Platelet monoamine oxidase and erythrocyte adenosine triphosphatase as biomarkers of necrotizing enterocolitis

封面


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

BACKGROUND: The diagnostics of necrotizing enterocolitis is a complex and often ineffective issue. Biomarkers reflecting key links in the pathogenesis of the disease may serve as early predictors of development, progression, and severe course of necrotizing enterocolitis.

AIM: To assess potentials of platelet monoamine oxidase activity and erythrocyte ATPase to predict the development of necrotizing enterocolitis in premature newborns.

METHODS: The present study had two stages and included 28 children who were treated at the Chelyabinsk Regional Children’s Clinical Hospital from November 2021 to December 2022. At the first stage, premature newborns were examined; among them a group of newborns with necrotizing enterocolitis IIB–IIIA-B was identified. Venous blood was used for testings. At the second stage, specimens obtained from the intestine during surgical interventions in newborns with surgical pathology were examined additionally as well.

RESULTS: Children with necrotizing enterocolitis showed a significant decrease in the specific activity of platelet monoamine oxidase which correlated with the activity of monoamine oxidase in gut specimens. The following changes were registered: decrease in the activity of magnesium adenosine triphosphatasein erythrocytes by 50–100% of the maximum enzyme activity in the control group; decrease of sodium-potassium adenosine triphosphatase activity y 4 times from the maximum values in the control group. There was also a significant increase in the activity of calcium adenosine triphosphatase activity in erythrocytes.

CONCLUSION: The obtained data allow to suggest that platelet monoamine oxidase in preterm newborns may potentially serve as an indicator of tissue and organ immaturity, rather than a marker of inflammation and oxidative damage. Changes in erythrocyte adenosine triphosphatase activity in preterm infants with surgical stages of necrotizing enterocolitis indicate a hypoxic hypoenergetic state, accompanied by high concentrations of intracellular calcium.

The obtained data are promising for developing new methods for diagnosis/prognosis of necrotizing enterocolitis in newborns.

全文:

受限制的访问

作者简介

Polina Vinel

South-Ural State Medical University

编辑信件的主要联系方式.
Email: vinelpolina@icloud.com
ORCID iD: 0000-0002-3745-3690
SPIN 代码: 6298-8131

MD

俄罗斯联邦, 64 Vorovskogo street, 454092 Chelyabinsk

Valentina Tsareva

South-Ural State Medical University; Chelyabinsk Regional Pediatric Hospital

Email: semenovatsareva@mail.ru
ORCID iD: 0000-0002-6695-7388
SPIN 代码: 7966-9068

MD, Cand. Sci. (Medicine)

俄罗斯联邦, 64 Vorovskogo street, 454092 Chelyabinsk; Chelyabinsk

Pavel Baboshko

Chelyabinsk Regional Pediatric Hospital

Email: 904306008@mail.ru
ORCID iD: 0009-0009-2627-0459
俄罗斯联邦, Chelyabinsk

Anton Sinitskii

South-Ural State Medical University

Email: Sinitskiyai@yandex.ru
ORCID iD: 0000-0001-5687-3976
SPIN 代码: 3681-1816

MD, Dr. Sci. (Medicine), Associate Professor

俄罗斯联邦, 64 Vorovskogo street, 454092 Chelyabinsk

Artem Kozhevnikov

South-Ural State Medical University

Email: vk_523@mail.ru
ORCID iD: 0009-0008-5400-3043

MD

俄罗斯联邦, 64 Vorovskogo street, 454092 Chelyabinsk

Alexandr Grunin

South-Ural State Medical University

Email: sasha_grunin@mail.ru
ORCID iD: 0009-0007-9327-7779

MD

俄罗斯联邦, 64 Vorovskogo street, 454092 Chelyabinsk

参考

  1. Tan X, Zhou Y, Xu L, et al. The predictors of necrotizing enterocolitis in newborns with low birth weight: A retrospective analysis. Medicine. 2022;101(7):e28789. doi: 10.1097/MD.0000000000028789
  2. Vinel PK, Tsareva VV, Sinitskiy AI, et al. Biomarkers of necrotizing enterocolitis through the prism of etiopathogenesis. Medical news of North Caucasus. 2023;18(2):211–218. EDN: HEHMIA doi: 10.14300/mnnc.2023.18051
  3. Gershon MD, Sherman DL, Pintar JE. Type-specific localization of monoamine oxidase in the enteric nervous system: Relationship to 5-hydroxytryptamine, neuropeptides, and sympathetic nerves. J Comp Neurol. 1990;301(2):191–213. doi: 10.1002/cne.903010205
  4. Nicotra A, Pierucci F, Parvez H, Senatori O. Monoamine oxidase expression during development and aging. Neurotoxicology. 2004;25(1-2):155–165. EDN: LNMWSN doi: 10.1016/S0161-813X(03)00095-0
  5. Lewinsohn R, Glover V, Sandler M. Development of benzylamine oxidase and monoamine oxidase A and B in man. Biochem Pharmacol. 1980;29(9):1221–1230. doi: 10.1016/0006-2952(80)90278-6
  6. Ramsay RR, Albreht A. Kinetics, mechanism, and inhibition of monoamine oxidase. J Neural Transm (Vienna). 2018;125(11):1659–1683. EDN: YPBYWP doi: 10.1007/s00702-018-1861-9
  7. Bond PA, Cundall RL. Properties of monoamine oxidase (MAO) in human blood platelets, plasma, lymphocytes and granulocytes. Clinica Chimica Acta. 1977;80(2):317–326. doi: 10.1016/0009-8981(77)90039-0
  8. Shulhan J, Dicken B, Hartling L, Larsen BM. Current knowledge of necrotizing enterocolitis in preterm infants and the impact of different types of enteral nutrition products. Adv Nutr. 2017;8(1):80–91. doi: 10.3945/an.116.013193
  9. Vinel PK, Grobovoy SI, Sinitskii AI, Kolesnikov OL. Modification of a spectrophotometric method for assessment of monoamine oxidase activity with 2,4-dinitrophenylhydrazine as a derivatizing reagent. Anal Biochem. 2021;(629):114294. doi: 10.1016/j.ab.2021.114294
  10. Bartolommei G, Moncelli MR, Tadini-Buoninsegni F. A method to measure hydrolytic activity of adenosine triphosphatases (ATPases). PLoS One. 2013;8(3):e58615. doi: 10.1371/journal.pone.0058615
  11. Roth JA, Young JG, Cohen DJ. Platelet monoamine oxidase activity in children and adolescents. Life Sci. 1976;18(9):919–924.doi: 10.1016/0024-3205(76)90409-4
  12. Cawthon RM, Pintar JE, Haseltine FP, Breakefield XO. Differences in the structure of A and B forms of human monoamine oxidase. J Neurochem. 1981;37(2):363–372. doi: 10.1111/j.1471-4159.1981.tb00464.x
  13. Sostek AJ, Sostek AM, Murphy DL, et al. Cord blood amine oxidase activities relate to arousal and motor functioning in human newborns. Life Sci. 1981;28(22):2561–2568. doi: 10.1016/0024-3205(81)90599-3
  14. Jones JB, Southgate J. Platelet monoamine oxidase activity in the human fetus. Dev Med Child Neurol. 1976;18(5):640–642. doi: 10.1111/j.1469-8749.1976.tb04209.x
  15. Lewinsohn R, Sandler M. Monoamine-oxidizing enzymes in human pregnancy. Clin Chim Acta. 1982;120(3):301–312. doi: 10.1016/0009-8981(82)90371-0
  16. Oreland L, Shaskan EG. Monoamine oxidase activity as a biological marker. Trends Pharmacol Sci. 1983;(4):339–341. doi: 10.1016/0165-6147(83)90432-7
  17. Stillwell W. An introduction to biological membranes: Composition, structure and function. 2 rev ed. Elsevier Science; 2016. 564 р.
  18. Bistritzer T, Berkovitch M, Rappoport MJ, et al. Sodium potassium adenosine triphosphatase activity in preterm and term infants and its possible role in sodium homeostasis during maturation. Arch Dis Child Fetal Neonatal Ed. 1999;81(3):F184–F187. doi: 10.1136/fn.81.3.f184
  19. Tian J, Xie ZJ. The Na-K-ATPase and calcium-signaling microdomains. Physiology (Bethesda). 2008;23(4):205–211. doi: 10.1152/physiol.00008.2008
  20. Auland ME, Morris MB, Roufogalis BD. Separation and characterization of two Mg2+-ATPase activities from the human erythrocyte membrane. Arch Biochem Biophys. 1994;312(1):272–277. doi: 10.1006/abbi.1994.1309
  21. Beleznay Z, Zachowski A, Devaux PF, Ott P. Characterization of the correlation between ATP-dependent aminophospholipid translocation and Mg(2+)-ATPase activity in red blood cell membranes. Eur J Biochem. 1997;243(1-2):58–65. EDN: FOZGWR doi: 10.1111/j.1432-1033.1997.58_1a.x
  22. Nozadze E, Arutinova N, Tsakadze L, et al. Molecular mechanism of Mg-ATPase activity. J Membr Biol. 2015;248(2):295–300. EDN: HVUIII doi: 10.1007/s00232-014-9769-2
  23. Bogdanova A, Makhro A, Wang J, et al. Calcium in red blood cells a perilous balance. Int J Mol Sci. 2013;14(5):9848–9872. EDN: RJSVQN doi: 10.3390/ijms14059848
  24. Zylinska L, Gulczynska E, Kozaczuk A. Changes in erythrocyte glutathione and plasma membrane calcium pump in preterm newborns treated antenatally with MgSO4. Neonatology. 2008;94(4):272–278. doi: 10.1159/000151646
  25. Ogbodo UC, Emeh JK, Neboh EE, et al. Estimation of intracellular magnesium concentrations and membrane atpase activities in the red blood cells of normal and sickle cell subjects in Enugu, Southeast Nigeria. Int J Biol Med Res. 2010;1(4):149–152.
  26. DOI: https://doi.org/10.17816/ps707

补充文件

附件文件
动作
1. JATS XML
下载
2. Fig. 1. Platelet monoamine oxidase activity: МАО-Б — monoamine oxidase B; Контроль — control group; НЭК — group of patients with necrotizing enterocolitis; * — differences are statistically significant compared to the control according to the Mann–Whitney criterion.

下载 (69KB)
索引源数据
3. Fig. 2. Erythrocyte sodium-potassium adenosine triphosphatase activity: Na/K-АТФ-аза — erythrocyte sodium-potassium adenosine triphosphatase; Контроль — control group; НЭК — group of patients with necrotizing enterocolitis; * — differences are statistically significant compared to the control according to the Mann–Whitney criterion.

下载 (70KB)
索引源数据
4. Fig. 3. Erythrocytes magnesium adenosine triphosphatase activity: Mg-АТФ-аза — erythrocyte magnesium adenosine triphosphatase; Контроль — control group; НЭК — group of patients with necrotizing enterocolitis; * — differences are statistically significant compared to the control according to the Mann–Whitney criterion.

下载 (68KB)
索引源数据
5. Fig. 4. Erythrocytes calcium adenosine triphosphatase activity: Ca-АТФ-аза — erythrocyte calcium adenosine triphosphatase; Контроль — control group; НЭК — group of patients with necrotizing enterocolitis; * — differences are statistically significant compared to the control according to the Mann–Whitney criterion.

下载 (73KB)
索引源数据

版权所有 © Vinel P.K., Tsareva V.V., Baboshko P.G., Sinitskii A.I., Kozhevnikov A.S., Grunin A.V., 2024

##common.cookie##