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Acute Cocaine Enhances Dopamine D2R Recognition and Signaling and Counteracts D2R Internalization in Sigma1R-D2R Heteroreceptor Complexes

Borroto-Escuela, Dasiel O. (author)
Karolinska Institutet
Narváez, Manuel (author)
Univ Malaga, Inst Invest Biomed Malaga, Fac Med, Malaga, Spain
Romero Fernández, Wilber (author)
Uppsala universitet,Beräkningsbiologi och bioinformatik,Science for Life Laboratory, SciLifeLab
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Pinton, Luca (author)
Karolinska Inst, Dept Neurosci, Biomed, Stockholm, Sweden
Wydra, Karolina (author)
Polish Acad Sci, Inst Pharmacol, Dept Drug Addict Pharmacol, Krakow, Poland
Filip, Malgorzata (author)
Polish Acad Sci, Inst Pharmacol, Dept Drug Addict Pharmacol, Krakow, Poland
Beggiato, Sarah (author)
Univ Ferrara, Dept Life Sci & Biotechnol SVEB, Ferrara, Italy
Tanganelli, Sergio (author)
Univ Ferrara, Dept Life Sci & Biotechnol SVEB, Ferrara, Italy
Ferraro, Luca (author)
Univ Ferrara, Dept Life Sci & Biotechnol SVEB, Ferrara, Italy
Fuxe, Kjell (author)
Karolinska Institutet
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 (creator_code:org_t)
2019-04-10
2019
English.
In: Molecular Neurobiology. - : Springer Science and Business Media LLC. - 0893-7648 .- 1559-1182. ; 56:10, s. 7045-7055
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The current study was performed to establish the actions of nanomolar concentrations of cocaine, not blocking the dopamine transporter, on dopamine D2 receptor (D2R)-sigma 1 receptor (delta 1R) heteroreceptor complexes and the D2R protomer recognition, signaling and internalization in cellular models. We report the existence of D2R-delta 1R heteroreceptor complexes in subcortical limbic areas as well as the dorsal striatum, with different distribution patterns using the in situ proximity ligation assay. Also, through BRET, these heteromers were demonstrated in HEK293 cells. Furthermore, saturation binding assay demonstrated that in membrane preparations of HEK293 cells coexpressing D2R and delta 1R, cocaine (1 nM) significantly increased the D2R B-max values over cells singly expressing D2R. CREB reporter luc-gene assay indicated that coexpressed delta 1R significantly reduced the potency of the D2R-like agonist quinpirole to inhibit via D2R activation the forskolin induced increase of the CREB signal. In contrast, the addition of 100 nM cocaine was found to markedly increase the quinpirole potency to inhibit the forskolin-induced increase of the CREB signal in the D2R-delta 1R cells. These events were associated with a marked reduction of cocaine-induced internalization of D2R protomers in D2R-delta 1R heteromer-containing cells vs D2R singly expressing cells as studied by means of confocal analysis of D2R-delta 1R trafficking and internalization. Overall, the formation of D2R-delta 1R heteromers enhanced the ability of cocaine to increase the D2R protomer function associated with a marked reduction of its internalization. The existence of D2R-delta 1R heteromers opens up a new understanding of the acute actions of cocaine.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

Cocaine
Sigma 1 receptor
Dopamine D2 receptor
Heteroreceptor complexes
Oligomerization
Dimerization
Substance use disorder

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