Skip to main content

Advertisement

Log in

Effect of handling on ATP utilization of cerebral Na,K-ATPase in rats with trimethyltin-induced neurodegeneration

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

Previously it was shown that for reduction of anxiety and stress of experimental animals, preventive handling seems to be one of the most effective methods. The present study was oriented on Na,K-ATPase, a key enzyme for maintaining proper concentrations of intracellular sodium and potassium ions. Malfunction of this enzyme has an essential role in the development of neurodegenerative diseases. It is known that this enzyme requires approximately 50% of the energy available to the brain. Therefore in the present study utilization of the energy source ATP by Na,K-ATPase in the frontal cerebral cortex, using the method of enzyme kinetics was investigated. As a model of neurodegeneration treatment with trimethyltin (TMT) was applied. Daily handling (10 min/day) of healthy rats and rats suffering neurodegeneration induced by administration of TMT in a dose of (7.5 mg/kg), at postnatal days 60–102 altered the expression of catalytic subunits of Na,K-ATPase as well as kinetic properties of this enzyme in the frontal cerebral cortex of adult male Wistar rats. In addition to the previously published beneficial effect on spatial memory, daily treatment of rats was accompanied by improved maintenance of sodium homeostasis in the frontal cortex. The key system responsible for this process, Na,K-ATPase, was able to utilize better the energy substrate ATP. In rats, manipulation of TMT-induced neurodegeneration promoted the expression of the α2 isoform of the enzyme, which is typical for glial cells. In healthy rats, manipulation was followed by increased expression of the α3 subunit, which is typical of neurons.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Data availability

The datasets generated during and/or analyzed during the current study are not publicly available but are available from the corresponding author on reasonable request.

References

  1. Skou JC (1957) The influence of some cations on an adenosine triphosphatase from peripheral nerves. Biochim Biophys Acta 23:394–401. https://doi.org/10.1016/0006-3002(57)90343-8

    Article  CAS  PubMed  Google Scholar 

  2. Alberts B, Johnson A, Lewis J et al (2002) Cell junctions. In: Molecular biology of the cell, 4th edn. Garland Science, New York. ISBN-10: 0-8153-4072-9

  3. Holm TH, Lykke-Hartmann K (2016) Insights into the pathology of the α3 Na+/K+-ATPase ion pump in neurological disorders; lessons from animal models. Front Physiol 7:1–12. https://doi.org/10.3389/fphys.2016.00209

    Article  Google Scholar 

  4. Liguri G, Taddei N, Nassi P et al (1990) Changes in Na+, K+-ATPase, Ca2+-ATPase and some soluble enzymes related to energy metabolism in brains of patients with Alzheimer’s disease. Neurosci Lett 112:338–342. https://doi.org/10.1016/0304-3940(90)90227-Z

    Article  CAS  PubMed  Google Scholar 

  5. Hattori N, Kitagawa K, Higashida T et al (1998) Cl−-ATPase and Na+/K+-ATPase activities in Alzheimer’s disease brains. Neurosci Lett 254:141–144. https://doi.org/10.1016/S0304-3940(98)00654-5

    Article  CAS  PubMed  Google Scholar 

  6. Paciorkowski AR, McDaniel SS, Jansen LA et al (2015) Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly. Epilepsia 56:422–430. https://doi.org/10.1111/epi.12914

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Singh SV, Fedorova OV, Wei W et al (2020) Na+, K+-ATPase α isoforms and endogenous cardiac steroids in prefrontal cortex of bipolar patients and controls. Int J Mol Sci 21:5912. https://doi.org/10.3390/ijms21165912

    Article  CAS  PubMed Central  Google Scholar 

  8. DeAndrade MP, Yokoi F, van Groen T et al (2011) Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism. Behav Brain Res 216:659–665. https://doi.org/10.1016/j.bbr.2010.09.009

    Article  CAS  PubMed  Google Scholar 

  9. Yin S, Ran Q, Yang J et al (2020) Nootropic effect of neferine on aluminium chloride–induced Alzheimer’s disease in experimental models. J Biochem Mol Toxicol. https://doi.org/10.1002/jbt.22429

    Article  PubMed  Google Scholar 

  10. Schneider Oliveira M, Flávia Furian A, Freire Royes LF et al (2004) Ascorbate modulates pentylenetetrazol-induced convulsions biphasically. Neuroscience 128:721–728. https://doi.org/10.1016/j.neuroscience.2004.07.012

    Article  CAS  PubMed  Google Scholar 

  11. Funck VR, Ribeiro LR, Pereira LM et al (2015) Contrasting effects of Na+, K+-ATPase activation on seizure activity in acute versus chronic models. Neuroscience 298:171–179. https://doi.org/10.1016/j.neuroscience.2015.04.031

    Article  CAS  PubMed  Google Scholar 

  12. Costa LG (1985) Inhibition of γ-[3H]aminobutyric acid uptake by organotin compounds in vitro. Toxicol Appl Pharmacol 79:471–479. https://doi.org/10.1016/0041-008X(85)90144-9

    Article  CAS  PubMed  Google Scholar 

  13. Viau V, Sharma S, Plotsky P, Meaney M (1993) Increased plasma ACTH responses to stress in nonhandled compared with handled rats require basal levels of corticosterone and are associated with increased levels of ACTH secretagogues in the median eminence. J Neurosci 13:1097–1105. https://doi.org/10.1523/JNEUROSCI.13-03-01097.1993

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Ferré P, Francisco Núñez J, García E et al (1995) Postnatal handling reduces anxiety as measured by emotionality rating and hyponeophagia tests in female rats. Pharmacol Biochem Behav 51:199–203. https://doi.org/10.1016/0091-3057(94)00419-J

    Article  PubMed  Google Scholar 

  15. Fenoglio KA, Brunson KL, Avishai-Eliner S et al (2005) Enduring, handling-evoked enhancement of hippocampal memory function and glucocorticoid receptor expression involves activation of the corticotropin-releasing factor type 1 receptor. Endocrinology 146:4090–4096. https://doi.org/10.1210/en.2004-1285

    Article  CAS  PubMed  Google Scholar 

  16. Boufleur N, Antoniazzi CTD, Pase CS et al (2013) Neonatal handling prevents anxiety-like symptoms in rats exposed to chronic mild stress: behavioral and oxidative parameters. Stress 16:321–330. https://doi.org/10.3109/10253890.2012.723075

    Article  CAS  PubMed  Google Scholar 

  17. Stara V, Mach M, Ujhazy E et al (2018) Beneficial effect of 6 weeks lasting handling of adult rats on spatial memory in experimental model of neurodegeneration. Interdiscip Toxicol 11:217–220. https://doi.org/10.2478/intox-2018-0020

    Article  PubMed  Google Scholar 

  18. Benetti SC, Silveira PP, Matté C et al (2010) Effects of a chronic exposure to a highly palatable diet and its withdrawal, in adulthood, on cerebral Na +, K + -ATPase and plasma S100B in neonatally handled rats. Int J Dev Neurosci 28:153–159. https://doi.org/10.1016/j.ijdevneu.2009.12.003

    Article  CAS  Google Scholar 

  19. Silveira PP, Portella AK, da Silva BC et al (2011) Association between Na+, K+-ATPase activity and the vulnerability/resilience to mood disorders induced by early life experience. Neurochem Res 36:2075–2082. https://doi.org/10.1007/s11064-011-0531-1

    Article  CAS  PubMed  Google Scholar 

  20. Noschang C, Krolow R, Arcego DM et al (2012) The influence of early life interventions on olfactory memory related to palatable food, and on oxidative stress parameters and Na+/K+-ATPase activity in the hippocampus and olfactory bulb of female adult rats. Neurochem Res 37:1801–1810. https://doi.org/10.1007/s11064-012-0793-2

    Article  CAS  PubMed  Google Scholar 

  21. Attwell D, Laughlin SB (2001) An energy budget for signaling in the grey matter of the brain. J Cereb Blood Flow Metab 21:1133–1145. https://doi.org/10.1097/00004647-200110000-00001

    Article  CAS  Google Scholar 

  22. Ferraz da Silva I, Freitas-Lima LC, Graceli JB, de Rodrigues LC (2018) Organotins in neuronal damage, brain function, and behavior: a short review. Front Endocrinol (Lausanne) 8:6–11. https://doi.org/10.3389/fendo.2017.00366

    Article  Google Scholar 

  23. Corvino V, Marchese E, Giannetti S et al (2012) The neuroprotective and neurogenic effects of neuropeptide Y administration in an animal model of hippocampal neurodegeneration and temporal lobe epilepsy induced by trimethyltin. J Neurochem 122:415–426. https://doi.org/10.1111/j.1471-4159.2012.07770.x

    Article  CAS  PubMed  Google Scholar 

  24. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254. https://doi.org/10.1016/0003-2697(76)90527-3

    Article  CAS  PubMed  Google Scholar 

  25. Lowry HO, Rosebrough NJ, Farr LA, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265–275

    Article  CAS  Google Scholar 

  26. Taussky HH, Shorr E (1953) A microcolorimetric method for the determination of inorganic phosphorus. J Biol Chem 202:675–685. https://doi.org/10.1017/CBO9781107415324.004

    Article  CAS  PubMed  Google Scholar 

  27. Gasparova Z, Janega P, Stara V, Ujhazy E (2012) Early and late stage of neurodegeneration induced by trimethyltin in hippocampus and cortex of male Wistar rats. Neuroendocrinol Lett 33:689–696

    CAS  PubMed  Google Scholar 

  28. Liu Z, Lv J, Zhang Z et al (2021) The main mechanisms of trimethyltin chloride-induced neurotoxicity: energy metabolism disorder and peroxidation damage. Toxicol Lett 345:67–76. https://doi.org/10.1016/j.toxlet.2021.04.008

    Article  CAS  PubMed  Google Scholar 

  29. Furuhashi K, Ogawa M, Suzuki Y et al (2008) Methylation of dimethyltin in mice and rats. Chem Res Toxicol 21:467–471. https://doi.org/10.1021/tx700320a

    Article  CAS  PubMed  Google Scholar 

  30. Costa R, Tamascia ML, Nogueira MD et al (2012) Handling of adolescent rats improves learning and memory and decreases anxiety. J Am Assoc Lab Anim Sci 51:548–553

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Poole T (1997) Happy animals make good science. Lab Anim 31:116–124. https://doi.org/10.1258/002367797780600198

    Article  CAS  PubMed  Google Scholar 

  32. de Freitas ML, de Oliveira CV, Mello FK et al (2018) Na+, K+-ATPase activating antibody displays in vitro and in vivo beneficial effects in the pilocarpine model of epilepsy. Neuroscience 377:98–104. https://doi.org/10.1016/j.neuroscience.2018.02.044

    Article  CAS  PubMed  Google Scholar 

  33. Juhaszova M, Blaustein MP (1997) Na+ pump low and high ouabain affinity subunit isoforms are differently distributed in cells. Proc Natl Acad Sci 94:1800–1805. https://doi.org/10.1073/pnas.94.5.1800

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. McGrail KM, Phillips JM, Sweadner KJ (1991) Immunofluorescent localization of three Na, K-ATPase isozymes in the rat central nervous system: both neurons and glia can express more than one Na, K-ATPase. J Neurosci 11:381–391

    Article  CAS  Google Scholar 

  35. Bøttger P, Glerup S, Gesslein B et al (2016) Glutamate-system defects behind psychiatric manifestations in a familial hemiplegic migraine type 2 disease-mutation mouse model. Sci Rep 6:22047. https://doi.org/10.1038/srep22047

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. de Arnaiz GR, Ordieres MGL (2014) Brain Na+, K+-ATPase activity in aging and disease. Int J Biomed Sci 10:85–102

    Google Scholar 

  37. Desfrere L, Karlsson M, Hiyoshi H et al (2009) Na, K-ATPase signal transduction triggers CREB activation and dendritic growth. Proc Natl Acad Sci 106:2212–2217. https://doi.org/10.1073/pnas.0809253106

    Article  PubMed  PubMed Central  Google Scholar 

  38. Moseley AE, Williams MT, Schaefer TL et al (2007) Deficiency in Na, K-ATPase isoform genes alters spatial learning, motor activity, and anxiety in mice. J Neurosci 27:616–626. https://doi.org/10.1523/JNEUROSCI.4464-06.2007

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Lingrel JB, Williams MT, Vorhees CV, Moseley AE (2007) Na, K-ATPase and the role of α isoforms in behavior. J Bioenerg Biomembr 39:385–389. https://doi.org/10.1007/s10863-007-9107-9

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The study was supported by Slovak Grant Agency: VEGA-2/0166/17, VEGA-2/0120/19, VEGA 2/0063/18, and ITMS-26230120006.

Author information

Authors and Affiliations

Authors

Contributions

ZG designed the study; VNS, DM, and EU performed the biological model; BK, NV, DS, and JV performed the analysis and evaluation of Na,K-ATPase expression and estimation of ATP utilization by Na,K-ATPase using the method of enzyme kinetics; ZG, BK, DS, and NV prepared the manuscript.

Corresponding author

Correspondence to Norbert Vrbjar.

Ethics declarations

Conflict of interest

No conflicts of interest, financial, or otherwise are declared by the authors.

Ethical approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed. All procedures with animals were performed in compliance with principles of laboratory animal care issued by EU Directive 2010/63/EU for animal experiments, proved and controlled by the State Veterinary and Food Administration of Slovak Republic (No. 4030/10-221), and with the agreement of the Ethical Committee of the Center of Experimental Medicine, Slovak Academy of Sciences. This article does not contain any studies involving human participants performed by any of the authors.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kalocayova, B., Snurikova, D., Vlkovicova, J. et al. Effect of handling on ATP utilization of cerebral Na,K-ATPase in rats with trimethyltin-induced neurodegeneration. Mol Cell Biochem 476, 4323–4330 (2021). https://doi.org/10.1007/s11010-021-04239-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11010-021-04239-6

Keywords

Navigation