Corticotropin‐releasing factor type‐2 receptor and corticotropin‐releasing factor‐binding protein coexist in rat ventral tegmental area nerve terminals originated in the lateral hypothalamic area. (28th November 2015)
- Record Type:
- Journal Article
- Title:
- Corticotropin‐releasing factor type‐2 receptor and corticotropin‐releasing factor‐binding protein coexist in rat ventral tegmental area nerve terminals originated in the lateral hypothalamic area. (28th November 2015)
- Main Title:
- Corticotropin‐releasing factor type‐2 receptor and corticotropin‐releasing factor‐binding protein coexist in rat ventral tegmental area nerve terminals originated in the lateral hypothalamic area
- Authors:
- Slater, Paula G.
Noches, Veronica
Gysling, Katia - Abstract:
- Abstract: There is significant functional evidence showing that corticotropin‐releasing factor type‐2 receptor (CRF2 R) and corticotropin‐releasing factor‐binding protein (CRF‐BP) regulate glutamatergic synapses onto ventral tegmental area (VTA) dopaminergic neurons. It has been shown that CRF requires CRF‐BP to potentiate N ‐methyl‐d ‐aspartate receptors in dopaminergic neurons through CRF2 R, and that increases glutamate release in cocaine‐treated rats through the activation of CRF2 R only by agonists with high affinity to CRF‐BP. Furthermore, this CRF‐mediated increase in VTA glutamate is responsible for stress‐induced relapse to cocaine‐seeking behaviour. However, there is a lack of anatomical evidence to explain the mechanisms of CRF actions in VTA. Thus, it was studied whether CRF2 R and CRF‐BP are expressed in VTA nerve terminals, using a synaptosomal preparation devoid of postsynaptic elements. The current results show that both proteins are co‐expressed in glutamatergic and γ‐aminobutyric acid (GABA)ergic VTA synaptosomes. A main glutamatergic input to the VTA that has been associated to addictive behaviour is originated in the lateral hypothalamic area (LHA). Thus, this study was focused in the LHA–VTA input using orexin as a marker of this input. The results show that CRF2 R and CRF‐BP mRNA and protein are expressed in the LHA, and that both proteins are present in orexin‐positive VTA synaptosomes. The results showing that CRF2 R and CRF‐BP are expressed in theAbstract: There is significant functional evidence showing that corticotropin‐releasing factor type‐2 receptor (CRF2 R) and corticotropin‐releasing factor‐binding protein (CRF‐BP) regulate glutamatergic synapses onto ventral tegmental area (VTA) dopaminergic neurons. It has been shown that CRF requires CRF‐BP to potentiate N ‐methyl‐d ‐aspartate receptors in dopaminergic neurons through CRF2 R, and that increases glutamate release in cocaine‐treated rats through the activation of CRF2 R only by agonists with high affinity to CRF‐BP. Furthermore, this CRF‐mediated increase in VTA glutamate is responsible for stress‐induced relapse to cocaine‐seeking behaviour. However, there is a lack of anatomical evidence to explain the mechanisms of CRF actions in VTA. Thus, it was studied whether CRF2 R and CRF‐BP are expressed in VTA nerve terminals, using a synaptosomal preparation devoid of postsynaptic elements. The current results show that both proteins are co‐expressed in glutamatergic and γ‐aminobutyric acid (GABA)ergic VTA synaptosomes. A main glutamatergic input to the VTA that has been associated to addictive behaviour is originated in the lateral hypothalamic area (LHA). Thus, this study was focused in the LHA–VTA input using orexin as a marker of this input. The results show that CRF2 R and CRF‐BP mRNA and protein are expressed in the LHA, and that both proteins are present in orexin‐positive VTA synaptosomes. The results showing that CRF2 R and CRF‐BP are expressed in the LHA–VTA input give anatomical support to suggest that this input plays a role in stress‐induced relapse to cocaine‐seeking behaviour. Abstract : Corticotropin releasing factor type‐2 receptor (CRF2 R) and CRF‐binding protein (CRF‐BP) mRNA and protein are expressed in ventral tegmental area (VTA) and lateral hypothalamic area (LHA). Both proteins co‐exist in glutamatergic and GABAergic, but not in cholinergic VTA nerve terminals. Furthermore, CRF2 R and CRF‐BP are present in VTA orexin‐positive varicosities (varicosome) and nerve terminals (synaptosome) of glutamatergic/orexinergic LHA neurons. … (more)
- Is Part Of:
- European journal of neuroscience. Volume 43:Number 2(2016:Jan.)
- Journal:
- European journal of neuroscience
- Issue:
- Volume 43:Number 2(2016:Jan.)
- Issue Display:
- Volume 43, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 43
- Issue:
- 2
- Issue Sort Value:
- 2016-0043-0002-0000
- Page Start:
- 220
- Page End:
- 229
- Publication Date:
- 2015-11-28
- Subjects:
- orexin -- synaptosomes -- syntaxin 1 -- VGLUT1 -- VGLUT2
Nervous system -- Periodicals
612.8 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1460-9568 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ejn.13113 ↗
- Languages:
- English
- ISSNs:
- 0953-816X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.731700
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2848.xml