Literature DB >> 2540626

Expression of the three opioid receptor subtypes mu, delta and kappa in guinea pig and rat brain cell cultures and in vivo.

J Barg1, R Levy, R Simantov.   

Abstract

Expression of the three opioid receptor subtypes mu, delta and kappa in aggregating cell cultures prepared from embryonic guinea pig or rat brains was compared with the in vivo expression of the receptors in the brain of developing and adult animals of the same species. At the day of culturing, one third of the receptors in the brain of guinea pig embryos were of the kappa type. In culture, however, the aggregating brain cells acquired within 14 days a high percentage (75%) of kappa receptors. As only 28% of the receptors in the adult guinea pig brain are of this subtype, an attempt was made to further analyse the specificity of this developmental process. In guinea pig, the 2-fold increase in kappa receptors in culture was accompanied with a decline in both the percentage and the density (per protein) of mu and delta subtypes. In contrast, a marked increase in delta receptors was observed in rat whole brain, forebrain or hindbrain cultures. Thus, the developmental pattern of the three receptor subtypes in rat brain cultures, but not in guinea pig, was similar to that in vivo. These and additional experiments suggest that at the developmental stage taken to prepare the cultures, neurons expressing opioid receptors were already programmed in the rat but not in guinea pig brain.

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Year:  1989        PMID: 2540626     DOI: 10.1016/0736-5748(89)90067-1

Source DB:  PubMed          Journal:  Int J Dev Neurosci        ISSN: 0736-5748            Impact factor:   2.457


  6 in total

Review 1.  Developmental opioid exposures: Neurobiological underpinnings, behavioral impacts, and policy implications.

Authors:  Samantha S Goldfarb; Gregg D Stanwood; Heather A Flynn; Devon L Graham
Journal:  Exp Biol Med (Maywood)       Date:  2019-10-20

2.  Dynorphins modulate DNA synthesis in fetal brain cell aggregates.

Authors:  A Gorodinsky; J Barg; M M Belcheva; R Levy; R J McHale; Z Vogel; C J Coscia
Journal:  J Neurochem       Date:  1995-10       Impact factor: 5.372

3.  kappa-Opioid agonist modulation of [3H]thymidine incorporation into DNA: evidence for the involvement of pertussis toxin-sensitive G protein-coupled phosphoinositide turnover.

Authors:  J Barg; M M Belcheva; J Rowiński; C J Coscia
Journal:  J Neurochem       Date:  1993-04       Impact factor: 5.372

4.  The prenatal development profile of expression of opioid peptides and receptors in the mouse brain.

Authors:  R A Rius; J Barg; W T Bem; C J Coscia; Y P Loh
Journal:  Brain Res Dev Brain Res       Date:  1991-02-22

5.  Evidence for the implication of phosphoinositol signal transduction in mu-opioid inhibition of DNA synthesis.

Authors:  J Barg; M M Belcheva; C J Coscia
Journal:  J Neurochem       Date:  1992-09       Impact factor: 5.372

6.  Beta-endorphin is a potent inhibitor of thymidine incorporation into DNA via mu- and kappa-opioid receptors in fetal rat brain cell aggregates in culture.

Authors:  J Barg; M Belcheva; R McHale; R Levy; Z Vogel; C J Coscia
Journal:  J Neurochem       Date:  1993-02       Impact factor: 5.372

  6 in total

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