Extracellular Na+ levels regulate formation and activity of the Nax/alpha1-Na+/K+ -ATPase complex in neuronal cells

Frontiers in Cellular Neuroscience

Volumn 8, Issue DEC, 2014, Pages

  Berret, Emmanuelle ^a   Smith, Pascal Y ^a   Henry, Melaine ^a   Soulet, Denis ^a,b   Hebert, Sebastien S ^a,b   Toth, Katalin ^b   Mouginot, Didier ^a,b   Drolet, Guy ^a,b  

^a Université Laval   (Canada)

^b UNIVERSITÉ LAVAL   (Canada)

Author keywords

Median preoptic nucleus; Nax channel; Na+ K+ ATPase; Salt diet; Sodium

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); SODIUM; SODIUM CHANNEL;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BRAIN NERVE CELL; CELL MEMBRANE PERMEABILITY; CEREBROSPINAL FLUID ANALYSIS; CONFOCAL MICROSCOPY; CONTROLLED STUDY; ELECTROPHYSIOLOGICAL PROCEDURES; ENVIRONMENTAL CHANGE; ENZYME ACTIVITY; ENZYME INDUCTION; EXTRACELLULAR FLUID; GENETIC TRANSFECTION; HOMEOSTASIS AND REGULATION; HYPERNATREMIA; IMAGE ANALYSIS; IMMUNOCYTOCHEMISTRY; MALE; NEURO2A CELL LINE; NEUROBLASTOMA CELL LINE; NONHUMAN; OSMOLALITY; PATCH CLAMP TECHNIQUE; PREOPTIC NUCLEUS; PROTEIN EXPRESSION; RAT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SALT INTAKE; SODIUM CELL LEVEL; SODIUM CONDUCTANCE;

EID: 84930641449     PISSN: 16625102     EISSN: None     Source Type: Journal    
DOI: 10.3389/fncel.2014.00413     Document Type: Article

References (31)

1. Antunes-Rodrigues, J., De Castro, M., Elias, L. L. K., Valença, M. M., and McCann, S. M. (2004). Neuroendocrine control of body fluid metabolism. Physiol. Rev. 84, 169-208. doi: 10.1152/physrev.00017.2003.
2. Berret, E., Nehme, B., Henry, M., Toth, K., Drolet, G., and Mouginot, D. (2013). Regulation of central Na+ detection requires the cooperative action of the Nax channel and a-1 isoform of the Na+/K+ - ATPase in the Na+-sensor neuronal population. J. Neurosci. 33, 3067-3078. doi: 10.1523/JNEUR0SCI.4801-12.2013
3. Costes, S. V., Daelemans, D., Cho, E. H., Dobbin, Z., Pavlakis, G., and Lockett, S. (2004). Automatic and quantitative measurement of protein-protein colocalization in live cells. Biophys. J. 86, 3993-4003. doi: 10.1529/biophysj.103.038422
4. Cox, P. S., Denton, D. A., Mouw, D. R., and Tarjan, E. (1987). Natriuresis induced by localized perfusion within the third cerebral ventricle of sheep. Am. J. Physiol. 252(1. Pt 2), R1-R6.
5. Denton, D. A., McKinley, M. J., andWeisinger, R. S. (1996). Hypothalamic integration of body fluid regulation. Proc. Natl. Acad. Sci. U.S.A. 93, 7397-7404. doi: 10.1073/pnas.93.14.7397.
6. Dooley, R., Harvey, B. J., andThomas, W. (2011). The regulation ofcell growth and survival by aldosterone. Front. Biosci. 16, 440-457. doi: 10.2741/3697.
7. Fitzsimons, J. T. (1998). Angiotensin, thirst, and sodium appetite. Physiol. Rev. 78, 583-686.
8. Geerling, J. C., Engeland, W. C., Kawata, M., and Loewy, A. D. (2006). Aldosterone target neurons in the nucleus tractus solitarius drive sodium appetite. J. Neurosci. 26, 411-417. doi: 10.1523/JNEUROSCI.3115-05.2006
9. Geerling, J. C., and Loewy, A.D.(2008). Central regulation of sodium appetite. Exp. Physiol. 93, 177-209. doi: 10.1113/expphysiol.2007.039891.
10. Grob, M., Drolet, G., and Mouginot, D. (2004). Specific Na+ sensors are functionally expressed in a neuronal population of the median preoptic nucleus of the rat. J. Neurosci. 24, 3974-3984. doi: 10.1523/JNEUROSCI.3720-03.2004.
11. Hiyama, T. Y., Watanabe, E., Okado, H., and Noda, M. (2004). The subfornical organ is the primary locus of sodium-level sensing by Na(x) sodium channels for the control of salt-intake behavior. J. Neurosci. 24, 9276-9281. doi: 10.1523/JNEUROSCI.2795-04.2004.
12. Hiyama, T. Y., Watanabe, E., Ono, K., Inenaga, K., Tamkun, M. M., Yoshida, S., et al. (2002). Na(x) channel involved in CNS sodium-level sensing. Nat. Neurosci. 5, 511-512. doi: 10.1038/nn0602-856.
13. Huang, B. S., and Leenen, F. H. (2002). Brain amiloride-sensitive Phe-Met-Arg- Phe-NH2-Gated Na+ Channels and Na+-Induced sympathoexcitation and hypertension. Hypertension 39, 557-561. doi: 10.1161/hy02t2.103004.
14. Huang, B. S., and Leenen, F. H. H. (1995). Brain ‘ouabain’ and desensitization of arterial baroreflex by high sodium in Dahl salt-sensitive rats. Hypertension 25, 372-376. doi: 10.1161/01.HYP.25.3.372.
15. Huang, B. S., and Leenen, F. H. H. (1998). Both brain angiotensin II and “ouabain” contribute to sympathoexcitation and hypertension in Dahl S rats on high salt intake. Hypertension 32, 1028-1033. doi: 10.1161/01.HYP.32.6.1028.
16. Huang, B. S., Van Vliet, B. N., and Leenen, F. H. H. (2004). Increases in CSF [Na+] precede the increases in blood pressure in Dahl S rats and SHR on a high-salt diet. Am. J. Physiol. Heart Circ. Physiol. 287, H1160-H1166. doi: 10.1152/ajpheart.00126.2004.
17. Hussy, N., Deleuze, C., Desarmenien, M. G., and Moos, F. C. (2000). Osmotic regulation of neuronal activity: a new role for taurine and glial cells in a hypothalamic neuroendocrine structure. Prog. Neurobiol. 62, 113-134. doi: 10.1016/S0301-0082(99)00071-4.
18. McKinley, M. J., Gerstberger, R., Mathai, M. L., Oldfield, B. J., and Schmid, H. (1999a). The lamina terminalis and its role in fluid and electrolyte homeostasis. J. Clin. Neurosci. 6, 289-301.
19. McKinley, M. J., Mathai, M. L., Pennington, G., Rundgren, M., and Vivas, L. (1999b). Effect of individual or combined ablation of the nuclear groups of the lamina terminalis on water drinking in sheep. Am. J. Physiol. 276(3. Pt 2), R673-R683.
20. McKinley, M. J., McAllen, R. M., Davern, P., Giles, M. E., Penschow, J., Sunn, N., et al. (2003). The sensory circumventricular organs of the mammalian brain. Adv. Anat. Embryol. Cell Biol. 172, III-XII, 1-122. doi: 10.1007/978-3-642-55532-9_1
21. Mouginot, D., Laforest, S., and Drolet, G. (2007). Challenged sodium balance and expression of angiotensin type 1A receptor mRNA in the hypothalamus of Wistar and Dahl rat strains. Regul. Pept. 142, 44-51. doi: 10.1016/j.regpep.2007.01.005.
22. Nehme, B., Henry, M., Mouginot, D., and Drolet, G. (2012). The expression pattern of the Na(+) Sensor, Na(X) in the hydromineral homeostatic network: a comparative study between the rat and mouse. Front. Neuroanat. 6:26. doi: 10.3389/fnana.2012.00026.
23. Noda, M. (2006). The subfornical organ, a specialized sodium channel, and the sensing of sodium levels in the brain. Neuroscientist 12, 80-91. doi: 10.1177/1073858405279683
24. Pietranera, L., Saravia, F. E., McEwen, B. S., Lucas, L. L., Johnson, A. K., and De Nicola, A. F. (2001). Changes in Fos expression in various brain regions during deoxycorticosterone acetate treatment: relation to salt appetite, vasopressin mRNA and the mineralocorticoid receptor. Neuroendocrinology 74, 396-406. doi: 10.1159/000054706.
25. Rahmouni, K., Barthelmebs, M., Grima, M., Imbs, J. L., and De Jong, W. (2002). Influence of sodium intake on the cardiovascular and renal effects of brain mineralocorticoid receptor blockade in normotensive rats. J. Hypertens. 20, 1829-1834. doi: 10.1097/00004872-200209000-00029.
26. Shimizu, H., Watanabe, E., Hiyama, T. Y., Nagakura, A., Fujikawa, A., Okado, H., et al. (2007). Glial Nax channels control lactate signaling to neurons for brain [Na+] sensing. Neuron 54, 59-72. doi: 10.1016/j.neuron.2007.03.014
27. Tanaka, J. (1989). Involvement of the median preoptic nucleus in the regulation of paraventricular vasopressin neurons by the subfornical organ in the rat. Exp. BrainRes. 76, 47-54. doi: 10.1007/BF00253622.
28. Thomas, W., and Harvey, B. J. (2011). Mechanisms underlying rapid aldosterone effects in the kidney. Annu. Rev. Physiol. 73, 335-357. doi: 10.1146/annurev-physiol-012110-142222.
29. Tremblay, C., Berret, E., Henry, M., Nehme, B., Nadeau, L., and Mouginot, D. (2011). Neuronal sodium leak channel is responsible for the detection of sodium in the rat median preoptic nucleus. J. Neurophysiol. 105, 650-660. doi: 10.1152/jn.00417.2010
30. Verbalis, J. G. (2003). Disorders of body water homeostasis. Best Pract. Clin. Endocrinol. Metab. 17, 471-503. doi: 10.1016/S1521-690X(03)00049-6.
31. Voisin, A. N., Drolet, G., and Mouginot, D. (2012). Intrinsic properties of the sodium sensor neurons in the rat median preoptic nucleus. Am. J. Physiol. Regul. Integr. Comp. Physiol. 303, R834-R842. doi: 10.1152/ajpregu.00260.2012