivarao DV, Mashimo H, Goyal RK. (2008). Pyloric sphincter dysfunction in nNOS-/- and W/Wv mutant mice: animal models of gastroparesis and duodenogastric reflux. Gastroenterology. 135(4):1258–1266. https://doi.org/10.1053/j.gastro.2008.06.039; PMid:18640116 PMCid:PMC2745304

Article received: Nov 14, 2018. Accepted for publication: Mar 04, 2019.