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http://purl.uniprot.org/citations/33960499http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33960499http://www.w3.org/2000/01/rdf-schema#comment"

Background

Alcohol excites neurons of the ventral tegmental area (VTA) and the release of dopamine from these neurons is a key event in ethanol (EtOH)-induced reward and reinforcement. Many mechanisms have been proposed to explain EtOH's actions on neurons of the VTA, but antagonists generally do not eliminate the EtOH-induced excitation of VTA neurons. We have previously demonstrated that the ion channel KCNK13 plays an important role in the EtOH-related excitation of mouse VTA neurons. Here, we elaborate on that finding and further assess the importance of KCNK13 in rats.

Methods

Rats (Sprague-Dawley and Fisher 344) were used in these studies. In addition to single-unit electrophysiology in brain slices, we used quantitative PCR and immunohistochemistry to discern the effects of EtOH and the brain slice preparation method on the expression levels of the Kcnk13 gene and KCNK13 protein.

Results

Immunohistochemistry demonstrated that the levels of KCNK13 were significantly reduced during procedures normally used to prepare brain slices for electrophysiology, with a reduction of about 75% in KCNK13 protein at the time that electrophysiological recordings would normally be made. Extracellular recordings demonstrated that EtOH-induced excitation of VTA neurons was reduced after knockdown of Kcnk13 using a small interfering RNA (siRNA) delivered via the recording micropipette. Real-time PCR demonstrated that the expression of Kcnk13 was altered in a time-dependent manner after alcohol withdrawal.

Conclusions

KCNK13 plays an important role in EtOH-induced stimulation of rat VTA neurons and is dynamically regulated by cell damage and EtOH exposure, and during withdrawal. KCNK13 is a novel alcohol-sensitive protein, and further investigation of this channel may offer new avenues for the development of agents useful in altering the rewarding effect of alcohol."xsd:string
http://purl.uniprot.org/citations/33960499http://purl.org/dc/terms/identifier"doi:10.1111/acer.14630"xsd:string
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/author"You C."xsd:string
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/author"Brodie M.S."xsd:string
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/author"Vandegrift B.J."xsd:string
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/name"Alcohol Clin Exp Res"xsd:string
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/pages"1348-1358"xsd:string
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/title"KCNK13 potassium channels in the ventral tegmental area of rats are important for excitation of ventral tegmental area neurons by ethanol."xsd:string
http://purl.uniprot.org/citations/33960499http://purl.uniprot.org/core/volume"45"xsd:string
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