Effects of SPAK knockout on sensorimotor gating, novelty exploration, and brain area-dependent expressions of NKCC1 and KCC2 in a mouse model of schizophrenia
- PMID: 25797415
- DOI: 10.1016/j.pnpbp.2015.03.007
Effects of SPAK knockout on sensorimotor gating, novelty exploration, and brain area-dependent expressions of NKCC1 and KCC2 in a mouse model of schizophrenia
Abstract
SPAK (Sterile 20/SPS1-related proline/alanine-rich kinase) is a protein kinase belonging to the mitogen-activated protein kinase (MAPK) superfamily that has been found to be extensively distributed across the body. The SPAK downstream substrates NKCC1 and KCC2 in the central nervous system are important in the interpretation of developmental mental disorders. The present study aimed to clarify the role of SPAK-NKCC1/KCC2 using a rodent schizophrenia-like model. The mouse paradigm of isolation rearing (IR) was employed, as it simulates the sensorimotor gating abnormalities of schizophrenia. SPAK transgenic mice were used and were divided into four groups: social-wild type, social-SPAK(-/-), isolation-wild type, and isolation-SPAK(-/-). The prepulse inhibition (PPI) test and the novel object recognition test (NORT) were used to measure schizophrenia-associated dysfunctions in gating ability and the novelty recognition, respectively. Finally, the protein expressions of NKCC1/KCC2 in the prefrontal cortex and hippocampus were detected to determine correlations with the behavioral data. Our results demonstrated that SPAK-null mice had superior PPI and novelty recognition relative to wild type controls, with a concomitant increase in KCC2 in the prefrontal cortex. IR disrupted PPI and NORT performances with an associated increase in KCC2. Furthermore, rearing environment and gene manipulation had mutually interactive effects, as the IR-induced effects on PPI and NORT were reversed by SPAK knockout, and the increase in KCC2 and the decreased in the NKCC1/KCC2 ratio in the prefrontal cortex induced by SPAK knockout were reversed by IR. Our data supported the gene-environment hypothesis and demonstrated the potential value of SPAK manipulation in future schizophrenia studies.
Keywords: NKCC(1)/KCC(2); Novelty recognition; Prepulse inhibition; Rearing environment; SPAK knockout.
Copyright © 2015 Elsevier Inc. All rights reserved.
Similar articles
-
Suppression of WNK1-SPAK/OSR1 Attenuates Bone Cancer Pain by Regulating NKCC1 and KCC2.J Pain. 2019 Dec;20(12):1416-1428. doi: 10.1016/j.jpain.2019.05.005. Epub 2019 May 11. J Pain. 2019. PMID: 31085334
-
Dietary salt intake regulates WNK3-SPAK-NKCC1 phosphorylation cascade in mouse aorta through angiotensin II.Hypertension. 2013 Nov;62(5):872-8. doi: 10.1161/HYPERTENSIONAHA.113.01543. Epub 2013 Sep 9. Hypertension. 2013. PMID: 24019400
-
STE20/SPS1-related proline/alanine-rich kinase is involved in plasticity of GABA signaling function in a mouse model of acquired epilepsy.PLoS One. 2013 Sep 13;8(9):e74614. doi: 10.1371/journal.pone.0074614. eCollection 2013. PLoS One. 2013. PMID: 24058604 Free PMC article.
-
What rodent models of deep brain stimulation can teach us about the neural circuit regulation of prepulse inhibition in neuropsychiatric disorders.Schizophr Res. 2018 Aug;198:45-51. doi: 10.1016/j.schres.2017.06.033. Epub 2017 Jun 27. Schizophr Res. 2018. PMID: 28663025 Review.
-
Neurogenesis and sensorimotor gating: bridging a microphenotype and an endophenotype.Curr Mol Med. 2015;15(2):129-37. doi: 10.2174/1566524015666150303002834. Curr Mol Med. 2015. PMID: 25732150 Review.
Cited by
-
High glucose-induced effects on Na+-K+-2Cl- cotransport and Na+/H+ exchange of blood-brain barrier endothelial cells: involvement of SGK1, PKCβII, and SPAK/OSR1.Am J Physiol Cell Physiol. 2021 Apr 1;320(4):C619-C634. doi: 10.1152/ajpcell.00177.2019. Epub 2021 Jan 6. Am J Physiol Cell Physiol. 2021. PMID: 33406028 Free PMC article.
-
Target inhibition of SPAK in choroid plexus attenuates T cell infiltration and demyelination in experimental autoimmune encephalomyelitis.J Neuroinflammation. 2025 Mar 13;22(1):80. doi: 10.1186/s12974-025-03407-5. J Neuroinflammation. 2025. PMID: 40082912 Free PMC article.
-
Regulatory control of the Na-Cl co-transporter NCC and its therapeutic potential for hypertension.Acta Pharm Sin B. 2021 May;11(5):1117-1128. doi: 10.1016/j.apsb.2020.09.009. Epub 2020 Sep 22. Acta Pharm Sin B. 2021. PMID: 34094823 Free PMC article. Review.
-
The CUL3/KLHL3-WNK-SPAK/OSR1 pathway as a target for antihypertensive therapy.Am J Physiol Renal Physiol. 2016 Jun 1;310(11):F1389-96. doi: 10.1152/ajprenal.00132.2016. Epub 2016 Apr 13. Am J Physiol Renal Physiol. 2016. PMID: 27076645 Free PMC article.
-
Quetiapine Ameliorates Schizophrenia-Like Behaviors and Protects Myelin Integrity in Cuprizone Intoxicated Mice: The Involvement of Notch Signaling Pathway.Int J Neuropsychopharmacol. 2015 Aug 1;19(2):pyv088. doi: 10.1093/ijnp/pyv088. Int J Neuropsychopharmacol. 2015. PMID: 26232790 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical