Research output: Contribution to journal › Article › peer-review
Na+,K+ - ATPase and Cardiotonic Steroids in Models of Dopaminergic System Pathologies. / Markina , Alisa A.; Kazanskaya, Rogneda B. ; Timoshina, Julia A. ; Zavialov, Vladislav A. ; Abaimov , Denis A. ; Volnova , Anna B. ; Fedorova, Tatiana N. ; Gainetdinov, Raul R. ; Lopachev , Alexander V. .
In: Biomedicines, Vol. 11, No. 7, 1820, 25.06.2023.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Na+,K+ - ATPase and Cardiotonic Steroids in Models of Dopaminergic System Pathologies
AU - Markina , Alisa A.
AU - Kazanskaya, Rogneda B.
AU - Timoshina, Julia A.
AU - Zavialov, Vladislav A.
AU - Abaimov , Denis A.
AU - Volnova , Anna B.
AU - Fedorova, Tatiana N.
AU - Gainetdinov, Raul R.
AU - Lopachev , Alexander V.
N1 - Markina, A.A.; Kazanskaya, R.B.; Timoshina, J.A.; Zavialov, V.A.; Abaimov, D.A.; Volnova, A.B.; Fedorova, T.N.; Gainetdinov, R.R.; Lopachev, A.V. Na+,K+-ATPase and Cardiotonic Steroids in Models of Dopaminergic System Pathologies. Biomedicines 2023, 11, 1820. https://doi.org/10.3390/biomedicines11071820
PY - 2023/6/25
Y1 - 2023/6/25
N2 - In recent years, enough evidence has accumulated to assert that cardiotonic steroids, Na+,K+-ATPase ligands, play an integral role in the physiological and pathophysiological processes in the body. However, little is known about the function of these compounds in the central nervous system. Endogenous cardiotonic steroids are involved in the pathogenesis of affective disorders, including depression and bipolar disorder, which are linked to dopaminergic system dysfunction. Animal models have shown that the cardiotonic steroid ouabain induces mania-like behavior through dopamine-dependent intracellular signaling pathways. In addition, mutations in the alpha subunit of Na+,K+-ATPase lead to the development of neurological pathologies. Evidence from animal models confirms the neurological consequences of mutations in the Na+,K+-ATPase alpha subunit. This review is dedicated to discussing the role of cardiotonic steroids and Na+,K+-ATPase in dopaminergic system pathologies—both the evidence supporting their involvement and potential pathways along which they may exert their effects are evaluated. Since there is an association between affective disorders accompanied by functional alterations in the dopaminergic system and neurological disorders such as Parkinson’s disease, we extend our discussion to the role of Na+,K+-ATPase and cardiotonic steroids in neurodegenerative diseases as well.
AB - In recent years, enough evidence has accumulated to assert that cardiotonic steroids, Na+,K+-ATPase ligands, play an integral role in the physiological and pathophysiological processes in the body. However, little is known about the function of these compounds in the central nervous system. Endogenous cardiotonic steroids are involved in the pathogenesis of affective disorders, including depression and bipolar disorder, which are linked to dopaminergic system dysfunction. Animal models have shown that the cardiotonic steroid ouabain induces mania-like behavior through dopamine-dependent intracellular signaling pathways. In addition, mutations in the alpha subunit of Na+,K+-ATPase lead to the development of neurological pathologies. Evidence from animal models confirms the neurological consequences of mutations in the Na+,K+-ATPase alpha subunit. This review is dedicated to discussing the role of cardiotonic steroids and Na+,K+-ATPase in dopaminergic system pathologies—both the evidence supporting their involvement and potential pathways along which they may exert their effects are evaluated. Since there is an association between affective disorders accompanied by functional alterations in the dopaminergic system and neurological disorders such as Parkinson’s disease, we extend our discussion to the role of Na+,K+-ATPase and cardiotonic steroids in neurodegenerative diseases as well.
KW - Na+,K+-ATPase
KW - cardiotonic steroids
KW - dopamine
KW - bipolar disorder
KW - depression
KW - neurodegeneration
M3 - Article
VL - 11
JO - Biomedicines
JF - Biomedicines
SN - 2227-9059
IS - 7
M1 - 1820
ER -
ID: 107029548